Details

Autor(en) / Beteiligte

• Higuchi, Takashi
• Oka, Shomi
• Furukawa, Hiroshi
• Nakamura, Minoru
• Komori, Atsumasa
• Abiru, Seigo
• Hashimoto, Satoru
• Shimada, Masaaki
• Yoshizawa, Kaname
• Kouno, Hiroshi
• Naganuma, Atsushi
• Ario, Keisuke
• Kaneyoshi, Toshihiko
• Yamashita, Haruhiro
• Takahashi, Hironao
• Makita, Fujio
• Yatsuhashi, Hiroshi
• Ohira, Hiromasa
• Migita, Kiyoshi

Titel

Role of deleterious single nucleotide variants in the coding regions of TNFAIP3 for Japanese autoimmune hepatitis with cirrhosis

Ist Teil von

• Scientific reports, 2019-05, Vol.9 (1), p.7925-7925, Article 7925

Ort / Verlag

England: Nature Publishing Group

Erscheinungsjahr

2019

Quelle

MEDLINE

Beschreibungen/Notizen

• Autoimmune hepatitis (AIH) is an autoimmune liver disease and cirrhosis is sometimes complicated with AIH at diagnosis, influencing its prognosis. TNFAIP3 gene encodes A20, an inhibitor of nuclear factor-κB pathway, and is a susceptibility gene for autoimmune diseases. We investigated deleterious variants in the coding regions of TNFAIP3 gene of Japanese AIH patients or those with cirrhosis. The deleterious variants in the coding regions of TNFAIP3 gene were analyzed by the cycle sequencing method and the frequencies of deleterious TNFAIP3 alleles of AIH or AIH with cirrhosis were compared with those of Japanese controls. The deleterious alleles in TNFAIP3 were not associated with AIH. A significant association was shown for the deleterious alleles in TNFAIP3 (P = 0.0180, odds ratio (OR) 4.28, 95% confidence interval (CI) 1.53-11.95) with AIH with cirrhosis at presentation. The serum IgM levels in AIH patients with deleterious alleles in TNFAIP3 were tended to be lower than those without (P = 0.0152, Q = 0.1216). The frequency of deleterious alleles in TNFAIP3 was higher in the AIH subset without the DRB1 risk alleles than that with (P = 0.0052, OR 5.10, 95%CI 1.55-16.74). The deleterious alleles in TNFAIP3were associated with AIH with cirrhosis.