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Trajectories of Health-Related Quality of Life and Perceived Social Support Among People Living With HIV Undergoing Antiretroviral Treatment: Does Gender Matter?

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The study examined the trajectories of health-related quality of life (HRQoL) and perceived social support (PSS) among people living with HIV (PLWH), with a special focus on gender differences. The participants included 252 PLWH (18% female) undergoing antiretroviral therapy. HRQoL (WHO Quality of Life-BREF; WHOQOL Group, 1998) and PSS (Berlin Social Support Scales; Schulz and Schwarzer, 2003) were measured three times at six-month intervals. Using a univariate approach, three trajectories of HRQoL and four trajectories of PSS were identified. Gender and relationship status were significant covariates for PSS only, with overrepresentation of single women in the increasing trajectory. The dual trajectory approach revealed a match in the decrease of HRQoL and PSS, but only for 31% of the sample. In fact, decreasing PSS co-occurred with increasing as well as stable HRQoL. There was no significant gender effect in this regard. Although a clear correspondence for decreasing trajectories exists, the findings also highlight a discrepancy between HRQoL and PSS changes that are unrelated to gender.
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Frontiers in Psychology | www.frontiersin.org 1 July 2019 | Volume 10 | Article 1664
ORIGINAL RESEARCH
published: 23 July 2019
doi: 10.3389/fpsyg.2019.01664
Edited by:
Sabrina Cipolletta,
University of Padova, Italy
Reviewed by:
Serena Giunta,
University of Palermo, Italy
Rytis Pakrosnis,
Vytautas Magnus University,
Lithuania
*Correspondence:
Ewa Gruszczyńska
egruszczynska@swps.edu.pl
Specialty section:
This article was submitted to
Health Psychology,
a section of the journal
Frontiers in Psychology
Received: 20 April 2019
Accepted: 02 July 2019
Published: 23 July 2019
Citation:
Gruszczyńska E and Rzeszutek M
(2019) Trajectories of Health-Related
Quality of Life and Perceived Social
Support Among People Living With
HIV Undergoing Antiretroviral
Treatment: Does Gender Matter?
Front. Psychol. 10:1664.
doi: 10.3389/fpsyg.2019.01664
Trajectories of Health-Related
Quality of Life and Perceived Social
Support Among People Living With
HIV Undergoing Antiretroviral
Treatment: Does Gender Matter?
EwaGruszczyńska1
* and MarcinRzeszutek 2
1 Faculty of Psychology, SWPS University of Social Sciences and Humanities, Warsaw, Poland, 2 Faculty of Psychology,
University of Warsaw, Warsaw, Poland
The study examined the trajectories of health-related quality of life (HRQoL) and perceived
social support (PSS) among people living with HIV (PLWH), with a special focus on gender
differences. The participants included 252 PLWH (18% female) undergoing antiretroviral
therapy. HRQoL (WHO Quality of Life-BREF; WHOQOL Group, 1998) and PSS (Berlin
Social Support Scales; Schulz and Schwarzer, 2003) were measured three times at
six-month intervals. Using a univariate approach, three trajectories of HRQoL and four
trajectories of PSS were identied. Gender and relationship status were signicant
covariates for PSS only, with overrepresentation of single women in the increasing
trajectory. The dual trajectory approach revealed a match in the decrease of HRQoL and
PSS, but only for 31% of the sample. In fact, decreasing PSS co-occurred with increasing
as well as stable HRQoL. There was no signicant gender effect in this regard. Although
a clear correspondence for decreasing trajectories exists, the ndings also highlight a
discrepancy between HRQoL and PSS changes that are unrelated to gender.
Keywords: health-related quality of life, perceived social support, people living with HIV, gender differences,
latent class growth curve
TRAJECTORIES OF HEALTH-RELATED QUALITY OF LIFE
AND PERCEIVED SOCIAL SUPPORT AMONG PEOPLE LIVING
WITH HIV UNDERGOING ANTIRETROVIRAL TREATMENT:
DOES GENDER MATTER?
Over the last two decades, cutting-edge progress has occurred in the treatment and prevention
of HIV infection, which has not only signicantly reduced mortality and morbidity among
people living with HIV (PLWH; Samji et al., 2013; Cohen et al., 2016) but has also been
attributed to signaling the end of the HIV/AIDS epidemic (Deeks et al., 2013; Carrico,
2019). However, the enormous progress in bio-medical care for PLWH did not directly
translate to the improvement of their psychological well-being. More specically, both in the
past (e.g., Bing et al., 2001) and at present, PLWH systematically declare lower levels of
Gruszczyńska and Rzeszutek Trajectories of Health-Related Quality of Life
Frontiers in Psychology | www.frontiersin.org 2 July 2019 | Volume 10 | Article 1664
well-being and higher psychological distress than the general
population (Miners et al., 2014), and especially worse health-
related quality of life (HRQoL) with respect to other chronic
diseases (Psaros et al., 2013).
Although a large number of studies have been conducted
on factors related to the HRQoL of these patients (e.g., Burgoyne
and Saunders, 2001; Hansen et al., 2009; Herrmann etal., 2013;
Bucciardini et al., 2014; Lifson et al., 2017; Mitchell et al.,
2017; Torres et al., 2018), they failed not only to provide a
consistent picture of the variables associated with the HRQoL
of PLWH but also to produce a convincing answer to the
aforementioned issue of low well-being among PLWH, especially
at a time when their life expectancies are similar to the general
population (Degroote et al., 2014). e only visible trend deals
with the fact that clinical factors have been historically considered
as the predominant predictor of the well-being of PLWH (Lubeck
and Fries, 1997), while there is now a growing recognition of
psychosocial factors as the major determinant of their quality
of life (Chida and Vedhara, 2009; Cooper et al., 2017). Some
authors underline that the plethora of inconclusive results in
research on HRQoL among PLWH is derived from methodological
shortcomings among most studies on this topic. Notably, the
literature is dominated by cross-sectional frameworks using the
variable-centered approach, which focuses only on the average
values for an entire study sample and neglects the heterogeneity
of well-being among PLWH and its relationship with
sociodemographic, clinical, and psychological characteristics
(Oberjé etal., 2015; Rzeszutek and Gruszczyńska, 2018). erefore,
the present study aims to overcome these methodological
drawbacks by applying a longitudinal design accompanied by
a person-centered perspective that allows for the identication
of subgroups with dierent levels of HRQoL and their changes
during time. Specically, we aim to enrich the literature by
focusing on the relatively understudied issue of gender-based
dierences in HRQoL among PLWH.
Surprisingly, although the global amount of HIV-infected
women is similar to the number of HIV-infected men, both
of which continue to grow worldwide (European Centre for
Disease Prevention and Control/WHO Regional Oce for
Europe, 2017), the majority of studies on HRQoL in HIV
infection were conducted on male populations only (e.g., Jia
et al., 2004; Liu et al., 2006; Song et al., 2016; Emuren et al.,
2017). us, research on HRQoL among HIV-infected women
remains scarce (e.g., McDonnell et al., 2000; Gielen et al.,
2001). In addition, authors examining gender dierences in
HRQoL in this patient group consequently observed lower
HRQoL among HIV-infected women than HIV-infected men
(e.g., Campsmith etal., 2003; Mrus etal., 2005; Chandra etal.,
2009). ere are several hypotheses on this consistent nding
that have pointed to the limited access to antiretroviral treatment
(ART) in some world regions (Penniman et al., 2007; Aziz
and Smith, 2011), more intense HIV-related stigma, and an
associated higher rate of mental disorders among HIV-infected
women than HIV-infected men (Campbell et al., 2006; Machtinger
et al., 2012; Geary et al., 2014). On the other hand, several
studies have demonstrated that females living with HIV exhibit
far greater adherence to treatment than their male counterparts
and therefore report better HIV-related clinical outcomes
(Collazos et al., 2007; Nicastri et al., 2007; Bor et al., 2015).
In considering the aforementioned ndings, it seems that no
comprehensive explanation for the observed gender dierences
in HRQoL among PLWH exists to date. As such, the present
study examines one variable that may provide important context
on this topic – social support (Carvalhal, 2010).
HIV/AIDS is a chronic disease that promotes
multidimensional psychological distress among PLWH, which
is now primarily associated with persistent HIV-related stigma
and social isolation (Rendina et al., 2018). Many studies have
observed that social support – particularly perceived social
support (PSS) – is one of the most important assets in coping
with HIV infection and related distress (e.g., Turner-Cobb
et al., 2002; Gonzalez et al., 2004; Earnshaw et al., 2015).
More specically, perceiving a high availability of support may
enhance adjustment to HIV infection directly through improved
adherence to treatment (e.g., Ashton etal., 2005; Alemu etal.,
2012) and also indirectly through buering the eect of
HIV-related stigma on mental functioning and quality of life
among these patients (Bekele et al., 2013; Breet et al., 2014).
Although the benecial eects of perceived support on
quality of life of PLWH are widely known, some authors have
recently become increasingly skeptical regarding this
unambiguously optimistic picture and have highlighted several
methodological shortcomings of existing studies conducted
using a cross-sectional framework, which is the most common
(Qiao et al., 2014). Consequently, it is dicult to solve the
egg or chicken dilemma in research on the link between perceived
social support and HRQoL among PLWH. Notably, existing
studies have been conducted in small samples (since the
implementation of a repeated measurement design among
PLWH may be challenging; Burgoyne and Renwick, 2004) or
using only a baseline assessment of PSS as a predictor for
HRQoL changes (Jia et al., 2005). us, the current literature
has not examined possible heterogeneity of the dual trajectories
of HRQoL and PSS. Furthermore, another topic that remains
understudied in the literature deals with gender dierences in
both PSS and HRQoL among PLWH (Gordillo et al., 2009).
