Serum level of full-length connective tissue growth factor reflects liver fibrosis stage in patients with Fontan-associated liver disease

• Published in: PloS one 2024-01, Vol.19 (1), p.e0296375-e0296375
• Main Authors: Kogiso, Tomomi, Takayanagi, Kayo, Ishizuka, Tsutomu, Otsuka, Motoyuki, Inai, Kei, Ogasawara, Yuri, Horiuchi, Kentaro, Taniai, Makiko, Tokushige, Katsutoshi
• Format: Article
• Language: English
• Subjects: Antibodies; Anticoagulants; Biology and Life Sciences; Biopsy; Cardiac catheterization; Care and treatment; Connective tissue; Connective tissue cells; Connective Tissue Growth Factor; Connective tissues; Correlation; Diagnosis; Disease control; Endothelial Cells; Enzyme-linked immunosorbent assay; Enzymes; Fatty liver; Fibrosis; Growth factors; Health aspects; Hospitals; Humans; Insulin resistance; Intubation; Liver; Liver - pathology; Liver cancer; Liver cirrhosis; Liver Cirrhosis - diagnosis; Liver Cirrhosis - etiology; Liver diseases; Medical research; Medicine and Health Sciences; Medicine, Experimental; Multivariate analysis; Non-alcoholic Fatty Liver Disease - pathology; Patients; Platelets; Research and Analysis Methods; Serum levels; Venous pressure; Viral antibodies; Womens health
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0296375

Chronic liver disease leads to liver fibrosis, and an accurate diagnosis of the fibrosis stage is crucial for medical management. Connective tissue growth factor (CTGF) is produced by endothelial cells and platelets and plays a central role in inducing fibrosis in various organs. In the present study, we tested the validity of measuring the serum levels of two types of CTGF to estimate the biopsy-confirmed liver fibrosis stage. We used two detection antibodies targeting the N- and C-terminal of CTGF to measure the serum levels of two forms of CTGF consisting of its full length and its N-terminal fragment. We analyzed the level of CTGF (via enzyme-linked immunosorbent assay) and the liver fibrosis stage in 38 patients with Fontan-associated liver disease (FALD) (26 cases of which were diagnosed pathologically). Correlations were determined by multivariate analysis and the area under the receiver operating characteristic curve. The 65 patients with nonalcoholic fatty liver disease (NAFLD) were included as a disease control group for examination. Full-length CTGF was significantly inversely correlated with liver fibrosis in patients with FALD. Although the platelet count was also associated with the liver fibrosis stage, full-length CTGF was more closely correlated with the fibrosis stage. Furthermore, the level of full-length CTGF was inversely associated with high central venous pressure. Conversely, the serum level of CTGF was not correlated with the fibrosis stage in NAFLD. The serum level of full-length CTGF may be useful for estimating the liver fibrosis stage in patients with FALD.