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Total insulinlike growth factor 1 and insulinlike growth factor binding protein levels, functional status, and mortality in older adults
Authors:Kaplan Robert C  McGinn Aileen P  Pollak Michael N  Kuller Lewis  Strickler Howard D  Rohan Thomas E  Xue XiaoNan  Kritchevsky Stephen B  Newman Anne B  Psaty Bruce M
Affiliation:From the Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York;;Cancer Prevention Research Unit, Departments of Medicine and Oncology, Lady Davis Research Institute of Jewish General Hospital and McGill University, Montreal, Quebec, Canada;;Department of Medicine and Epidemiology, Cardiovascular Health Research Unit, University of Pittsburgh, Pittsburgh, Pennsylvania;;Sticht Center on Aging, School of Medicine, Wake Forest University, Winston-Salem, North Carolina;;Department of Medicine, University of Pittsburgh, Pittsburgh Pennsylvania;and;Departments of Epidemiology, Medicine and Health Services, University of Washington, Seattle, Washington.
Abstract:OBJECTIVES: To assess the association between total insulinlike growth factor (IGF)‐1, IGF binding protein‐1 (IGFBP‐1), and IGFBP‐3 levels and functioning and mortality in older adults. DESIGN: Cohort study. SETTING/PARTICIPANTS: One thousand one hundred twenty‐two individuals aged 65 and older without prior cardiovascular disease events participating in the Cardiovascular Health Study. MEASUREMENTS: Baseline fasting plasma levels of IGF‐1, IGFBP‐1, and IGFBP‐3 (defined as tertiles, T1‐T3) were examined in relationship to handgrip strength, time to walk 15 feet, development of new difficulties with activities of daily living (ADLs), and mortality. RESULTS: Higher IGFBP‐1 predicted worse handgrip strength (P‐trendT1‐T3<.01) and slower walking speed (P‐trendT1‐T3=.03), lower IGF‐1 had a borderline significant association with worse handgrip strength (P‐trendT1‐T3=.06), and better grip strength was observed in the middle IGFBP‐3 tertile than in the low or high tertiles (P=.03). Adjusted for age, sex, and race, high IGFBP‐1 predicted greater mortality (P‐trendT1‐T3<.001, hazard ratio (HR)T3vsT1=1.48, 95% confidence interval (CI)=1.15–1.90); this association was borderline significant after additional confounder adjustment (P‐trendT1‐T3=.05, HRT3vsT1=1.35, 95% CI=0.98–1.87). High IGFBP‐1 was associated with greater risk of incident ADL difficulties after adjustment for age, sex, race, and other confounders (P‐trendT1‐T3=.04, HRT3vsT1=1.40, CI=1.01–1.94). Neither IGF‐1 nor IGFBP‐3 level predicted mortality or incident ADL difficulties. CONCLUSION: In adults aged 65 and older, high IGFBP‐1 levels were associated with greater risk of mortality and poorer functional ability, whereas IGF‐1 and IGFBP‐3 had little association with these outcomes.
Keywords:disability    insulinlike growth factor (IGF)    older adults
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