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Effect of Vitamin D Supplementation on Weight Loss, Glycemic Indices, and Lipid Profile in Obese and Overweight Women: A Clinical Trial Study

Authors:

Abstract

Introduction Vitamin D (vit D) deficiency has defined as a health problem worldwide. World Health Organization (WHO) has declared that obesity is an epidemic of the 21st century. Previous studies have shown that obesity may increase the risk of Vit D deficiency. Furthermore, other studies have demonstrated that vit D insufficiency was accompanied with higher risk of type 2 diabetes, cardiovascular diseases, hypertension, and obesity. The aim of this study was to survey the effect of vit D supplementation on weight loss among overweight and obese women aged 20–40 years in Isfahan. Methods This double-blind clinical trial was done on 50 overweight and obese women who were divided into two groups, in which one group received vit D supplements and the other group received placebo. Intervention group received vit D with dozes 50,000 IU/w for 6 weeks. The levels of total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-c), high-density lipoprotein cholesterol (HDL-c), fasting blood sugar (FBS), insulin (ins), homeostasis model assessment of ins resistance (IR), C-reactive protein (CRP), height, weight (WT), waist circumference (WC), hip circumference (HC), and blood pressure (BP) were measured before and after intervention. Results After using vit D supplementation for 6 weeks, WT, WC, and body mass index (BMI) were decreased significantly and serum vit D increased significantly compared to control group (P < 0.001). Other factors including TC, TG, LDL-c, HDL-c, FBS, CRP, ins, IR, and waist to hip ratio (WHR) did not change significantly (P > 0.05). Conclusions After 6 weeks of intervention, the means of WT, BMI, WC, and HC decreased significantly. Previous studies have shown that vit D deficiency was more prevalence in obese people and there was an inverse association among vit D with BMI and WC. The relationship between vit D and lipid profiles such as glycemic indexes, anthropometric indexes, CRP, and BP is not clear and needs more study in the future.
1© 2018 International Journal of Preventive Medicine | Published by Wolters Kluwer - Medknow
Introduction
Vitamin D (vit D) deciency is considered
as a health problem worldwide. Nowadays,
vit D deciency has involved more than
half of people worldwide.[1] The prevalence
of vit D deciency in Tehran and Isfahan
was estimated about 81/3% and 70/16%,
respectively.[2] vit D plays an important role
in calcium metabolism, maintenance of the
skeleton, control of cell proliferation and
differentiation, and immunity.[3] Recently,
it has been shown that vit D deciency
has a strong relationship with increased
risk of type 2 diabetes, cardiovascular
disease (CVD) as well as CVD risk
factors such as hypertension and
obesity.[4] Obesity was recognized as an
epidemic of the 21st century by World
Health Organization (WHO)[5] and it is a
serious health problem worldwide.[5,6] Since
Address for correspondence:
Dr. Mohammad Hasan Entezari,
Department of Clinical
Nutrition/Community
Nutrition/Food Science and
Technology, Food Security
Research Center, School of
Nutrition and Food Science,
Isfahan University of Medical
Sciences, Isfahan, Iran.
E‑mail: entezari@hlth.mui.ac.ir
Abstract
Introduction: Vitamin D (vit D) deciency has dened as a health problem worldwide. World
Health Organization (WHO) has declared that obesity is an epidemic of the 21st century. Previous
studies have shown that obesity may increase the risk of Vit D deciency. Furthermore, other studies
have demonstrated that vit D insufciency was accompanied with higher risk of type 2 diabetes,
cardiovascular diseases, hypertension, and obesity. The aim of this study was to survey the effect
of vit D supplementation on weight loss among overweight and obese women aged 20–40 years in
Isfahan. Methods: This double‑blind clinical trial was done on 50 overweight and obese women
who were divided into two groups, in which one group received vit D supplements and the other
group received placebo. Intervention group received vit D with dozes 50,000 IU/w for 6 weeks.
The levels of total cholesterol (TC), triglyceride (TG), low‑density lipoprotein cholesterol (LDL‑c),
high‑density lipoprotein cholesterol (HDL‑c), fasting blood sugar (FBS), insulin (ins), homeostasis
model assessment of ins resistance (IR), C‑reactive protein (CRP), height, weight (WT), waist
circumference (WC), hip circumference (HC), and blood pressure (BP) were measured before and
after intervention. Results: After using vit D supplementation for 6 weeks, WT, WC, and body mass
index (BMI) were decreased signicantly and serum vit D increased signicantly compared to control
group (P < 0.001). Other factors including TC, TG, LDL‑c, HDL‑c, FBS, CRP, ins, IR, and waist to
hip ratio (WHR) did not change signicantly (P > 0.05). Conclusions: After 6 weeks of intervention,
the means of WT, BMI, WC, and HC decreased signicantly. Previous studies have shown that vit
D deciency was more prevalence in obese people and there was an inverse association among vit
D with BMI and WC. The relationship between vit D and lipid proles such as glycemic indexes,
anthropometric indexes, CRP, and BP is not clear and needs more study in the future.
Keywords: Blood pressure, cholesterol, high‑density lipoprotein, low‑density lipoprotein,
triglyceride, Vitamin D supplementation, weight loss, glycemic indices
Effect of Vitamin D Supplementation on Weight Loss, Glycemic Indices,
and Lipid Prole in Obese and Overweight Women: A Clinical Trial Study
Original Article
Zahra Sadat
Khosravi,
Marzieh Kafeshani1,
Parastoo Tavasoli,
Akbar Hassan Zadeh2,
Mohammad Hassan
Entezari1
Departments of Clinical
Nutrition and 1Clinical
Nutrition/Community Nutrition/
Food Science and Technology,
Food Security Research Center,
School of Nutrition and Food
Science, Isfahan University of
Medical Sciences, Isfahan, Iran,
2Department of Epidemiology
and Biostatic, School of Health,
Isfahan University of Medical
Sciences, Isfahan, Iran
How to cite this article: Khosravi ZS, Kafeshani M,
Tavasoli P, Hassan Zadeh A, Entezari MH. Effect
of Vitamin D supplementation on weight loss,
glycemic indices, and lipid prole in obese and
overweight women: A clinical trial study. Int J Prev
Med 2018;9:63.