Current Study
In considering the aforementioned research gaps, the aim of
our study was three-fold. First, we aimed to examine whether
heterogeneity of univariate change of HRQoL and PSS exists
among PLWH, and if these trajectories are also gender-related,
both with and without other possible sociodemographic and
clinical covariates. en, the probability of following a given
pattern of the dual trajectories of HRQoL and PSS was explored.
Specically, wewere interested in the co-occurrence of trajectories
with the same direction of change, under the assumption of
existing cross-sectional studies that a decrease or an increase
in HRQoL corresponds to relevant changes in PSS. Finally,
weexamined whether any gender dierences in joint probability
for dual trajectories existed, supposing that combinations of
changes may not be equally distributed due to gender-related
patterns of social exchange as well as the social consequences
of being diagnosed with HIV.
Gruszczyńska and Rzeszutek Trajectories of Health-Related Quality of Life
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MATERIALS AND METHODS
Participants and Procedure
e participants were 252 persons with conrmed HIV-positive
results undergoing antiretroviral therapy in an outpatient clinic.
e majority of them were men, which is typical based on
the gender-related prevalence rate of HIV infection in Europe
and the United States (Joint United Nations Programme on
HIV/AIDS (UNAIDS), 2018). Detailed characteristics of the
sample are provided in Tab l e 1 .
e study design was longitudinal, with three measurements
at 6-month intervals. Aer written informed consent was
obtained from a participant, they lled in the self-descriptive
questionnaire provided. For the next two measurements, they
were approached during their control visit in the outpatient
clinic aer establishing the date via phone or email, based on
their preference. All longitudinal data were collected by trained
research assistants using a “paper-and-pencil” approach.
Participation in the study was voluntary. e study was approved
by the institutional ethics committee.
Measures
Health-related quality of life was assessed using the WHO
Quality of Life-BREF (WHOQOL-BREF), developed under a
WHO initiative for cross-cultural assessment (WHOQOL Group,
1998). e tool consists of 26 items to measure four domains:
physical health, psychological health, social relationships, and
environment. Each item is rated on a ve-point Likert scale
(scores ranged from 1 to 5), and raw scores were used. Since
correlations between domains in our study were stable and
moderate (from 0.48 to 0.69), and followed the research indicating
a possibility of assessing global HRQoL using this tool (Harsha
et al., 2016), the overall indicator was obtained by summing
and averaging all item scores. Higher values indicate a higher
quality of life. e reliability, measured by the Cronbach’s α
coecient, was 0.93, 0.92, and 0.92, from the rst to third
wave, respectively.
Perceived social support was measured using the relevant
subscale of eight items from the Berlin Social Support Scales
developed by Schulz and Schwarzer (2003). The answers
are provided on a Likert-type scale, from 1 (not true at
all) to 4 (entirely true), then summed and averaged. The
higher scores indicate higher PSS. The Cronbach’s α coefficient
was 0.93, 0.92, and 0.92, for first, second, and third
measurement, respectively.
Data Analysis
We started the analysis with univariate latent class growth
curve models to examine how HRQoL and PSS changed in
our sample during the study period. From 1- to 5-class
solutions were tested separately for HRQoL and PSS, and
error variances and covariances were freely estimated across
classes. e optimal solution was identied on the basis of
several criteria widely identied in the literature (Nylund
et al., 2007). Namely, we used Akaike as well as Bayesian
information criterion (AIC and BIC, respectively), including
the sample size-adjusted BIC (SABIC). e model with lower
values was favored. Next, entropy as a measure of accuracy
of classication was taken into consideration; in this case,
the model with higher values was favored (Celeux and
Soromenho, 1996). Finally, sample proportion per class was
analyzed, since classes with very few individuals may besample-
specic and dicult to replicate. e practical rule is to favor
a model with a fewer number of classes when at least one
class has a frequency of less than 5% of the sample size
(Hipp and Bauer, 2006). Time was coded as 0 for the rst
measurement, 0.5 for the second, and 1 for the third (Biesanz
et al., 2004). Both linear and quadratic trends were explored,
but wedid not present them further since all quadratic terms
were revealed as insignicant.
To identify covariates of trajectories, the bias-adjusted three-
step analysis (Vermunt and Magidson, 2016) was implemented
in order (1) to separate modeling trajectories from their
relationship with other variables and (2) to correct for
probabilistic classication to classes. Namely, when univariate
models were established (e.g., the number, shape, and membership
of trajectories were xed), weexamined whether any dierences
existed in predicting this membership based on sociodemographic
and clinical variables. We started with gender and then added
other covariates to determine if they would modify the
gender eect.
In the next step, joint probabilities were computed since
we used two sets of trajectories (one for HRQoL and the other
for PSS). Specically, we were interested in the probability of
belonging to a given trajectory of HRQoL when simultaneously
being a member of a given trajectory of PSS. Finally, by means
of multinomial logistic regression, we assessed whether the
probability of being a member of each combination of HRQoL
and PSS trajectories was the same for women and men, both
with and without additional covariates. All analyses were performed
using IBM SPSS Statistics version 25 (IBM Corp, 2016) and
LatentGOLD version 5.1 (Vermunt and Magidson, 2016).
TABLE 1 | Sociodemographic and clinical variables in the studied sample
(N=252).
Variable N (%)
Gender
Male 208 (82.5)
Female 44 (17.5)
Age in years (M±SD) 39.03±10.40
Marital status
Married 147 (58.3)
Single 105 (41.7)
Education
Basic vocational 109 (43.3)
Secondary and university degree 143 (56.7)
HIV/AIDS status
HIV+ only 215 (85.3)
HIV/AIDS 37 (14.7)
HIV infection duration in years (M±SD) 7.23±6.23
Antiretroviral treatment (ART) duration in
years (M±SD)
5.82±5.25
CD4 count 575.48±2248.89
M, mean; SD, standard deviation.
Gruszczyńska and Rzeszutek Trajectories of Health-Related Quality of Life
Frontiers in Psychology | www.frontiersin.org 4 July 2019 | Volume 10 | Article 1664
RESULTS
Descriptive Statistics and Missing Values
Table 2 presents basic descriptive statistics for repeated measures
of HRQoL and PSS. e dropout due to longitudinal design
was 41% of the sample between the rst and last measurements.
Missing data analysis suggested that the pattern of missingness
can betreated as random (Little’s MCAR test: χ2= 53.32, df=54,
p = 0.50); therefore, the option that included all available data
was chosen, with missing values for indicators being handled
by the maximum likelihood function (Vermunt and Magidson,
2016). Furthermore, regarding sociodemographic and clinical
variables, there were also no signicant dierences between
completers and non-completers. However, the result for gender
was on the edge of signicance (χ2 = 3.95, df = 1, p = 0.05),
suggesting a tendency of higher dropout among women than men.
Heterogeneity of Change: HRQoL and PSS
Univariate Trajectories
e model t criteria indicate that model with three trajectories
was the best tted to the HRQoL data (see Tab l e 3). Specically,
although all the informative criteria indices scored lower
with every added class, the drop in value became smaller.
For models with more than three classes, the smallest class had
only four members, which suggests the existence of outliners.
Finally, entropy was relatively stable across all models, indicating
that the perfect classication of participants was challenging.
Average posterior probabilities were 0.79, 0.93, and 0.81 for classes
1, 2, and 3, respectively. is solution is plotted in Figure 1.
e starting points diered signicantly across trajectories
(overall Wald statistics =14101.81, p < 0.001; for all pairwise
comparisons p<0.001). e rst class was the most numerous,
containing 45.6% of the sample, for whom HRQoL signicantly
decreased during the study period (slope = −0.13, z = 2.55,
p < 0.02). e second class, with the lowest and most stable
HRQoL (slope = −0.08, z = −0.86, ns), was represented by
29.4% of the sample. Finally, the third class included 25% of
PLWH and exhibited the highest and increasing HRQoL
(slope = 0.12, z = 1.98, p < 0.05).
For PSS, the 4-class solution was chosen as the best tted
to the data due to the lowest BIC and SABIC values, and
highest accuracy of classication, while retaining a reasonable
size for the smallest class. Moreover, this decision was supported
by visibly worse performance on all these criteria by the 5-class
model (see Tabl e 3 ). Average posterior probabilities ranged
from 0.78 for class 2 to 0.89 for class 1. Figure 2 presents
the obtained trajectories. e majority of the sample (63.1%)
was allocated to the rst class and exhibited decreasing PSS
trajectory (slope = −0.19, z = −2.21, p < 0.05) with a middle
starting point. e second class consisted of PLWH (14.3% of
the sample) with a slightly higher starting point and increasing
PSS (slope = 0.21, z = 2.36, p < 0.05). e highest and stable
trajectory was represented by 15.1% of the sample, identied
as class 3. On the other side was the smallest class 4 (7.5%
of the sample) with the lowest and stable PSS, albeit with a
noticeable tendency to decrease (slope= −0.23, z= −1.08, ns).
Gender as a Covariate of Univariate
Trajectories
When gender was added to the models as the only predictor
of class membership, it was insignicant for both HRQoL
TABLE 3 | Summary of model selection indices of latent class growth curve analysis: Unconditional univariate models for health-related quality of life (HRQoL) and
perceived social support (PSS).
Model BIC AIC SABIC Number of
parameters
Entropy Smallest class
N (%) Frequency
HRQoL
1-Class 3467.27 3456.69 3457.76 3
2-Class 3334.58 3309.88 3312.39 7 0.61 39.3 99
3-Class 3285.87 3247.04 3251.00 11 0.63 25.0 63
4-Class 3262.65 3209.71 3215.09 15 0.64 1.6 4
5-Class 3256.24 3189.18 3196.00 19 0.62 1.6 4
PSS
1-Class 4039.37 4028.78 4029.86 3
2-Class 3824.25 3799.55 3802.06 7 0.84 26.2 60
3-Class 3751.05 3712.22 3716.18 11 0.62 15.9 40
4-Class 3727.09 3674.15 3679.54 15 0.71 7.5 19
5-Class 3738.32 3671.26 3678.08 19 0.57 15.1 38
BIC, Bayesian information criterion; AIC, Akaike’s information criterion; SABIC, sample-size adjusted BIC.
