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Genetic Determinants and Genotype-Phenotype Correlations in Vietnamese Patients With Dilated Cardiomyopathy

Vy Nguyen, Minh Thu Tran Vu, Thi Nam Phuong, Thi Huynh Nga Tran, Thi Hao, Thi My Hanh Nguyen, Bao Nam Tran Huynh, Lan Anh Lé, Ngoc Thieu Nguyen Pham, Thi Dieu Ai Nguyen, Thi My Nuong Nguyen, Ngoc Hong Phuong Le, Vinh Pham Nguyen, Thuy Duong Ho Huynh

2021Circulation Journal22 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Dilated cardiomyopathy (DCM) is an important cause of heart failure and cardiac transplantation. This study determined the prevalence of DCM-associated genes and evaluated the genotype-phenotype correlation in Vietnamese patients. METHODS AND RESULTS: This study analyzed 58 genes from 230 patients. The study cohort consisted of 64.3% men; age at diagnosis 47.9±13.7 years; familial (10.9%) and sporadic DCM (82.2%). The diagnostic yield was 23.5%, 44.0% in familial and 19.6% in sporadic DCM.TTNtruncating variants (TTNtv) were predominant (46.4%), followed byTPM1,DSP,LMNA,MYBPC3,MYH6,MYH7,DES,TNNT2,ACTC1,ACTN2,BAG3,DMD,FKTN,PLN,TBX5,RBM20,TCAP(2-6%). Familial DCM, genotype-positive andTTNtv-positive patients were younger than those with genotype-negative and sporadic DCM. Genotype-positive patients displayed a decreased systolic blood pressure and left ventricular wall thickness compared to genotype-negative patients. Genotype-positive patients, particularly those withTTNtv, had a family history of DCM, higher left atrial volume index and body mass index, and lower right ventricle-fractional area change than genotype-negative patients. Genotype-positive patients reached the combined outcomes more frequently and at a younger age than genotype-negative patients. Major cardiac events occurred more frequently in patients positive with genes other thanTTNtv. CONCLUSIONS: The study findings provided an overview of Vietnamese DCM patients' genetic profile and suggested that management of environmental factors may be beneficial for DCM patients.

Topics & Concepts

Dilated cardiomyopathyGenotypePhenotypeVietnameseCardiomyopathyGeneticsMedicineCardiologyInternal medicineBiologyGeneHeart failureLinguisticsPhilosophyCardiomyopathy and Myosin StudiesCongenital heart defects researchCardiac electrophysiology and arrhythmias
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