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After excluding the 11 HCC cases diagnosed at baseline, the remaining 136 patients were evaluated for HCC development during long-term follow-up. Of interest, development of HCC was find more observed in 14/34 (41.2%) of the patients positive for COMP at baseline compared to only 5/102 (4.9%) of the patients negative for COMP at baseline (P = 0.008). In addition, 14 out of the 19 (73.7%) patients who developed HCC on follow-up had tested positive for COMP prior to the diagnosis of HCC. Similarly, in the subgroup of non-HCC patients with advanced fibrosis (moderate, severe fibrosis or cirrhosis) as it was determined by liver biopsy (n = 39), development of HCC was observed in 6/11 (54.5%) of COMP positive patients at baseline compared to 4/28 (14.3%) of COMP negative patients at baseline (P analysis of patients according to cartilage oligomeric matrix protein antigen values (cartilage oligomeric matrix protein-positive vs cartilage oligomeric matrix protein-negative). Only, three patients, that were cartilage oligomeric matrix ... While there was a trend for more rapid development of decompensation in COMP positive compared to COMP negative patients (Figure ?(Figure3B),3B), this difference did not reach click here statistical significance (P = 0.149). In contrast, the Kaplan-Meier analysis in cirrhotic non-HCC patients during long-term follow-up (n = 70) revealed a significant difference regarding the development of HCC between COMP-positive (14/25; 56%) and COMP-negative (5/45; 11.1%) cirrhotic patients (Figure ?(Figure3C).3C). Moreover, COMP-positive patients demonstrated a statistically higher incidence of liver-related deaths (17/39; 43.6%) compared to COMP-negative patients (22/108; 20.4%) (Figure ?(Figure3D).3D). Similarly, Kaplan-Meier analysis in the sub-group of patients with available histological data at baseline that were followed-up (n = 84), revealed that B3GAT3 COMP-positive patients at baseline had a higher incidence of development of HCC (P = 0.001) and liver-related deaths (P

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