TABLE 2 | Descriptive statistics for health-related quality of life (HRQoL) and
perceived social support (PSS).
Variable Range Mean SD Skewness Kurtosis
HRQoL
Time 1 1.42–4.92 3.75 0.57 −0.82 0.99
Time 2 1.58–4.92 3.74 0.56 −0.59 0.61
Time 3 1.27–4.81 3.66 0.58 −0.65 1.47
PSS
Time 1 1–4 2.31 0.68 −0.84 0.561
Time 2 1–3 2.26 0.71 −0.75 −0.37
Time 3 1–3 2.22 0.72 −0.75 −0.29
SD, standard deviation; sample size for Time 1, Time 2, and Time 3 was 252, 201, 149,
respectively.
Gruszczyńska and Rzeszutek Trajectories of Health-Related Quality of Life
Frontiers in Psychology | www.frontiersin.org 5 July 2019 | Volume 10 | Article 1664
(W = 4.71, ns) and PSS (W = 3.25, ns). When all the other
covariates were included in the mode (i.e., age, education,
relationship status, CD4 count, duration of being diagnosed
with HIV infection, duration of antiretroviral therapy and being
in the AIDS stage) for HRQoL, trajectories of gender remained
insignicant. Signicant eects were observed for age (W=7.11,
p < 0.05) and education (W = 8.77, p < 0.02). Specically,
PLWH in the decreasing HRQoL trajectory were older than
the other two trajectories (41.2 vs. 36.8 and 37.7years of age,
respectively), and PLWH in the increasing HRQoL trajectory
were better educated than those with the stable HRQoL trajectory.
For PSS, both gender (W=674.39, p<0.001) and relationship
status (W = 9.02, p < 0.05) were signicant correlates of PSS
trajectories. us, an interaction of these variables was examined,
revealing a signicant eect between classes 1 and 2 (W=196.56,
p < 0.001). Compared to the decreasing trajectory, there was
overrepresentation of single women in the increasing PSS trajectory.
Dual Trajectories of HRQoL and PSS:
Gender Differences
Table 4 illustrates joint probability while accounting for both
sets of heterogonous trajectories (i.e., for HRQoL and PSS
simultaneously). It is evident that no clear correspondence exists
between the trajectories of HRQoL and PSS. Although the
highest probability was noted for the dual decreasing trajectory
(0.31), the relatively high probability also points to the
simultaneous membership of stable HRQoL and decreasing PSS.
Likewise, approximately 11% of PLWH followed the increasing
HRQoL and decreasing PSS trajectories concurrently. However,
no members in the lowest and stable PSS reported an increase
in HRQoL.
Finally, considering joint probability, gender dierences were
examined with control for all the other sociodemographic and
clinical variables. Wefocused on the dual trajectories combining
the decreasing PSS and all HRQoL trajectories, since for all
the other combinations the frequency was below 10% of the
sample (see Tab l e 4 ). e results of multinomial logistic
regression with dual decreasing trajectories as a reference
category showed no signicant eect of gender alone (χ2= 3.88,
df =2, p = 0.14) nor of any of the remaining variables when
added to the model (χ2 = 20.12, df = 16, p = 0.22).
DISCUSSION
e rst aim of our study was partly achieved (i.e., wemanaged
to observe the heterogeneity of change in HRQoL and PSS
among PLWH), but no systematic gender dierences were
found with regard to these trajectories. Specically, weidentied
three classes of HRQoL, and their members diered in terms
of age and education only; therefore, clinical variables did
not predict class membership. us, our study ts the current
trend of HRQoL research, which points to the diminishing
role of HIV-related clinical factors as determinants of quality
of life for PLWH (Cooper et al., 2017). In a time of great
progress in HIV/AIDS treatment and prevention HIV, infection
has lost its fatal character and became a chronic and manageable
health problem (Deeks etal., 2013). erefore, it is unsurprising
that socially valid resources such as education can be a
signicant predictor of HRQoL trajectories, which is in line
with other studies (albeit cross-sectional and variable-centered;
e.g., Degroote et al., 2014; O’Leary et al., 2014). Moreover,
we observed that older age was related to decreasing HRQoL
trajectories, even if they started from a relatively high level.
is corresponds to existing research on elderly PLWH who
compared to younger PLWH faced more problems and
impediments in their daily functioning due to higher HIV-related
stigma (Emlet, 2006) as well as diculties in distinguishing
physical HIV symptoms from those associated with aging
(Guaraldi et al., 2011; Morgan et al., 2012).
However, one of the most important (yet null) results
deals with the lack of gender dierences in HRQoL change
among our participants. Specically, our nding may revise
the long-lasting and relatively persistent trend in the literature,
which points to lower HRQoL among female PLWH than
male PLWH based on cross-sectional data only (e.g.,
Campsmith et al., 2003; Mrus et al., 2005; Solomon et al.,
2008; Chandra et al., 2009). Some authors observed that
gender dierences in HRQoL within this patient group may
be apparent, i.e., they disappeared aer careful adjustment
of the results with regard to some clinical (e.g., longer illness
duration; Ruiz-Perez et al., 2009) or sociodemographic data
(worse employment and education status; Rzeszutek, 2017).
In other words, lower quality of life among female PLWH
FIGURE 2 | Results of latent class growth curve analysis for perceived social
support (unconditional model).
FIGURE 1 | Results of latent class growth curve analysis for health-related
quality of life (unconditional model).
Gruszczyńska and Rzeszutek Trajectories of Health-Related Quality of Life
Frontiers in Psychology | www.frontiersin.org 6 July 2019 | Volume 10 | Article 1664
does not necessarily reect their more dicult or dierent
adjustment to HIV/AIDS in comparison to male PLWH but
may rather be a result of other factors that have not been
carefully controlled for in other studies (Bogart et al., 2011;
Rzeszutek, 2017).
However, the results for PSS do not support this explanation.
Namely, the null eect for gender became signicant only
when other covariates were included in the model, resulting
in gender and relationship status being identied as correlates
of PSS trajectory membership. For a single woman, there
was a higher probability of belonging to the increasing PSS
trajectory than to the decreasing one, even if the starting
points of both trajectories were only slightly dierent. Notably,
this is inconsistent with results concerning female PLWH
(Li etal., 2016), but it corresponds to research demonstrating
that relationship status may have dierent consequences for
men and women, with men beneting more from marriage
(Nock, 1998). Among PLWH, men also benet more from
social support, while women are more likely to seek it
(Gordillo et al., 2009; Bekele et al., 2013). us, being a
single woman is not necessarily a disadvantageous condition
in this context. Such individuals may eectively receive
support from other sources that do not require HIV disclosure,
and they may also be less prone to abuse from an intimate
partner (Machtinger et al., 2012). However, we lack data
on the relationship status of these women at the time of
diagnosis; therefore, it cannot be excluded that they had
been infected by a partner in a heterosexual relationship.
e decision to besingle could thus bea deliberate consequence
of this mode of transmission – the most frequent among
women in Europe and the United States (Crepaz etal., 2017;
European Centre for Disease Prevention and Control/WHO
Regional Oce for Europe, 2017). Nonetheless, since no
relevant published data exist with which to compare this
gender-relationship status interaction, it could represent a
sample-specic association. As such, this topic requires
further research.
e obtained combinations of dual trajectories added to a
complexity of change in HRQoL and PSS among PLWH.
Although the probability of being a member of dual decreasing
trajectories was the highest, only 31% of the sample could
be assigned to this group. us, some factors may indeed
be responsible for the simultaneous change of both HRQoL
and PSS; however, they do not respond in the same manner
across the entire sample, since co-occurrence of the matching
change direction in both variables was rather modest. is is
especially pronounced within decreasing PSS, where weidentied
three combinations of dual trajectories: (1) congruent decreasing
PSS and HRQoL, (2) decreasing PSS and increasing HRQoL,
and (3) decreasing PSS with stable HRQoL. erefore, a few
non-exclusive explanations are possible for this mixture of
HRQoL and PSS change.
First, it is likely that an interrelation exists between PSS
and HRQoL (Burgoyne and Renwick, 2004) causing a downward
spiral over time. In this case, some general factors may broadly
aect the functioning of PLWH. e natural candidates are
those related to sociodemographic resources and clinical
characteristics; however, this group did not dier in this respect
from the other combinations of trajectories. e primary
explanation for this null eect could be that we did not assess
the change of these characteristics, only baselines. Nevertheless,
this result is congruent with most studies, which show its
modest role in the functioning of PLWH aer the inception
of ART (Torres et al., 2018). Second, for some PLWH, an
increase in HRQoL may result in reduced perceived support
since it is no longer needed to the same extent. Also, this
shi in perception may additionally serve to conserve self-
ecacy (Warner etal., 2011), which is of particular importance
for patients with chronic diseases that have a stigmatized
social reception, thereby further improving quality of life (Li
et al., 2011). Finally, in the third case (i.e., for PLWH with
decreasing PSS and stable HRQoL), these two processes may
have dierent temporal dynamics, as a change in PSS likely
proceeded changes in HRQoL (Jia et al., 2005). It would
berather exceptional to maintain such an incongruent dynamic-
static status in light of ndings that suggest cross-sectionally
lower PSS is related to lower HRQoL among PLWH (Douaihy
and Singh, 2001; Burgoyne and Renwick, 2004). Interestingly,
being a member of each of these groups remained unrelated
not only to gender but also to the other sociodemographic
and clinical variables.
ere are several strengths of this study, including the
longitudinal and person-centered approach with a relatively
large clinical sample and three measurement points. However,
certain limitations must benoted. First, this is a correlational
study based on self-descriptive data; thus, no causal interpretation
is allowed. Additionally, the separation of the univariate trajectory
classes for HRQoL was only acceptable. Moreover, since the
HRQoL measurement covered social domain, signicant overlap
with social support is likely to occur, which may lead to an
overestimation of the relationship between these variables.
