TY - JOUR
T1 - Association Between Mortality and Heritability of the Scale of Aging Vigor in Epidemiology
AU - The Long Life Family Study Research Group
AU - Sanders, Jason L.
AU - Singh, Jatinder
AU - Minster, Ryan L.
AU - Walston, Jeremy D.
AU - Matteini, Amy M.
AU - Christensen, Kaare
AU - Mayeux, Richard
AU - Borecki, Ingrid B.
AU - Perls, Thomas
AU - Newman, Anne B.
N1 - Funding Information:
Conflict of Interest: The authors declare no conflict of interest. LLFS has grant support from the National Institutes of Health, Department of Health and Human Services, through the National Institute on Aging (Grants 5U01AG023744, 5U01AG023755, 5U01AG023749, 5U01AG023746, 5U01AG023712). Author Contributions: Sanders, Walston, Matteini, Newman: conception and design. Christensen, Mayeux, Borecki, Perls, Newman: acquisition of data. Sanders, Singh, Minster, Newman: analysis and interpretation of data. Sanders, Minster, Newman: drafting of manuscript. Sanders, Singh, Minster, Walston, Matteini, Christensen, Mayeux, Borecki, Perls, Newman: critical revision of the manuscript. Singh, Minster: statistical analysis. Walston, Matteini, Christensen, Mayeux, Borecki, Perls, Newman: obtaining funding; supervision; administrative, technical, or materials support. All authors had access to data at all times. Sponsor's Role: The investigators retained full independence in the conduct of this research.
Publisher Copyright:
© 2016, Copyright the Authors Journal compilation © 2016, The American Geriatrics Society
PY - 2016/8/1
Y1 - 2016/8/1
N2 - Objectives: To investigate the association between mortality and heritability of a rescaled Fried frailty index, the Scale of Aging Vigor in Epidemiology (SAVE), to determine its value for genetic analyses. Design: Longitudinal, community-based cohort study. Setting: The Long Life Family Study (LLFS) in the United States and Denmark. Participants: Long-lived individuals (N = 4,875, including 4,075 genetically related individuals) and their families (N = 551). Measurements: The SAVE was administered to 3,599 participants and included weight change, weakness (grip strength), fatigue (questionnaire), physical activity (days walked in prior 2 weeks), and slowness (gait speed); each component was scored 0, 1, or 2 using approximate tertiles, and summed (range 0 (vigorous) to 10 (frail)). Heritability was determined using a variance component–based family analysis using a polygenic model. Association with mortality in the proband generation (N = 1,421) was calculated using Cox proportional hazards mixed-effect models. Results: Heritability of the SAVE was 0.23 (P <.001) overall (n = 3,599), 0.31 (P <.001) in probands (n = 1,479), and 0.26 (P <.001) in offspring (n = 2,120). In adjusted models, higher SAVE scores were associated with higher mortality (score 5–6: hazard ratio (HR) = 2.83, 95% confidence interval (CI) = 1.46–5.51; score 7–10: HR = 3.40, 95% CI = 1.72–6.71) than lower scores (0–2). Conclusion: The SAVE was associated with mortality and was moderately heritable in the LLFS, suggesting a genetic component to age-related vigor and frailty and supporting its use for further genetic analyses.
AB - Objectives: To investigate the association between mortality and heritability of a rescaled Fried frailty index, the Scale of Aging Vigor in Epidemiology (SAVE), to determine its value for genetic analyses. Design: Longitudinal, community-based cohort study. Setting: The Long Life Family Study (LLFS) in the United States and Denmark. Participants: Long-lived individuals (N = 4,875, including 4,075 genetically related individuals) and their families (N = 551). Measurements: The SAVE was administered to 3,599 participants and included weight change, weakness (grip strength), fatigue (questionnaire), physical activity (days walked in prior 2 weeks), and slowness (gait speed); each component was scored 0, 1, or 2 using approximate tertiles, and summed (range 0 (vigorous) to 10 (frail)). Heritability was determined using a variance component–based family analysis using a polygenic model. Association with mortality in the proband generation (N = 1,421) was calculated using Cox proportional hazards mixed-effect models. Results: Heritability of the SAVE was 0.23 (P <.001) overall (n = 3,599), 0.31 (P <.001) in probands (n = 1,479), and 0.26 (P <.001) in offspring (n = 2,120). In adjusted models, higher SAVE scores were associated with higher mortality (score 5–6: hazard ratio (HR) = 2.83, 95% confidence interval (CI) = 1.46–5.51; score 7–10: HR = 3.40, 95% CI = 1.72–6.71) than lower scores (0–2). Conclusion: The SAVE was associated with mortality and was moderately heritable in the LLFS, suggesting a genetic component to age-related vigor and frailty and supporting its use for further genetic analyses.
KW - epidemiology
KW - frailty
KW - genetics
KW - longevity
KW - phenotype
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U2 - 10.1111/jgs.14190
DO - 10.1111/jgs.14190
M3 - Article
C2 - 27294813
AN - SCOPUS:84982272990
SN - 0002-8614
VL - 64
SP - 1679
EP - 1683
JO - Journal of the American Geriatrics Society
JF - Journal of the American Geriatrics Society
IS - 8
ER -