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Perceived Social Support, Loneliness, and Later Life Telomere Length
Following Wartime Captivity
Jacob Y. Stein, Yafit Levin, and Yael Lahav
Tel-Aviv University
Orit Uziel
Rabin Medical Center, Petah Tikva, Israel and
Tel-Aviv University
Heba Abumock
Rabin Medical Center, Petah Tikva, Israel
Zahava Solomon
Tel-Aviv University
Objectives: Telomere length (TL) is a robust indicator of cellular aging. TL erosion has been associated
with exposure to social and traumatic stressors. Loneliness and perceived social support are strongly
linked to increased morbidity and mortality, but have yet to be investigated in relation to TL after extreme
stress. The present study examined whether loneliness and lack of perceived social support following
wartime captivity may be associated with TL as repatriated prisoners of war (ex-POWs) enter old age and
contribute to its prediction. Method: A cohort of Israeli ex-POWs from the 1973 Yom Kippur War (n⫽
83) were assessed. Questionnaires were utilized to assess loneliness and perceived social support 18 years
after the repatriation (T1), and Southern blotting was used to measure TL 24 years later (T2). A
zero-order Pearson correlation test and a hierarchical regression analysis were utilized in order to
examine the research questions. Results: Loneliness and lack of perceived social support each signifi-
cantly predicted shorter TL in later life, and together added 25.8% to the overall explained variance.
Conclusions: This is the first study to empirically demonstrate that loneliness and lack of perceived
social support in early adulthood may be associated with shorter TL during transition to old age in a
population that has endured extreme stress. Although the study design precludes causal inferences,
several psychobiological mechanisms may explain the findings. The potential clinical significance of
social deficits for longevity and heath in related populations is therefore addressed, and an agenda for
future investigations is suggested.
Keywords: telomeres, wartime captivity, loneliness, social support, stress
Supplemental materials: http://dx.doi.org/10.1037/hea0000669.supp
Telomeres are DNA nucleoprotein complexes located at the
ends of chromosomes that protect the stability and integrity of the
chromosomes (e.g., prevent the end of the linear chromosomal
DNA from being recognized as a broken end; Blackburn, Epel, &
Lin, 2015). Telomeres shorten with every consecutive DNA rep-
lication, and therefore telomere length (TL) is considered a robust
marker of cellular aging (e.g., Müezzinler, Zaineddin, & Brenner,
2013). Shorter telomeres are associated with a weaker immune
system and altogether higher vulnerability to age related diseases
and mortality (e.g., Kaszubowska, 2008). Moreover, evidence in-
dicates that this relation is reciprocal: telomere shortening can both
facilitate disease etiology and progression and be a result of age-
related diseases (Blackburn et al., 2015). Notwithstanding, the mech-
anisms of telomere attrition and its association with morbidity and
mortality remain only partially understood. In this respect, the role
that stress-related factors play in this process is rapidly gaining re-
searchers’ attention.
The link between stressful and traumatic experiences and TL
erosion has been initially identified in vitro in relation to caregiver
stress (e.g., Epel et al., 2004). Recent studies have also demon-
strated that TL shortening is associated with combat stress (e.g.,
Bersani et al., 2016;Zhang et al., 2014), social stressors (e.g.,
Oliveira et al., 2016), and childhood stressors (e.g., Price, Kao,
Burgers, Carpenter, & Tyrka, 2013), to name but a few. Studies
This article was published Online First September 10, 2018.
Jacob Y. Stein, Yafit Levin, and Yael Lahav, Bob Shapell School of
Social Work, and I-Core Research Center for Mass Trauma, Tel Aviv
University; Orit Uziel, Laboratory for Telomere Biology, Felsenstein
Medical Research Center, Rabin Medical Center, Petah Tikva, Israel,
and Sackler School of Medicine, Tel-Aviv University; Heba Abumock,
Laboratory for Telomere Biology, Felsenstein Medical Research Cen-
ter, Rabin Medical Center, Petah Tikva, Israel; Zahava Solomon, Bob
Shapell School of Social Work, and I-Core Research Center for Mass
Trauma, Tel Aviv University.
This research was supported by the I-CORE Program of the Planning
and Budgeting Committee and The Israel Science Foundation (Grant
1916/12).
Correspondence concerning this article should be addressed to Jacob Y.
Stein, Bob Shapell School of Social Work, I-CORE Research Center for
Mass Trauma, Tel Aviv University, P.O. Box 39040, Ramat Aviv, Tel-
Aviv 69978, Israel. E-mail: cobisari@gmail.com
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© 2018 American Psychological Association 2018, Vol. 37, No. 11, 1067–1076
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