19th century, the prevalence of obesity has
increased along with changes in diets and
lifestyle factors.[7] WHO estimated that at
least 300 million adults are obese and more
than 1 billion are overweight worldwide.[7,8]
It is proved that 3.4 million of obese and
overweight people are died due to obesity
and comorbidities including hypertension,
type 2 diabetes, stroke, CVD, some type
of cancer such as prostate, breast, ovary,
cervix, colon, and gallbladder every
year.[5,9] In addition, obesity is related
with hypercholesterolemia, osteoarthritis,
gastroesophageal reux, sleep apnea, and
kidney chronic disease.[10] Furthermore, this
issue becomes a general health problem
In Iran. The prevalence of obesity and
overweight was 42% in men and 57% in
women in 2005, and it was anticipated
to reach 54% and 74% among men and
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DOI:
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Khosravi, et al.: Vitamin D supplementation, weight loss, glycemic indices, and lipid prole
International Journal of Preventive Medicine 2018, 9: 632
women, respectively by 2015.[11] A study In Iran showed
that obesity in women are more than twice than men.[12]
In a performed study in Isfahan, all women over than
65 years had abdominal obesity.[13] Lifestyle modication
such as proper exercise is the best and cheapest way for
decreasing the obesity. In addition, diet plays a key role in
weight loss programs.[7] Today’s attention toward the role
of vit D in chronic diseases such as obesity is increasing.
Based on several studies, obese and overweight people
mostly have a lower levels of vit D than those who have
less body fat.[14] Some studies suggested that obesity
increased risk of vit D deciency[15] whereas other studies
shown that insufcient levels of vit D could increase
the risk of type 2 diabetes, CVD, and risks such as
hypertension and obesity.[16] A previous study has shown
that vit D deciency is more common in obese people.
It was seen that there is an inverse association
among vit D with body mass index (BMI) and waist
circumference (WC).[4,17‑20] However, conicting results
had been seen such as a study among Iranian individuals
aged 20–64 years with BMI of 24.2 ± 3.8 (57% female)
which has not shown signicant association between
serum levels of vit D and BMI.[4] In this study, we tried
to perform a comprehensive assessment about the effects
of vit D supplementation and body weight as well as other
anthropometric measurements, BP, lipid prole, glycemic
indices, and C‑reactive protein (CRP) among Iranian
women. Therefore, our main purpose was to examine the
effect of vit D on weight loss in obese and overweight
women aged 20–40 years in Isfahan.
Methods
Subjects
This double‑blind clinical trial study was performed
among overweight and obese women in Isfahan
endocrine and metabolism center, and other participants
were female students of Isfahan University of Medical
Science. Convenient method was used to enroll
participants to the study. The following inclusion criteria
was used to select participants: 20–40 years females,
BMI higher than 25 (obese and overweight), nonsmoking,
no history of diabetes, no hyperthyroids and hypothyroids,
no participation in other weight loss programs, no weight
loss during two past months, regular menstrual cycle,
and no pregnancy. The general questionnaire included
information about demographic characteristics such as
location, education level, marital status and the number
of pregnancy and children. In addition, we asked other
questions about physical activity, the duration and times
of sleep, consumption of supplements, and being on a
special of diet. After giving general overview about this
study, all individuals provided informed written consent.
Study design
The aim of this double‑blind clinical trial study was to
evaluate the effect of vit D supplementation on weight
loss in 20–40 years obese and overweight women in
Isfahan. The enough sample size was 25 person in each
group that calculated according to the following formula
N = (z1+z2 2s²/d². In this formula, α was considered
0.05 and β was 80%. Hence, we recruited 75 persons to
compensate potential losses during 6 weeks at follow‑up.
After that, individuals were randomly divided into two
groups (intervention and control) and received vit D
supplements and placebo, respectively. The participants
continued their usual diet during the study. The
intervention follow‑up was 6 weeks that began from May
21, 2013 to July 5, 2013. At the rst visit, we gave 6 pearls
of vit D supplements to intervention group and 6 pearls of
placebo to the controls and we asked them to eat one per
week. Supplements were made in Zahravi pharmaceutical
company, Tabriz, Iran. The dozens of supplements were
50,000 IU and placebo had the same shape, color, and
packaging with given supplement. In addition, at the rst
meeting, food record has been explained to the individuals
and they were asked to prepare it for 3 days including one
weekend and 2 week days. Furthermore, the individuals
were asked to report their physical activity during one
selected week. In addition, participants recorded their
daily amount of sun exposure from sunrise till sunset.
The levels of total cholesterol (TC), triglyceride (TG),
low‑density lipoprotein cholesterol (LDL‑c), high‑density
lipoprotein cholesterol (HDL‑c), fasting blood
sugar (FBS), insulin (ins), homeostasis model assessment
of ins resistance (HOMA‑IR), CRP, vit D, height (ht),
WT, WC, blood pressure (BP), and BMI were measured
at the beginning and the end of study. Furthermore,
anthropometric indicators and BP were measured. ht
was measured by tape without shoes, nearest to the
0.1 cm, and for weight, we used a Beshel model digital
scale (Germany) nearest to the 0.1 kg that individuals
wore light clothing with no shoes. BMI was calculated
with this formula, BMI = weight (kg)/height² (m). BMI
between 24/9 and 29/9 was dened as overweight and
more than 29/9 was dened obese. Individuals’s BP
was measured by trained personnel using a mercury
sphygmomanometer, after 10 min of rest in a sitting
position.
Biochemical analysis
Blood samples were taken in a sitting position following
12–14 h overnight fasting before and after the intervention.
FBS, lipid proles, and CRP were measured by biochemical
autoanalyzer A15 with Biosystem kit (made by Spain).
ELISA method was used to determine concentration of vit
D and ins. In addition, we obtained the ins sensitivity with
using this formula: (fasting ins [micro unit/ml] * fasting
glucose [micro mol/l]/22.5).[8]
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Khosravi, et al.: Vitamin D supplementation, weight loss, glycemic indices, and lipid prole
International Journal of Preventive Medicine 2018, 9: 63 3
Statistical analysis
Normal distributions of all variables were analyzed by the
Kolmogorov–Smirnov test and by evaluating the histogram
curves. All variables had normal distribution. Analyses
were performed with independent t‑test and paired t‑test.
The data were analyzed with SPSS version 20 (IBM,
Armonk, NY, USA). The signicance was considered 0.05.
