Association between idiopathic pulmonary fibrosis and coronary artery disease: a case-control study and cohort analysis

Association between idiopathic pulmonary fibrosis and coronary artery disease: a case-control study and cohort analysis

Authors

  • Won-Young Kim Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
  • Yejin Mok Institute for Health Promotion; Department of Epidemiology and Health Promotion, Graduate School of Public Health, Yonsei University, Seoul, Korea
  • Go Woon Kim Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
  • Soo-Jin Baek Health Insurance Policy Research Institute, National Health Insurance Corporation, Seoul, Korea
  • Young Duk Yun Health Insurance Policy Research Institute, National Health Insurance Corporation, Seoul, Korea
  • Sun Ha Jee Institute for Health Promotion; Department of Epidemiology and Health Promotion, Graduate School of Public Health, Yonsei University, Seoul, Korea
  • Dong Soon Kim Asan Medical Center, University of Ulsan

Keywords:

Coronary artery disease, IPF, Incidence, Risk factors

Abstract

Background: Although the increased risk of coronary artery disease (CAD) in the patients with idiopathic pulmonary fibrosis (IPF) has been reported, there was few detailed information on the risk factors for CAD in IPF. The aim of this study was to investigate the prevalence of CAD in IPF with analysis of other risk factors. Methods: The subjects were 460 patients (mean age, 65 years; 79% male; 74% current or ex-smoker) diagnosed as IPF at Asan Medical Center and 1,925 controls matched with age, gender, smoking habits, and date of IPF diagnosis from the cohort of Korean Heart Study. Cardiovascular risk factors and prevalence of CAD in both groups were compared and the incidence of newly developed CAD during follow-up was also analyzed. Results: IPF group was more diabetic, and control group had a higher proportion of hypertension and hypercholesterolemia. The prevalence of CAD in IPF group (7%) was two times higher than that of control group (3%). Multivariate analysis revealed that age (OR, 1.04; 95% CI, 1.02-1.07), hypertension (OR, 2.13; 95% CI, 1.36-3.33), hypercholesterolemia (OR, 3.85; 95% CI, 2.51-5.88), and IPF (OR, 2.64; 95% CI, 1.68-4.14) were significant risk factors for CAD. During follow-up (median: 2.5 years for IPF and 4.4 years for controls), the incidence of newly diagnosed CAD was higher in the patients with IPF (6.8%) compared to controls (2.8%) (RR, 1.92; 95% CI, 1.08-3.43). Conclusions: IPF itself was an independent risk factor for CAD after the adjustment of age, hypertension, diabetes, and hypercholesterolemia.

Author Biographies

Won-Young Kim, Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

Yejin Mok, Institute for Health Promotion; Department of Epidemiology and Health Promotion, Graduate School of Public Health, Yonsei University, Seoul, Korea

Go Woon Kim, Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

Soo-Jin Baek, Health Insurance Policy Research Institute, National Health Insurance Corporation, Seoul, Korea

Young Duk Yun, Health Insurance Policy Research Institute, National Health Insurance Corporation, Seoul, Korea

Sun Ha Jee, Institute for Health Promotion; Department of Epidemiology and Health Promotion, Graduate School of Public Health, Yonsei University, Seoul, Korea

Dong Soon Kim, Asan Medical Center, University of Ulsan

Professor, Medicine

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Published

05-01-2015

Issue

Section

Original Articles: Clinical Research

How to Cite

1.
Kim W-Y, Mok Y, Kim GW, Baek S-J, Yun YD, Jee SH, et al. Association between idiopathic pulmonary fibrosis and coronary artery disease: a case-control study and cohort analysis. Sarcoidosis Vasc Diffuse Lung Dis [Internet]. 2015 Jan. 5 [cited 2025 Jun. 22];31(4):289-96. Available from: https://mattioli1885journals.com/index.php/sarcoidosis/article/view/3340