1. Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction.
- Author
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Kumar S, Mishra A, Srivastava A, Bhatt M, Garg N, Agarwal SK, Pande S, and Mittal B
- Subjects
- Aged, Alleles, Case-Control Studies, Connectin genetics, Coronary Artery Disease diagnosis, Coronary Artery Disease physiopathology, Female, Gene Expression, Heterozygote, Homozygote, Humans, Male, Middle Aged, Muscle Proteins genetics, Polymerase Chain Reaction, Polymorphism, Genetic, Stroke Volume, Troponin T genetics, Ventricular Dysfunction, Left diagnosis, Ventricular Dysfunction, Left physiopathology, Base Sequence, Carrier Proteins genetics, Coronary Artery Disease genetics, Genetic Predisposition to Disease, Sequence Deletion, Ventricular Dysfunction, Left genetics
- Abstract
Mutations in sarcomeric genes are common genetic cause of cardiomyopathies. An intronic 25-bp deletion in cardiac myosin binding protein C (MYBPC3) at 3' region is associated with dilated and hypertrophic cardiomyopathies in Southeast Asia. However, the frequency of sarcomeric gene polymorphisms and associated clinical presentation have not been established with left ventricular dysfunction (LVD). Therefore, the aim of the present study was to explore the association of MYBPC3 25-bp deletion, titin (TTN) 18 bp I/D, troponin T type 2 (TNNT2) 5 bp I/D and myospryn K2906N polymorphisms with LVD. This study includes 988 consecutive patients with angiographically confirmed coronary artery disease (CAD) and 300 healthy controls. Among the 988 CAD patients, 253 with reduced left ventricle ejection fraction (LVEF≤45%) were categorized as LVD. MYBPC3 25-bp deletion, TTN 18 bp I/D and TNNT2 5 bp I/D polymorphisms were determined by direct polymerase chain reaction method, while myospryn K2906N polymorphism by TaqMan assay. Our results showed that MYBPC3 25-bp deletion polymorphism was significantly associated with elevated risk of LVD (LVEF <45) (healthy controls versus LVD: OR=3.85, P <0.001; and nonLVD versus LVD: OR=1.65, P = 0.035), while TTN 18 bp I/D, TNNT2 5 bp I/D and myospryn K2906N polymorphisms did not show any significant association with LVD. The results also showed that MYBPC3 25-bp deletion polymorphism was significantly associated with other parameters of LV remodelling, i.e. LV dimensions (LV end diastole dimension, LVEDD: P = 0.037 and LV end systolic dimension, LVESD: P = 0.032). Our data suggests that MYBPC3 25-bp deletion may play significant role in conferring LVD as well as CAD risk in north Indian population.
- Published
- 2016
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