Independent t‑test and Chi‑square was used  to comparison
the general characteristics of participants.
Results
From 75 potentially eligible participants, 6 persons were
excluded due to the personal reasons, 8 persons had
normal serum levels of vit D, and 5 blood specimens
were devastated due to the laboratory personnel mistake.
We could not take blood from 3 participants because
of high weight. Hence, they were eliminated. Finally,
we had 53 individuals that 26 of them were assigned
to intervention group and 27 of them were entered into
control group. The baseline characteristics of 53 obese and
overweight women are shown in Table 1. Anthropometric
variables of participants are presented in Table 2.
According to data, there were no signicantly differences
in baseline anthropometric variables between intervention
and control groups except WC which was signicantly
higher (P = 0.04) in intervention group. The analysis showed
that in intervention group, the means of weight, BMI, and
WC were reduced signicantly (73.2 ± 7.6–71.6 ± 7.7,
28 ± 2.7–27.2 ± 2.8, 90.4 ± 7.2–88 ± 7.5, respectively)
(P < 0.001), but WHR (0.85 ± 0.05–0.84 ± 0.06) did
not change signicantly [Table 2]. As it has shown in
Table 3, there were no differences in means of dietary
energy, macronutrient, and micronutrient such as vit D of
participants between two groups. Biochemical variables
were reported in Table 4. The assessment of biochemical
markers (HDL‑c, LDL‑c, TC, TG, FBS, Ins, HOMA‑IR) in
two groups shown that there were no signicant differences
in all of the biochemical variables (P > 0.05), except for
the vit D that was 21.9 ± 6.5 in intervention and 18.1 ± 4.8
in control groups (P < 0.01). The mean of differences in
anthropometric and laboratory variables were presented
in Table 5. After calculating the mean of differences in
two groups, it was cleared that intervention with the vit
D (P < 0.001) decreased the means of weight (1.6 ± 1.3),
BMI (0.6 ± 0.5), and WC (2.3 ± 1.1) and increased
the mean of vit D (62 ± 29, P < 0.001). Furthermore,
after adjusting for age, the means of the vit D was
signicant (83.49 ± 5.43, 34.2 ± 5.33 P = 0.001).
Discussion
The ndings of this double‑blind clinical trial study in obese
and overweight women aged 20–40 years showed that
supplementation of the vit D with dozes 50,000 IU/w for
6 weeks reduced signicantly the mean of BMI, weight, WC,
and on the other hand, it increased signicantly the level of
vit D in comparison with the control group. However, there
were no signicant effect of the vit D on other factors such
Table 1: Baseline characteristics of the participants
Parameter Intervention
(n=260)
Control
(n=27)
P*
Age 29.1±9.6 26.9±9.1 0.4
The number of children 1.0±1.3 0.48±0.93 0.06
Job (%)
Homeworker 30.80 25.90 0.54
Student 53.80 66.70
Employee 15.40 7.4
Marital status (%)
Single 53.80 33.3 0.13
Married 46.20 66.70
Education level (%)
Less than high school 3.8 11.10 0.24
High school and higher 46.2 18.50
College education and higher 50.00 70.40
Physical activity (min/week) 874.8±697.1 604.5±643.4 0.14
Sun exposure (min/day) 49.6±40 61.5±49.3 0.34
*P<0.05 is signicant; obtained from independent t‑test and
χ2, Values are mean±SD. SD=Standard deviation
Table 2: Anthropometric variables of the participants
Variables Intervention
(n=26)
Control
(n=27)
P*,‡
Weight (kg)
Baseline 73.2±7.6 70.3±9 0.02
End 71.6±7.7 70.3±9
P*0.001 0.81
Height 162±7 158.8±6 0.8
BMI (kg/m²)
Baseline 28±2.7 27.8±2.6 0.91
End 27.2±2.8 27.8±2.7 0.4
P*0.001 0.81
WC (cm)
Baseline 90.4±7.2 86±8 0.04
End 88±7.5 86.3±8.5 0.42
P*0.001 0.27
WHR
Baseline 0.85±0.05 0.81±0.05 0.4
End 0.84±0.06 0.82±0.06 0.4
P*0.23 0.44
SBP (mmHg)
Baseline 112.7±8.5 112.5±5 0.9
End 112.3±10 112±6.5 0.8
P*0.8 0.6
DBP (mmHg)
Baseline 80±6.5 78.5±8.5 0.4
End 78±5 76±6 0.2
P*0.15 0.17
*P<0.05 is signicant, Values are mean±SD, For comparison of
between‑group differences by an independent t‑test. BMI=Body
mass index, WC=Waist circumference, WHR=Waist to hip ratio,
SBP=Systolic blood pressure, DBP=Diastolic blood pressure,
SD=Standard deviation
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Khosravi, et al.: Vitamin D supplementation, weight loss, glycemic indices, and lipid prole
International Journal of Preventive Medicine 2018, 9: 634
as hip circumference (HC), WHR, SBP, diastolic BP (DBP),
lipid proles, glycemic indexes, and CRP. Supplemental
interventions on women aged 20–40 years were our study
target because they were as mothers and had an important
role in prevalence of chronic diseases and therefore health
of society. The result of this study demonstrated that
supplementation of the vit D in obese and overweight
women reduced signicantly the mean of weight, BMI, and
WC. Previous studies had shown that the vit D deciency
is more prevalent in obese people and there was an inverse
association between vit D, BMI, and WC.[3,4,9,11,13‑21] Vashi
et al. showed that 1 kg/m² increase in BMI was associated
with signicantly reduced vit D level (42% ng/ml).[22] In
another study, there was a signicant inverse relationship
after adjusting all confounding that associated with vit
D and BMI.[23] However, conicting results have been
seen[3,17,24] such as a study on Iranian 20–64 years with BMI
24.2 ± 3.8 (57% female) which had not shown signicant
association between the level of vit D and BMI. Probably,
its main reason was BMI, which was 24.2 and in the normal
