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      Impact of coronary artery revascularization on long-term outcome in hypertrophic cardiomyopathy patients: a nationwide population-based cohort study

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          Abstract

          Limited data are available on the long-term outcomes in patients with hypertrophic cardiomyopathy (HCM) patients with significant coronary artery disease (CAD) requiring revascularization. We investigated the risk of cardiovascular outcomes in HCM patients who underwent coronary revascularization compared to the control group without HCM. HCM patients aged ≥ 20 years were enrolled from the Korean National Health Insurance Database. Information on the diagnosis and previous medical history was obtained from the claims data. Cardiovascular outcomes were identified during 8-year after coronary revascularization in HCM patients (HCM group) and matched controls without HCM (non-HCM control group). A total of 431 patients in the HCM group and 1968 in the non-HCM control group were analyzed. The risk of all-cause death, cardiovascular death, sudden cardiac death (SCD), ischemic stroke, and hospitalization due to heart failure was significantly higher in the HCM group than in the non-HCM group, with prominent risk increase of cardiovascular death (adjusted hazard ratio [HR] 2.27, 95% confidence interval [CI] 1.63–3.15, P < 0.001) and ischemic stroke (adjusted HR 2.38, 95% CI 1.55–3.64, P < 0.001). Beyond 1-year after revascularization, the HCM group still had a significantly higher risk of cardiovascular death, SCD, and ventricular fibrillation/tachycardia compared to the non-HCM group. Mortality and major cardiovascular outcomes occurred more frequently in HCM patients with significant CAD requiring revascularization, compared to the matched non-HCM control group. Active and regular surveillance for concomitant risk factors and relevant intervention are warranted in HCM patients at increased risk for CAD.

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          Most cited references31

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          2019 ESC Guidelines for the diagnosis and management of chronic coronary syndromes

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            2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy

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              Hypertrophic cardiomyopathy.

              Hypertrophic cardiomyopathy is a common inherited cardiovascular disease present in one in 500 of the general population. It is caused by more than 1400 mutations in 11 or more genes encoding proteins of the cardiac sarcomere. Although hypertrophic cardiomyopathy is the most frequent cause of sudden death in young people (including trained athletes), and can lead to functional disability from heart failure and stroke, the majority of affected individuals probably remain undiagnosed and many do not experience greatly reduced life expectancy or substantial symptoms. Clinical diagnosis is based on otherwise unexplained left-ventricular hypertrophy identified by echocardiography or cardiovascular MRI. While presenting with a heterogeneous clinical profile and complex pathophysiology, effective treatment strategies are available, including implantable defibrillators to prevent sudden death, drugs and surgical myectomy (or, alternatively, alcohol septal ablation) for relief of outflow obstruction and symptoms of heart failure, and pharmacological strategies (and possibly radiofrequency ablation) to control atrial fibrillation and prevent embolic stroke. A subgroup of patients with genetic mutations but without left-ventricular hypertrophy has emerged, with unresolved natural history. Now, after more than 50 years, hypertrophic cardiomyopathy has been transformed from a rare and largely untreatable disorder to a common genetic disease with management strategies that permit realistic aspirations for restored quality of life and advanced longevity. Copyright © 2013 Elsevier Ltd. All rights reserved.
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                Author and article information

                Contributors
                cardiman73@gmail.com , hkkim73@snu.ac.kr
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                19 April 2023
                19 April 2023
                2023
                : 13
                : 6412
                Affiliations
                [1 ]GRID grid.412484.f, ISNI 0000 0001 0302 820X, Division of Cardiology, Department of Internal Medicine, Seoul National University College of Medicine, Cardiovascular Center, , Seoul National University Hospital, ; 101 Daehak-Ro, Jongno-Gu, Seoul, 03080 Korea
                [2 ]GRID grid.263765.3, ISNI 0000 0004 0533 3568, Department of Statistics and Actuarial Science, , The Soongsil University, ; Seoul, Republic of Korea
                [3 ]GRID grid.412480.b, ISNI 0000 0004 0647 3378, Cardiovascular Center and Department of Internal Medicine, , Seoul National University Bundang Hospital, ; Seongnam, Gyeonggi Republic of Korea
                [4 ]GRID grid.412484.f, ISNI 0000 0001 0302 820X, Division of Cardiology, Department of Internal Medicine, , Seoul National University Hospital Healthcare System Gangnam Center, ; Seoul, Republic of Korea
                Article
                33344
                10.1038/s41598-023-33344-3
                10115788
                37076510
                f4e0fe9b-a892-44cb-bab4-b03883db7575
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 25 November 2022
                : 12 April 2023
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                © The Author(s) 2023

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                cardiology,cardiovascular biology
                Uncategorized
                cardiology, cardiovascular biology

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