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Polymorphism of CONNEXIN37 gene is a risk factor for ischemic stroke in Han Chinese population.

AbstractBACKGROUND:
Stroke has a high fatality and disability rate, and is one of the main burdens to human health. It is thus very important to identify biomarkers for the development of effective approaches for the prevention and treatment of stroke. Connexin37 is an anti-inflammatory cytokine and is involved in chronic inflammation and atherosclerosis. Recent studies have found that CONNEXIN37 gene variations are associated with atherosclerosis diseases, such as coronary heart disease and stroke, but its association with stroke in distinct human populations remains to be determined. We report here the analysis of the association of the single nucleotide polymorphisms (SNPs) of CONNEXIN37 with ischemic stroke in Han Chinese population.
METHODS:
Two SNPs of CONNEXIN37 gene were analyzed in 385 ischemic stroke patients and 362 hypertension control patients using ligase detection reaction (LDR) method.
RESULTS:
Logistic regression analysis demonstrated that, AG and GG genotypes of SNP rs1764390 and CC genotype of rs1764391 of CONNEXIN37 were associated with an increased risk of ischemic stroke, and that G allele of rs1764390 is a risk factor for ischemic stroke. Further, we found that SNP rs1764390 and SNP rs1764391 in CONNEXIN37 were associated with ischemic stroke under additive/dominant model, and recessive/dominant model, respectively.
CONCLUSION:
Our results indicate that CONNEXIN37 gene polymorphism is an ischemic stroke risk factor in Northern Han Chinese.
AuthorsHong Li, Shasha Yu, Rui Wang, Zhaoqing Sun, Xinghu Zhou, Liqiang Zheng, Zhihua Yin, Yingxian Sun
JournalLipids in health and disease (Lipids Health Dis) Vol. 17 Issue 1 Pg. 72 (Apr 10 2018) ISSN: 1476-511X [Electronic] England
PMID29631604 (Publication Type: Journal Article)
Chemical References
  • Connexins
Topics
  • Asian People (genetics)
  • Brain Ischemia (genetics)
  • Case-Control Studies
  • Connexins (genetics)
  • Gene Frequency
  • Haplotypes (genetics)
  • Humans
  • Hypertension (genetics)
  • Linkage Disequilibrium
  • Polymorphism, Single Nucleotide
  • Stroke (genetics)
  • Gap Junction alpha-4 Protein

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