range. In addition, it could be another reason that only 48%
of individuals had vit D deciency.[17] In some studies,
the inverse association between vit D and WC has been
seen.[22,25] In one of these studies, vit D also had a signicant
association with HC.[25] In Seo’s study only, this association
between vit D and WC has been seen in women.[14]
Our study did not have a signicant effect on FBS, ins, and
HOMA‑IR. A study in 2012 has not found any signicant
effect on FBS and HOMA‑IR with supplementation of
vit D with dozes 1000 IU/d during 1 year.[26] In another
study, there was no signicant relationship between vit
D and HOMA‑IR because of participants were healthy
overweight adults with normal FBS.[3] From this aspect, it
was similar to our study. Furthermore, in several studies,
vit D did not have a relationship with fasting ins, IR,
and fasting glucose.[20,27‑30] Of course in some studies, vit
D had an inverse effect on HOMA‑IR, fasting ins, and
FBS.[16,18] We could not nd any signicant effect of vit
D; this effect may be seen in long‑term studies. In this
study, we could not nd any role of vit D on the lipid
prole such as TG, TC, HDL‑c, and LDL‑c. Result of
this study were approved by previous studies.[31‑33] In
Moghassemi and Marjani’s study of Iran, after 12 weeks
supplementation with the vit D, lipid prole did not
change signicantly.[31] Also, in a randomly clinical trial
on women has not found any changes in lipid prole that
it maybe related to short duration of study and dose
of the vit D.[23] In addition, some studies such as Women
Health Initiative that had longer duration and dose of the
vit D was 200 IU that take it twice a week for 7 years
has not found changes in lipid prole.[33] In several
Table 3: Dietary intake of participants before study
Nutrient Intervention
(n=26)
Control
(n=27)
P*,‡
Energy (kcal) 2096±6.3 2117±661 0.9
Carbohydrate (g) 292±107 300±157 0.8
Protein (g) 83±36 102.5±89 0.5
Fat (g) 73.5±31 78.5±77 0.3
Saturated fatty acid (g) 20±8 24.5±23 0.4
Polyunsaturated fatty acid (g) 21.5±12 22±15 0.8
Monounsaturated fatty acid (g) 32.2±118 42±214 0.7
Fiber soluble (g) 0.5±0.2 0.8±1.5 0.3
Fiber insoluble (g) 4.5±8 6±12.5 0.5
Calcium (mg) 841±363 899±646 0.7
Vitamin D (Ug) 1.4±1.9 1.3±2 0.93
*P<0.05 is signicant, Values are mean±SD, For comparison of
between‑group differences by an independent t‑test. SD=Standard
deviation
Table 4: Biochemical variables in participants
Variable Intervention
(n=26)
Control
(n=27)
P*,‡
HDL‑C (mg/dl)
Baseline 42.8±11.5 48.7±16 0.1
End 42.8±8.7 44.3±10 0.5
P0.1 0.7
LDL‑C (mg/dl)
Baseline 89.5±25 91.4±27 0.8
End 92.7±25.5 87.5±21.2 0.4
P0.3 0.3
TC (mg/dl)
Baseline 184.3±37 188.7±42.5 0.7
End 184±34 176.5±28 0.4
P0.9 0.07
FBS (mg/dl)
Baseline 96.8±12 101±13 0.2
End 90.5±9.5 91.2±12 0.8
P0.01 0.003
TG (mg/dl)
Baseline 118±90 109.5±56 0.7
End 120.5±111 100±48 0.4
P0.8 0.1
Vitamin D (nmol/l)
Baseline 22±6.5 18±5 0.01
End 84±30.5 34±24 0.001
P0.001 0.001
Insulin (mg/dl)
Baseline 10.2±6 9.5±5 0.6
End 13±8 10±6 0.1
P0.09 0.5
HOMA‑IR (mU/l)
Baseline 2.4±1.5 2.4±1.1 0.84
End 2.9±1.9 2.2±1.5 0.16
P0.25 0.7
*P<0.05 is signicant, Values are mean±SD, For comparison
of between‑group differences by an independent t‑test for
comparison of within‑group differences by an paired t‑test.
TC=Total cholesterol, TG=Triglyceride, LDL‑C=Low‑density
lipoprotein cholesterol, HDL‑C=High‑density lipoprotein
cholesterol, FBS=Fasting blood sugar, SD=Standard deviation,
HOMA‑IR=Homeostasis model assessment of insulin resistance
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Khosravi, et al.: Vitamin D supplementation, weight loss, glycemic indices, and lipid prole
International Journal of Preventive Medicine 2018, 9: 63 5
studies, similar results were obtained.[20,22,26] However,
some studies have found inverse results such as Kim
et al. that after supplementation of the vit D only, HDL‑c
was reduced signicantly.[30] in another study LDL‑c
and TG decreased signicantly[34] but HDL‑c increased
signicantly.[35] In a similar study, after consuming the
supplementation of vit D with dozes 300 IU/d for 3 years,
LDL‑c and TG increased signicantly but TC and HDL‑c
reduced signicantly[36] A meta‑analysis was conducted
on the effects of vit D supplementation on lipid prole.
showed that only LDL was changed signicantly after the
intervention.[25] Overall, there are contradictory results
for the effect of the vit D on lipid proles, so more
investigations are necessary in the future. We have not
seen a signicant relationship between supplementation of
the vit D and BP in our study. A clinical study in Germany
supplementation of the vit D with dozes 100,000 IU did
not cause any changes in BP.[37] In a meta‑analysis that
included 10 interventional studies, after supplementation
of the vit D, no signicant effects was found in systolic
and DBP.[38] As well as several other studies have not
reported the effect of vit D on BP.[26,39,40] Of course, a
study has reported an inverse relationship between vit D
levels and systolic BP in men,[19] but probably, its main
reason was individuals’ age because the aim society in this
study were the individuals with age higher than 65 years
and mostly had a high BP but participants in our study
were individuals with age 20–40 years that mostly had a
normal BP. Another possible reason was the difference in
gender.
