TY - JOUR
T1 - Does salivary telomere length explain race/ethnic differences in aging?
AU - Brown, Lauren
AU - García, Catherine
AU - Ailshire, Jennifer
N1 - Funding Information:
This research was supported by the National Institute on Aging (NIA) of the National Institutes of Health, Multidisciplinary Training Grant award in Gerontology at the University of Southern California (grant number T32AG0037), the NIA Training Grant award to Institute for Social Research at University of Michigan (grant number T32AG000221), the NIA Aging Research Dissertation Award to Increase Diversity (grant number R36AG057949), and NIA Grant R00AG039528. We would like to acknowledge Michael H. Esposito for creating the Figure for this paper using R Version 3.53.
Publisher Copyright:
© 2020 Society for Biodemography and Social Biology.
PY - 2020
Y1 - 2020
N2 - Telomere length (TL) is a biomarker that can be used to characterize variability in aging and may explain race/ethnic differences in aging. Yet, it remains unclear if TL is related to aging-associated health risks in multi-ethnic populations or if it explains race/ethnic differences in health. We examine whether salivary TL (STL) explains any of the race/ethnic variability in 15 indicators of high-risk biological, physical, and cognitive health among 4,074 White, Black, and Latinx older adults ages 54+ in the 2008 Health and Retirement Study. TL was assayed from saliva using quantitative PCR (T/S ratio). Decomposition analyses from logistic regression models show variation in STL does not account for any of the observed race/ethnic differences health. In age-adjusted, race-stratified models, STL was associated with HDL, total cholesterol, and lung function among Whites, but was not associated with any markers of health among Black or Latinx groups. In this diverse national sample of older adults, STL does not account for race/ethnic differences in late life health, is associated with relatively few indicators of health among Whites, and is not associated with indicators of health among Black or Latinx groups. STL may not be a useful biomarker for understanding racial/ethnic differences in population aging among older adults.
AB - Telomere length (TL) is a biomarker that can be used to characterize variability in aging and may explain race/ethnic differences in aging. Yet, it remains unclear if TL is related to aging-associated health risks in multi-ethnic populations or if it explains race/ethnic differences in health. We examine whether salivary TL (STL) explains any of the race/ethnic variability in 15 indicators of high-risk biological, physical, and cognitive health among 4,074 White, Black, and Latinx older adults ages 54+ in the 2008 Health and Retirement Study. TL was assayed from saliva using quantitative PCR (T/S ratio). Decomposition analyses from logistic regression models show variation in STL does not account for any of the observed race/ethnic differences health. In age-adjusted, race-stratified models, STL was associated with HDL, total cholesterol, and lung function among Whites, but was not associated with any markers of health among Black or Latinx groups. In this diverse national sample of older adults, STL does not account for race/ethnic differences in late life health, is associated with relatively few indicators of health among Whites, and is not associated with indicators of health among Black or Latinx groups. STL may not be a useful biomarker for understanding racial/ethnic differences in population aging among older adults.
KW - aging
KW - biomarkers
KW - ethnicity
KW - race
KW - telomere length
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U2 - 10.1080/19485565.2020.1798736
DO - 10.1080/19485565.2020.1798736
M3 - Article
C2 - 33335644
AN - SCOPUS:85096914209
SN - 1948-5565
VL - 65
SP - 351
EP - 369
JO - Biodemography and Social Biology
JF - Biodemography and Social Biology
IS - 4
ER -