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Published on: April 1, 2019
[Association of ADAMTS-1 gene polymorphisms with ischemic stroke caused by large artery atherosclerosis]
Chenling Lyu1, Yawen Chen, Min Zhu
1Department of Neurology, Taizhou Hospital Affiliated to Wenzhou Medical University, Taizhou, Zhejiang 317000, P.R. China. jinxp155@aliyun.com.
Insights
Polymorphisms in the ADAMTS-1 gene, specifically rs402007, are linked to large artery atherosclerosis ischemic stroke. The C allele may increase susceptibility to this stroke subtype.
Area of Science:
- Genetics
- Neurology
- Cardiovascular Disease
Background:
- Large artery atherosclerosis (LAA) is a significant cause of ischemic stroke.
- Genetic factors play a role in the development of LAA-related ischemic stroke.
- The ADAMTS-1 gene is a potential candidate gene influencing vascular disease.
Purpose of the Study:
- To investigate the association between specific polymorphisms in the ADAMTS-1 gene and ischemic stroke caused by LAA.
- To identify potential genetic risk factors for LAA-related ischemic stroke.
Main Methods:
- Genotyping of single nucleotide polymorphisms (SNPs) rs416905 (T/C) and rs402007 (G/C) in the ADAMTS-1 gene.
- Polymerase chain reaction and DNA sequencing were used for genotyping.
- Comparison of genotype and allele frequencies between 767 patients with LAA ischemic stroke and 506 controls.
Main Results:
- Significant differences in the frequencies of the rs402007 GC+CC genotype and C allele were observed between patients and controls.
- Binary logistic regression confirmed the significant association of rs402007 polymorphisms with LAA ischemic stroke (P=0.001, OR=1.521).
- rs416905 and rs402007 SNPs were in complete linkage disequilibrium.
Conclusions:
- Polymorphisms in the ADAMTS-1 gene, particularly at the rs402007 locus, are associated with ischemic stroke due to LAA.
- The C allele of the rs402007 polymorphism may represent a susceptibility factor for LAA-related ischemic stroke.
Objective:
To assess the association of a disintegrin and metallo-proteinase with thrombospondin type 1 motifs (ADAMTS-1) gene polymorphism and ischemic stroke caused by large artery atherosclerosis (LAA).
Methods:
In total 767 patients and 506 controls were recruited. Single nucleotide polymorphisms (SNPs) rs416905 (T/C) and rs402007 (G/C) of the ADAMTS-1 gene were genotyped by polymerase chain reaction and DNA sequencing.
Results:
Frequencies of the rs402007 GC+CC genotype and the C allele were significantly different between the two groups (68.84% vs. 60.67%, χ2=9.012, P=0.003, OR=1.432; 45.24% vs. 38.54%, χ2=11.208, P=0.001, OR=1.318). Binary logistic regression has confirmed that the above difference was significant (P=0.001, OR=1.521, 95%CI: 1.183-1.955). The frequencies of TC+CC and GC+CC genotypes were similar between the two groups, and so was it with the C allele. The two SNPs had been in complete linkage disequilibrium (D'=1.0, r2=1.0).
Conclusion:
The rs416905 and rs402007 polymorphisms of the ADAMTS-1 gene may be associated with ischemic stroke caused by LAA. The C allele of the rs402007 locus may be a susceptibility factor for this subtype of stroke.
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