AccScience Publishing / JCTR / Volume 7 / Issue 4 / DOI: 10.18053/jctres.07.202104.010
ORIGINAL ARTICLE

The genetics of cardiac failure: Role of a G protein-coupled receptor polymorphism in therapeutic response in an Indian population

Sudha Ramalingam1 * Shanmugasundaram Radhakrishnan2 Tamilarasu Kaliappan2 Rajendiran Gopalan2 Meenu Subrahmanian1 Ramalingam Sankaran1 *
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1 PSG Center for Molecular Medicine and Therapeutics, PSG Institute of Medical Sciences and Research, Coimbatore, Tamil Nadu, India
2 Department of Cardiology, PSG Hospitals, Coimbatore, Tamil Nadu, India
Received: 12 March 2021 | Revised: 11 April 2021 | Accepted: 16 June 2021 | Published online: 30 July 2021
© 2021 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution -Noncommercial 4.0 International License (CC-by the license) ( https://creativecommons.org/licenses/by-nc/4.0/ )
Abstract

Background and aim:  The incidence of heart failure (HF) is rising to epidemic proportions in developing countries like India. A lack of adequate Indian studies underscores the importance of pursuing research into HF in an Indian population. G protein-coupled receptor kinase 5 (GRK5) Gln41>Leu (rs2230345) polymorphism was reported as a genetic modifier associated with survival in HF patients. A prospective study was conducted to investigate the association of GRK5 Gln41>Leu polymorphism with response to β-blocker therapy in Indian HF patients.
Methods: HF patients (n=584) were recruited for the study. The patients were genotyped by tetra-primerbased allele specific PCR and confirmed with Sanger sequencing. The HF patients were evaluated for GRK5 gene expression and followed-up for ~3 years. Drug dosages, cardiac output and hospitalization-free survival were evaluated as study outcomes. HF subgroups (i.e.,systolic or diastolic dysfunction, biventricular dysfunction and pulmonary artery hypertension)were also analyzed in association with hospital-free survival.
Results: HF patients showed genotype frequencies of AT (15%) and TT (1%). AT/TT genotype carriers showed downregulated GRK5 gene expression and significant reduction in carvedilol drug dosage (p=0.0001). Moreover, AT/TT genotype carriers on β-blockers showed improved ejection fraction from 27% to 36% (p=0.0007) and increased hospitalization-free survival in comparison to other HF patients. HF patients with AA genotype showed an increased rate of hospital admission in comparison with patients with the AT/TT genotype. HF subgroups with the AT/TT genotype showed an increased hospitalization-free survival versus subgroups with the AA genotype.
Conclusions: GRK5 Gln41>Leu polymorphism in response to β-blocker therapy improved cardiac function in HF patients.
Relevance for patients: This study presents a comprehensive clinicofunctional pharmacogenetic characterization of GRK5 Gln41>Leu polymorphism in a cohort of Indian HF patients. GRK5 Gln41>Leu polymorphism can confer improved cardiac function and reduce hospitalization, thus improving the quality of life in HF patients.

Conflict of interest
The authors declare no conflict of interest.
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