1. Coronary Artery Disease Without Standard Cardiovascular Risk Factors.
- Author
-
Yamamoto K, Natsuaki M, Morimoto T, Shiomi H, Takeji Y, Yamaji K, Matsumura-Nakano Y, Yoshikawa Y, Yamamoto E, Fuki M, Kato E, Yamashita Y, Yaku H, Nakatsuma K, Watanabe H, Matsuda M, Tamura T, Inoko M, Mabuchi H, Shirotani M, Eizawa H, Ishii K, Inada T, Onodera T, Shinoda E, Yamamoto T, Toyofuku M, Takahashi M, Sakamoto H, Miki S, Aoyama T, Suwa S, Sato Y, Furukawa Y, Ando K, Kadota K, Nakagawa Y, and Kimura T
- Subjects
- Acute Coronary Syndrome surgery, Age Factors, Aged, Aged, 80 and over, Atrial Fibrillation epidemiology, Body Mass Index, Cause of Death, Chronic Disease, Coronary Artery Disease surgery, Female, Heart Disease Risk Factors, Humans, Male, Middle Aged, Myocardial Revascularization, Neoplasms epidemiology, Proportional Hazards Models, ST Elevation Myocardial Infarction surgery, Sex Factors, Time-to-Treatment statistics & numerical data, Acute Coronary Syndrome epidemiology, Coronary Artery Disease epidemiology, Diabetes Mellitus epidemiology, Dyslipidemias epidemiology, Hypertension epidemiology, Mortality, ST Elevation Myocardial Infarction epidemiology, Smoking epidemiology
- Abstract
Recently, one observational study showed that patients with ST-segment elevation myocardial infarction (STEMI) without standard cardiovascular risk factors were associated with increased mortality compared with patients with risk factors. This unexpected result should be evaluated in other populations including those with non-ST-segment elevation acute coronary syndrome (NSTE-ACS) and chronic coronary syndrome (CCS). Among 30,098 consecutive patients undergoing first coronary revascularization in the CREDO-Kyoto PCI/CABG (Coronary Revascularization Demonstrating Outcome Study in Kyoto Percutaneous Coronary Intervention/Coronary Artery Bypass Grafting) registry cohort-2 and 3, we compared clinical characteristics and outcomes between patients with and without risk factors stratified by their presentation (STEMI n = 8,312, NSTE-ACS n = 3,386, and CCS n = 18,400). Patients with risk factors were defined as having at least one of the following risk factors: hypertension, dyslipidemia, diabetes, and current smoking. The proportion of patients without risk factors was low (STEMI: 369 patients [4.4%], NSTE-ACS: 110 patients [3.2%], and CCS: 462 patients [2.5%]). Patients without risk factors compared with those with risk factors more often had advanced age, low body weight, and malignancy and less often had history of atherosclerotic disease and prescription of optimal medical therapy. In patients with STEMI, patients without risk factors compared with those with risk factors were more often women and more often had atrial fibrillation, long door-to-balloon time, and severe hemodynamic compromise. During a median of 5.6 years follow-up, patients without risk factors compared with those with risk factors had higher crude incidence of all-cause death. After adjusting confounders, the mortality risk was significant in patients with CCS (hazard ratio [HR] 1.22, 95% confidence interval [CI] 1.01 to 1.49, p = 0.04) but not in patients with STEMI (HR 1.06, 95% CI 0.89 to 1.27, p = 0.52) and NSTE-ACS (HR 1.07, 95% CI, 0.74 to 1.54, p = 0.73). In conclusion, among patients undergoing coronary revascularization, patients without standard cardiovascular risk factors had higher crude incidence of all-cause death compared with those with at least one risk factor. After adjusting confounders, the mortality risk was significant in patients with CCS but not in patients with STEMI and NSTE-ACS., Competing Interests: Disclosures Dr. Morimoto receives lecturer's fees from Bayer, Daiichi Sankyo, Japan Lifeline, Kyocera, Mitsubishi Tanabe, Novartis, and Toray; the manuscript fees from Bristol-Myers Squibb and Kowa; and served advisory boards for Asahi Kasei, Boston Scientific, Bristol-Myers Squibb, and Sanofi. Dr. Shiomi receives personal fees from Abbott Vascular, Boston Scientific, and Daiichi Sankyo. Dr. Kato receives honoraria from AstraZeneca, Amgen, Bayer, Boehringer Ingelheim, Bristol-Meyers Squibb, Daiichi Sankyo, Merck Sharp & Dohme KK, Ono Pharmaceutical, Pfizer, Takeda, Tanabe-Mitsubishi; and research fund from Abbott Vascular, and Ono Pharmaceutical. Dr. Furukawa receives honoraria from Ono Pharmaceutical, Novartis, Daiichi Sankyo, Bayer, Otsuka Pharmaceutical, Kowa, Takeda, Sumitomo Dainippon Pharma, Pfizer, Bristol-Myers Squibb, and Sanofi. Dr. Nakagawa receives grant from Abbott Vascular and Boston Scientific, and personal fees from Abbott Vascular, Bayer, Boston Scientific, Bristol-Myers Squibb, and Daiichi Sankyo. Dr. Kimura receives personal fees from Abbott Vascular, Abiomed, Astellas, Astellas Amgen BioPharma, AstraZeneca, Bayer, Boston Scientific, Boehringer Ingelheim, Bristol-Myers Squibb, Chugai Pharmaceutical, Edwards Lifescience, Eisai, Daiichi Sankyo, Interscience, Japan Society for the Promotion of Science, Kowa, Kowa Pharmaceutical, Lifescience, Medical Review, Merck Sharp & Dohme, MSD Life Science Foundation, Mitsubishi Tanabe Pharma, Novartis Pharma, Ono Pharmaceutical, OrbusNeich, Otsuka Pharmaceutical, Pharmaceuticals and Medical Devices Agency, Philips, Public Health Research Foundation, Sanofi, Sumitomo Dainippon Pharma, Takeda Pharmaceutical, Terumo, Toray, and Tsumura. The remaining authors have no conflicts of interest to declare., (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Published
- 2022
- Full Text
- View/download PDF