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Mutation location effect on severity of phenotype during exercise testing in type 1 long-QT syndrome: impact of transmembrane and C-loop location.
J Cardiovasc Electrophysiol ; 24(9): 1015-20, 2013 Sep.
Article em En | MEDLINE | ID: mdl-23691991
ABSTRACT

BACKGROUND:

Targeted mutation site-specific differences have correlated C-loop missense mutations with worse outcomes and increased benefit of beta-blockers in LQT1. This observation has implicated the C-loop region as being mechanistically important in the altered response to sympathetic stimulation known to put patients with LQT1 at risk of syncope and sudden cardiac death.

OBJECTIVE:

The objective of this study was to determine if there is mutation site-specific response to sympathetic stimulation and beta-blockers using exercise testing.

METHODS:

This study is a retrospective review of LQT1 patients undergoing exercise testing at 3 academic referral centers.

RESULTS:

A total of 123 patients (age 28 ± 17 years, 59 male) were studied including 34 patients (28%) with C-loop mutations. There were no significant differences in supine, standing, peak exercise and 1-minute recovery QTc duration between patients with C-loop mutations and patients with alternate mutation sites. In 37 patients that underwent testing on and off beta-blockers, beta-blocker use was associated with a significant reduction in supine, standing and peak exercise QTc. This difference was not seen in the small group of patients (7/37) with C-loop mutations. There was no difference in QTc at 1 and 4 minutes into recovery.

CONCLUSIONS:

Genetically confirmed LQT1 patients in this study cohort with C-loop mutations did not demonstrate the expected increase in QTc in response to exercise, or resultant response to beta-blocker. The apparent increased risk of cardiac events associated with C-loop mutation sites and the marked benefit received from beta-blocker therapy are not reflected by exercise-mediated effects on QTc in this study population.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Mutação de Sentido Incorreto / Síndrome de Romano-Ward / Canal de Potássio KCNQ1 / Teste de Esforço Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Mutação de Sentido Incorreto / Síndrome de Romano-Ward / Canal de Potássio KCNQ1 / Teste de Esforço Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2013 Tipo de documento: Article