TY - JOUR
T1 - IL12B rs6887695 polymorphism and interaction with alcohol intake in the risk of ulcerative colitis in Japan
AU - Japan Ulcerative Colitis Study Group
AU - Miyake, Yoshihiro
AU - Tanaka, Keiko
AU - Nagata, Chisato
AU - Furukawa, Shinya
AU - Andoh, Akira
AU - Yokoyama, Tetsuji
AU - Yoshimura, Naoki
AU - Mori, Kenichiro
AU - Ninomiya, Tomoyuki
AU - Yamamoto, Yasunori
AU - Takeshita, Eiji
AU - Ikeda, Yoshio
AU - Saito, Mitsuru
AU - Ohashi, Katsuhisa
AU - Imaeda, Hirotsugu
AU - Kakimoto, Kazuki
AU - Higuchi, Kazuhide
AU - Nunoi, Hiroaki
AU - Mizukami, Yuji
AU - Suzuki, Seiyuu
AU - Hiraoka, Sakiko
AU - Okada, Hiroyuki
AU - Kawasaki, Keitarou
AU - Higashiyama, Masaaki
AU - Hokari, Ryota
AU - Miura, Hiromasa
AU - Miyake, Teruki
AU - Kumagi, Teru
AU - Kato, Hiromasa
AU - Hato, Naohito
AU - Sayama, Koji
AU - Hiasa, Yoichi
N1 - Funding Information:
This work was supported by Health and Labour Sciences Research Grants, Research on Intractable Diseases from the Ministry of Health, Labour, and Welfare, Japan (grant number H27-nanchitou[nan]-ippan-033), and the Japan Intractable Diseases Research Foundation. The funding sources did not have a role in the trial design or manuscript preparation.
Publisher Copyright:
© 2022
PY - 2022/7
Y1 - 2022/7
N2 - Background: The interleukin (IL)-23/Th17 pathway plays a critical role in ulcerative colitis (UC). The IL-12p40 subunit, which is shared by IL-23 and IL-12, is encoded by the IL12B gene. The current case-control study investigated the association between IL12B SNP rs6887695 and the UC risk. 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.
AB - Background: The interleukin (IL)-23/Th17 pathway plays a critical role in ulcerative colitis (UC). The IL-12p40 subunit, which is shared by IL-23 and IL-12, is encoded by the IL12B gene. The current case-control study investigated the association between IL12B SNP rs6887695 and the UC risk. 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.
KW - Alcohol consumption
KW - Gene-environment interaction
KW - IL12B polymorphism
KW - Japanese
KW - Ulcerative colitis
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U2 - 10.1016/j.cyto.2022.155901
DO - 10.1016/j.cyto.2022.155901
M3 - Article
C2 - 35567898
AN - SCOPUS:85129993973
SN - 1043-4666
VL - 155
JO - Cytokine
JF - Cytokine
M1 - 155901
ER -