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Vascular endothelial growth factor A polymorphisms are associated with increased risk of coronary heart disease: a

Yafeng Wang1, Qiuyu Huang2, Jianchao Liu3

  • 1Cardiovascular Department, The Second Clinical Medical College of Fujian Medical University, Quanzhou, Fujian, China.

Oncotarget
|April 22, 2017
PubMed

Insights

Genetic variations in vascular endothelial growth factor (VEGFA) are linked to coronary heart disease (CHD) risk. Specific VEGFA polymorphisms (rs699947, rs3025039, rs2010963) were identified as significant risk factors for developing CHD.

Area of Science:

  • Cardiovascular Genetics
  • Molecular Epidemiology
  • Biomedical Research

Background:

  • Coronary heart disease (CHD) arises from complex genetic and environmental interactions.
  • Vascular Endothelial Growth Factor (VEGFA) plays a crucial role in vascular biology.
  • Identifying genetic risk factors for CHD is vital for understanding disease pathogenesis.

Purpose of the Study:

  • To investigate the association between specific VEGFA gene polymorphisms (rs699947 C>A, rs3025039 C>T, rs2010963 G>C) and the risk of developing CHD.
  • To conduct a comprehensive meta-analysis to pool existing evidence on VEGFA polymorphisms and CHD risk.
  • To explore potential ethnic and CHD subtype-specific associations.

Main Methods:

  • Systematic literature search of EMBASE and PubMed databases.
  • Meta-analysis of ten publications comprising 22 trials.
  • Inclusion of 2097 cases and 2867 controls.
  • Calculation of Odds Ratios (ORs) with 95% Confidence Intervals (CIs) to assess genetic associations.

Main Results:

  • A significant association was found between VEGFA rs699947 C>A polymorphism and increased CHD risk.
  • VEGFA rs3025039 C>T polymorphism also showed a significant association with CHD risk.
  • VEGFA rs2010963 G>C polymorphism was associated with myocardial infarction (MI) risk.

Conclusions:

  • The VEGFA rs699947 C>A, rs3025039 C>T, and rs2010963 G>C polymorphisms are identified as risk factors for CHD.
  • These findings highlight the role of VEGFA genetic variations in CHD susceptibility.
  • Further large-scale, well-designed studies are recommended to validate these genetic associations.

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