Influence of the β-fibrinogen-455G/A polymorphism on development of ischemic stroke and coronary heart disease

Lian Gu1, Wenhui Liu2, Yan Yan1

  • 1Department of Neurology, First Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning, Guangxi, China.

Thrombosis Research
|January 23, 2014
PubMed

Insights

The β-fibrinogen-455G/A polymorphism is linked to increased risk of ischemic stroke (IS) and coronary heart disease (CHD). This genetic factor, particularly the A allele, shows higher susceptibility in Asian populations for IS.

Area of Science:

  • Genetics and Cardiovascular Disease
  • Molecular Epidemiology
  • Vascular Biology

Background:

  • Ischemic stroke (IS) and coronary heart disease (CHD) are leading global causes of mortality.
  • Previous studies on the β-fibrinogen-455G/A (FGB-455G/A) polymorphism and IS/CHD risk have yielded inconsistent results.

Purpose of the Study:

  • To conduct a meta-analysis investigating the association between the FGB-455G/A polymorphism and susceptibility to IS and CHD.
  • To clarify the genetic contribution of this polymorphism to vascular disorders.

Main Methods:

  • A comprehensive literature search was performed across PubMed, Embase, and four Chinese databases up to July 2013.
  • Data from 45 studies (7238 cases, 7395 controls) were analyzed using Stata 11.2.
  • Pooled odds ratios (OR) with 95% confidence intervals (CI) and cumulative meta-analysis were employed to assess genetic associations and temporal trends.

Main Results:

  • The FGB-455G/A polymorphism is associated with an increased risk of IS (OR=1.518, 95%CI=1.279-1.802) under the dominant model.
  • Subgroup analysis revealed a significantly elevated risk of IS associated with the A allele in Asians (OR=1.700, 95%CI=1.417-2.040) but not in Caucasians.
  • A significant association was also found between the FGB-455G/A polymorphism and CHD risk (OR=1.802, 95%CI=1.445-2.246).

Conclusions:

  • The FGB-455G/A polymorphism is a contributing factor to the susceptibility of individuals to ischemic stroke.
  • This genetic polymorphism also plays a role in the development of coronary heart disease.
  • The findings highlight the importance of genetic variations in fibrinogen for vascular disease risk.
Abstract

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