Galectin-9 as a new biomarker of acute-on-chronic liver failure.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
27 Sep 2024
Historique:
received: 05 06 2024
accepted: 17 09 2024
medline: 28 9 2024
pubmed: 28 9 2024
entrez: 27 9 2024
Statut: epublish

Résumé

Galectin-9 (Gal-9) expression in patients with acute-on-chronic liver failure and its correlation with prognosis remain unclear. This study investigated the relationship between liver failure prognosis and Gal-9 expression analysis in patients with acute-on-chronic liver failure. Patients with acute-on-chronic liver failure attributable to hepatitis B and those with chronic hepatitis B were included in this single-center prospective cohort study. The Gal-9 levels in the acute-on-chronic liver failure group were significantly higher than those in the chronic hepatitis B group, and there was an upregulation of Gal-9 and T-cell immunoglobulin domain and mucin domain-3 expressions in peripheral blood T cells. Gal-9 was localized in the regenerative areas of liver tissues in patients with acute-on-chronic liver failure, co-localizing with Kupffer cells. Kaplan-Meier survival curves showed that patients with Gal-9 levels < 9.6 ng/ml had a worse prognosis, with the area under the receiver operating characteristic curve (AUC-ROC) being similar to that of the Model for End-Stage Liver Disease score. The combined ROC curve of the two had better predictive performance, with an AUC of 0.945. High Gal-9 levels in liver regenerative areas can serve as a prognostic marker, indicating a better prognosis for patients with hepatitis B virus-acute-on-chronic liver failure.

Identifiants

pubmed: 39333198
doi: 10.1038/s41598-024-73397-6
pii: 10.1038/s41598-024-73397-6
doi:

Substances chimiques

Galectins 0
LGALS9 protein, human 0
Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

22303

Subventions

Organisme : National Key Research and Development Program of China,China
ID : 2021YFC2301801

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Jun Ling (J)

Hepatology Department, The Fifth Medical Center of Chinese PLA General Hospital, No. 100, Xisi Huanzhong Road, Beijing, 10039, China.

Shaoli You (S)

Hepatology Department, The Fifth Medical Center of Chinese PLA General Hospital, No. 100, Xisi Huanzhong Road, Beijing, 10039, China.

Weiwei Chen (W)

Infectious Disease Department, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, 10039, China.

Xinxin Yang (X)

Infectious Disease Department, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, 10039, China.

Yiwen Xv (Y)

Hepatology Department, The Fifth Medical Center of Chinese PLA General Hospital, No. 100, Xisi Huanzhong Road, Beijing, 10039, China.

Bing Zhu (B)

Hepatology Department, The Fifth Medical Center of Chinese PLA General Hospital, No. 100, Xisi Huanzhong Road, Beijing, 10039, China. zhubing302@163.com.

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