<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bhatt SP</submitter><funding>NIA NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>NINR NIH HHS</funding><funding>NIH</funding><funding>NIH HHS</funding><pagination>359-366</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11892675</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(3)</volume><pubmed_abstract>&lt;b>Rationale:&lt;/b> Chronic lung diseases are associated with increased risk of mortality due to coronary heart disease (CHD). Nonetheless, the population attributable fraction (PAF) of lung function impairment relative to other established cardiovascular risk factors is unclear. &lt;b>Objectives:&lt;/b> To evaluate the PAF of low lung function for CHD mortality &lt;b>Methods:&lt;/b> We harmonized and pooled lung function and clinical data across eight U.S. general population cohorts. Impaired lung function was defined as forced expiratory volume in 1 second (FEV&lt;sub>1&lt;/sub>) and/or forced vital capacity ≤ 95% predicted on baseline spirometry. The association between CHD mortality and risk factors was assessed using cause-specific proportional hazards and Fine-Gray proportional subdistribution hazard mo</pubmed_abstract><journal>Annals of the American Thoracic Society</journal><pubmed_title>Low Lung Function Is Associated with High Population Attributable Fraction for Cardiovascular Mortality.</pubmed_title><pmcid>PMC11892675</pmcid><funding_grant_id>N01 HC085083</funding_grant_id><funding_grant_id>N01 HC085082</funding_grant_id><funding_grant_id>N01 HC085081</funding_grant_id><funding_grant_id>RC1 HL100543</funding_grant_id><funding_grant_id>R01 HL109301</funding_grant_id><funding_grant_id>N01 HC085086</funding_grant_id><funding_grant_id>N01 HC095166</funding_grant_id><funding_grant_id>HHSN268201700004I</funding_grant_id><funding_grant_id>N01 HC095165</funding_grant_id><funding_grant_id>N01 HC095168</funding_grant_id><funding_grant_id>N01 HC095167</funding_grant_id><funding_grant_id>N01 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HL130627</funding_grant_id><funding_grant_id>HHSN268201200036C</funding_grant_id><funding_grant_id>HHSN268201800012I</funding_grant_id><funding_grant_id>HHSN268201700002C</funding_grant_id><funding_grant_id>R01 HL157634</funding_grant_id><funding_grant_id>R01 HL155576</funding_grant_id><funding_grant_id>R01 HL109315</funding_grant_id><funding_grant_id>R21 HL129924</funding_grant_id><funding_grant_id>75N92023D00004</funding_grant_id><funding_grant_id>R01 HL077612</funding_grant_id><funding_grant_id>75N92023D00005</funding_grant_id><funding_grant_id>R01 HL093081</funding_grant_id><funding_grant_id>75N92023D00006</funding_grant_id><funding_grant_id>75N92023D00002</funding_grant_id><funding_grant_id>HHSN268201700005I</funding_grant_id><funding_grant_id>75N92023D00003</funding_grant_id><funding_grant_id>N01 HC095159</funding_grant_id><funding_grant_id>HHSN268201700001I</funding_grant_id><funding_grant_id>HHSN268201700005C</funding_grant_id><funding_grant_id>HHSN268201800015I</funding_grant_id><funding_grant_id>HHSN268201800011C</funding_grant_id><funding_grant_id>HHSN268201700001C</funding_grant_id><funding_grant_id>HHSN268201800011I</funding_grant_id><funding_grant_id>N01 HC085079</funding_grant_id><funding_grant_id>UH3 HL155806</funding_grant_id><funding_grant_id>R01 HL109319</funding_grant_id><funding_grant_id>U01 HL130114</funding_grant_id><pubmed_authors>Schwartz JE</pubmed_authors><pubmed_authors>Balte PP</pubmed_authors><pubmed_authors>O'Connor GT</pubmed_authors><pubmed_authors>Wu C</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Jaeger BC</pubmed_authors><pubmed_authors>Oelsner EC</pubmed_authors><pubmed_authors>White WB</pubmed_authors><pubmed_authors>Chaves PH</pubmed_authors><pubmed_authors>Bhatt SP</pubmed_authors><pubmed_authors>Lloyd-Jones D</pubmed_authors><pubmed_authors>Kalhan R</pubmed_authors><pubmed_authors>Yende S</pubmed_authors><pubmed_authors>Newman AB</pubmed_authors><pubmed_authors>Divo MJ</pubmed_authors><pubmed_authors>Couper D</pubmed_authors><pubmed_authors>Umans JG</pubmed_authors><pubmed_authors>Jacobs DR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low Lung Function Is Associated with High Population Attributable Fraction for Cardiovascular Mortality.</name><description>&lt;b>Rationale:&lt;/b> Chronic lung diseases are associated with increased risk of mortality due to coronary heart disease (CHD). Nonetheless, the population attributable fraction (PAF) of lung function impairment relative to other established cardiovascular risk factors is unclear. &lt;b>Objectives:&lt;/b> To evaluate the PAF of low lung function for CHD mortality &lt;b>Methods:&lt;/b> We harmonized and pooled lung function and clinical data across eight U.S. general population cohorts. Impaired lung function was defined as forced expiratory volume in 1 second (FEV&lt;sub>1&lt;/sub>) and/or forced vital capacity ≤ 95% predicted on baseline spirometry. The association between CHD mortality and risk factors was assessed using cause-specific proportional hazards and Fine-Gray proportional subdistribution hazard mo</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-07-16T23:28:51.502Z</modification><creation>2026-07-12T03:11:17.708Z</creation></dates><accession>S-EPMC11892675</accession><cross_references><pubmed>39447115</pubmed><doi>10.1513/AnnalsATS.202407-715OC</doi><doi>10.1513/annalsats.202407-715oc</doi></cross_references></HashMap>