Association between polymorphisms in microRNAs and ischemic stroke in an Asian population: evidence based on 6,083

Donghua Zou1, Chunbin Liu1, Qian Zhang1

  • 1Department of Stroke Center, The Fifth Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China, drweijinru@126.com.

Abstract

Insights

Genetic variations in miR-146a and miR-149 are linked to increased ischemic stroke (IS) risk in Asian populations. However, miR-196a2 and miR-499 polymorphisms showed no significant association with IS.

Area of Science:

  • Genetics
  • Molecular Biology
  • Neurology

Background:

  • MicroRNA (miRNA) gene polymorphisms have been implicated in ischemic stroke (IS) pathogenesis.
  • Previous studies on specific miRNA polymorphisms (miR-146a, miR-196a2, miR-149, miR-499) and IS risk have yielded inconsistent findings.

Purpose of the Study:

  • To conduct a meta-analysis investigating the association between four specific miRNA polymorphisms and ischemic stroke risk.
  • To clarify the inconsistent results regarding the role of these polymorphisms in IS susceptibility.

Main Methods:

  • A meta-analysis was performed, pooling data from 14 case-control studies.
  • The analysis included a total of 6,083 IS cases and 7,248 controls from Asian populations.
  • Four polymorphisms (miR-146a rs2910164, miR-196a2 rs11614913, miR-149 rs2292832, miR-499 rs3746444) were assessed across various genetic models.

Main Results:

  • The GG genotype of miR-146a (rs2910164) was associated with an increased risk of IS under the recessive model (OR=1.20, P=0.03).
  • The CC genotype of miR-149 (rs2292832) showed an increased IS risk in both recessive (OR=1.28, P=0.005) and homozygous (OR=1.31, P=0.004) models.
  • No significant association between miR-196a2 (rs11614913) or miR-499 (rs3746444) polymorphisms and IS risk was observed in any genetic model.

Conclusions:

  • The GG genotype of miR-146a and the CC genotype of miR-149 may increase susceptibility to ischemic stroke in Asian populations.
  • Polymorphisms in miR-196a2 and miR-499 do not appear to be associated with IS risk in this population.
  • Further large-scale, well-designed studies are recommended to validate these findings.

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