Key result
Genetic screening in Indian DCM patients reveals ~40% familial inheritance alongside LMNA and MYH7 variants.
Observational (n=80)
Genetic screening in Indian patients with dilated cardiomyopathy identified a 40% rate of familial inheritance and pathogenic variants in LMNA and MYH7.
Reports demographic/genetic profiles in Indian DCM patients; hypothesis-generating and should not yet change practice.
Background: Dilated Cardiomyopathy (DCM) is a genetic disorder where a heterogeneous group of cardiac-muscles are involved and is characterized by ventricular dilatation, impaired systolic function, reduced myocardial contractility with left ventricular ejection fraction (LVEF) less than 40%. Our study aims to report the Demographic, Clinical and Genetic profile of Indian Dilated Cardiomyopathy patients. Methodology: All patients were recruited with prior written informed consent and are of Indian origin. Results: In a total of 80 DCM patients, the prevalence was higher among males. In males, mean age of onset was comparatively less than females. In this cohort, 40% had familial inheritance. Sixty two percent of DCM patients belong to NYHA functional class II with ejection fraction (EF) ranging between 21-30% and, around one third of the patients had atrial fibrillation (AF). Genetic screening revealed a novel splice site mutation LMNA (c.639+ G>C) and a rare variant MYH7 (c.2769 C>T) in a patient and insilico analysis of both variants suggested functional changes that were considered pathogenic. We report 3% and 4% occurance of variants, each in LMNA and MYH7, where as reported frequencies of these genes are 6% LMNA and 4% MYH7. Conclusions: DCM is often familial and all possible candidate genes should be screened to identify mutations. Such type of exercise may help in the identification of mechanistic pathways. Next generation sequencing platforms may play an important role in this respect in future.
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Rao et al. (2015) conducted an observational in Dilated Cardiomyopathy (n=80). Genetic screening was evaluated on Occurrence of LMNA and MYH7 variants. Genetic screening in 80 Indian patients with dilated cardiomyopathy revealed a 3% and 4% occurrence of variants in LMNA and MYH7, respectively, with 40% demonstrating familial inheritance.
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