Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/12669
Title: Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy
Authors: Velicki, Lazar
Jakovljevic, Professor Djordje
Preveden A.
Golubovic, Mladjan
Bjelobrk M.
Ilic A.
Stojsic S.
Barlocco F.
Tafelmeier M.
Okwose N.
Tesic, Milorad
Brennan P.
Popovic D.
Ristić Fira A.
Macgowan G.
Filipovic, Nenad
Maier L.
Olivotto I.
Journal: BMC Cardiovascular Disorders
Issue Date: 1-Dec-2020
Abstract: © 2020, The Author(s). Background: Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease that affects approximately one in 500 people. HCM is a recognized genetic disorder most often caused by mutations involving myosin-binding protein C (MYBPC3) and β-myosin heavy chain (MYH7) which are responsible for approximately three-quarters of the identified mutations. Methods: As a part of the international multidisciplinary SILICOFCM project (www.silicofcm.eu) the present study evaluated the association between underlying genetic mutations and clinical phenotype in patients with HCM. Only patients with confirmed single pathogenic mutations in either MYBPC3 or MYH7 genes were included in the study and divided into two groups accordingly. The MYBPC3 group was comprised of 48 patients (76%), while the MYH7 group included 15 patients (24%). Each patient underwent clinical examination and echocardiography. Results: The most prevalent symptom in patients with MYBPC3 was dyspnea (44%), whereas in patients with MYH7 it was palpitations (33%). The MYBPC3 group had a significantly higher number of patients with a positive family history of HCM (46% vs. 7%; p = 0.014). There was a numerically higher prevalence of atrial fibrillation in the MYH7 group (60% vs. 35%, p = 0.085). Laboratory analyses revealed normal levels of creatinine (85.5 ± 18.3 vs. 81.3 ± 16.4 µmol/l; p = 0.487) and blood urea nitrogen (10.2 ± 15.6 vs. 6.9 ± 3.9 mmol/l; p = 0.472) which were similar in both groups. The systolic anterior motion presence was significantly more frequent in patients carrying MYH7 mutation (33% vs. 10%; p = 0.025), as well as mitral leaflet abnormalities (40% vs. 19%; p = 0.039). Calcifications of mitral annulus were registered only in MYH7 patients (20% vs. 0%; p = 0.001). The difference in diastolic function, i.e. E/e′ ratio between the two groups was also noted (MYBPC3 8.8 ± 3.3, MYH7 13.9 ± 6.9, p = 0.079). Conclusions: Major findings of the present study corroborate the notion that MYH7 gene mutation patients are presented with more pronounced disease severity than those with MYBPC3.
URI: https://scidar.kg.ac.rs/handle/123456789/12669
Type: Article
DOI: 10.1186/s12872-020-01807-4
SCOPUS: 85097319687
Appears in Collections:Faculty of Engineering, Kragujevac
[ Google Scholar ]

Page views(s)

16

Downloads(s)

2

Files in This Item:
File Description SizeFormat 
10.1186-s12872-020-01807-4.pdf858.73 kBAdobe PDFThumbnail
View/Open


Items in SCIDAR are protected by copyright, with all rights reserved, unless otherwise indicated.