Even if conceptually relevant, only weak and highly similar
correlation has been noted across all the domains1. is indicates
already well-recognized dierence among perceived social
support, satisfaction with social support, and their correlates
and outcomes (Vangelisti, 2009). Next, although the sample
reects the gender-related prevalence of HIV infection in
1
We would like to thank the anonymous reviewer for this comment. e time-
averaged correlations with PSS for each domain of HRQoL were as follows:
0.25 for somatic domain, 0.40 for psychological domain, 0.40 for social domain,
and 0.43 for environmental domain.
TABLE 4 | Joint probability of membership for dual trajectories of health-related
quality of life (HRQoL) and perceived social support (PSS).
HRQoL PSS
Decreasing Increasing High
stable
Low
stable
Total
Decreasing 0.32 0.05 0.06 0.03 0.46
Stable 0.20 0.03 0.01 0.05 0.29
Increasing 0.11 0.06 0.08 0.00 0.25
Total 0.63 0.14 0.15 0.08 1
Gruszczyńska and Rzeszutek Trajectories of Health-Related Quality of Life
Frontiers in Psychology | www.frontiersin.org 7 July 2019 | Volume 10 | Article 1664
Europe and United States, the study could be underpowered
to detect gender dierences. Furthermore, since there was a
tendency for higher dropout among women, a recruitment
bias cannot be excluded, though it was not observed in a
careful examination of the general pattern of missingness.
Finally, it must be underlined that the ndings are restricted
only to PLWH who are formally diagnosed and under medical
treatment, which is a typical characteristic for most studies
with clinical samples.
Despite these limitations, our study adds to the HIV/AIDS
literature by investigating the heterogeneity of change in
HRQoL and PSS with a special emphasis on gender dierences.
e present study demonstrates the complexity of dual changes
and identies groups of PLWH with mismatched HRQoL
and PSS trajectories. e limited role of baseline
sociodemographic and clinical characteristics of PLWH in
predicting these changes was also highlighted, particularly a
lack of signicant dierences between men and women. In
fact, the ndings may suggest that gender is no longer a
crucial factor beyond their HRQoL and PSS change if aer
being diagnosed access to treatment is equal.
DATA AVAILABILITY
e datasets for this study will not bemade publicly available
because although anonymized, it concerns sensitive issues (being
infected with HIV). e informed consent did not include
the consent to the publication of the data.
ETHICS STATEMENT
All procedures performed in this study were in accordance
with the ethical standards of the Research Ethics Committee
of the University of Economics and Human Sciences, Warsaw,
Poland, and with the 1964 Helsinki declaration and its later
amendments or comparable ethical standards. Informed consent
was obtained from all individual participants included in the
study. e protocol was approved by the Research Ethics
Committee of the University of Economics and Human Sciences,
Warsaw, Poland.
AUTHOR CONTRIBUTIONS
EG and MR conceived the study, designed the study, supervised
the data collection and database organization, conducted the
interpretation of the data, draed, and revised the manuscript.
EG conducted the statistical analysis. EG and MR approved
the submitted version of the manuscript.
FUNDING
is study was funded by the National Science Center, Poland,
research project no. 2016/23/D/HS6/02943. Open access of this
article was nanced by the Ministry of Science and Higher
Education in Poland under the 2019–2022 program “Regional
Initiative of Excellence, project number 012/RID/2018/19.
REFERENCES
Alemu, H., Haile, D., Tsui, A., Ahmed, S., and Shewamare, A. (2012). Eect
of depressive symptoms and social support on weight and CD4 count increase
at HIV clinic in Ethiopia. AIDS Care 24, 866–876. doi: 10.1080/0954
0121.2011.648160
Ashton, E., Vosvick, M., Chesney, M., Gore-Felton, C., Koopman, C., O’Shea, K.,
et al. (2005). Social support and maladaptive coping as predictors of the
change in physical health symptoms among persons living with HIV/AIDS.
AIDS Patient Care STDs 19, 587–598. doi: 10.1089/apc.2005.19.587
Aziz, M., and Smith, K. (2011). Challenges and successes in linking HIV-
infected women to care in the United States. Clin. Infect. Dis. 52, 231–237.
doi: 10.1093/cid/ciq047
Bekele, T., Rourke, S., Tucker, R., Greene, S., Sobota, M., Koornstra, J., et al.
(2013). Direct and indirect eects of perceived social support on health-
related quality of life in persons living with HIV/AIDS. AIDS Care 25,
337–346. doi: 10.1080/09540121.2012.701716
Biesanz, J. C., Deeb-Sossa, N., Papadakis, A. A., Bollen, K. A., and Curran, P. J.
(2004). e role of coding time in estimating and interpreting growth curve
models. Psychol. Methods 9, 30–52. doi: 10.1037/1082-989X.9.1.30
Bing, E. G., Burnam, M. A., Longshore, D., Fleishman, J. A., Sherbourne, C.
D., London, A. S., et al. (2001). Psychiatric disorders and drug use among
human immunodeciency virus infected adults in the United States. Arch.
Gen. Psychiatry 58, 721–728. doi: 10.1001/archpsyc.58.8.721
Bogart, L. M., Wagner, G. J., Galvan, F. H., Landrine, H., Klein, D. J., and
Sticklor, L. A. (2011). Perceived discrimination and mental health symptoms
among black men with HIV. Cult. Divers. Ethn. Minor. Psychol. 17, 295–302.
doi: 10.1037/a0024056
Bor, J., Rosen, S., Chimbindi, N., Haber, N., Herbst, K., Mutevedzi, T., et al.
(2015). Mass HIV treatment and sex disparities in life expectancy: demographic
surveillance in rural South Africa. PLoS Med. 12:e1001905. doi: 10.1371/
journal.pmed.1001905
Breet, E., Kagee, A., and Seedat, S. (2014). HIV-related stigma and symptoms
of post-traumatic stress disorder and depression in HIV-infected individuals:
does social support play a mediating or moderating role? AIDS Care 26,
947–951. doi: 10.1080/09540121.2014.901486
Bucciardini, R., Pugliese, K., Weimer, L., Digregorio, M., Fragola, V., and
Mancini, M. (2014). Relationship between health-related quality of life
measures and high HIV viral load in HIV-infected triple-class-experienced
patients. HIV Clin. Trials 15, 176–183. doi: 10.1310/hct1504-176
Burgoyne, R., and Renwick, R. (2004). Social support and quality of life over
time among adults living with HIV in the HAART era. Soc. Sci. Med. 58,
1353–1366. doi: 10.1016/S0277-9536(03)00314-9
Burgoyne, R., and Saunders, D. (2001). Quality of life among urban Canadian
HIV/AIDS clinic outpatients. Int. J. STD AIDS 12, 505–512. doi: 10.1328/
a03564056
Campbell, C., Nair, S., and Maimane, M. (2006). AIDS stigma, sexual moralities
and the policing of women and youth in South Africa. Fem. Rev. 83,
132–138. doi: 10.1057/palgrave.fr.9400285
Campsmith, M., Nakashima, A., and Davidson, A. (2003). Self-reported health-
related quality of life in persons with HIV infection: results from a multi-site
interview project. Health Qual. Life Outcomes 1:12. doi: 10.1186/1477-7525-1-12
Carrico, A. W. (2019). Getting to zero: targeting psychiatric comorbidities as
drivers of the HIV/AIDS epidemic. Int. J. Behav. Med. 26, 1–2. doi: 10.1007/
s12529-019-09771-w
Carvalhal, A. (2010). Are women a dierent group of HIV-infected individuals?
Arch. Womens Ment. Health 13, 181–183. doi: 10.1007/s00737-010-0167-1
Celeux, G., and Soromenho, G. (1996). An entropy criterion for assessing the
number of clusters in a mixture model. J. Classif. 13, 195–212. doi: 10.1007/
BF01246098
Gruszczyńska and Rzeszutek Trajectories of Health-Related Quality of Life
Frontiers in Psychology | www.frontiersin.org 8 July 2019 | Volume 10 | Article 1664
Chandra, P., Satyanarayana, V., Satishchandra, P., Satish, K., and Kumar, M.
(2009). Do men and women with HIV dier in their quality of life? A
study from South India. AIDS Behav. 13, 110–117. doi: 10.1007/s10461-
008-9434-9
Chida, Y., and Vedhara, K. (2009). Adverse psychosocial factors predict poorer
prognosis in HIV disease: a meta-analytic review of prospective investigations.
Brain Behav. Immun. 23, 434–445. doi: 10.1016/j.bbi.2009.01.013
Cohen, M. S., Chen, Y. Q., McCauley, M., Gamble, T., Hosseinipour, M. C.,
Kumarasamy, N., et al. (2016). Antiretroviral therapy for the prevention of
HIV-1 transmission. N. Engl. J. Med. 375, 830–839. doi: 10.1056/
NEJMoa1600693
Collazos, J., Asensi, V., and Carto, J. (2007). Sex dierences in the clinical,
immunological and virological parameters of HIV-infected patients treated
with HAART. AIDS 21, 835–843. doi: 10.1097/QAD.0b013e3280b0774a
Cooper, V., Clatworthy, J., Harding, R., Whetham, J., and Consortium, E. (2017).
