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Impact of Neuroeffector Adrenergic Receptor Polymorphisms on Incident Ventricular Fibrillation During Acute Myocardial Ischemia. | LitMetric

AI Article Synopsis

  • Research indicates that genetic variations in cardiac adrenergic receptors may influence the risk of developing ventricular fibrillation (VF) during ST-segment-elevation myocardial infarction (STEMI).
  • In a study involving 953 patients, specific polymorphisms were analyzed to see how they impacted VF occurrence, with 19 out of 156 genetic constructs linked to lower VF risk.
  • Notably, the Gly49 and Del322-325 variants were associated with reduced VF risk, potentially due to their effects on norepinephrine release and biased signaling, providing insights that could inform future treatment approaches.

Article Abstract

Background Cardiac adrenergic receptor gene polymorphisms have the potential to influence risk of developing ventricular fibrillation (VF) during ST-segment-elevation myocardial infarction, but no previous study has comprehensively investigated those most likely to alter norepinephrine release, signal transduction, or biased signaling. Methods and Results In a case-control study, we recruited 953 patients with ST-segment-elevation myocardial infarction without previous cardiac history, 477 with primary VF, and 476 controls without VF, and genotyped them for Arg389Gly and Ser49Gly, Gln27Glu and Gly16Arg, and Ins322-325Del. Within each minor allele-containing genotype, haplotype, or 2-genotype combination, patients with incident VF were compared with non-VF controls by odds ratios (OR) of variant frequencies referenced against major allele homozygotes. Of 156 investigated genetic constructs, 19 (12.2%) exhibited significantly (<0.05) reduced association with incident VF, and none was associated with increased VF risk except for Gly389 homozygotes in the subset of patients not receiving β-blockers. Gly49 carriers (prevalence 23.0%) had an OR (95% CI) of 0.70 (0.49-0.98), and the 322-325 deletion (Del) carriers (prevalence 13.5%) had an OR of 0.61 (0.39-0.94). When present in genotype combinations (8 each), both Gly49 carriers (OR, 0.67 [0.56-0.80]) and Del carriers (OR, 0.57 [0.45- 0.71]) were associated with reduced VF risk. Conclusions In ST-segment-elevation myocardial infarction, the adrenergic receptor minor alleles Gly49, whose encoded receptor undergoes enhanced agonist-mediated internalization and β-arrestin interactions leading to cardioprotective biased signaling, and Del322-325, whose receptor causes disinhibition of norepinephrine release, are associated with a lower incidence of VF. Registration URL: https://clinicaltrials.gov; Unique identifier: NCT00859300.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10111522PMC
http://dx.doi.org/10.1161/JAHA.122.025368DOI Listing

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