Claire C Cutting, Jonathan A Rose, Ann-Marcia C Tukpah, Noriaki Wada, Mizuki Nishino, Sean Kalra, Matthew R Moll, Michael H Cho, Edwin K Silverman, Gregory L Kinney, Harry B Rossiter, Heida Bjarnadottir, Valborg Gudmundsdottir, Sigurdur Sigurdsson, Gunnar Gudmundsson, Vilmundur Gudnason, George R Washko, Matthew J Budoff, Hiroto Hatabu, Gary M Hunninghake, Rachel K Putman
{"title":"肺间质异常、冠心病和死亡率。","authors":"Claire C Cutting, Jonathan A Rose, Ann-Marcia C Tukpah, Noriaki Wada, Mizuki Nishino, Sean Kalra, Matthew R Moll, Michael H Cho, Edwin K Silverman, Gregory L Kinney, Harry B Rossiter, Heida Bjarnadottir, Valborg Gudmundsdottir, Sigurdur Sigurdsson, Gunnar Gudmundsson, Vilmundur Gudnason, George R Washko, Matthew J Budoff, Hiroto Hatabu, Gary M Hunninghake, Rachel K Putman","doi":"10.1183/13993003.02286-2024","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Interstitial lung abnormalities (ILA) share common risk factors with coronary heart disease (CHD), including increased age and cigarette smoking, however the relationship between ILA and CHD has not been well described.</p><p><strong>Methods: </strong>Participants from the Genetic Epidemiology of Chronic Obstructive Pulmonary Disease study (COPDGene) and Age Gene/Environment Susceptibility (AGES)-Reykjavik studies with ILA assessment, clinical CHD, and coronary artery calcium (CAC) data were included. In both cohorts, CHD was defined by clinical history and additionally by CAC>100. Multivariable logistic regression assessed the relationship between ILA and CHD; Cox proportional hazards models were used to assess mortality associated with ILA and CHD.</p><p><strong>Results: </strong>9% of subjects with CHD had ILA in both COPDGene and AGES-Reykjavik. Subjects with ILA had increased odds of CHD defined by clinical history in COPDGene (odds ratio [OR] 1.6, 95% confidence interval [CI]: 1.2 to 2.0, <i>p</i><0.001) and AGES-Reykjavik (OR 1.6, 1.2 to 2.0, <i>p</i><0.001), similar results were seen with CAC>100. In both COPDGene and AGES-Reykjavik, participants with CHD and ILA had a greater risk of death compared to those with CHD but without ILA (hazard ratio [HR] 2.0, 95% CI: 1.4 to 2.7, <i>p</i><0.001) and (HR 1.3, 95% CI: 1.1 to 1.4, <i>p</i><0.001), respectively. In AGES-Reykjavik, among participants with CHD, ILA was associated with an over 9-fold increase in the odds of a respiratory death (OR=9.6, 95% CI 3.2, 29, p<0.0001).</p><p><strong>Conclusion: </strong>ILA are a common co-occurrence with CHD and associated with worse mortality, suggesting that ILA are a clinically important comorbidity in patients with CHD.</p>","PeriodicalId":12265,"journal":{"name":"European Respiratory Journal","volume":" ","pages":""},"PeriodicalIF":16.6000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interstitial Lung Abnormalities, Coronary Heart Disease, and Mortality.\",\"authors\":\"Claire C Cutting, Jonathan A Rose, Ann-Marcia C Tukpah, Noriaki Wada, Mizuki Nishino, Sean Kalra, Matthew R Moll, Michael H Cho, Edwin K Silverman, Gregory L Kinney, Harry B Rossiter, Heida Bjarnadottir, Valborg Gudmundsdottir, Sigurdur Sigurdsson, Gunnar Gudmundsson, Vilmundur Gudnason, George R Washko, Matthew J Budoff, Hiroto Hatabu, Gary M Hunninghake, Rachel K Putman\",\"doi\":\"10.1183/13993003.02286-2024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Interstitial lung abnormalities (ILA) share common risk factors with coronary heart disease (CHD), including increased age and cigarette smoking, however the relationship between ILA and CHD has not been well described.</p><p><strong>Methods: </strong>Participants from the Genetic Epidemiology of Chronic Obstructive Pulmonary Disease study (COPDGene) and Age Gene/Environment Susceptibility (AGES)-Reykjavik studies with ILA assessment, clinical CHD, and coronary artery calcium (CAC) data were included. In both cohorts, CHD was defined by clinical history and additionally by CAC>100. Multivariable logistic regression assessed the relationship between ILA and CHD; Cox proportional hazards models were used to assess mortality associated with ILA and CHD.