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http://purl.uniprot.org/citations/29360590http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
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Objective

To investigate the association between single nucleotide polymorphisms or haplotypes of the COL4A1 gene and the risk of intracerebral hemorrhage (ICH).

Methods

We conducted a case-control study that included 181 patients from the Chinese Han population with hypertensive ICH and 197 hypertension patients without ICH. Genomic DNA was extracted by DNA extraction kit, and the 6 single nucleotide polymorphism genotypes of the COL4A1 gene were detected with a MassARRAY Analyzer. Unphased 3.1.4 and SPSS 19.0 were used to analyze the association between alleles, genotypes, and haplotypes of the COL4A1 gene and the risk of ICH.

Results

Compared with the control group, patients in the ICH group were significantly younger. There were no differences in gender, diabetes, hyperlipidemia, current smoking, and alcohol consumption between the 2 groups. Our association analysis showed that the rs3742207 A, rs11069830 A, and rs679505 A alleles were association factors of the risks of ICH; rs11069830 AA, rs544012 AC, and rs679505 AA genotypes were association factors of the risk of ICH; AA haplotype (rs3742207-rs11069830) was an association factor of the risk of ICH. After adjusting age and gender by multivariate logistic regression, the rs544012 AC and rs679505 AA genotypes were independently associated with the risk of ICH.

Conclusions

Our study showed that the rs544012 AC and rs679505 AA genotypes were independently associated with the risk of ICH in the Chinese Han population and that the AA haplotype (rs3742207-rs11069830) in the COL4A1 gene may be related to the risk of ICH in the Chinese Han population; these conclusions need further confirmation in future studies with larger samples."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.org/dc/terms/identifier"doi:10.1016/j.wneu.2018.01.072"xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/author"He S."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/author"Li H."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/author"Lin S."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/author"Liu M."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/author"Yang J."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/author"Zheng J."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/author"Xia C."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/author"You C."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/date"2018"xsd:gYear
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/name"World Neurosurg"xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/pages"e527-e533"xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/title"Genetic Variations of the COL4A1 Gene and Intracerebral Hemorrhage Risk: A Case-Control Study in a Chinese Han Population."xsd:string
http://purl.uniprot.org/citations/29360590http://purl.uniprot.org/core/volume"112"xsd:string
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