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Association between Beta Adrenergic Receptor Polymorphism and Ischemic Stroke: A Meta-Analysis

BACKGROUND AND PURPOSE: The purpose of this meta-analysis was to determine the precise association between beta-2 adrenergic receptor (β2AR) polymorphism and Ischemic stroke. METHODS: Published case control studies on association between β2AR and ischemic stroke were searched from electronic databas...

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Detalles Bibliográficos
Autores principales: Kumar, Amit, Prasad, Manya, Kumar, Pradeep, Yadav, Arun Kumar, Pandit, Awadh Kishor, Kathuria, Prachi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Stroke Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460333/
https://www.ncbi.nlm.nih.gov/pubmed/26060801
http://dx.doi.org/10.5853/jos.2015.17.2.138
Descripción
Sumario:BACKGROUND AND PURPOSE: The purpose of this meta-analysis was to determine the precise association between beta-2 adrenergic receptor (β2AR) polymorphism and Ischemic stroke. METHODS: Published case control studies on association between β2AR and ischemic stroke were searched from electronic databases. Pooled Odds ratio and 95% Confidence interval were calculated by using software RevMan version 5.2. RESULTS: A total of three studies involving 1,642 cases and 1,673 controls, which were published from 2007 to 2014, were subjected to meta-analysis for allelic association and 518 cases and 510 controls for genotypic association. Pooled analysis of two studies for genotypic association suggested that subjects carrying Gln27Glu polymorphism of β2AR had an increased risk for Ischemic stroke under recessive model (OR 2.09; 95% CI; 1.20 to 3.64) and under dominant model (OR 1.47; 95% CI 1.14 to 1.90). Pooled analysis of three studies for allelic association showed a significantly higher Glu27 allele of β2AR in the patients with ischemic stroke (OR 1.58; 95% CI; 1.38 to 1.81). CONCLUSIONS: The present meta-analysis suggests that Gln27Glu polymorphism of β2AR gene is associated with increased risk for ischemic stroke.