We could not nd any effect of the vit D on CRP in our
study. In a study on the healthy population, vit D had no
effect on CRP.[26] Forooghi et al. in Iran have not found
effect of vit D on CRP too.[41] Furthermore, another
studies had similar results. In some studies, an inverse
association has been seen between vit D and CRP. It means
that supplementation of the vit D can reduce CRP.[42,43] In
an interventional study on obese people, CRP increased
signicantly.[16] According to the previous studies, the
reason of the vit D deciency in obesity has not cleared yet
but some mechanisms has proposed these reasons for the
relationship between vit D and obesity: trapped of the vit D
in adipose tissue that makes less bioavailability for convert
to the form of 1,25(OH)2D.[10] In a study vit D deciency
was accompanied with abdominal obesity. Therefore, vit
D is lower in serum of obese people, and therefore, its
bioavailability reduces for these individuals.[16] The role
of vit D in causing IR has not cleared yet. Some studies
have suggested that vit D may have benecial effects
on ins responsiveness by stimulating expression of ins
receptors[44] or regulating calcium homeostasis which
is necessary for intracellular ins‑mediated processes.[45]
As regard to the obesity is the most common cause of
ins‑resistance, the relation between vit D and IR might
be the result of increased body size.[16] We could not nd
the effect of vit D on lipid proles, glycemic indexes,
CRP, and BP in this study. Some studies have reported
these effects which were mostly due to the weight loss
and BMI reduction that improved these factors. The
possible effect of vit D on BP may be related to regulation
the renin–angiotensin system, suppression the spread of
proliferation of vascular smooth muscle cells, improvement
IR, modication extended‑dependent cells to endothelium
and inhibition of anticoagulant activity and hypertrophy of
myocardial cells.[46] Possibility mechanism for the effect
of vit D in CRP reduction is that vit D receptors are in
more than 37 body tissues that effect on these organs by
their receptors and regulate pro‑inammatory mechanisms
and systematic inammation in the body. Vit D receptors
are located in the nucleus of macrophages. Some of these
macrophages produce cytokines, especially Tumor necrosis
factor (TNF)‑α. TNF‑α expression signicantly depends
on the effect of NF‑β. Increased vit D inhibits the protein
expression of NF‑β and reduces the expression of NF‑β and
thus reduces the level of TNF‑α. In addition, vit D binds
to receptors on monocytes and so produce in ammatory
cytokines, CRP and reduces systemic in ammation.[41]
We performed this study as an interventional that gave us
a more acceptable result. We included women aged 20–
40 years that were at risk for vit D de ciency had more
exposure to disease in the future.
Limitations
The short duration of the study and increase in the levels
of the vit D in control group were our limitation. One of
Table 5: The mean of differences in anthropometric and
biochemical variables
Variable Intervention
(n=26)
Control
(n=27)
P*,‡
Weight (kg) −1.6±1.3 0.05±1 0.001
BMI −0.61±0.5 0.02±0.5 0.001
WC (cm) −2.3±1 0.3±1.5 0.001
WHR 0.01±0.04 −0.0008±0.03 0.22
HDL‑C (mg/dl) 0.003±8 −4.4±12.5 0.13
LDL‑C (mg/dl) 3.17±17.5 −4±19 0.17
TC (mg/dl) −0.3±26 −12.2±33.5 0.15
FBS (mg/dl) −6.35±12 −9.5±15.5 0.4
TG (mg/dl) 2.5±48.5 −9±34.5 0.3
Vitamin D 62±29 15.7±22 0.001
Insulin (mg/dl) 3±8 0.66±6 0.27
HOMA‑IR (mU/l) 0.5±2.1 −0.11±1.5 0.23
SBP (mmHg) −0.5±8 −0.75±7 0.9
DBP (mmHg) −2.3±8 −2.6±9.6 0.9
*P<0.05 is signicant, Values are mean±SD, For comparison
of between‑group differences by an independent t‑test. TC=Total
cholesterol, TG=Triglyceride, LDL‑C=Low‑density lipoprotein
cholesterol, HDL‑C=High‑density lipoprotein cholesterol,
FBS=Fasting blood sugar, SBP=Systolic blood pressure,
DBP=Diastolic blood pressure, HOMA‑IR=Homeostasis
model assessment of insulin resistance, BMI=Body mass index,
WC=Waist circumference, WHR=Waist to hip ratio
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Khosravi, et al.: Vitamin D supplementation, weight loss, glycemic indices, and lipid prole
International Journal of Preventive Medicine 2018, 9: 636
the possible causes of this increase can be attributed to
the seasons. With the arrival of summer, the amount and
intensity of the sun increases, and spontaneously, levels
of vit D increases. Entrance healthy obese individuals
with normal laboratory indexes may be the reason for not
signicant effects. The authors declared that there is no
conict of interest.
Conclusions
Overall supplementation of the vit D with dozes
50,000 IU/w for 6 weeks in obese and overweight women
aged 20–40 years reduced in the mean of BMI, weight,
and WC signicantly and vit D increased signicantly
compared to the control group.
Financial support and sponsorship
Nil.
Conicts of interest
There are no conicts of interest.
Received: 13 Oct 15 Accepted: 15 Dec 17
Published: 20 Jul 18
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... Moreover, in our study, vitamin D sup-plementation increased irisin levels in blood and testicular tissue supernatants. Possible reasons why vitamin D supplementation may increase irisin amounts may be due to 1) increasing antioxidant capacity, 2) preventing weight loss through regulating insulin sensitivity, and 3) helping the capacity of irisin-secreting tissues by preventing apoptosis in cells [54][55][56] . ...
... Vitamin D supplementation eliminates these complications. It probably makes this by regulating the antioxidant capacity, increasing insu- lin sensitivity and preventing apoptosis, which is what we have suggested above [54][55][56] . This explains why the atrophic tubule structure and the congestion around the seminiferous tubules observed in the testicular tissues of the rats in the diabetes group were not observed in the testicular tissues of the rats in the diabetes+vitamin D group. ...
