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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.
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.
Background:
Ischemic stroke (IS) and coronary heart disease (CHD) are two vascular disorders that are a common cause of death worldwide. Several studies have assessed the association of the β-fibrinogen-455G/A (FGB-455G/A) polymorphism and risk of IS and CHD, but the results are still inconsistent. Our study aimed to investigate whether the FGB-455G/A polymorphism was associated with susceptibility to IS and CHD by using meta-analysis.
Methods:
Relevant studies were identified from PubMed, Embase and four Chinese database up to July 2013.Data were analyzed and processed by Stata 11.2. A pooled OR with 95% CI was calculated to estimate the strength of the genetic association. Cumulative meta-analysis was performed to assess the tendency of pooled OR over time.
Results:
45 studies based on a total of 7238 cases and 7395 controls were included in our meta-analysis. The results indicated that the FGB-455G/A polymorphism is associated with the risk of IS when compared with the dominant model (OR=1.518, 95%CI=1.279-1.802 for AA+GA vs. GG). In the subgroup analysis by ethnicity, significantly elevated risks were associated with the A allele in Asians (OR=1.700, 95%CI=1.417-2.040), but not in Caucasians (OR=0.942, 95%CI=0.813-1.091). Both the hypertension and non-hypertension subgroups reached significant results, but no significance was found when stratified according to sex or subtype of IS. Results indicate that the FGB-455G/A polymorphism is associated with CHD (OR=1.802, 95%CI=1.445-2.246).
Conclusion:
Our meta-analysis suggests that the FGB-455G/A polymorphism contributes to susceptibility to IS and CHD.
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