4.4 Article

Heterogeneity of healthy aging: comparing long-lived families across five healthy aging phenotypes of blood pressure, memory, pulmonary function, grip strength, and metabolism

期刊

GEROSCIENCE
卷 41, 期 4, 页码 383-393

出版社

SPRINGER
DOI: 10.1007/s11357-019-00086-y

关键词

Familial longevity; Healthy aging

资金

  1. National Institute on Aging at National Institutes of Health [U01-AG023712, U01-AG23744, U01-AG023746, U01AG023749, U01-AG023755]
  2. Epidemiology of Aging training grant at the University of Pittsburgh (National Institute on Aging at National Institutes of Health) [T32-AG0001810]
  3. National Institute on Aging of the National Institutes of Health [P01 AG043352]
  4. National Institute of Aging [R01 AG023629, P30 AG024827]

向作者/读者索取更多资源

Five healthy aging phenotypes were developed in the Long Life Family Study to uncover longevity pathways and determine if healthy aging across multiple systems clustered in a subset of long-lived families. Using blood pressure, memory, pulmonary function, grip strength, and metabolic measures (body mass index, waist circumference and fasting levels of glucose, insulin, triglycerides, lipids, and inflammatory markers), offspring were ranked according to relative health using gender-, age-, and relevant confounder-adjusted z-scores. Based on our prior work, families met a healthy aging phenotype if >= 2 and >= 50% of their offspring were exceptionally healthy for that respective phenotype. Among 426 families, only two families met criteria for three healthy aging phenotypes and none met criteria for four or more healthy aging phenotypes. Using Spearman correlation, the proportion of offspring within families with exceptionally healthy pulmonary function was correlated with the proportion of offspring within families with exceptional strength (r = 0.19, p = 0.002). The proportion of offspring within families meeting the healthy blood pressure and metabolic phenotypes were also correlated (r = 0.14, p = 0.006), and more families were classified as meeting healthy blood pressure and metabolic phenotypes (Kappa = 0.10, p = 0.02), as well as the healthy pulmonary and blood pressure phenotypes than expected by chance (Kappa = 0.09, p = 0.03). Other phenotypes were weakly correlated (|r| <= 0.07) with low pairwise agreement (Kappa <= 0.06). Among these families selected for familial longevity, correspondence between healthy aging phenotypes was weak, supporting the heterogeneous nature of longevity and suggesting biological underpinnings of each individual phenotype should be examined separately to determine their shared and unique determinants.

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