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

cholangitis propensity score quality of life serum albumin

Journal

JGH open : an open access journal of gastroenterology and hepatology
ISSN: 2397-9070
Titre abrégé: JGH Open
Pays: Australia
ID NLM: 101730833

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 08 02 2022
revised: 10 05 2022
accepted: 08 06 2022
entrez: 5 8 2022
pubmed: 6 8 2022
medline: 6 8 2022
Statut: epublish

Résumé

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. 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. 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; 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.

Sections du résumé

Background and Aim UNASSIGNED
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 UNASSIGNED
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 UNASSIGNED
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;
Conclusion UNASSIGNED
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.

Identifiants

pubmed: 35928695
doi: 10.1002/jgh3.12789
pii: JGH312789
pmc: PMC9344586
doi:

Types de publication

Journal Article

Langues

eng

Pagination

577-586

Informations de copyright

© 2022 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

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Auteurs

Naruhiro Kimura (N)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Toru Setsu (T)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Yoshihisa Arao (Y)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Norihiro Sakai (N)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Yusuke Watanabe (Y)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Hiroyuki Abe (H)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Hiroteru Kamimura (H)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Akira Sakamaki (A)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Takeshi Yokoo (T)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Kenya Kamimura (K)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Atsunori Tsuchiya (A)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Akihiko Osaki (A)

Division of Gastroenterology and Hepatology Niigata City General Hospital Niigata Japan.

Kentarou Igarashi (K)

Division of Gastroenterology and Hepatology Niigata City General Hospital Niigata Japan.

Nobuo Waguri (N)

Division of Gastroenterology and Hepatology Niigata City General Hospital Niigata Japan.

Masahiko Yanagi (M)

Division of Gastroenterology and Hepatology JA Niigata Kouseiren Ojiya General Hospital Niigata Japan.

Toru Takahashi (T)

Division of Gastroenterology and Hepatology JA Niigata Kouseiren Ojiya General Hospital Niigata Japan.

Soichi Sugitani (S)

Division of Gastroenterology and Hepatology JA Niigata Kouseiren Murakami General Hospital Niigata Japan.

Yuka Kobayashi (Y)

Division of Gastroenterology and Hepatology JA Niigata Kouseiren Ngaoka Chuo General Hospital Niigata Japan.

Masaaki Takamura (M)

Division of Gastroenterology and Hepatology JA Niigata Kouseiren Ngaoka Chuo General Hospital Niigata Japan.

Akira Yoshikawa (A)

Division of Gastroenterology and Hepatology JA Niigata Kouseiren Ngaoka Chuo General Hospital Niigata Japan.

Toru Ishikawa (T)

Division of Gastroenterology and Hepatology Saiseikai Niigata Hospital Niigata Japan.

Toshiaki Yoshida (T)

Division of Gastroenterology and Hepatology Saiseikai Niigata Hospital Niigata Japan.

Toshiaki Watanabe (T)

Division of Gastroenterology and Hepatology Watanabe Clinic Niigata Japan.

Hitoshi Bannai (H)

Division of Gastroenterology and Hepatology Niigata Saiseikai Sanjo Hospital Niigata Japan.

Tomoyuki Kubota (T)

Division of Gastroenterology and Hepatology Niigata Rinko Hospital Niigata Japan.

Kazuhiro Funakoshi (K)

Division of Gastroenterology and Hepatology Niigata Prefecture Central Hospital Niigata Japan.

Hiroto Wakabayashi (H)

Division of Gastroenterology and Hepatology Takeda General Hospital Fulushima Japan.

So Kurita (S)

Division of Gastroenterology and Hepatology Niigata Cancer Center Hospital Niigata Japan.

Norio Ogata (N)

Division of Gastroenterology and Hepatology Niigata Cancer Center Hospital Niigata Japan.

Masashi Watanabe (M)

Division of Gastroenterology and Hepatology Niigata Prefecture Shibata Hospital Niigata Japan.

Yuhsaku Mita (Y)

Division of Gastroenterology and Hepatology Niigata Minami Hospital Niigata Japan.

Shigeki Mori (S)

Division of Gastroenterology and Hepatology Niitsu Medical Center Hospital Niigata Japan.

Motoya Sugiyama (M)

Division of Gastroenterology and Hepatology Sugiyama Internal Medicine Clinic Niigata Japan.

Toru Miyajima (T)

Division of Gastroenterology and Hepatology JA Niigata Kouseiren Toyosaka Hospital Niigata Japan.

Sumio Takahashi (S)

Division of Gastroenterology and Hepatology JA Niigata Medical Center Niigata Japan.

Shuichi Sato (S)

Division of Gastroenterology and Hepatology Kido Hospital Niigata Japan.

Kisei Ishizuka (K)

Division of Gastroenterology and Hepatology Niigata Shirone General Hospital Niigata Japan.

Hironobu Ohta (H)

Division of Gastroenterology and Hepatology Niigata Shirone General Hospital Niigata Japan.

Yutaka Aoyagi (Y)

Division of Gastroenterology and Hepatology JA Niigata Medical Center Niigata Japan.

Shuji Terai (S)

Division of Gastroenterology and Hepatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.

Classifications MeSH