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Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese
期刊文章   開放取用(OA)   同儕審查

Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese

Tatsuya Furuichi, Koichi Maeda, Chung-Tei Chou, Yu-Fen Liu, Ting-Chun Liu, Yoshinari Miyamoto, Atsushi Takahashi, Kanji Mori, Katsunori Ikari, Naoyuki Kamatani, …
Journal of Human Genetics, 卷.53(5), 頁碼.419-424
05/2008
PMID: 18299954

摘要

ANKH Ankylosing spondylitis Association MSX2 Single-nucleotide polymorphism markers Genetics (clinical) Genetics
Several genes have been implicated in the etiology of ankylosing spondylitis (AS); however, the significance of these genes except HLA-B27 remains to be elucidated. In this study, we examined the association of AS with novel candidate genes and previously reported genes other than HLA-B27. We examined a total of 45 single nucleotide polymorphisms (SNPs) in 15 genes by a sequential screening. We first genotyped 170 Japanese AS patients and 896 controls for the SNPs (first screen). Then, we genotyped eight SNPs with P < 0.05 in the first screen for 108 additional Japanese patients (second screen). We checked the replication of the association of the most significant SNP by genotyping 219 Taiwanese AS patients and 185 controls. When the first and second screens were combined, four SNPs showed nominal significance of P < 0.05. An intronic SNP (IVS1 + 996G > A) in MSX2, a novel candidate gene, showed the most significant association (P = 0.0030). The association was not replicated in our Taiwanese population; however, there was the same trend with the Japanese population in the allelic frequency distribution of the SNP. In the genes previously reported to have association with AS, only one synonymous SNP, c.963T > G in ANKH, showed a marginal association in the Japanese population (P = 0.045). © 2008 The Japan Society of Human Genetics and Springer.

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https://doi.org/10.1007/s10038-008-0265-3檢視
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