Shorter Leukocyte Telomere Length in Midlife Women with Poor Sleep Quality
Author(s) -
Aric A. Prather,
Eli Puterman,
Jue Lin,
Aoife O’Donovan,
Jeffrey Krauss,
A. Janet Tomiyama,
Elissa S. Epel,
Elizabeth H. Blackburn
Publication year - 2011
Publication title -
journal of aging research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.564
H-Index - 43
eISSN - 2090-2212
pISSN - 2090-2204
DOI - 10.4061/2011/721390
Subject(s) - medicine , telomere , sleep quality , gerontology , sleep (system call) , psychiatry , genetics , insomnia , gene , biology , computer science , operating system
Background . Accumulating evidence supports leukocyte telomere length (LTL) as a biological marker of cellular aging. Poor sleep is a risk factor for age-related disease; however, the extent to which sleep accounts for variation in LTL is unknown. Methods . The present study examined associations of self-reported sleep duration, onset latency, and subjective quality with LTL in a community-dwelling sample of 245 healthy women in midlife (aged 49–66 years). Results . While sleep duration and onset latency were unrelated to LTL, women reporting poorer sleep quality displayed shorter LTL ( r = 0.14, P = 0.03), independent of age, BMI, race, and income ( b = 55.48, SE = 27.43, P = 0.04). When analyses were restricted to participants for whom sleep patterns were chronic, poorer sleep quality predicted shorter LTL independent of covariates and perceived psychological stress. Conclusions . This study provides the first evidence that poor sleep quality explains significant variation in LTL, a marker of cellular aging.
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