Intergenerational effects of maternal lifetime stressor exposure on offspring telomere length in Black and White women.
Pubmed ID: 36457292
Pubmed Central ID: PMC10235210
Journal: Psychological medicine
Publication Date: Oct. 1, 2023
MeSH Terms: Humans, Adult, Female, Adolescent, Middle Aged, Young Adult, Child, Prospective Studies, Telomere, Pregnancy, Intergenerational Relations, White People, Black or African American, Maternal Exposure, Mothers, Telomere Shortening
Grants: R01 HD073568, R56 AG059677, R01 AG059677, R00 AG062778, R56 HL141878, R25 HL145817, T32 HL007444, K99 AG062778, K12 HD051958
Authors: Lin J, Epel ES, Laraia BA, Tomiyama AJ, Guan J, Parker JE, Mayer SE, Hamlat E, Brownell K, Price C, Mujahid M, Slavich GM
Cite As: Mayer SE, Guan J, Lin J, Hamlat E, Parker JE, Brownell K, Price C, Mujahid M, Tomiyama AJ, Slavich GM, Laraia BA, Epel ES. Intergenerational effects of maternal lifetime stressor exposure on offspring telomere length in Black and White women. Psychol Med 2023 Oct;53(13):6171-6182. Epub 2022 Dec 2.
Studies:
Abstract
BACKGROUND: Although maternal stressor exposure has been associated with shorter telomere length (TL) in offspring, this literature is based largely on White samples. Furthermore, timing of maternal stressors has rarely been examined. Here, we examined how maternal stressors occurring during adolescence, pregnancy, and across the lifespan related to child TL in Black and White mothers. METHOD: Mothers (112 Black; 110 White; <i>M</i><sub>age</sub> = 39) and their youngest offspring (<i>n</i> = 222; <i>M</i><sub>age</sub> = 8) were part of a larger prospective cohort study, wherein mothers reported their stressors during adolescence (assessed twice during adolescence for the past year), pregnancy (assessed in midlife for most recent pregnancy), and across their lifespan (assessed in midlife). Mother and child provided saliva for TL measurement. Multiple linear regression models examined the interaction of maternal stressor exposure and race in relation to child TL, controlling for maternal TL and child gender and age. Race-stratified analyses were also conducted. RESULTS: Neither maternal adolescence nor lifespan stressors interacted with race in relation to child TL. In contrast, greater maternal pregnancy stressors were associated with shorter child TL, but this effect was present for children of White but not Black mothers. Moreover, this effect was significant for financial but not social pregnancy stressors. Race-stratified models revealed that greater financial pregnancy stressors predicted shorter telomeres in offspring of White, but not Black mothers. CONCLUSIONS: Race and maternal stressors interact and are related to biological aging across generations, but these effects are specific to certain races, stressors, and exposure time periods.