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Genetic polymorphism of ITGA2 C807T can increase the risk of ischemic stroke.

AbstractBACKGROUND:
The role of genetic variants in the pathogenesis of stroke has not been fully elucidated. Several studies have been examined the association of the Integrin alpha2 (ITGA2) gene-C807T (rs1126643) polymorphism with ischemic stroke susceptibility. However, the results of these studies are inconsistent. In order to explore this association more deeply, we performed a meta-analysis.
METHODS:
We collected case-control studies concerning the relationship between the C807T polymorphism and ischemic stroke, and odd ratios (OR) with corresponding 95% confidence intervals (CI) were used to describe the relationships. Inconsistency index (I(2)) and Cochran's Q statistic were used to check heterogeneity. Publication bias was tested by funnel plots and Egger's test.
RESULTS:
Fifteen studies with 2242 cases and 2408 controls were included. Our meta-analysis results indicated an association between the C807T polymorphism and the risk of ischemic stroke in the overall population, Asians and the subgroup of hospital-based people. However, statistically association was not observed for Caucasians and non-hospitalized individuals.
CONCLUSIONS:
The ITGA2 gene C807T polymorphism may be a susceptible predictor of the risk of ischemic stroke. More data are needed to elucidate the relationship further.
AuthorsGuangliang Wu, Yujing Xi, Li Yao, Li Su, Yan Yan, Minzhi Li, Lian Gu
JournalThe International journal of neuroscience (Int J Neurosci) Vol. 124 Issue 11 Pg. 841-51 (Nov 2014) ISSN: 1563-5279 [Electronic] England
PMID24397542 (Publication Type: Journal Article, Meta-Analysis)
Chemical References
  • Integrin alpha2
Topics
  • Asian People (genetics)
  • Brain Ischemia (complications, genetics)
  • Case-Control Studies
  • Genetic Association Studies
  • Genetic Predisposition to Disease (genetics)
  • Hospitalization (statistics & numerical data)
  • Humans
  • Integrin alpha2 (genetics)
  • Polymorphism, Single Nucleotide (genetics)
  • Publication Bias (statistics & numerical data)
  • Stroke (complications, genetics)
  • White People (genetics)

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