Improved Liver Function After Sustained Virologic Response Enhanced Prognosis in Hepatitis C with Compensated Advanced Liver Fibrosis.


Journal

Digestive diseases and sciences
ISSN: 1573-2568
Titre abrégé: Dig Dis Sci
Pays: United States
ID NLM: 7902782

Informations de publication

Date de publication:
05 2023
Historique:
received: 13 01 2022
accepted: 16 07 2022
medline: 28 4 2023
pubmed: 17 12 2022
entrez: 16 12 2022
Statut: ppublish

Résumé

Liver function can be improved in patients with chronic hepatitis C virus (HCV) infection who achieved sustained virologic response (SVR) with direct-acting antiviral (DAA) treatment. However, to our knowledge, the impact of liver function improvement after SVR on prognosis has not been investigated. A total of 716 patients with chronic HCV infection and compensated advanced liver fibrosis who began receiving DAA treatment between September 2014 and August 2018 in 25 Japanese hospitals and achieved SVR were enrolled. The median age was 73 years, and 336 (47%) and 380 (53%) patients had albumin-bilirubin (ALBI) grade 1 and grade 2, respectively. Improvement to ALBI grade 1 at 1 year after the end of treatment (EOT) was observed in 76% of the patients with baseline ALBI grade 2. Among 380 patients with baseline ALBI grade 2, alanine aminotransferase (ALT) levels ≥ 40 U/L (p < 0.001) and modified ALBI (mALBI) grade 2a (p < 0.001) were significantly associated with improvement to ALBI grade 1 at 1 year after EOT in multivariate analysis. During the median observation period of 51.8 months, 4 and 10 patients with baseline ALBI grade 1 and 2, respectively, died. In patients with baseline ALBI grade 2, only the absence of improvement to ALBI grade 1 at 1 year after EOT was significantly associated with all-cause mortality in univariate analysis. Baseline ALT levels and mALBI grade were significantly associated with improvement in liver function after SVR. Patients whose liver function improved after SVR could have better prognosis.

Sections du résumé

BACKGROUND AND AIM
Liver function can be improved in patients with chronic hepatitis C virus (HCV) infection who achieved sustained virologic response (SVR) with direct-acting antiviral (DAA) treatment. However, to our knowledge, the impact of liver function improvement after SVR on prognosis has not been investigated.
METHODS
A total of 716 patients with chronic HCV infection and compensated advanced liver fibrosis who began receiving DAA treatment between September 2014 and August 2018 in 25 Japanese hospitals and achieved SVR were enrolled.
RESULTS
The median age was 73 years, and 336 (47%) and 380 (53%) patients had albumin-bilirubin (ALBI) grade 1 and grade 2, respectively. Improvement to ALBI grade 1 at 1 year after the end of treatment (EOT) was observed in 76% of the patients with baseline ALBI grade 2. Among 380 patients with baseline ALBI grade 2, alanine aminotransferase (ALT) levels ≥ 40 U/L (p < 0.001) and modified ALBI (mALBI) grade 2a (p < 0.001) were significantly associated with improvement to ALBI grade 1 at 1 year after EOT in multivariate analysis. During the median observation period of 51.8 months, 4 and 10 patients with baseline ALBI grade 1 and 2, respectively, died. In patients with baseline ALBI grade 2, only the absence of improvement to ALBI grade 1 at 1 year after EOT was significantly associated with all-cause mortality in univariate analysis.
CONCLUSIONS
Baseline ALT levels and mALBI grade were significantly associated with improvement in liver function after SVR. Patients whose liver function improved after SVR could have better prognosis.

Identifiants

pubmed: 36526814
doi: 10.1007/s10620-022-07629-y
pii: 10.1007/s10620-022-07629-y
doi:

Substances chimiques

Antiviral Agents 0
Bilirubin RFM9X3LJ49
Albumins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2115-2122

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Références

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Auteurs

Yuki Tahata (Y)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Ryotaro Sakamori (R)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Ryoko Yamada (R)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Takahiro Kodama (T)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Hayato Hikita (H)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Hideki Hagiwara (H)

Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.

Masahide Oshita (M)

Ikeda Municipal Hospital, Ikeda, Osaka, Japan.

Yasuharu Imai (Y)

Ikeda Municipal Hospital, Ikeda, Osaka, Japan.

Naoki Hiramatsu (N)

Osaka Rosai Hospital, Sakai, Osaka, Japan.

Eiji Mita (E)

National Hospital Organization Osaka National Hospital, Osaka, Osaka, Japan.

Akira Kaneko (A)

Minoh City Hospital, Minoh, Osaka, Japan.

Masanori Miyazaki (M)

Osaka Police Hospital, Osaka, Osaka, Japan.

Kazuyoshi Ohkawa (K)

Osaka International Cancer Institute, Osaka, Osaka, Japan.

Taizo Hijioka (T)

National Hospital Organization Osaka Minami Medical Center, Kawachinagano, Osaka, Japan.

Hiroyuki Fukui (H)

Yao Municipal Hospital, Yao, Osaka, Japan.

Toshifumi Ito (T)

Japan Community Healthcare Organization Osaka Hospital, Osaka, Osaka, Japan.

Keiji Yamamoto (K)

National Hospital Organization Minami Wakayama Medical Center, Tanabe, Wakayama, Japan.

Yoshinori Doi (Y)

Otemae Hospital, Osaka, Osaka, Japan.

Yuichi Yoshida (Y)

Suita Municipal Hospital, Suita, Osaka, Japan.

Yukinori Yamada (Y)

Kaizuka City Hospital, Kaizuka, Osaka, Japan.

Takayuki Yakushijin (T)

Osaka General Medical Center, Osaka, Osaka, Japan.

Tomohide Tatsumi (T)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Tetsuo Takehara (T)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan. takehara@gh.med.osaka-u.ac.jp.

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