TY - JOUR
T1 - Disease susceptibility genes shared by primary biliary cirrhosis and Crohn's disease in the Japanese population
AU - Aiba, Yoshihiro
AU - Yamazaki, Keiko
AU - Nishida, Nao
AU - Kawashima, Minae
AU - Hitomi, Yuki
AU - Nakamura, Hitomi
AU - Komori, Atsumasa
AU - Fuyuno, Yuta
AU - Takahashi, Atsushi
AU - Kawaguchi, Takaaki
AU - Takazoe, Masakazu
AU - Suzuki, Yasuo
AU - Motoya, Satoshi
AU - Matsui, Toshiyuki
AU - Esaki, Motohiro
AU - Matsumoto, Takayuki
AU - Kubo, Michiaki
AU - Tokunaga, Katsushi
AU - Nakamura, Minoru
N1 - Publisher Copyright:
© 2015 The Japan Society of Human Genetics.
PY - 2015/9/29
Y1 - 2015/9/29
N2 - We previously identified TNFSF15 as the most significant susceptibility gene at non-HLA loci for both primary biliary cirrhosis (PBC) and Crohn's diseases (CD) in the Japanese population. The aim of this study is to identify further disease susceptibility genes shared by PBC and CD. We selected 15 and 33 genetic variants that were significantly associated with PBC and CD, respectively, based on previously reported genome-wide association studies of the Japanese population. Next, an association study was independently performed for these genetic variants in CD (1312 CD patients and 3331 healthy controls) and PBC (1279 PBC patients and 1015 healthy controls) cohorts. Two CD susceptibility genes, ICOSLG rs2838519 and IL12B rs6556412, were also nominally associated with susceptibility to PBC (P=3.85 × 10 -2 and P=8.40 × 10 -3, respectively). Three PBC susceptibility genes, CXCR5 rs6421571, STAT4 rs7574865 and NFKB1 rs230534, were nominally associated with susceptibility to CD (P=2.82 × 10 -2, P=3.88 × 10 -2 and P=2.04 × 10 -2, respectively). The effect of ICOSLG and CXCR5 variants were concordant but the effect of STAT4, NFKB1 and IL12B variants were discordant for PBC and CD. TNFSF15 and ICOSLG-CXCR5 might constitute a shared pathogenic pathway in the development of PBC and CD in the Japanese population, whereas IL12B-STAT4-NFKB1 might constitute an opposite pathogenic pathway, reflecting the different balance between Th1 and Th17 in the two diseases.
AB - We previously identified TNFSF15 as the most significant susceptibility gene at non-HLA loci for both primary biliary cirrhosis (PBC) and Crohn's diseases (CD) in the Japanese population. The aim of this study is to identify further disease susceptibility genes shared by PBC and CD. We selected 15 and 33 genetic variants that were significantly associated with PBC and CD, respectively, based on previously reported genome-wide association studies of the Japanese population. Next, an association study was independently performed for these genetic variants in CD (1312 CD patients and 3331 healthy controls) and PBC (1279 PBC patients and 1015 healthy controls) cohorts. Two CD susceptibility genes, ICOSLG rs2838519 and IL12B rs6556412, were also nominally associated with susceptibility to PBC (P=3.85 × 10 -2 and P=8.40 × 10 -3, respectively). Three PBC susceptibility genes, CXCR5 rs6421571, STAT4 rs7574865 and NFKB1 rs230534, were nominally associated with susceptibility to CD (P=2.82 × 10 -2, P=3.88 × 10 -2 and P=2.04 × 10 -2, respectively). The effect of ICOSLG and CXCR5 variants were concordant but the effect of STAT4, NFKB1 and IL12B variants were discordant for PBC and CD. TNFSF15 and ICOSLG-CXCR5 might constitute a shared pathogenic pathway in the development of PBC and CD in the Japanese population, whereas IL12B-STAT4-NFKB1 might constitute an opposite pathogenic pathway, reflecting the different balance between Th1 and Th17 in the two diseases.
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U2 - 10.1038/jhg.2015.59
DO - 10.1038/jhg.2015.59
M3 - Article
C2 - 26084578
AN - SCOPUS:84942793285
SN - 1434-5161
VL - 60
SP - 525
EP - 531
JO - Jinrui idengaku zasshi. The Japanese journal of human genetics
JF - Jinrui idengaku zasshi. The Japanese journal of human genetics
IS - 9
ER -