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Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry

LR. Lopes, MA. Losi, N. Sheikh, C. Laroche, P. Charron, J. Gimeno, JP. Kaski, AP. Maggioni, L. Tavazzi, E. Arbustini, D. Brito, J. Celutkiene, A. Hagege, A. Linhart, J. Mogensen, JM. Garcia-Pinilla, T. Ripoll-Vera, H. Seggewiss, E. Villacorta, A....

. 2022 ; 9 (1) : 42-53. [pub] 2022Dec13

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc22032192

Grantová podpora
MR/T005181/1 Medical Research Council - United Kingdom
Medical Research Council - United Kingdom
British Heart Foundation - United Kingdom

E-zdroje Online Plný text

NLK ProQuest Central od 2016-10-01 do Před 1 rokem
Health & Medicine (ProQuest) od 2016-10-01 do Před 1 rokem

AIMS: The interaction between common cardiovascular risk factors (CVRF) and hypertrophic cardiomyopathy (HCM) is poorly studied. We sought to explore the relation between CVRF and the clinical characteristics of patients with HCM enrolled in the EURObservational Research Programme (EORP) Cardiomyopathy registry. METHODS AND RESULTS: 1739 patients with HCM were studied. The relation between hypertension (HT), diabetes (DM), body mass index (BMI), and clinical traits was analysed. Analyses were stratified according to the presence or absence of a pathogenic variant in a sarcomere gene. The prevalence of HT, DM, and obesity (Ob) was 37, 10, and 21%, respectively. HT, DM, and Ob were associated with older age (P<0.001), less family history of HCM (HT and DM P<0.001), higher New York Heart Association (NYHA) class (P<0.001), atrial fibrillation (HT and DM P<0.001; Ob p = 0.03) and LV (left ventricular) diastolic dysfunction (HT and Ob P<0.001; DM P = 0.003). Stroke was more frequent in HT (P<0.001) and mutation-positive patients with DM (P = 0.02). HT and Ob were associated with higher provocable LV outflow tract gradients (HT P<0.001, Ob P = 0.036). LV hypertrophy was more severe in Ob (P = 0.018). HT and Ob were independently associated with NYHA class (OR 1.419, P = 0.017 and OR 1.584, P = 0.004, respectively). Other associations, including a higher proportion of females in HT and of systolic dysfunction in HT and Ob, were observed only in mutation-positive patients. CONCLUSION: Common CVRF are associated with a more severe HCM phenotype, suggesting a proactive management of CVRF should be promoted. An interaction between genotype and CVRF was observed for some traits.

2nd Department of Internal Cardiovascular Medicine General University Hospital and 1st Medical Faculty Charles University Opletalova 38 Prague 110 00 Czech Republic

APHP Centre de Référence des Maladies Cardiaques Héréditaires Assistance Publique Hôpitaux de Paris ICAN Hôpital Pitié Salpêtrière 47 83 Bd de l'Hôpital Paris 75013 France

Assistance Publique Hôpitaux de Paris Hôpital Européen Georges Pompidou Département de Cardiologie Paris France and Université Paris Descartes Sorbonne Paris Cité Paris 75006 France

Cardiology Department of Cardiological Thoracic and Vascular Sciences and Public Health University of Padova Via 8 Febbraio 2 Padova 35122 Italy

CCUL Faculdade de Medicina Universidade de Lisboa Av Prof Egas Moniz MB Lisbon 1649 028 Portugal

Centre for Inherited Cardiovascular Diseases Fondazione IRCCS Policlinico San Matteo Viale Camillo Golgi Pavia 27100 Italy

Centre for Inherited Cardiovascular Diseases Great Ormond Street Hospital London WC1N 3JH UK

Clinic of Cardiac and Vascular Diseases Institute of Clinical Medicine Faculty of Medicine Vilnius University Universiteto g 3 Vilnius 01513 Lithuania

Department of Advanced Biomedical Sciences University Federico 2 Corso Umberto 1 40 Naples 80138 Italy

Department of Cardiology and Division of Cardiovascular Sciences Guy's and St Thomas' Hospitals and King's College London Strand London WC2R 2LS UK

Department of Cardiology Odense University Hospital J B Winsløws Vej 4 Odense 5000 Denmark

EORP European Society of Cardiology Sophia Antipolis France

Hospital Clínico Universitario Virgen de la Arrixaca Ctra Madrid Cartagena Murcia 30120 El Spain

Inherited Cardiovascular Disease Unit Son Llatzer University Hospital and IdISBa Palma de Mallorca Spain

Institute of Cardiovascular Science University College London Gower St London WC1E 6BT UK

Maria Cecilia Hospital GVM Care and Research Via Corriera 1 Cotignola 48033 RA Italy

Member of National Centers of expertise for familial cardiopathies CIBERCV Salamanca Spain

Serviço de Cardiologia Centro Hospitalar Universitário Lisboa Norte Lisbon 1169 050 Portugal

Serviço de Cardiologia Hospital Garcia de Orta Av Torrado da Silva Almada 2805 267 Portugal

Sorbonne Université Inserm UMR1166 15 21 Rue de l'École de Médecine Paris 75006 France

St Bartholomew's Hospital Barts Heart Centre Barts Health NHS Trust Whitechapel Rd London E1 1BB UK

State Research Institute Centre for Innovative Medicine Vilnius Lithuania

Unidad de Insuficiencia Cardiaca y Cardiopatías Familiares Servicio de Cardiología Hospital Universitario Virgen de la Victoria IBIMA Málaga and Ciber Cardiovascular Instituto de Salud Carlos 3 Madrid Spain

Universitätsklinikum Würzburg Deutsches Zentrum für Herzinsuffizienz Am Schwarzenberg 15 Haus 15A 97078 Wurzburg Germany

Citace poskytuje Crossref.org

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