|Title||Dynamics and heterogeneity in the process of human frailty and aging: evidence from the U.S. older adult population.|
|Publication Type||Journal Article|
|Year of Publication||2010|
|Authors||Yang, Y, Lee, LC|
|Journal||J Gerontol B Psychol Sci Soc Sci|
|Date Published||2010 Mar|
|Keywords||Aged, Aged, 80 and over, Aging, Cohort Studies, Female, Frail Elderly, Humans, Male, Surveys and Questionnaires, United States|
OBJECTIVES: This study investigated the dynamics and heterogeneity of the frailty index (FI) conceived as a systemic indicator of biological aging in the community-dwelling older adult population in the United States.
METHODS: We used panel data on multiple birth cohorts from the Health and Retirement Survey 1993-2006 and growth curve models to estimate age trajectories of the FI and their differences by sex, race, and socioeconomic status (SES) within cohorts.
RESULTS: The FI for cohorts born before 1942 exhibit quadratic increases with age and accelerated increases in the accumulation of health deficits. More recent cohorts exhibit higher average levels of and rates of increment in the FI than their predecessors do at the same ages. Females, non-Whites, and individuals with low education and income exhibit greater degrees of physiological deregulation than their male, White, and high-SES counterparts at any age. Patterns of sex, race, and SES differentials in rates of aging vary across cohorts.
DISCUSSION: Adjusting for social behavioral factors, the analysis provides evidence for physiological differences in the aging process among recent cohorts of older adults, points to the need for biological explanations of female excess in general system damage, and reveals the insufficiency of any single mechanism for depicting the racial and SES differences in the process of physiological deterioration.
|User Guide Notes|
|Endnote Keywords|| |
Frailty index/Deficits accumulation/Biological aging/Heterogeneity of frailty/age trajectories
|Endnote ID|| |
|Alternate Journal||J Gerontol B Psychol Sci Soc Sci|
|PubMed Central ID||PMC2981448|
|Grant List||R24 HD050924 / HD / NICHD NIH HHS / United States |
P30 AG-12857 / AG / NIA NIH HHS / United States