JGH Open (Aug 2022)

Cumulative risk of developing a new symptom in patients with primary biliary cholangitis and its impact on prognosis

  • Naruhiro Kimura,
  • Toru Setsu,
  • Yoshihisa Arao,
  • Norihiro Sakai,
  • Yusuke Watanabe,
  • Hiroyuki Abe,
  • Hiroteru Kamimura,
  • Akira Sakamaki,
  • Takeshi Yokoo,
  • Kenya Kamimura,
  • Atsunori Tsuchiya,
  • Akihiko Osaki,
  • Kentarou Igarashi,
  • Nobuo Waguri,
  • Masahiko Yanagi,
  • Toru Takahashi,
  • Soichi Sugitani,
  • Yuka Kobayashi,
  • Masaaki Takamura,
  • Akira Yoshikawa,
  • Toru Ishikawa,
  • Toshiaki Yoshida,
  • Toshiaki Watanabe,
  • Hitoshi Bannai,
  • Tomoyuki Kubota,
  • Kazuhiro Funakoshi,
  • Hiroto Wakabayashi,
  • So Kurita,
  • Norio Ogata,
  • Masashi Watanabe,
  • Yuhsaku Mita,
  • Shigeki Mori,
  • Motoya Sugiyama,
  • Toru Miyajima,
  • Sumio Takahashi,
  • Shuichi Sato,
  • Kisei Ishizuka,
  • Hironobu Ohta,
  • Yutaka Aoyagi,
  • Shuji Terai

DOI
https://doi.org/10.1002/jgh3.12789
Journal volume & issue
Vol. 6, no. 8
pp. 577 – 586

Abstract

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Abstract Background and Aim Symptoms of primary biliary cholangitis (PBC) frequently impair one's quality of life (QOL). Nonetheless, with improved treatment, the prognosis of PBC also improves. QOL plays an important role in patients with PBC. In this study, we aimed to reevaluate the transition of new symptom development in PBC and its predictive factors. Methods This retrospective multicenter study enrolled 382 patients with PBC for symptom analysis. The impact of a newly developed symptom on PBC prognosis was investigated by Kaplan–Meier analysis with propensity score matching and logistic progression analysis. Results The cumulative risk of developing a new symptom after 10 and 20 years of follow‐up was 7.6 and 28.2%, and specifically that of pruritus, which was the most common symptom, was 6.7 and 23.3%, respectively. In Cox hazard risk analysis, serum Alb level (hazard ratio [HR], 1.097; 95% confidence interval [CI], 1.033–1.165; P = 0.002), the serum D‐Bil level (HR, 6.262; 95% CI, 2.522–15.553, P < 0.001), and Paris II criteria (HR, 0.435; 95% CI, 0.183–1.036; P = 0.037) were significant independent predictors of a new symptom. Kaplan–Meier analysis showed that the overall survival and liver‐related death were not significant between patients with and without a new symptom. Conclusion The cumulative risk of new symptom development is roughly 30% 20 years after diagnosis and could be predicted by factors including serum albumin levels, serum D‐Bil level, and Paris II criteria.

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