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Objective: Diabetes is an important endocrinological disease that has an increasing incidence in the world and affects all biological tissues including testicles. Therefore, this study aimed to reveal the histological and biochemical effects of vitamin D on irisin, apoptosis, total antioxidant status (TAS), and total oxidant status (TOS) in testicular tissues of rats with experimental diabetes. Materials and methods: 41 male Wistar rats, 8-10 weeks old, weighing between 200-220 g, were included in the study as the following groups: control group (n=7; no treatment), sham group [only sodium citrate buffer (SCB)] [n=7; single dose 0.1 Molar (M) SCB given intraperitoneally (i.p)], vitamin D group (n=7; 50 IU/day given orally), diabetes group [n=10; single dose 50 mg/kg Streptozotocin (STZ) dissolved in 0.1 M SCB and given i.p (tail vein blood glucose level above 250 mg/dl after 72 hours)] and diabetes+vitamin D group [n=10, single dose 50 mg/kg STZ, dissolved in 0.1 M SCB and given i.p (tail vein blood glucose level above 250 mg/dl after 72 hours) and when diabetes occurs, oral vitamin D administration of 50 IU/day)]. At the end of the 8 weeks experiment, blood was drawn from the tail vein of all rats, they were sacrificed and testicular tissues were taken. While the amount of irisin in the blood and testicular tissue supernatants was analyzed with the Enzyme-Linked Immunosorbent Assay (ELISA) method, TAS and TOS measurements were analyzed with the REL method, testicular tissues were analyzed histopathologically, immunohistochemically, and with the TUNEL method. Results: When the diabetes group was compared with the control and sham groups, it was reported that the amounts of blood and tissue supernatant irisin and TAS significantly decreased and the TOS was significantly increased; a statistically significant increase in irisin and TAS of blood and tissue supernatants and a significant decrease in TOS were detected when diabetes+vitamin D and diabetes groups were compared among themselves. Similar results were obtained in the immunohistochemical studies. Tissue expressions of irisin decreased in the diabetes group compared to the control and sham groups, while the application of vitamin D increased the tissue expressions of irisin. Additionally, when the numbers of apoptotic cells were compared, it was reported that apoptotic cells in the diabetes group increased significantly compared to the control and sham groups, and vitamin D administration significantly decreased the number of apoptotic cells. Conclusions: Taken together, vitamin D administration to diabetic rats decreased the number of apoptotic cells and increased the amount of irisin. Vitamin D had an effective role in maintaining the physiological integrity of rat testicular tissues, so vitamin D may be a potent agent to be used in the treatment of diabetes in the future.
... As a result, vitamin D may lower cholesterol, triglyceride, and LDL levels by enhancing calcium absorption 72,73 . Other investigations 18,74 , however, have found no significant link between vitamin D levels in NAFLD patients and abnormalities in the lipid profile. ...
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... Regarding lipid profiles, the combination group showed a significant decline in serum levels of cholesterol, triglycerides, and LDL, along with a significant increase in HDL levels at 45 days of the treatment period ( Figure 2). Metformin has been reported to have positive effects on lipid profiles, reducing serum levels of cholesterol, triglycerides, and LDL while increasing HDL levels [29]. A study unveiled that metformin counters IR by preventing weight gain, reducing hyperinsulinemia, and maintaining the lipid profile. ...
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Objective: The association between nutrient intake and obesity and coronary problems has received great attention. So, this study aimed to examine the association between vitamin D, calcium, and magnesium intake and obesity and coronary indices. Methods: A total of 491 male and female university employees (18-64 years) were randomly included in a cross-sectional study. Blood samples were drawn, and the lipid profile was analyzed. Different anthropometrics were measured. Obesity and coronary indices were calculated based on standard formulas. A 24-h recall was used to measure the average dietary intake of vitamin D, calcium, and magnesium. Results: For the total sample, vitamin D had a significantly weak correlation with the abdominal volume index (AVI) and weight-adjusted waist index (WWI). However, calcium intake had a significant moderate correlation with the AVI and a weak correlation with the conicity index (CI), body roundness index (BRI), body adiposity index (BAI), WWI, lipid accumulation product (LAP), and atherogenic index of plasma (AIP). In males, there was a significant weak correlation between calcium and magnesium intake and the CI, BAI, AVI, WWI, and BRI. Additionally, magnesium intake had a weak correlation with the LAP. In female participants, calcium and magnesium intake had a weak correlation with CI, BAI, AIP, and WWI. Additionally, calcium intake showed a moderate correlation with the AVI and BRI and a weak correlation with the LAP. Conclusion: Magnesium intake had the greatest impact on coronary indices. Calcium intake had the greatest impact on obesity indices. Vitamin D intake had minimal effects on obesity and coronary indices.
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Background and Aim Evidence shows that vitamin D deficiency and obesity are associated with impaired physical and mental health. This study aims to investigate the effect of Pilates and vitamin D supplementation on quality of life and mental health of overweight men. Methods & Materials This is a randomized clinical trial with a pre-test/post-test design. Fifty overweight men were selected by a convenience sampling method and were randomly divided into four groups of control, exercise, supplementation, and exercise+supplementation. The exercise and combined groups performed 8 weeks of Pilates at an intensity of 50-75% of heart rate reserve, three sessions per week. The supplementation and combined groups received 50,000 IU vitamin D capsule once per week. Assessment tools were the 36-item Short Form survey (SF-36) and the General Health Questionnaire (GHQ). The data were analyzed by paired t-test, one-way ANOVA and Kruskal-Wallis test. P˂0.05 was statistically significant. Ethical Considerations This study was approved by the research ethics committee of Islamic Azad University, Babol Branch, Iran (Code: IR.IAU.BABOL.REC.1398.088). Results Vitamin D status in subjects was lower than normal (<30 ng/mL) at baseline. Eight weeks of Pilates alone, vitamin D intake alone, and the combined intervention led to a significant increase in SF-36 (10.57%, 9.26% and 15.75%, respectively) and GHQ (12.66%, 10.72% and 17.90%, respectively). However, the effect of combined intervention was higher on the SF-36 (P<0.001) and GHQ (P<0.001) scores compared to two other interventions. Conclusion It seems Pilates alone, vitamin D supplementation alone, and their combination can improve the quality of life and mental health in overweight people with vitamin D deficiency, where the combined intervention is more effective.
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This book is the result of a collective effort to present and develop knowledge in all scientific areas. We would like to thank all participants in this magnificent interdisciplinary work, firstly. We would also like to remind you that the idea of this connection and conversation between diverse areas, all correlated with the improvement of science, is done internationally, preferring to eliminate borders to reach the largest number of people and spread knowledge. In this sense, we quote Bobbio, who says that borders are a great obstacle to reaching all those who are different and that people are people no matter their nationality when he talks about the diffusion of human rights. In this way, this book, despite being indexed in a platform, can reach everyone and fulfill its role of developing and flourishing in different places without excluding people. Finally, we hope, dear reader, that you find this book pertinent, and if you feel instigated, you can contribute to our mission and spread the knowledge through future submissions.
