| Literature DB >> 12750963 |
Taku Yoneyama1,2, Hidetoshi Kasuya1, Hideaki Onda1, Hiroyuki Akagawa1,2, Nobuyoshi Jinnai3,2, Toshiaki Nakajima2, Tomokatsu Hori1, Ituro Inoue4.
Abstract
We previously performed a genome-wide linkage study of intracranial aneurysm (IA) and found positive evidence of linkage at chromosomes 5q22-31, 7q11, and 14q22. In the present study, we focus on 5q31, where three candidate genes, fibroblast growth factor 1 (FGF1), fibrillin 2 (FBN2), and lysyl oxidase gene ( LOX) lie, and evaluate associations with IA. Genomic DNAs were obtained from 172 IA patients and 192 controls. Association analysis was performed with ten, five, and four single-nucleotide polymorphisms (SNPs) identified in FGF1, FBN2, and LOX, respectively. A difference in allelic frequency was observed for only the SNP at intron 4 in FGF1 (chi(2)=4.44, df=1, P=0.035). Although a haplotype association was observed with the combination of ten SNPs in FGF1 (chi(2)=16.04, df=1, P=0.00006), significant haplotype associations were not observed when haplotypes were constructed with the three, two, and four SNPs in FGF1 according to the linkage disequilibrium structure. No associations of FBN2 and LOX with IA were detected in the present study.Entities:
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Year: 2003 PMID： 12750963 DOI： 10.1007/s10038-003-0030-6
Source DB: PubMed Journal: J Hum Genet ISSN： 1434-5161 Impact factor: 3.172