4.6 Article

Frailty index as a predictor of all-cause and cause-specific mortality in a Swedish population-based cohort

期刊

AGING-US
卷 9, 期 12, 页码 2629-2646

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/aging.101352

关键词

frailty; early risk marker; competing risks; cardiovascular disease mortality; cancer mortality

资金

  1. NIH [R01 AG04563, AG10175, AG028555]
  2. MacArthur Foundation Research Network on Successful Aging
  3. Swedish Council for Working Life and Social Research (FAS/FORTE) [97:0147:1B, 2009-0795]
  4. Swedish Research Council [825-2007-7460, 825-2009-6141, 521-2013-8689, 2015-03255]
  5. JPND/Swedish Research Council [2015-06796]
  6. FORTE [2013-2292]
  7. Loo & Hans Osterman Foundation
  8. Foundation for Geriatric Diseases
  9. Magnus Bergwall Foundation
  10. Strategic Research Program in Epidemiology at Karolinska Institutet
  11. Swedish Research Council [2015-06796] Funding Source: Swedish Research Council
  12. Vinnova [2015-06796] Funding Source: Vinnova

向作者/读者索取更多资源

Frailty is a complex manifestation of aging and associated with increased risk of mortality and poor health outcomes. However, younger individuals (under 65 years) are less-studied in this respect. Also, the relationship between frailty and cause-specific mortality in community settings is understudied. We used a 42-item Rockwood-based frailty index (FI) in the Swedish Adoption/Twin Study of Aging (n=1477; 623 men, 854 women; aged 29-95 years) and analyzed its association with all-cause and cause-specific mortality in up to 30-years of follow-up. Deaths due to cardiovascular disease (CVD), cancer, dementia and other causes were considered as competing risks. The FI was independently associated with increased risk for all-cause mortality in younger (<65 years; HR per increase in one deficit 1.11, 95% CI 1.07-1.17) and older (>= 65 years; HR 1.07, 95% CI 1.04-1.10) women and in younger men (HR 1.05, 95% CI 1.01-1.10). In cause-specific mortality analysis, the FI was strongly predictive of CVD mortality in women (HR per increase in one deficit 1.13, 95% CI 1.09-1.17), whereas in men the risk was restricted to deaths from other causes (HR 1.07, 95% CI 1.01-1.13). In conclusion, the FI is a strong mortality predictor especially among younger individuals and its associations with cause-specific mortality are sex-specific.

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