Measuring quality of life among people living with HIV: a systematic review
of reviews. Health Qual. Life Outcomes 15:220. doi: 10.1186/s12955-017-0778-6
Crepaz, N., Dong, X., Chen, M., and Hall, H. I. (2017). Examination of HIV
infection through heterosexual contact with partners who are known to
be HIV infected in the United States. AIDS 31, 1641–1644. doi: 10.1097/
QAD.0000000000001526
Deeks, S., Lewin, S., and Havlir, D. (2013). e end of AIDS: HIV infection
as a chronic disease. Lancet 382, 1525–1533. doi: 10.1016/S0140-
6736(13)61809-7
Degroote, S., Vogelaers, D., and Vandijck, D. (2014). What determines health-
related quality of life among people living with HIV: an updated review
of the literature. Arch. Public Health 72:40. doi: 10.1186/2049-3258-72-40
Douaihy, A., and Singh, N. (2001). Factors aecting quality of life in patients
with HIV infection. AIDS Read. 11, 444–449.
Earnshaw, V., Lang, S., Lippitt, M., Jin, H., and Chaudoir, S. (2015). HIV
stigma and physical health symptoms: do social support, adaptive coping,
and/or identity centrality act as resilience resources? AIDS Behav. 19, 41–49.
doi: 10.1007/s10461-014-0758-3
Emlet, C. (2006). A comparison of HIV stigma and disclosure patterns between
older and younger adults living with HIV/AIDS. AIDS Patient Care STDs
20, 350–358. doi: 10.1089/apc.2006.20.350
Emuren, L., Welles, S., Evans, A. A., Polansky, M., Okulicz, J. F., Macalino,
G., et al. (2017). Health-related quality of life among military HIV patients
on antiretroviral therapy. PLoS One. 12:e0178953. doi: 10.1371/journal.
pone.0178953
European Centre for Disease Prevention and Control/WHO Regional Oce
for Europe (2017). HIV/AIDS surveillance in Europe 2017–2016 data. Stockholm:
ECDC.
Geary, C., Parker, W., Rogers, S., Haney, E., Njihia, C., and Haile, A. (2014).
Gender dierences in HIV disclosure, stigma, and perceptions of health.
AIDS Care 26, 1419–1425. doi: 10.1080/09540121.2014.921278
Gielen, A., McDonnell, K., Campo, P., and Faden, R. (2001). Quality of life
among women living with HIV: the importance violence, social support,
and self-care behaviors. Soc. Sci. Med. 52, 315–322. doi: 10.1016/
S0277-9536(00)00135-0
Gonzalez, J., Penedo, F., Antoni, M., Dura, R., Pherson-Baker, S., and Ironson, G.
(2004). Social support, positive states of mind, and HIV treatment adherence
in men and women living with HIV/AIDS. Health Psychol. 23, 413–418.
doi: 10.1037/0278-6133.23.4.413
Gordillo, V., Fekete, E., Platteau, T., Antoni, M., Schneiderman, N., and
Nostlinger, C. (2009). Emotional support and gender in people living with
HIV: eects on psychological well-being. J. Behav. Med. 32, 523–531. doi:
10.1007/s10865-009-9222-7
Guaraldi, G., Orlando, G., and Zona, S. (2011). Premature age-related co-
morbidities among HIV-infected persons compared with the general population.
Clin. Infect. Dis. 53, 1120–1126. doi: 10.1093/cid/cir627
Hansen, N., Vaughan, E., Cavanaugh, C., Connell, C. M., and Sikkema, K.
(2009). Health-related quality of life in bereaved HIV-positive adults:
relationships between HIV symptoms, grief, social support, and axis II
indication. Health Psychol. 28, 249–257. doi: 10.1037/a0013168
Herrmann, S., McKinnon, E., Hyland, N., Lalanne, C., Mallal, S., Nolan, D.,
et al. (2013). HIV-related stigma and physical symptoms have a persistent
inuence on health-related quality of life in Australians with HIV infection.
Health Qual. Life Outcomes 11:56. doi: 10.1186/1477-7525-11-56
Hipp, J. R., and Bauer, D. J. (2006). Local solutions in the estimation of growth
mixture models. Psychol. Methods 11, 36–53. doi: 10.1037/1082-989X.11.1.36
IBM Corp (2016). IBM SPSS statistics for windows. Version 24. Armonk, NY:
IBM Corp (Released 2016).
Jia, H., Uphold, C. R., Wu, S., Chen, G. J., and Duncan, P. W. (2005). Predictors
of changes in health-related quality of life among men with HIV infection
in the HAART era. AIDS Patient Care STDs 19, 395–405. doi: 10.1089/
apc.2005.19.395
Jia, H., Uphold, C., Wu, S., Reid, K., Findley, K., and Duncan, P. (2004).
Health-related quality of life among men with HIV infection: eects of
social support, coping, and depression. AIDS Patient Care STDs 18, 594–603.
doi: 10.1089/apc.2004.18.594
Joint United Nations Programme on HIV/AIDS (UNAIDS) (2018). UNAIDS
DATA 2018. Available at: http://www.unaids.org/sites/default/les/media_asset/
unaids-data-2018_en.pdf (Accessed March, 19 2019).
Li, X., Huang, L., Wang, H., Fennie, K. P., He, G., and Williams, A. B. (2011).
Stigma mediates the relationship between self-ecacy, medication adherence,
and quality of life among people living with HIV/AIDS in China. AIDS
Patient Care STDs 25, 665–671. doi: 10.1089/apc.2011.0174
Li, L., Lin, C., Liang, L. J., and Ji, G. (2016). Exploring coping and social
support with gender and education among people living with HIV in China.
AIDS Behav. 20, 317–324. doi: 10.1007/s10461-015-1232-6
Lifson, A. R., Grund, B., Gardner, E. M., Kaplan, R., Denning, E., Engen, N.,
et al. (2017). Improved quality of life with immediate versus deferred initiation
of antiretroviral therapy in early asymptomatic HIV infection. AIDS 31,
953–963. doi: 10.1097/QAD.0000000000001417
Liu, C., Ostrow, D., Detels, R., Hu, Z., Johnson, L., Kingsley, L., et al. (2006).
Impacts of HIV infection and HAART use on quality of life. Qual. Life
Res. 15, 941–949. doi: 10.1007/s11136-005-5913-x
Lubeck, D., and Fries, J. (1997). Assessment of quality of life in early stage
HIV-infected persons: data from the AIDS time-oriented health outcome
study (ATHOS). Qual. Life Res. 6, 494–506. doi: 10.1023/A:1018404014821
Machtinger, E., Wilson, T., Haberer, J., and Weiss, D. (2012). Psychological
trauma and PTSD in HIV-positive women: a meta-analysis. AIDS Behav.
16, 2091–2100. doi: 10.1007/s10461-011-0127-4
McDonnell, K., Gielen, A., Wu, A., Campo, P., and Faden, R. (2000). Measuring
health related quality of life among women living with HIV. Qual. Life Res.
9, 931–940. doi: 10.1023/A:1008909919456
Miners, A., Phillips, A., Kreif, N., Rodger, A., Speakman, A., Fisher, M., et al.
(2014). Health-related quality-of-life of people with HIV in the era of
combination antiretroviral treatment: a cross-sectional comparison with the
general population. Lancet HIV 1, e32–e40. doi: 10.1016/S2352-3018(14)70018-9
Mitchell, M., Nguyen, T., Isenberg, S., Maragh-Bass, A., Keruly, J., and Knowlton, A.
(2017). Psychosocial and service use correlates of health-related quality of
life among a vulnerable population living with HIV/AIDS. AIDS Behav. 21,
1580–1587. doi: 10.1007/s10461-016-1589-1
Morgan, E., Iudicello, J., and Weber, E. (2012). Synergistic eects of HIV
infection and older age on daily functioning. J. Acquir. Immune Dec. Syndr.
61, 341–348. doi: 10.1097/QAI.0b013e31826bfc53
Mrus, J., Williams, P., Tsevat, J., Cohn, S., and Wu, A. (2005). Gender dierences
in health-related quality of life in patients with HIV/AIDS. Qual. Life Res.
14, 479–491. doi: 10.1007/s11136-004-4693-z
Nicastri, E., Leone, S., Angeletti, C., Palmesano, L., Sarmati, L., Chiesi, A.,
et al. (2007). Sex issues in HIV-1-infected persons during highly active
antiretroviral therapy: a systematic review. J. Antimicrob. Chemother. 60,
724–732. doi: 10.1093/jac/dkm302
Nock, S. (1998). Marriage in men’s lives. Oxford, New York.
Nylund, K., Asparouhov, T., and Muthén, B. O. (2007). Deciding on the number
of classes in latent class analysis and growth mixture modeling: a Monte
Carlo simulation study. Struct. Equ. Model. 14, 535–569. doi: 10.1080/
10705510701575396
O’Leary, A., Jemmott, J. B., Stevens, R., Rutledge, S. E., and Icard, L. D. (2014).
Optimism and education buer the eects of syndemic conditions on HIV
status among African American men who have sex with men. AIDS Behav.
18, 2080–2088. doi: 10.1007/s10461-014-0708-0
Oberjé, E., Dima, A., van Hulzen, A. W., Prins, J., and de Bruin, M. (2015).
Looking beyond health-related quality of life: predictors of subjective well-
being among people living with HIV in the Netherlands. AIDS Behav. 19,
1398–1407. doi: 10.1007/s10461-014-0880-2
Gruszczyńska and Rzeszutek Trajectories of Health-Related Quality of Life
Frontiers in Psychology | www.frontiersin.org 9 July 2019 | Volume 10 | Article 1664
Penniman, T. V., Taylor, S. L., Bird, C. E., Beckman, R., Collins, R. L., and
Cunningham, W. (2007). e associations of gender, sexual identity and
competing needs with healthcare utilization among people with HIV/AIDS.
