Expression and Clinical Significance of Decoy Receptor 3 in Acute-on-Chronic Liver Failure

Author:

Lin Su1ORCID,Wu Bing2,Lin Yehong1,Wang Mingfang1,Zhu Yueyong1ORCID,Jiang Jiaji1ORCID,Zhang Lurong34ORCID,Lin Jianhua2ORCID

Affiliation:

1. Liver Center, The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian 350005, China

2. Fujian Key Lab of Individualized Active Immunotherapy and Key Lab of Radiation Biology of Fujian Province Universities, Fuzhou 350005, China

3. Department of Radiation Oncology, College of Medicine, University of Florida, Gainesville, Florida 32610, USA

4. Lab of Radiation Biology, Fujian Provincial Tumor Hospital, Fuzhou 350006, China

Abstract

Aims. To explore the expression level and clinical significance of decoy receptor 3 (DcR3) in patients with acute-on-chronic liver failure (ACLF).Methods. Serum DcR3 levels were measured by enzyme-linked immunosorbent assay (ELISA) in 76 patients with ACLF and 41 non-ACLF patients with chronic liver disease. Blood routine and liver functions were accessed for their correlations with DcR3.Results. Serum DcR3 in ACLF patients was significantly higher than that in non-ACLF patients. It was positively correlated with neutrophilic granulocyte, aspartate aminotransferase, prothrombin time, and international standardized ratio, but negatively correlated with platelet and serum albumin. At the early stage, the level of DcR3 was not significantly different between the survival and nonsurvival group of ACLF. However, at the late stage, DcR3 increased in nonsurvival and gradually decreased in survivals. The baseline DcR3 could not sufficiently predict the outcome of ACLF, while the change of DcR3 within the first week displayed a better predictive value than model for end-stage liver disease (MELD) score.Conclusions. DcR3 was highly expressed in patients with ACLF and correlated with several clinical indices. Dynamic change of DcR3 might predict the prognosis of ACLF.

Funder

International Science & Technology Cooperation Program of China

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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