TY - JOUR
T1 - Autoantibody status and histological variables influence biochemical response to treatment and long-term outcomes in Japanese patients with primary biliary cirrhosis
AU - Nakamura, Minoru
AU - Kondo, Hisayoshi
AU - Tanaka, Atsushi
AU - Komori, Atsumasa
AU - Ito, Masahiro
AU - Yamamoto, Kazuhide
AU - Ohira, Hiromasa
AU - Zeniya, Mikio
AU - Hashimoto, Etsuko
AU - Honda, Masao
AU - Kaneko, Shuichi
AU - Ueno, Yoshiyuki
AU - Kikuchi, Kentaro
AU - Shimoda, Shinji
AU - Harada, Kenichi
AU - Arai, Kuniaki
AU - Miyake, Yasuhiro
AU - Abe, Masanori
AU - Taniai, Makiko
AU - Saibara, Toshiji
AU - Sakisaka, Shotaro
AU - Takikawa, Hajime
AU - Onji, Morikazu
AU - Tsubouchi, Hirohito
AU - Nakanuma, Yasuni
AU - Ishibashi, Hiromi
N1 - Publisher Copyright:
© 2015 John Wiley & Sons, Ltd.
PY - 2015/8/1
Y1 - 2015/8/1
N2 - Aim: The aim of the present study is to evaluate the factors influencing biochemical response to treatment and the value of biochemical response for predicting long-term outcomes in Japanese patients with primary biliary cirrhosis (PBC). Methods: Biochemical response to ursodeoxycholic acid (UDCA) or UDCA plus bezafibrate was defined as good (≤upper limit of normal [ULN]), fair (≤1.5×ULN) or poor (>1.5×ULN) at 2 years after initiation of UDCA treatment. Associations between various factors (including age, sex, autoantibody status and histological variables at baseline), biochemical response to treatment and long-term outcomes were evaluated in 164 Japanese PBC patients. Results: Anti-gp210 positivity and a higher bile duct loss score were significant risk factors for worse alkaline phosphatase (ALP) response (odds ratios [OR], 2.78 and 1.85, respectively). Age, anti-gp210 positivity and anticentromere positivity were significant risk factors for worse alanine aminotransferase (ALT) response (OR, 1.05, 4.0 and 2.77, respectively). Anti-gp210 positivity and a higher hepatitis score were significant risk factors for worse immunoglobulin (Ig)M response (OR, 2.10 and 2.06, respectively). Worse ALP and IgM response were significant risk factors for progression to late-stage disease without jaundice (OR, 2.27 and 2.32, respectively). Worse ALT response was a significant risk factor for progression to late-stage disease with persistent jaundice (OR, 11.11). Conclusion: Biochemical response to treatment at 2 years, which is influenced by autoantibody status and histological variables at baseline, can predict long-term outcomes in Japanese patients with PBC.
AB - Aim: The aim of the present study is to evaluate the factors influencing biochemical response to treatment and the value of biochemical response for predicting long-term outcomes in Japanese patients with primary biliary cirrhosis (PBC). Methods: Biochemical response to ursodeoxycholic acid (UDCA) or UDCA plus bezafibrate was defined as good (≤upper limit of normal [ULN]), fair (≤1.5×ULN) or poor (>1.5×ULN) at 2 years after initiation of UDCA treatment. Associations between various factors (including age, sex, autoantibody status and histological variables at baseline), biochemical response to treatment and long-term outcomes were evaluated in 164 Japanese PBC patients. Results: Anti-gp210 positivity and a higher bile duct loss score were significant risk factors for worse alkaline phosphatase (ALP) response (odds ratios [OR], 2.78 and 1.85, respectively). Age, anti-gp210 positivity and anticentromere positivity were significant risk factors for worse alanine aminotransferase (ALT) response (OR, 1.05, 4.0 and 2.77, respectively). Anti-gp210 positivity and a higher hepatitis score were significant risk factors for worse immunoglobulin (Ig)M response (OR, 2.10 and 2.06, respectively). Worse ALP and IgM response were significant risk factors for progression to late-stage disease without jaundice (OR, 2.27 and 2.32, respectively). Worse ALT response was a significant risk factor for progression to late-stage disease with persistent jaundice (OR, 11.11). Conclusion: Biochemical response to treatment at 2 years, which is influenced by autoantibody status and histological variables at baseline, can predict long-term outcomes in Japanese patients with PBC.
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U2 - 10.1111/hepr.12423
DO - 10.1111/hepr.12423
M3 - Article
AN - SCOPUS:84937513916
SN - 1386-6346
VL - 45
SP - 846
EP - 855
JO - Hepatology Research
JF - Hepatology Research
IS - 8
ER -