J. Natl. Med. Assoc. 99, 419–427.
Psaros, C., O’Cleirigh, C., Bullis, J., Markowitz, S., and Safren, S. (2013). e
inuence of psychological variables on health related quality of life among
HIV positive individuals with a history of intravenous drug use. J. Psychoactive
Drugs 45, 304–312. doi: 10.1080/02791072.2013.825030
Qiao, S., Li, X., and Stanton, B. (2014). Social support and HIV-related risk
behaviors: a systematic review of the global literature. AIDS Behav. 18,
419–441. doi: 10.1007/s10461-013-0561-6
Rendina, H., Brett, M., and Parsons, J. (2018). e critical role of internalized
HIV-related stigma in the daily negative aective experiences of HIV-positive
gay and bisexual men. J. Aect. Disord. 227, 289–297. doi: 10.1016/j.
jad.2017.11.005
Ruiz-Perez, I., Olry, A., del Castilloc, L., Bano, J., Ruz, M., and Jimeneze,
A. (2009). No differences in quality of life between men and
womenundergoing HIV antiretroviral treatment. Impact of demographic,
clinical and psychosocial factors. AIDS Care 21, 943–952. doi:
10.1080/09540120802612840
Rzeszutek, M. (2017). Health-related quality of life and coping strategies among
people living with HIV: the moderating role of gender. Arch. Womens Ment.
Health 21, 247–257. doi: 10.1007/s00737-017-0801-2
Rzeszutek, M., and Gruszczyńska, E. (2018). Positive and negative aect change
among people living with HIV: a one-year prospective study. Int. J. Behav.
Med. 26, 28–37. doi: 10.1007/s12529-018-9741-0
Samji, H., Cescon, A., Hogg, R. S., Modur, S. P., Altho, K. N., Buchacz, K.,
et al. (2013). Closing the gap: Increases in life expectancy among treated
HIV-positive individuals in the United States and Canada. PLoS One 18,
144–156. doi: 10.1371/journal.pone.0081355
Schulz, U., and Schwarzer, R. (2003). Soziale Unterstützung bei der
Krankheitsbewältigung: Die Berliner Social Support Skalen (BSSS). Diagnostica
49, 73–82. doi: 10.1026//0012-1924.49.2.73
Solomon, S., Venkatesh, K., Brown, L., Verma, P., Cecelia, A., Daly, C., et al.
(2008). Gender-related dierences in quality of life domains of persons
living with HIV/AIDS in South India in the era prior to greater access to
antiretroviral therapy. AIDS Patient Care and STDs 22, 999–1005. doi: 10.1089/
apc.2008.0040
Song, B., Yan, C., Lin, Y., Fuxiang, W., and Wang, L. (2016). Health-related
quality of life in HIV-infected men who have sex with men in China: a
Cross-sectional study. Med. Sci. Monit. 22, 2859–2870. doi: 10.12659/
MSM.897017
Torres, T. S., Harrison, L. J., La Rosa, A. M., Cardoso, S. W., Zheng, L.,
Ngongondo, M., et al. (2018). Quality of life improvement in resource-
limited settings aer one year of second-line antiretroviral therapy use among
adult men and women. AIDS 32, 583–593. doi: 10.1097/QAD.0000000000001738
Turner-Cobb, J. M., Gore-Felton, C., Marouf, F., Koopman, C., Kim, P., et al.
(2002). Coping, social support, and attachment style as psychosocial correlates
of adjustment in men and women with HIV/AIDS. J. Behav. Med. 25,
337–353. doi: 10.1023/A:1015814431481
Vangelisti, A. L. (2009). Challenges in conceptualizing social support. J. Soc.
Pers. Relat. 26, 39–51. doi: 10.1177/0265407509105520
Vermunt, J. K., and Magidson, J. (2016). Technical guide for latent GOLD 5.1:
Basic, advanced, and syntax. Belmont, CA: Statistical Innovations.
Warner, L., Ziegelmann, J., Schüz, B., Wurm, S., Tesch-Roemer, C., and
Schwarzer, R. (2011). Maintaining autonomy despite multimorbidity: self-
ecacy and the two faces of social support. Eur. J. Ageing 8, 3–12. doi:
10.1007/s10433-011-0176-6
WHOQOL Group (1998). Development of the World Health Organization
WHOQOL-BREF quality of life assessment. Psychol. Med. 28, 551–558. doi:
10.1017/S0033291798006667
Conict of Interest Statement: e authors declare that the research was conducted
in the absence of any commercial or nancial relationships that could beconstrued
as a potential conict of interest.
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... Malleable constructs that fluctuate over time ("state-like") could be more promising targets for intervention than more stable constructs ("traitlike"). Some research has suggested that positive affect [31], quality of life [33], and social support fluctuate [33] over 1 year in middle-aged PWH; however, these studies are limited by their relatively restricted time frame, lack of HIV− comparisons, and general measures of positive and/ or negative constructs. ...
... Malleable constructs that fluctuate over time ("state-like") could be more promising targets for intervention than more stable constructs ("traitlike"). Some research has suggested that positive affect [31], quality of life [33], and social support fluctuate [33] over 1 year in middle-aged PWH; however, these studies are limited by their relatively restricted time frame, lack of HIV− comparisons, and general measures of positive and/ or negative constructs. ...
... The current study investigated general, group-level changes in internal strengths and socioemotional support; however, unique trajectories of positive psychological attributes among subgroups of PWH have been observed in other studies [31,33] and may identify who is more likely to improve in internal strengths and socioemotional support over time. Unsurprisingly, depressive symptoms were negatively associated with both factors and may dampen psychological resilience. ...
Article
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Positive psychological attributes are associated with better health outcomes, yet few studies have identified their underlying constructs and none have examined their temporal trajectories in clinical vs. non-clinical samples. From data collected over 4 years from people with HIV (PWH) and HIV-uninfected (HIV−) participants, we identified two latent factors (internal strengths; socioemotional support) based on responses to seven positive psychological attributes. Internal strengths increased over 4 years for PWH, but not for HIV− comparisons. Socioemotional support did not change significantly in either group. Lower internal strengths and worse socioemotional support were related to greater depressive symptoms. We speculate that improvement in internal strengths in PWH could reflect their being in care, but this requires further study to include PWH not in care. Given the apparent malleability of internal strengths and their association with improved health outcomes, these attributes can serve as promising intervention targets for PWH.
... Other studies comparing younger, middle-aged, and older adults indicated that older women had greater decrements in physical, psychological, and environmental domains and sexual activity, more bodily pain, emotional stress, social isolation, and greater poverty than older men (Hsieh et al., 2022). However, other studies found no significant gender differences in HRQOL (Gruszczyńska & Rzeszutek, 2019;Rzeszutek, 2018). ...
... Women had worse HRQOL independently of whether they lived in a capital city or a metropolitan region (Silva et al., 2017), regardless of the presence of non-communicable chronic diseases (Höfelmann et al., 2018), and with high levels of stress (Dumith et al., 2022). However, other studies have shown no differences in HRQOL associated with the gender of the participants (Gruszczyńska & Rzeszutek, 2019;Rzeszutek, 2018). ...
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Gender, as a social determinant of health, can favor social and health inequalities that compromise the health-related quality of life (HRQOL) in people living with HIV/AIDS (PLWHA). This study aims to compare HRQOL in women and men with HIV in Brazil and identify factors associated with their physical and mental health. Two hundred eighteen men and 101 women with HIV completed a sociodemographic and clinical questionnaire, the 36-item Short Form Health Survey (SF-36v2), the HIV/AIDS-Targeted Quality of Life (HAT-QOL), and the WHOQOL-HIV BREF. HRQOL scores were compared with the Mann-Whitney U test, and multiple linear regression analyses were used to identify factors related to Physical and Mental Health (PCS and MCS of SF-36v2). Women had worse HRQOL than men in all three instruments. Models for Physical Health (Women: R² = 0.56, p < .001; Men: R² = 0.552, p < .001) and Mental Health (Women: R² = 0.602, p < .001; Men: R² = 0.600, p < .001) showed gender-related differences. Overall Function (Women: Beta = 0.496; Men: Beta = 0.387) and Level of Independence (Women: Beta = 0.375; Men: Beta = 0.305) were the domains that best predicted Physical Health in both genders. Environment in women (Beta = − 0.289) and Psychological in men (Beta = 0.372) were the domains that best predicted Mental Health. Significant HRQOL and physical and mental health differences were associated with gender in PLWHA in Brazil.
... Patients' perceived and reported health aspects beyond objectively quantified clinical parameters are summarized as health-related quality of life (HRQL). PLWH consistently report lower HRQL than HIVnegative individuals despite antiretroviral therapy and viral suppression [2,3]. Albeit the role of HIV-associated complications and side effects of ART on HRQL, psychosocial factors related to stigma, socioeconomic status, and limited access to social support may be other key determinants of HRQL [4][5][6]. ...
... Additionally, PLWH with lower education had lower scores in the two domains, roleand social functioning. Sociodemographic factors have shown a high impact on the HRQL in PLWH, suggesting the need for more social support [2,35]. Overall, social support may help reduce the effects of HIV-related stigmatization within the context of economic insecurity [4]. ...
Article
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Purpose Liver-related comorbidities can impair the health-related quality of life (HRQL) in people living with human immunodeficiency virus (HIV) (PLWH). However, the role of hepatic steatosis and significant fibrosis in PLWH remains incompletely characterized. Therefore, the aim of this study was to explore the association of hepatic steatosis and significant fibrosis on the HRQL using the medical outcomes study HIV health survey (MOS-HIV) in PLWH. Methods A total of 222 PLWH were included in the final analysis of this cohort study. Metabolic comorbidities, socioeconomic factors, and HIV-related parameters were assessed. Hepatic steatosis and fibrosis were measured using vibration-controlled transient elastography (VCTE). The MOS-HIV survey, containing two summary scores (physical health summary (PHS) and mental health summary (MHS)) and ten domains, was used to assess the HRQL. Clinical predictors were identified using multivariable linear regression models. Results The majority of this cohort was male, and the median age was 52 years, with a high prevalence of hepatic steatosis ( n = 81, 36.5%). Significant fibrosis was present in 7.7% ( n = 17). The mean PHS and MHS scores were 52.7 ± 9.5 and 51.4 ± 10.5, respectively. The lowest scores were in the general health perception (GHP) and energy/fatigue (EF) domains. A high BMI and waist circumference were associated with a poor PHS score. Lower education, unemployment, arterial hypertension, and significant fibrosis remained independent predictors of an impaired HRQL. Conclusion Metabolic comorbidities, significant fibrosis, and a lower socioeconomic status may negatively affect the HRQL in PLWH. Considering the negative impact of significant fibrosis on the outcome, counseling and preventive measures according to current guidelines are recommended in this subgroup of PLWH.
