ArticleJournal of molecular neuroscience : MN2015
Association of GWAS-Supported Variants rs2200733 and rs6843082 on Chromosome 4q25 with Ischemic Stroke in the Southern Chinese Han Population.
Article in Journal of molecular neuroscience : MN, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 12 citations in OpenAlex.
- Obstructive sleep apnea and genotype rs6843082 as a risk factor for cerebrovascular accident.Scientific reports · 2024Article
- Association Between rs2200733 Polymorphism of PITX2 Gene and the Risk of Atrial Fibrillation.Anatolian journal of cardiology · 2023Article
- Influence of the rs6736 Polymorphism on Ischemic Stroke Susceptibility in Han Chinese Individuals via the Disruption of miR-7-1 Binding to the C14orf119 Gene.Journal of molecular neuroscience : MN · 2022Article
- Stroke Genomics: Current Knowledge, Clinical Applications and Future Possibilities.Brain sciences · 2022Review
- Variants rs2200733 and rs6843082 Show Different Associations in Asian and Non-Asian Populations With Ischemic Stroke.Frontiers in genetics · 2022Article
- Potential Common Genetic Risks of Sporadic Parkinson's Disease and Amyotrophic Lateral Sclerosis in the Han Population of Mainland China.Frontiers in neuroscience · 2021Article
- Polymorphism of rs3737597 in DISC1 Gene on Chromosome 1q42.2 in sALS Patients: a Chinese Han Population Case-Control Study.Molecular neurobiology · 2017Article
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Authors and funding
8 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Genome-wide association studies (GWAS) have revealed two single-nucleotide polymorphisms (SNPs) on chromosome 4q25, rs2200733, and rs6843082, associated with ischemic stroke (IS) in Caucasians. However, subsequent validation studies have remained controversial. The current study aims to evaluate the associations between rs2200733, rs6843082, and IS in the southern Chinese Han population. A total of 1632 subjects were recruited in this case-control study. Genotyping for rs2200733 and rs6843082 was conducted in the Sequenom MassARRAY iPLEX platform. The genetic association of the rs2200733 and rs6843082 polymorphisms with IS was estimated using the PLINK program. Our results show that the SNP rs2200733 and rs6843082 have no significant associations with IS in additive, dominant, recessive, and allelic models (all p > 0.050). However, the results also indicate that the rs2200733 polymorphism is associated with systolic blood pressure (SBP) in IS patients in both the additive model (p adj = 0.002) and the recessive model (p adj = 0.002) after correcting for age. Meanwhile, the rs6843082 polymorphism showed a significant association with serum total cholesterol (TC) in IS individuals in the additive model (p adj = 0.017) and the dominant model (p adj = 0.023). These findings suggest that the SNP rs2200733 and rs6843082 on chromosome 4q25 may be not associated with IS susceptibility in southern Han Chinese. As for IS-related quantitative traits, the rs2200733 and rs6843082 polymorphisms might influence SBP and TC in IS patients, respectively.
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