PMID- 26207169 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20150724 LR - 20240323 IS - 1948-5182 (Print) IS - 1948-5182 (Electronic) VI - 7 IP - 14 DP - 2015 Jul 18 TI - Cartilage oligomeric matrix protein: A novel non-invasive marker for assessing cirrhosis and risk of hepatocellular carcinoma. PG - 1875-83 LID - 10.4254/wjh.v7.i14.1875 [doi] AB - AIM: To assess serum cartilage oligomeric matrix protein (COMP) as a marker of cirrhosis and risk of progression to hepatocellular carcinoma (HCC). METHODS: A COMP enzyme-linked immunosorbent assay was used to test 187 patients with chronic liver diseases at the time point of first evaluation. The selected patients included 72 with chronic hepatitis B infection, 75 with chronic hepatitis C infection, 22 with primary biliary cirrhosis, 7 with autoimmune hepatitis type 1, and 11 with alcoholic liver disease. Demographic, biochemical, histological and clinical characteristics of the patients were recorded at the first evaluation. One hundred and forty-seven patients were followed for a median [interquartile range (IQR)] duration of 96.5 (102) mo. The clinical, biochemical and histological data, as well as the development of cirrhosis, HCC according to internationally accepted criteria and in case of death, a liver-related cause during the follow-up period, were recorded at the electronic database of our clinic. COMP determination was also performed in 43 healthy individuals who served as the control study group. RESULTS: COMP positivity (> 15 U/L) was detected in 22%-36% among chronic liver disease groups. Strikingly, almost 83% of COMP-positive patients were cirrhotic at baseline, independently of cause of liver disease. Among the patients who developed HCC during follow-up, 73.7% (14/19) were COMP positive at baseline. COMP positivity was significantly associated with older age (P < 0.001), advanced fibrosis (P = 0.001) and necroinflammatory activity (P = 0.001), higher aspartate aminotransferase (P < 0.001), alanine aminotransferase (P < 0.02), gamma-glutamyl transpeptidase (P = 0.003), alkaline phosphatase (P = 0.001), bilirubin (P < 0.05), international normalized ratio (P = 0.002) and alpha-fetoprotein levels (P < 0.02), and lower albumin (P < 0.001), and platelet count (P = 0.008). COMP levels [median (IQR)] were significantly higher in cirrhotics compared to non-cirrhotics [13.8 (7.9) U/L vs 9.8 (4.6) U/L, respectively; P < 0.001]. On multivariate logistic regression analysis, COMP-positivity was independently associated only with cirrhosis (OR = 4.40, 95%CI: 1.33-14.69, P = 0.015). Kaplan-Meier analysis showed that COMP positivity was significantly associated with HCC development (P = 0.007) and higher incidence of liver-related death (P < 0.001). CONCLUSION: Elevated COMP levels are strongly associated with cirrhosis and HCC progression. Serum COMP is a new promising non-invasive biomarker for HCC risk assessment in surveillance programs. FAU - Norman, Gary L AU - Norman GL AD - Gary L Norman, Zakera Shums, Inova Diagnostics, Inc., San Diego, CA 92131, United States. FAU - Gatselis, Nikolaos K AU - Gatselis NK AD - Gary L Norman, Zakera Shums, Inova Diagnostics, Inc., San Diego, CA 92131, United States. FAU - Shums, Zakera AU - Shums Z AD - Gary L Norman, Zakera Shums, Inova Diagnostics, Inc., San Diego, CA 92131, United States. FAU - Liaskos, Christos AU - Liaskos C AD - Gary L Norman, Zakera Shums, Inova Diagnostics, Inc., San Diego, CA 92131, United States. FAU - Bogdanos, Dimitrios P AU - Bogdanos DP AD - Gary L Norman, Zakera Shums, Inova Diagnostics, Inc., San Diego, CA 92131, United States. FAU - Koukoulis, George K AU - Koukoulis GK AD - Gary L Norman, Zakera Shums, Inova Diagnostics, Inc., San Diego, CA 92131, United States. FAU - Dalekos, George N AU - Dalekos GN AD - Gary L Norman, Zakera Shums, Inova Diagnostics, Inc., San Diego, CA 92131, United States. LA - eng PT - Journal Article PL - United States TA - World J Hepatol JT - World journal of hepatology JID - 101532469 PMC - PMC4506945 OTO - NOTNLM OT - Biomarker OT - Cirrhosis OT - Enzyme-linked immunosorbent assay OT - Hepatic fibrosis OT - Hepatocellular carcinoma OT - Viral hepatitis EDAT- 2015/07/25 06:00 MHDA- 2015/07/25 06:01 PMCR- 2015/07/18 CRDT- 2015/07/25 06:00 PHST- 2015/04/14 00:00 [received] PHST- 2015/05/29 00:00 [revised] PHST- 2015/06/30 00:00 [accepted] PHST- 2015/07/25 06:00 [entrez] PHST- 2015/07/25 06:00 [pubmed] PHST- 2015/07/25 06:01 [medline] PHST- 2015/07/18 00:00 [pmc-release] AID - 10.4254/wjh.v7.i14.1875 [doi] PST - ppublish SO - World J Hepatol. 2015 Jul 18;7(14):1875-83. doi: 10.4254/wjh.v7.i14.1875.