... While social support has been proved effectively protecting both physical and mental health (12). This relative relationship does not change according to gender (13). A previous study also indicated that the odds of participating in HIV risk behaviors decreased with social support (14). ...
Article
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This study focused on the mental health of people living with HIV(PLWHIV) and explored their relationship between loneliness and perceived social support, health related quality of life (HRQoL) with a method of structural equation model. We collected clinical and psychological data from consecutively enrolled PLWHIV. A total of 201 PLWHIVs were enrolled and measured with self-reporting survey instruments of UCLA Loneliness Scale, Self-Rating Depression Scale, Self-Rating Anxiety Scale, Social Support Ratio Scale and Short Form Health Survey-36. The levels of loneliness, depression, anxiety, perceived social support and HRQoL were assessed. PLWHIV enrolled were divided into two groups of loneliness and non-loneliness based on their UCLA Loneliness Scale scores. Multivariable analysis indicated that being married is a protective factor associated with loneliness (OR = 0.226; P = 0.032). We further found the loneliness group had a higher level of depression (P < 0.001) and anxiety (P < 0.001), but lower level of HRQoL (P < 0.001) than the non-loneliness group. We found there was a positive linear correlation between social support and HRQoL among the enrolled PLWHIVs (r² = 0.0592; P = 0.0005). A structural equation model (SEM) was established to evaluate whether the loneliness played as a mediation role between social support and HRQoL. The model showed loneliness as a mediation from social support leading to a decrease of HRQoL. Our findings showed a potential psychological pathway from social support to HRQoL, suggesting the need for interventions focusing on social support may improve poor HRQoL lead by loneliness.
... Furthermore, good levels of QOL cores were also positively associated with family support. This is also in agreement with the results of a study that examined the Trajectories of Health-Related Quality of Life and Perceived Social Support Among People Living with HIV Undergoing ART [28]. The finding may be due to social support that can enhance patients adherence to the medication [29,30] and associated with enhanced HRQOL [31]. ...
Article
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Background People living with HIV/AIDS (PLWHA) are frequently confronted with severe social issues such as rejection, abandonment, criticism, and stigma. This would negatively affect their quality of life. Several studies have been conducted so far to assess factors affecting the health-related quality of life among people living with HIV/AIDS who are on antiretroviral therapy (ART) in Ethiopia. However, to our knowledge, there is no previous study that has summarized the results of the studies that investigated health-related quality of life (HRQOL) among PLWHA in Ethiopia. Therefore, the purpose of this review was to estimate the pooled prevalence of HRQOL and its association with social support among people living with HIV/AIDS (PLWHA) on ART in Ethiopia. Methods A systematic search was carried out using several electronic databases (PubMed, Science Direct, Web of Science, and Cochrane electronic), Google Scholar, Google, and a manual search of the literature on health-related quality of life among people living with HIV/AIDS who are on ART. A Microsoft Excel data extraction sheet was used to extract pertinent data from an individual study. To assess the heterogeneity of primary articles, the Cochrane Q test statistics and the I2 test were carried out, and a random effects meta-analysis was used to estimate the pooled prevalence of HRQOL. Result Out of the 493 articles reviewed, ten with a total of 3257 study participants were eligible for meta-analysis. The pooled prevalence of HRQOL among people living with HIV/AIDS who are on antiretroviral therapy in Ethiopia was 45.27%. We found that strong perceived social support was significantly associated with higher levels of subjectively perceived HRQOL. PLWHA who were on ART and had good social support were four times more likely to report higher HRQOL when compared to their counterparts [AOR = 4.01, 95% CI 3.07–5.23]. Conclusion A substantial number of PLWHA had poor HRQOL in Ethiopia. Social support was significantly associated with HRQOL among people living with HIV/AIDS. Hence, it’s recommended to encourage suitable intervention at every follow-up visit, and psycho-social support is also warranted to improve the quality of life.
... Increasing social support increases the quality of life of HIV/AIDS persons [40]. Social support is significant predictor of quality of life [41] [42] [43]. It is significantly associated with better quality of life, minimizes the depressive symptoms among HIV/AIDS patients [44]. ...
... Increasing social support increases the quality of life of HIV/AIDS persons [40]. Social support is significant predictor of quality of life [41] [42] [43]. It is significantly associated with better quality of life, minimizes the depressive symptoms among HIV/AIDS patients [44]. ...
... The findings of that study were that both physical and mental HRQoL were negatively associated with the presence of any unmet basic need, a highly prevalent (87%) condition in our sample. With respect to HRQoL, there have been very few publications addressing this outcome over time in persons living with HIV [37]. ...
Article
Full-text available
Despite significant advances in antiretroviral therapy, unmet basic needs can negatively impact health-related quality of life (HRQoL) in people living with HIV, especially as they age. We aimed to examine the effect of unmet basic needs across age groups on changes in HRQoL over a 4-year period in persons with HIV. Physical and mental HRQoL scores from the Positive Spaces, Healthy Spaces cohort interviewed in 2006 (n = 538), 2007 (n = 506), and 2009 (n = 406) were examined across three age groups according to their unmet needs for food, clothing, and housing. Individual growth curve model analyses were used to investigate changes over time, adjusting for demographics, employment, living conditions, social supports, HIV status, and health behavior risks. Low scores on physical and mental HRQoL were positively associated with higher number of unmet basic needs (β = -6.40, standard error (SE) = 0.87, p < 0.001 and β = -7.39, SE = 1.00, p < 0.001, respectively). There was a slight improvement in physical and mental HRQoL over 4 years in this HIV cohort, but the burden of unmet basic needs took its toll on those over 50 years of age. Regularly assessing unmet basic needs is recommended given the impact these can have on HRQOL for people living with HIV. Recognition of unmet needs is vital, as is the development of timely interventions.
Article
Purpose: Given the steady rise in HIV incidence among South Asian women in Canada their health-related challenges and disability are not well understood. Our aim was to understand the ‘lived experiences’ of disability among South Asian women living with HIV in Southern Ontario, Canada. Methods: We conducted a qualitative study using an interpretive phenomenological approach. We recruited immigrant South Asian women living with HIV in Ontario and conducted one-on-one semi structured interviews. Following the first interview, participants were invited to participate in a second interview. Interviews were audio recorded and transcribed verbatim. Results: Eight participants completed the first interview; six completed a second interview (14 interviews total). The mean age of participants was 47.1 years (standard deviation (sd)=5.8) and mean length of time since HIV diagnosis was 15.1 years (sd=6.7). We identified two overarching themes, “experiencing disability” and “experiencing discrimination”. Apart from the physical and mental health impairments, the complex intersection of illness, gender, ethnicity, HIV-stigma and discrimination influenced disability experiences. Conclusion: Understanding the disability experiences of marginalized women living with HIV through a phenomenological lens can help to facilitate the development of culturally safe treatment approaches and health care policies to lessen disability and improve their quality of life.
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An interdisciplinary description of the cognitive and emotional functioning of HIV-infected individuals treated according to the latest world standards. The authors summarize the results of many years of pioneering research in Poland on the impact of aging on the course of HIV infection, characterizing the neuropsychological functioning of HIV+ subjects and analyzing the state of brain structures and activity in relation to the neuropsychological and chemosensory functions of the project participants.
Article
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Purpose The aim of this study was to investigate the heterogeneity of changes in affective states, i.e., positive (PA) and negative (NA) affect, as well as the sociodemographic and clinical covariates of these changes among people living with HIV (PLWH) in a 1-year prospective study. Method Participants were 141 ambulatory patients (15% female) with a confirmed diagnosis of HIV infection who were undergoing antiretroviral treatment. Their affective states were assessed three times, with 6-month intervals, using the positive and negative general affect scale (PANAS-X). Sociodemographic (gender, age, relationship status, education, employment) and clinical variables (CD4 count assessed via self-report, HIV/AIDS status, time since HIV diagnosis and antiretroviral treatment duration) were also obtained. Results Heterogeneity of changes was present only for NA, whereas PA decreased gradually in the whole sample. Time since diagnosis was unrelated to baseline affect levels as well as affect level changes. Additionally, the trajectories of NA and PA were independent of each other. The significant correlates of trajectories were gender and CD4 counts, both baseline CD4 levels and CD4 changes. Conclusion This study adds to the literature by describing affect changes among PLWH and identifying potential correlates of these changes, particularly CD4 count and gender. As such, these findings point to the potential clinical significance of further research on the roles of these variables.
