Familial aggregation of the aging process: biological age measured in young adult offspring as a predictor of parental mortality

被引:0
作者
Ilona Shapiro
Daniel W. Belsky
Salomon Israel
Iaroslav Youssim
Yechiel Friedlander
Hagit Hochner
机构
[1] Braun School of Public Health,Department of Epidemiology and Butler Columbia Aging Center
[2] The Hebrew University of Jerusalem,Department of Psychology
[3] Columbia University Mailman School of Public Health,undefined
[4] The Hebrew University of Jerusalem,undefined
来源
GeroScience | 2023年 / 45卷
关键词
Cohort study; Biological age; Aging; Mortality; Familial aggregation; Intergenerational associations;
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学科分类号
摘要
Measures of biological age (BA) integrate information across organ systems to quantify “biological aging,” i.e., inter-individual differences in aging-related health decline. While longevity and lifespan aggregate in families, reflecting transmission of genes and environments across generations, little is known about intergenerational continuity of biological aging or the extent to which this continuity may be modified by environmental factors. Using data from the Jerusalem Perinatal Study (JPS), we tested if differences in offspring BA were related to mortality in their parents. We measured BA using biomarker data collected from 1473 offspring during clinical exams in 2007–2009, at age 32 ± 1.1. Parental mortality was obtained from population registry data for the years 2004–2016. We fitted parametric survival models to investigate the associations between offspring BA and parental all-cause and cause-specific mortality. We explored potential differences in these relationships by socioeconomic position (SEP) and offspring sex. Participants’ BAs widely varied (SD = 6.95). Among those measured to be biologically older, parents had increased all-cause mortality (HR = 1.10, 95% CI: 1.08, 1.13), diabetes mortality (HR = 1.19, 95% CI: 1.08, 1.30), and cancer mortality (HR = 1.07, 95% CI: 1.02, 1.13). The association with all-cause mortality was stronger for families with low compared with high SEP (Pinteraction = 0.04) and for daughters as compared to sons (Pinteraction < 0.001). Using a clinical-biomarker-based BA estimate, observable by young adulthood prior to the onset of aging-related diseases, we demonstrate intergenerational continuity of the aging process. Furthermore, variation in this familial aggregation according to household socioeconomic position (SEP) at offspring birth and between families of sons and daughters proposes that the environment alters individuals’ aging trajectory set by their parents.
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页码:901 / 913
页数:12
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  • [1] Vos T(2012)Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010 The Lancet 380 2163-2196
  • [2] Flaxman AD(1988)Biomarkers of aging Exp Gerontol 23 223-239
  • [3] Naghavi M(1947)Biologic versus chronologic age J Gerontol 2 217-227
  • [4] Lozano R(2013)The hallmarks of aging Cell 153 1194-1217
  • [5] Michaud C(2014)Geroscience: linking aging to chronic disease Cell 159 709-713
  • [6] Ezzati M(1989)Improving the precision of biological age determinations. Part 1: a new approach to calculating biological age Exp Gerontol 24 289-300
  • [7] Baker GT(1988)Assessment of biological age by principal component analysis Mech Ageing Dev 46 1-18
  • [8] Sprott RL(2017)Selection of an optimal set of biomarkers and comparative analyses of biological age estimation models in Korean females Arch Gerontol Geriatr 70 84-91
  • [9] Benjamin H(2018)DNA methylation-based biomarkers and the epigenetic clock theory of ageing Nat Rev Genet 19 371-384
  • [10] López-Otín C(2015)Homeostatic dysregulation proceeds in parallel in multiple physiological systems Aging Cell 14 1103-1112