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Chronic diseases continue to globally represent the top cause of death. Although their aetiology is diverse, anthropogens (including factors related to modern lifestyles or behaviours) are considered common risk factors for meta-inflammation and activation of the inflammatory-oxidative cascade involved in the development and progression of many chronic diseases. The interaction of individuals’ genetic background and/or epigenetic changes with exposure to anthropogens and chemicals may represent the early stages of the pathogenesis of chronic diseases such as cancer and cardiovascular diseases, etc. Time-depending variations in anthropogens exposure (particularly during critical exposure windows) can play a key role in their pathophysiology. Since all these elements contribute differently across individuals for the development of chronic diseases, personalized medicine should consider all the responsible factors involved in the development and progression of these diseases in order to optimize their management and treatment. In addition, the identification of the main risk factors associated with meta-inflammation can make a real difference for providing appropriate and disease-tailored health services. The goal of this Research Topic is to identify new mechanisms involved in the pathogenesis of chronic diseases and to highlight how lifestyle, nutritional and environmental interventions (apart from specific pharmacologic treatments), can influence the prognosis of such diseases. New approach methodologies (NAMs) can serve to identify specific new targets for personalized interventions that should be translated into clinical studies for proving their efficacy and safety. This Research Topic is aimed to identify the newest research in the field of personalized medicine in chronic diseases including, but not limited to, genomic medicine. Here, we will focus primarily on the following themes: • Role of meta-inflammation and inflammatory-oxidative cascade in certain chronic diseases and possible preventive strategies • Nutritional status and nutritional interventions for the prevention and management of chronic diseases • Nutritional intervention (e.g., use of nutraceuticals) as a complement to the standard pharmacological treatments for chronic diseases We welcome you to contribute to this collection with Mini-reviews, Reviews, Perspectives, Protocols, General Commentaries, and Original Research Articles on the topic.
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Abstract: Vitamin D is a steroid prohormone synthesized in the skin following ultraviolet exposure and also achieved through supplemental or dietary intake. While there is strong evidence for its role in maintaining bone and muscle health, there has been recent debate regarding the role of vitamin D deficiency in hypertension based on conflicting epidemiological evidence. Thus, we conducted a scoping systematic literature review and meta-analysis of all observational studies published up to early 2014 in order to map trends in the evidence of this association. Mixed-effect meta-analysis was performed to pool risk estimates from ten prospective studies (n=58,262) (pooled risk for incident hypertension, relative risk [RR] =0.76 (0.63–0.90) for top vs bottom category of 25-hydroxyvitamin D [25OHD]) and from 19 cross-sectional studies (n=90,535) (odds ratio [OR] =0.79 (0.73–0.87)). Findings suggest that the better the assessed quality of the respective study design, the stronger the relationship between higher 25OHD levels and hypertension risk (RR =0.67 (0.51–0.88); OR =0.77 (0.72–0.89)). There was significant heterogeneity among the findings for both prospective and cross-sectional studies, but no evidence of publication bias was shown. There was no increased risk of hypertension when the participants were of older age or when they were vitamin D deficient. Younger females showed strong associations between high 25OHD levels and hypertension risk, especially in prospective studies (RR =0.36 (0.18–0.72); OR =0.62 (0.44–0.87)). Despite the accumulating evidence of a consistent link between vitamin D and blood pressure, these data are observational, so questions still remain in relation to the causality of this relationship. Further studies either combining existing raw data from available cohort studies or conducting further Mendelian analyses are needed to determine whether this represents a causal association. Large randomized controlled trials are also needed to determine whether vitamin supplementation may be beneficial in the prevention or the treatment of hypertension. Keywords: 25OHD, high blood pressure, meta-analysis, prospective, cross-sectional, blood pressure
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The purpose of this study was to investigate the effects of vitamin D supplementation and circuit training on body composition, abdominal fat, blood lipids, and insulin resistance in T2D and vitamin D deficient elderly women. Fifty-two elderly women were randomly assigned to either the vitamin D supplementation with circuit training group (D+T: n = 15), the circuit training group (T: n = 13), the vitamin D supplementation group (D: n = 11), or the control group (CON: n = 13). The subjects in D took vitamin D supplements at 1,200 IU per day for 12 weeks; the subjects in T exercised 3 to 4 times per week, 25 to 40 minutes per session for 12 weeks; and the subjects in D+T participated in both treatments. Subjects in CON were asked to maintain normal daily life pattern for the duration of the study. Body composition, abdominal fat, blood lipids, and surrogate indices for insulin resistance were measured at pre- and post-test and the data were compared among the four groups and between two tests by utilizing two-way ANOVA with repeated measures. The main results of the present study were as follows: 1) Body weight, fat mass, percent body fat, and BMI decreased significantly in T, whereas there were no significant changes in the variables in D and CON. Lean body mass showed no significant changes in all groups. 2) TFA and SFA decreased significantly in T, whereas there were no significant changes in the variables in D and CON. The other abdominal fat related variables showed no significant changes in all groups. 3) TC, TG, HDL-C, and LDL-C showed improvements in T, whereas there were no significant changes in the variables in D and CON. 4) Fasting glucose, fasting insulin, and HOMA-IR tended to be lower in D+T. It was concluded that the 12 weeks of vitamin D supplementation and circuit training would have positive effects on abdominal fat and blood lipid profiles in T2D and vitamin D deficient elderly women. Vitamin D supplementation was especially effective when it was complemented with exercise training.
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Nutritional status influences bone health spinal cord injury (SCI). This study evaluates serum levels of 25-hydroxy-vitamin-D and calcium along with dietary intakes in patients with chronic SCI. Total of 160 patients participated in this investigation. Dietary intakes were assessed by semi-quantitative food-frequency questionnaire. Serum calcium, phosphorus and 25(OH)-vitamin-D level were measured. Mean of serum calcium and 25(OH)-vitamin-D were 9.54 ± 0.64 mg/dl (standard error of the mean [SE]: 0.05) and 13.6 ± 10.99 μg/dl (SE: 0.9), respectively. Dairy intake was below recommended amount (1.8 ± 0.74 per serving (SE: 0.06), recommended: 4). A high prevalence (53.1%) of Vitamin D deficiency (25(OH) Vitamin D <13 ng/ml) was found. This study shows below adequate intake of calcium and Vitamin D in Iranian patients with SCI. These results insist on the importance of dietary modifications among these patients.
