<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>119</viewCount><searchCount>0</searchCount></scores><additional><submitter>Jiang M</submitter><funding>NIA NIH HHS</funding><pagination>2629-2646</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5764396</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(12)</volume><pubmed_abstract>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 (&lt;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.</pubmed_abstract><journal>Aging</journal><pubmed_title>Frailty index as a predictor of all-cause and cause-specific mortality in a Swedish population-based cohort.</pubmed_title><pmcid>PMC5764396</pmcid><funding_grant_id>R01 AG028555</funding_grant_id><funding_grant_id>R01 AG010175</funding_grant_id><pubmed_authors>Kuja-Halkola R</pubmed_authors><pubmed_authors>Jylhava J</pubmed_authors><pubmed_authors>Karlsson I</pubmed_authors><pubmed_authors>Pedersen NL</pubmed_authors><pubmed_authors>Hagg S</pubmed_authors><pubmed_authors>Jiang M</pubmed_authors><pubmed_authors>Foebel AD</pubmed_authors><view_count>119</view_count></additional><is_claimable>false</is_claimable><name>Frailty index as a predictor of all-cause and cause-specific mortality in a Swedish population-based cohort.</name><description>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 (&lt;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.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Dec</publication><modification>2021-02-21T03:44:18Z</modification><creation>2019-03-27T00:14:51Z</creation></dates><accession>S-EPMC5764396</accession><cross_references><pubmed>29273703</pubmed><doi>10.18632/aging.101352</doi></cross_references></HashMap>