Possible genetic implications in the response to cardiac resynchronisation therapy in a patient affected by heart failure

Possible genetic implications in the response to cardiac resynchronisation therapy in a patient affected by heart failure

Authors

  • Natalia Pezzali Cardiologia, Dipartimento di Medicina Sperimentale e Applicata, Università e Spedali Civili di Brescia
  • Marco Metra Cardiologia, Dipartimento di Medicina Sperimentale e Applicata, Università e Spedali Civili di Brescia
  • Livio Dei Cas Cardiologia, Dipartimento di Medicina Sperimentale e Applicata, Università e Spedali Civili di Brescia

DOI:

https://doi.org/10.7175/cmi.v5i2.507

Keywords:

Heart failure, Cardiac resynchronisation therapy, Genetic polymorphisms

Abstract

This report presents a case of a patient with idiopathic dilated cardiomyopathy and severe left ventricular systolic dysfunction who underwent cardiac resynchronisation therapy (CRT). During the follow-up a progressive increase in left ventricular ejection fraction was observed, as well as clinical improvement. No cardiovascular events occurred during the follow-up, except for appropriate Implantable Cardioverter Defibrillator (ICD) bursts for fast ventricular tachycardia. Genotyping for adrenoceptor gene polymorphisms detected that the patient was Glu27Glu homozygous carrier. There’s a large interindividual variability in response to CRT. Despite attempts to identify factors having an impact on this therapy, only QRS duration is accepted according to guidelines. Beta-adrenoceptors polymorphisms, modulating sympathetic drive in heart failure and left ventricular remodelling, may have a role in identifying patients with a better response to CRT, in order to target and individualise the patients’ treatment.

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Published

2011-06-15

Issue

Section

Case report
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