Predictors of right ventricular function and size in patients with hypertrophic cardiomyopathy.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
03 12 2020
Historique:
received: 15 09 2020
accepted: 17 11 2020
entrez: 4 12 2020
pubmed: 5 12 2020
medline: 18 3 2021
Statut: epublish

Résumé

We investigated factors associated with right ventricular (RV) function and size in hypertrophic cardiomyopathy (HCM) patients. Two hundred fifty-three consecutive HCM patients and 20 healthy volunteers underwent cardiac magnetic resonance examination. In addition to measuring RV function (ejection fraction-RVEF) and size (end-diastolic volume-RVEDV), each image was inspected for the presence of RV and left ventricular (LV) hypertrophy, and the maximal wall thickness of the left and right ventricles was recorded. HCM patients had higher RVEF and lower RVEDV than healthy volunteers and similar RV mass. The mean RV wall thickness was higher in HCM patients than in controls. LV late gadolinium enhancement (LGE) was present in 89.7% of patients, and RV LGE was present in 3.1% of patients (p < 0.0001). Univariate and multivariable analyses revealed that LVEF, peak LV outflow tract gradient, LV LGE, maximal LV wall thickness, and tricuspid regurgitation (TR) volume by magnetic resonance imaging were positive predictors of RVEF. In addition to TR volume, the only independent predictor of RVEF < 45% was LVEF (odds ratio = 0.80, 95% confidence interval 0.67-0.95). Multivariable analysis revealed that LVEDV and TR volume were positive predictors of RVEDV, whereas negative predictors were RVEF, maximal RV wall thickness, LV LGE, and age. Neither estimated systolic pulmonary artery pressure nor TR grade by echocardiography proved to be predictors of RVEF. There were no differences in either the maximal RV wall thickness or the maximal left ventricular (LV) wall thickness in patients stratified according to NYHA functional class (p = 0.93 and p = 0.15, respectively). There were no differences in mean RV wall thickness in patients categorised based on the number of clinical risk factors for sudden cardiac death (SCD), i.e., non-sustained ventricular tachycardia, family history of SCD, or unexplained syncope (p = 0.79). On the other hand, there was a weak positive association between RV hypertrophy and the estimated probability of SCD at 5 years (rho = 0.16, p = 0.01). RV systolic dysfunction measured as decreased RVEF was uncommon in HCM and was associated with poor LV systolic function. LV also had a significant impact on RV size.

Identifiants

pubmed: 33273702
doi: 10.1038/s41598-020-78245-x
pii: 10.1038/s41598-020-78245-x
pmc: PMC7713380
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

21054

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Auteurs

Mateusz Śpiewak (M)

Magnetic Resonance Unit, Department of Radiology, National Institute of Cardiology, ul. Alpejska 42, 04-628, Warsaw, Poland. mspiewak@ikard.pl.

Mariusz Kłopotowski (M)

Department of Interventional Cardiology and Angiology, National Institute of Cardiology, Warsaw, Poland.

Łukasz Mazurkiewicz (Ł)

Department of Cardiomyopathies, National Institute of Cardiology, Warsaw, Poland.

Ewa Kowalik (E)

Department of Congenital Heart Diseases, National Institute of Cardiology, Warsaw, Poland.

Joanna Petryka-Mazurkiewicz (J)

Department of Coronary Artery Disease and Structural Heart Diseases, National Institute of Cardiology, Warsaw, Poland.

Barbara Miłosz-Wieczorek (B)

Magnetic Resonance Unit, Department of Radiology, National Institute of Cardiology, ul. Alpejska 42, 04-628, Warsaw, Poland.

Anna Klisiewicz (A)

Department of Congenital Heart Diseases, National Institute of Cardiology, Warsaw, Poland.

Adam Witkowski (A)

Department of Interventional Cardiology and Angiology, National Institute of Cardiology, Warsaw, Poland.

Magdalena Marczak (M)

Magnetic Resonance Unit, Department of Radiology, National Institute of Cardiology, ul. Alpejska 42, 04-628, Warsaw, Poland.

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