IL12B rs6887695 polymorphism and interaction with alcohol intake in the risk of ulcerative colitis in Japan.
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Miyake Yoshihiro, Tanaka Keiko, Nagata Chisato, Furukawa Shinya, Andoh Akira, Yokoyama Tetsuji, Yoshimura Naoki, Mori Kenichiro, Ninomiya Tomoyuki, Yamamoto Yasunori, Takeshita Eiji, Ikeda Yoshio, Saito Mitsuru, Ohashi Katsuhisa, Imaeda Hirotsugu, Kakimoto Kazuki, Higuchi Kazuhide, Nunoi Hiroaki, Mizukami Yuji, Suzuki Seiyuu, Hiraoka Sakiko, Okada Hiroyuki, Kawasaki Keitarou, Higashiyama Masaaki, Hokari Ryota, Miura Hiromasa, Miyake Teruki, Kumagi Teru, Kato Hiromasa, Hato Naohito, Sayama Koji, Hiasa Yoichi, Japan Ulcerative Colitis Study Group
Аннотация
METHODS: There were 384 cases within 4 years of UC diagnosis and 661 controls who were enrolled. Adjustments were made for sex, age, pack-years of smoking, alcohol consumption, history of appendicitis, family history of UC, education level, and body mass index.
RESULTS: Subjects with the GG IL12B SNP rs6887695 genotype had a significantly increased risk of UC compared with those with the CC genotype (adjusted odds ratio [AOR], 1.60; 95% confidence interval [CI], 1.08-2.36). This positive association was also significant using the additive and recessive models (AOR, 1.25; 95% CI, 1.03-1.52; AOR, 1.50; 95% CI, 1.08-2.09, respectively). An independent inverse relationship was observed between ever alcohol consumption and the UC risk in those with the CC genotype while no significant association was found in those with at least one G allele (P for interaction = 0.0008).
CONCLUSIONS: IL12B SNP rs6887695 was significantly associated with UC. The influence of alcohol consumption might rely on rs6887695.