</p><p><strong>Results: </strong>9% of subjects with CHD had ILA in both COPDGene and AGES-Reykjavik. Subjects with ILA had increased odds of CHD defined by clinical history in COPDGene (odds ratio [OR] 1.6, 95% confidence interval [CI]: 1.2 to 2.0, <i>p</i><0.001) and AGES-Reykjavik (OR 1.6, 1.2 to 2.0, <i>p</i><0.001), similar results were seen with CAC>100. In both COPDGene and AGES-Reykjavik, participants with CHD and ILA had a greater risk of death compared to those with CHD but without ILA (hazard ratio [HR] 2.0, 95% CI: 1.4 to 2.7, <i>p</i><0.001) and (HR 1.3, 95% CI: 1.1 to 1.4, <i>p</i><0.001), respectively. In AGES-Reykjavik, among participants with CHD, ILA was associated with an over 9-fold increase in the odds of a respiratory death (OR=9.6, 95% CI 3.2, 29, p<0.0001).</p><p><strong>Conclusion: </strong>ILA are a common co-occurrence with CHD and associated with worse mortality, suggesting that ILA are a clinically important comorbidity in patients with CHD.</p>\",\"PeriodicalId\":12265,\"journal\":{\"name\":\"European Respiratory Journal\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":16.6000,\"publicationDate\":\"2025-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Respiratory Journal\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1183/13993003.02286-2024\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"RESPIRATORY SYSTEM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Respiratory Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1183/13993003.02286-2024","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RESPIRATORY SYSTEM","Score":null,"Total":0}
Interstitial Lung Abnormalities, Coronary Heart Disease, and Mortality.
Background: Interstitial lung abnormalities (ILA) share common risk factors with coronary heart disease (CHD), including increased age and cigarette smoking, however the relationship between ILA and CHD has not been well described.
Methods: Participants from the Genetic Epidemiology of Chronic Obstructive Pulmonary Disease study (COPDGene) and Age Gene/Environment Susceptibility (AGES)-Reykjavik studies with ILA assessment, clinical CHD, and coronary artery calcium (CAC) data were included. In both cohorts, CHD was defined by clinical history and additionally by CAC>100. Multivariable logistic regression assessed the relationship between ILA and CHD; Cox proportional hazards models were used to assess mortality associated with ILA and CHD.
Results: 9% of subjects with CHD had ILA in both COPDGene and AGES-Reykjavik. Subjects with ILA had increased odds of CHD defined by clinical history in COPDGene (odds ratio [OR] 1.6, 95% confidence interval [CI]: 1.2 to 2.0, p<0.001) and AGES-Reykjavik (OR 1.6, 1.2 to 2.0, p<0.001), similar results were seen with CAC>100. In both COPDGene and AGES-Reykjavik, participants with CHD and ILA had a greater risk of death compared to those with CHD but without ILA (hazard ratio [HR] 2.0, 95% CI: 1.4 to 2.7, p<0.001) and (HR 1.3, 95% CI: 1.1 to 1.4, p<0.001), respectively. In AGES-Reykjavik, among participants with CHD, ILA was associated with an over 9-fold increase in the odds of a respiratory death (OR=9.6, 95% CI 3.2, 29, p<0.0001).
Conclusion: ILA are a common co-occurrence with CHD and associated with worse mortality, suggesting that ILA are a clinically important comorbidity in patients with CHD.
期刊介绍:
The European Respiratory Journal (ERJ) is the flagship journal of the European Respiratory Society. It has a current impact factor of 24.9. The journal covers various aspects of adult and paediatric respiratory medicine, including cell biology, epidemiology, immunology, oncology, pathophysiology, imaging, occupational medicine, intensive care, sleep medicine, and thoracic surgery. In addition to original research material, the ERJ publishes editorial commentaries, reviews, short research letters, and correspondence to the editor. The articles are published continuously and collected into 12 monthly issues in two volumes per year.