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Objective: We evaluated improvement of quality of life (QoL) after one year of second-line antiretroviral therapy (ART) use in resource-limited settings (RLS) among adult men and women, comparing two randomized treatment arms. Design: ACTG A5273 was a randomized clinical trial of second-line ART comparing lopinavir/ritonavir (LPV/r) + raltegravir (RAL) with LPV/r + nucleos(t)ide reverse transcriptase inhibitors (NRTIs) in participants failing a non-nucleoside reverse transcriptase inhibitor (NNRTI)-containing regimen at 15 sites in 9 RLS. Participants completed the ACTG SF-21 which has 8 QoL domains with a standard score ranging from 0 (worst) to 100 (best). Methods: Differences in QoL by randomized arm, as well as by demographic and clinical variables, were evaluated by regression models for baseline and week 48 QoL scores fitted using the generalized estimating equations method (GEE). Results: 512 individuals (49% male, median age 39 years) were included. 512 and 492 participants had QoL assessments at baseline and week 48, respectively. QoL improved significantly from week 0 to 48 (p < 0.001 for all domains). There was no significant difference between treatment arms for any domain. Individuals with higher VL and lower CD4 at baseline had lower mean QoL at baseline but larger improvements such that mean QoL was similar at week 48. Conclusions: Improvements in QoL were similar after starting second-line ART of LPV/r combined with either RAL or NRTIs in RLS. QoL scores at baseline were lower among participants with worse disease status prior to starting second-line, but after one year similar QoL scores were achieved.
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The aim of the study was to explore gender differences in the level of health-related quality of life (HRQoL) and coping strategies among people living with the human immunodeficiency virus (HIV) (PLWH). In particular, the moderating role of participants’ gender on the relationship between coping strategies and HRQoL was explored, while controlling for socio-medical data. A total of 444 HIV-infected men and 86 HIV-infected women were recruited to participate in the study. This was a cross-sectional study with the HRQoL assessed by the World Health Organization (WHO) Quality of Life-BREF (WHOQOL-BREF) and the coping strategies measured by the Brief COPE inventory. Although the HIV-infected men and HIV-infected women differed in terms of some HRQoL domains, these differences disappeared in the regression analysis after controlling for socio-demographic data (employment and higher education). In addition, several statistically significant interactions between participants’ gender and coping strategies in relation to HRQoL domains were observed. Future research on gender differences in HRQoL among PLWH should take into account unique differences between HIV-infected men and HIV-infected women across, not only in respect to socio-medical factors but also regarding psychosocial variables.
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AimA systematic review of reviews was conducted to identify and appraise brief measures of health-related quality of life (HRQoL) that have been used in peer-reviewed research with people living with HIV. Methods The review was conducted in two stages: 1) search of electronic databases to identify systematic reviews of tools used to measure HRQoL in adults living with HIV, published since the year 2000; 2) selection of HRQol scales from those identified in the reviews. Inclusion criteria included scales that could be self-administered in 10 min or less, covering at least 3 domains of quality of life (physical function, social/role function and mental/emotional function). For generic scales, inclusion criteria included the availability of normative data while for HIV-specific scales, patient input into the development of the scale was required. ResultsTen reviews met the inclusion criteria. Nine generic scales met the inclusion criteria: the EuroQol five dimensions questionnaire (EQ-5D); Health Utilities Index; McGill Quality of Life questionnaire; Medical Outcomes Study (MOS) Short Form (SF)-12; SF-36; World Health Organisation Quality of Life (WHOQOL- BREF), Questions of Life Satisfaction (FLZM) and SF-20. Available psychometric data supported the EQ-5D and SF-36. Seven HIV-specific scales met the inclusion criteria: the AIDS Clinical Trials Group (ACTG)-21; HIV-QL-31; MOS-HIV; Multidimensional Quality of Life Questionnaire for Persons with HIV/AIDS (MQOL-HIV), PROQOL-HIV, Symptom Quality of Life Adherence (HIV-SQUAD) and the WHOQOL-HIV BREF. Of the HIV -specific measures, the MOS-HIV was considered to have the most well-established psychometric properties, however limitations identified in the reviews included insufficient input from people living with HIV in the development of the scale, cross-cultural relevance and continued applicability. Two relatively new measures, the WHOQOL-HIV BREF and PROQOL-HIV, were considered to have promising psychometric properties and may have more relevance to people living with HIV. Conclusion The findings highlight the need for further validation of HRQoL measures in people living with HIV. The choice of one measure over another is likely to be influenced by the purpose of the quality of life assessment and the domains of HRQoL that are most relevant to the specific research or clinical question.
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Background: Research suggests that HIV stigma exerts a detrimental impact on the mental health of HIV-positive gay and bisexual men (GBM). We sought to better understand these processes by examining two forms of HIV stigma (i.e., anticipated and internalized) at two levels (i.e., individual and situational) in association with daily negative affective experiences. Methods: We conducted a 21-day twice-daily ecological momentary assessment study of 51 HIV-positive GBM. Twice-daily stigma measures were disaggregated into individual-level averages and situational fluctuations, and we utilized multilevel models to examine both concurrent and time-lagged effects of HIV stigma on anxious affect, depressed affect, anger, fatigue, and emotion dysregulation. Results: Situational experiences of internalized HIV stigma were associated with increased levels of anxious and depressed affect, anger, and emotion dysregulation in both concurrent and time-lagged analyses. Situational experiences of anticipated HIV stigma were only associated with anger and only within concurrent analyses. Individual-level internalized HIV stigma was associated with anxious affect and emotion dysregulation in both concurrent and time-lagged models, and with depressed affect and fatigue in time-lagged models. Limitations: The small and high-risk sample limits generalizability and results should be replicated in larger and more diverse samples. Conclusions: These findings suggest that, independent of the effects of individual-level stigma, situational experiences of internalized HIV stigma are associated with increases in event-level negative affective experiences. A combination of individually-delivered and mobile interventions may be successful at reducing the impact of internalized HIV stigma on negative affect and emotion dysregulation.
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Objective The aims of this study were: (i) to determine the factors associated with HRQOL at baseline in our cohort, and (ii) to evaluate if there are differences in baseline HRQOL measures by antiretroviral treatment. Methods The Short Form 36 (SF-36) was administered between 2006 and 2010 among members of the United States HIV Natural History Study cohort (NHS), and participants who completed the SF-36 were included in the study. Physical component summary (PCS) and mental component summary (MCS) scores were computed based on standard algorithms. Multivariate linear regression models were constructed for PCS and MCS to estimate the association between selected variables and HRQOL scores. Results Antiretroviral therapy (ART) was not independently associated with HRQOL scores. Factors associated with PCS were CD4+ count < 200 cells/mm³ (β = -5.84, 95% CI: -7.63, -4.06), mental comorbidity (β = -2.82, 95% CI: -3.79, -1.85), medical comorbidity (β = -2.51, 95% CI: -3.75, -1.27), AIDS diagnosis (β = -2.38, 95% CI: -3.79, -0.98). Others were gender, military rank, marital status, and age. Factors independently associated with MCS were CD4+ count < 200 cells/mm³ (β = -1.93, 95% CI: -3.85, -0.02), mental comorbidity (β = -6.25, 95% CI: -7.25, -5.25), age (β = 0.37, 95% CI: 0.14, 0.60), and being African American (β = 1.55, 95% CI: 0.63, 2.47). Conclusion Among military active duty and beneficiaries with HIV, modifiable factors associated with HRQOL measures included advanced HIV disease, and mental or medical comorbidity. Addressing these factors may improve quality of life of HIV-infected individuals in the NHS cohort.
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Among people living with HIV/AIDS (PLHIV), health-related quality of life (HRQOL) is an important clinical metric of perceived well-being. Baseline data from the BEACON study (N = 383) were used to examine relationships between HRQOL and negative social support, HIV-related stigma, viral suppression, and physical and mental health service use among a vulnerable population of low-income, urban PLHIV who currently or formerly used substances, and were primarily African American. Factor analyses and structural equation modeling indicated that increases in negative social support, stigma, mental health care visits and HIV physician visits were associated with lower HRQOL, while viral suppression was associated with greater HRQOL. The association between negative social support and HRQOL suggests the importance of intervening at the dyad or network levels to shape the type of social support being provided to PLHIV. HIV-related stigma is another negative social factor that is prevalent in this sample and could be addressed by intervention. Results indicate that greater mental and physical health service use can be used to identify individuals with lower HRQOL. Therefore, findings increase an understanding of HRQOL in this understudied population and have implications for designing interventions to improve HRQOL among PLHIV.
Article
: Using data from the National HIV Surveillance System, we examined HIV infections diagnosed between 2010 and 2015 attributed to heterosexual contact with partners previously known to be HIV infected. More than 4 in 10 HIV infections among heterosexual males and 5 in 10 HIV infections among heterosexual females were attributed to this group. Findings may inform the prioritization of prevention and care efforts and resource allocation modeling for reducing new HIV infection among discordant partnerships.
Article
Objective: To determine if immediate compared to deferred initiation of antiretroviral therapy (ART) in healthy persons living with HIV (PLWH) had a more favorable impact on health-related quality of life (QOL), or self-assessed physical, mental and overall health status. Design: QOL was measured in START (Strategic Timing of Antiretroviral Therapy), which randomized healthy ART naive PLWH with >500 CD4+ cells/μl from 35 countries to immediate versus deferred ART. Methods: At baseline, months 4 and 12, then annually, participants completed a visual analogue scale (VAS) for "perceived current health" and the Short-Form 12-Item Health Survey version 2 from which were computed: (1) General health (GH) perception; (2) Physical Component Summary (PCS), and (3) Mental Component Summary (MCS); the VAS and GH were rated from 0 = lowest to 100 = highest. Results: QOL at study entry was high (mean scores: VAS = 80.9, GH = 72.5, PCS = 53.7, MCS = 48.2). Over a mean follow-up of 3 years, changes in all QOL measures favored the immediate group (p < 0.001); estimated differences were: VAS = 1.9, GH = 3.6, PCS = 0.8, MCS = 0.9. When QOL changes were assessed across various demographic and clinical subgroups, treatment differences continued to favor the immediate group. QOL was poorer in those experiencing primary outcomes; however, when excluding those with primary events, results remained favorable for immediate ART recipients. Conclusions: In an international randomized trial in ART-naive participants with >500 CD4+ cells/μl, there were modest but significant improvements in self-assessed QOL among those initiating ART immediately compared to deferring treatment, supporting patient-perceived health benefits of initiating ART as soon as possible after an HIV diagnosis.