<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Verna EC</submitter><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><pagination>582-90</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7979413</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>42(5)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Pentraxin-2 (PTX-2), a serum protein, inhibits inflammation and fibrosis, and recombinant PTX-2 is being tested as an anti-fibrotic agent.&lt;h4>Aim&lt;/h4>To evaluate the association between serum PTX-2 levels and fibrosis stage in patients with non-alcoholic fatty liver disease (NAFLD).&lt;h4>Methods&lt;/h4>Serum pentraxin-2 levels were compared between four groups of well-characterised patients including NAFLD with no fibrosis, NAFLD with mild-moderate fibrosis (stage 1-2), NAFLD with advanced fibrosis (stage 3-4), and age-sex matched non-NAFLD controls.&lt;h4>Results&lt;/h4>Sixty subjects were included in the study. The mean age was 58.9 years, 68% were male and 58% were Caucasian. In univariate analysis, serum PTX-2 levels significantly decreased from non-NAFLD controls to mild NAFLD with no fibrosis, to NAFLD with mild-moderate fibrosis and were lowest in patients with NAFLD and advanced fibrosis, in a dose-dependent manner (P &lt; 0.0001). In multivariable-adjusted analyses controlling for age, sex, albumin, and CRP, the results remained consistent and statistically significant. Serum PTX-2 level had an AUROC of 0.84 (95% CI: 0.71-0.97) for the diagnosis of NAFLD, and an AUROC of 0.77 (95% CI: 0.65-0.90) for the diagnosis of advanced fibrosis in NAFLD. Serum PTX-2 levels also decreased with increasing liver stiffness as estimated by magnetic resonance elastography (r = -0.31, P = 0.02).&lt;h4>Conclusions&lt;/h4>PTX-2 levels are significantly lower in patients with NAFLD compared to non-NAFLD controls, and decline further in patients with advanced fibrosis. PTX-2 may therefore be both a biomarker of disease and a potential target for anti-fibrotic therapy with the recombinant pentraxin-2.</pubmed_abstract><journal>Alimentary pharmacology &amp; therapeutics</journal><pubmed_title>Novel association between serum pentraxin-2 levels and advanced fibrosis in well-characterised patients with non-alcoholic fatty liver disease.</pubmed_title><pmcid>PMC7979413</pmcid><funding_grant_id>K23 DK090303</funding_grant_id><funding_grant_id>K23-DK090303</funding_grant_id><pubmed_authors>Bettencourt R</pubmed_authors><pubmed_authors>Verna EC</pubmed_authors><pubmed_authors>Loomba R</pubmed_authors><pubmed_authors>Valasek MA</pubmed_authors><pubmed_authors>Nguyen P</pubmed_authors><pubmed_authors>Patel J</pubmed_authors><pubmed_authors>Brenner DA</pubmed_authors><pubmed_authors>Hernandez C</pubmed_authors><pubmed_authors>Kisselva T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Novel association between serum pentraxin-2 levels and advanced fibrosis in well-characterised patients with non-alcoholic fatty liver disease.</name><description>&lt;h4>Background&lt;/h4>Pentraxin-2 (PTX-2), a serum protein, inhibits inflammation and fibrosis, and recombinant PTX-2 is being tested as an anti-fibrotic agent.&lt;h4>Aim&lt;/h4>To evaluate the association between serum PTX-2 levels and fibrosis stage in patients with non-alcoholic fatty liver disease (NAFLD).&lt;h4>Methods&lt;/h4>Serum pentraxin-2 levels were compared between four groups of well-characterised patients including NAFLD with no fibrosis, NAFLD with mild-moderate fibrosis (stage 1-2), NAFLD with advanced fibrosis (stage 3-4), and age-sex matched non-NAFLD controls.&lt;h4>Results&lt;/h4>Sixty subjects were included in the study. The mean age was 58.9 years, 68% were male and 58% were Caucasian. In univariate analysis, serum PTX-2 levels significantly decreased from non-NAFLD controls to mild NAFLD with no fibrosis, to NAFLD with mild-moderate fibrosis and were lowest in patients with NAFLD and advanced fibrosis, in a dose-dependent manner (P &lt; 0.0001). In multivariable-adjusted analyses controlling for age, sex, albumin, and CRP, the results remained consistent and statistically significant. Serum PTX-2 level had an AUROC of 0.84 (95% CI: 0.71-0.97) for the diagnosis of NAFLD, and an AUROC of 0.77 (95% CI: 0.65-0.90) for the diagnosis of advanced fibrosis in NAFLD. Serum PTX-2 levels also decreased with increasing liver stiffness as estimated by magnetic resonance elastography (r = -0.31, P = 0.02).&lt;h4>Conclusions&lt;/h4>PTX-2 levels are significantly lower in patients with NAFLD compared to non-NAFLD controls, and decline further in patients with advanced fibrosis. PTX-2 may therefore be both a biomarker of disease and a potential target for anti-fibrotic therapy with the recombinant pentraxin-2.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Sep</publication><modification>2025-04-25T19:31:31.854Z</modification><creation>2025-04-06T07:58:21.22Z</creation></dates><accession>S-EPMC7979413</accession><cross_references><pubmed>26119353</pubmed><doi>10.1111/apt.13292</doi></cross_references></HashMap>