4.7 Article

Socioeconomic Disadvantage and the Pace of Biological Aging in Children

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PEDIATRICS
卷 147, 期 6, 页码 -

出版社

AMER ACAD PEDIATRICS
DOI: 10.1542/peds.2020-024406

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资金

  1. National Institutes of Health [R01HD083613, R01HD092548]
  2. Jacobs Foundation
  3. German Research Foundation
  4. Russell Sage Foundation Biology and Social Science [1810-08987]
  5. National Institute on Aging [R01AG066887, R01AG061378]
  6. Canadian Institute for Advanced Research Child and Brain Development Network
  7. Eunice Kennedy Shriver National Institute of Child Health and Human Development [5-R24-HD042849]
  8. National Institutes of Health (NIH)

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This study found that children growing up in socioeconomically disadvantaged environments experience accelerated biological aging compared to children in more affluent environments. Factors such as Latinx ethnicity, advanced puberty, higher BMI, and tobacco exposure were associated with faster biological aging. However, the relationship between socioeconomic disadvantage and accelerated aging remained significant even after controlling for these factors.
BACKGROUND AND OBJECTIVES: Children who grow up in socioeconomic disadvantage face increased burden of disease and disability throughout their lives. One hypothesized mechanism for this increased burden is that early-life disadvantage accelerates biological processes of aging, increasing vulnerability to subsequent disease. To evaluate this hypothesis and the potential impact of preventive interventions, measures are needed that can quantify early acceleration of biological aging in childhood. METHODS: Saliva DNA methylation and socioeconomic circumstances were measured in N = 600 children and adolescents aged 8 to 18 years (48% female) participating in the Texas Twin Project. We measured pace of biological aging using the DunedinPoAm DNA methylation algorithm, developed to quantify the pace-of-aging-related decline in system integrity. We tested if children in more disadvantaged families and neighborhoods exhibited a faster pace of aging as compared with children in more affluent contexts. RESULTS: Children living in more disadvantaged families and neighborhoods exhibited a faster DunedinPoAm-measured pace of aging (r = 0.18; P = .001 for both). Latinx-identifying children exhibited a faster DunedinPoAm-measured pace of aging compared with both White- and Latinx White-identifying children, consistent with higher levels of disadvantage in this group. Children with more advanced pubertal development, higher BMI, and more tobacco exposure exhibited faster a faster DunedinPoAm-measured pace of aging. However, DunedinPoAm- measured pace of aging associations with socioeconomic disadvantage were robust to control for these factors. CONCLUSIONS: Children growing up under conditions of socioeconomic disadvantage exhibit a faster pace of biological aging. DNA methylation pace of aging might be useful as a surrogate end point in evaluation of programs and policies to address the childhood social determinants of lifelong health disparities.

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