[Associations of the MicroRNA-143/145 Polymorphisms with Cardiovascular Risk Factors and the Severity of Coronary

Yun Chen1, Zhi Luo1, Wei Zeng1

  • 1Department of Cardiology,Affiliated Hospital,College of Preclinical Medicine,North Sichuan Medical College,Nanchong,Sichuan 637000,China.

Insights

The rs353292 polymorphism in microRNA-143/145 is linked to higher cardiovascular risk factors like triglycerides, glucose, and hs-CRP. This genetic variation may increase the risk of myocardial infarction in Chinese individuals.

Area of Science:

  • Genetics
  • Cardiovascular Disease
  • Biochemistry

Background:

  • MicroRNA (miR)-143/145 gene polymorphisms are implicated in cardiovascular disease.
  • Understanding their role in cardiovascular risk factors and coronary heart disease (CHD) severity is crucial.

Purpose of the Study:

  • To investigate the association between miR-143/145 polymorphisms (rs353292 and rs4705343) and cardiovascular risk factors.
  • To evaluate the impact of these polymorphisms on the severity of coronary heart disease (CHD) in the Chinese Han population.

Main Methods:

  • Genotyping of rs353292 and rs4705343 polymorphisms using polymerase chain reaction-restriction fragment length polymorphism.
  • Analysis of 380 CHD patients and 163 healthy controls.
  • Comparison of physiological, biochemical parameters, and myocardial infarction (MI) incidence across genotypes.

Main Results:

  • The rs353292 TT genotype was associated with higher serum triglycerides and glucose levels in controls.
  • In CHD patients, the rs353292 TT genotype correlated with elevated hypersensitive C-reactive protein (hs-CRP) and a higher frequency of MI.
  • The rs4705343 polymorphism showed no significant association with CHD risk or severity.

Conclusions:

  • The T allele of rs353292 polymorphism is linked to increased serum hs-CRP levels in CHD patients.
  • This polymorphism may influence myocardial infarction occurrence and progression via miR-143/145 regulation of CRP.
  • The rs4705343 polymorphism is not associated with CHD risk or severity.

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