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The prevalence of obesity has increased worldwide, and approximately 25%-35% of the adult population is obese in some countries. The excess of body fat is associated with adverse health consequences. Considering the limited efficacy of diet and exercise in the current obese population and the use of bariatric surgery only for morbid obesity, it appears that drug therapy is the only available method to address the problem on a large scale. Currently, pharmacological obesity treatment options are limited. However, new antiobesity drugs acting through central nervous system pathways or the peripheral adiposity signals and gastrointestinal tract are under clinical development. One of the most promising approaches is the use of peptides that influence the peripheral satiety signals and brain-gut axis such as GLP-1 analogs. However, considering that any antiobesity drug may affect one or several of the systems that control food intake and energy expenditure, it is unlikely that a single pharmacological agent will be effective as a striking obesity treatment. Thus, future strategies to treat obesity will need to be directed at sustainable weight loss to ensure maximal safety. This strategy will probably require the coadministration of medications that act through different mechanisms.
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Obesity is a major public health issue. This review updates the evidence on the effectiveness of behavioural and pharmacologic treatments for overweight and obesity in adults. We updated the search conducted in a previous review. Randomized trials of primary-care-relevant behavioural (diet, exercise and lifestyle) and pharmacologic (orlistat and metformin) with or without behavioural treatments in overweight and obese adults were included if 12-month, postbaseline data were provided for weight outcomes. Studies reporting harms were included regardless of design. Data were extracted and pooled wherever possible for 5 weight outcomes, 6 secondary health outcomes and 4 adverse events categories. We identified 68 studies, most consisted of short-term (≤ 12 mo) treatments using diet (n = 8), exercise (n = 4), diet and exercise (n = 10), lifestyle (n = 19), orlistat (n = 25) or metformin (n = 4). Compared with the control groups, intervention participants had a greater weight loss of -3.02 kg (95% confidence interval [CI] -3.52 to -2.52), a greater reduction in waist circumference of -2.78 cm (95% CI -3.34 to -2.22) and a greater reduction in body mass index of -1.11 kg/m(2) (95% CI -1.39 to -0.84). The relative risk for loss of ≥ 5% body weight was 1.77 (95% CI 1.58-1.99, [number needed to treat 5, 95% CI 4-7]), and the relative risk for loss of ≥ 10% body weight was 1.91 (95% CI 1.69-2.16, [number needed to treat 9, 95% CI 7-12]). Incidence of type 2 diabetes was lower among pre-diabetic intervention participants (relative risk 0.62 [95% CI 0.50-0.77], number needed to treat 17 [95% CI 13-29]). With prevalence rates for type 2 diabetes on the rise, weight loss coupled with a reduction in the incidence of type 2 diabetes could potentially have a significant benefit on population health and a possible reduction in need for drug treatments for glycemic control. There is moderate quality evidence that behavioural and pharmacologic plus behvioural, treatments for overweight and obesity in adults lead to clinically important reductions in weight and incidence of type 2 diabetes in pre-diabetic populations. Registration: PROSPERO no. CRD42012002753.
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The prevalence of normal-weight adults is decreasing, and the proportion in excessive weight categories (body mass index ≥ 25) is increasing. In this review, we sought to identify interventions to prevent weight gain in normal-weight adults. We searched multiple databases from January 1980 to June 2013. We included randomized trials of primary care-relevant behavioural, complementary or alternative interventions for preventing weight gain in normal-weight adults that reported weight change at least 12 months after baseline. We included any studies reporting harms. We planned to extract and pool data for 4 weight outcomes, 6 secondary health outcomes and 5 adverse events categories. One small study provided moderate-quality evidence. The 12-month program, which used education and financial strategies and was offered more than 25 years ago in the United States, was successful in stabilizing weight and producing weight loss. More intervention participants maintained their baseline weight or lost weight than controls (82% v. 56%, p < 0.0001), and program participants maintained their weight better than controls by showing greater weight reduction by the end of the intervention (mean difference adjusted for height -0.82, 95% confidence interval -1.57 to -0.06, kg). No evidence was available for sustained effects or for any other weight outcomes, secondary outcomes or harms. We were unable to determine whether behavioural interventions led to weight-gain prevention and improved health outcomes in normal-weight adults. Given the importance of primary prevention, and the difficulty of losing weight and maintaining weight loss, this paucity of evidence is surprising and leaves clinicians and public health practitioners with unclear direction. Registration: PROSPERO no. CRD42012002753.
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Vitamin D deficiency is now recognized as a pandemic. The major cause of vitamin D deficiency is the lack of appreciation that sun exposure in moderation is the major source of vitamin D for most humans. Very few foods naturally contain vitamin D, and foods that are fortified with vitamin D are often inadequate to satisfy either a child's or an adult's vitamin D requirement. Vitamin D deficiency causes rickets in children and will precipitate and exacerbate osteopenia, osteoporosis, and fractures in adults. Vitamin D deficiency has been associated with increased risk of common cancers, autoimmune diseases, hypertension, and infectious diseases. A circulating level of 25-hydroxyvitamin D of >75 nmol/L, or 30 ng/mL, is required to maximize vitamin D's beneficial effects for health. In the absence of adequate sun exposure, at least 800–1000 IU vitamin D3/d may be needed to achieve this in children and adults. Vitamin D2 may be equally effective for maintaining circulating concentrations of 25-hydroxyvitamin D when given in physiologic concentrations.
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High plasma level of P-selectin is associated with the development of venous thromboembolism (VTE). Furthermore, supplementation of vitamin D could decrease thrombotic events. Hence, this study was designed to examine whether the administration of vitamin D can influence the plasma level of P-selectin in patients with VTE. In the randomized controlled trial, 60 patients with confirmed acute deep vein thrombosis and/or pulmonary embolism (PE) were randomized into the intervention (n = 20) and control (n = 40) groups. The intervention arm was given an intramuscular single dose of 300 000 IU vitamin D3. Plasma level of 25-hydroxy vitamin D, P-selectin, and high-sensitive C-reactive protein (hs-CRP) was measured at baseline and 4 weeks after. The plasma level of P-selectin (95% confidence interval = -5.99 to -1.63, P = .022) and hs-CRP (P = .024) significantly declined in vitamin D-treated group, while only hs-CRP was significantly decreased in the control group (P = .011). However, the magnitude of these reductions was not statistically significant. This study could not support the potential benefit of the high-dose vitamin D on plasma level of P-selectin and hs-CRP in patients with VTE. © The Author(s) 2015.