Research Article Details

Article ID: A15775
PMID: 28715286
Source: Scand J Clin Lab Invest
Title: Effects of lifestyle intervention on soluble CD163, a macrophage activation marker, in patients with non-alcoholic fatty liver disease.
Abstract: OBJECTIVE: Liver macrophages play an important role in the pathogenesis of non-alcoholic fatty liver disease (NAFLD). Soluble CD163 (sCD163), a macrophage-specific biomarker, reflects disease activity in the range of liver diseases. The impact of lifestyle intervention on sCD163 in adult NAFLD patients has not been investigated. MATERIAL AND METHODS: We assessed 126 NAFLD patients participating in a lifestyle intervention study for sCD163 concentrations at baseline, after the three-month intervention period, and at long-term follow-up after 12 and 24&#8201;months. RESULTS: The median sCD163 concentration at baseline was 2.59&#8201;mg/L (IQR&#8201;=&#8201;1.78-3.63&#8201;mg/L). There was a significant decrease in sCD163 from baseline to three months follow-up (-0.64&#8201;mg/L, p&#8201;<&#8201;.001) with no difference between the four study groups (p&#8201;=&#8201;.6). At 12 and 24&#8201;months follow-up, the sCD163 concentrations had returned to baseline level (p&#8201;=&#8201;.3 and p&#8201;=&#8201;.1). Baseline sCD163 correlated with liver biomarkers and metabolic variables. There was a significantly greater decrease in sCD163 in patients who had a decrease in alanine aminotransferase (ALT) compared with patients with unchanged or increased ALT (-0.76&#8201;mg/L vs. -0.41&#8201;mg/L, p&#8201;=&#8201;.02), and in patients with a decrease in HOMA-IR compared with individuals with no decrease (-0.86&#8201;mg/L vs. -0.55&#8201;mg/L, p&#8201;=&#8201;.03). CONCLUSION: sCD163 is associated with markers of liver necro-inflammation and glucose homoeostasis in NAFLD. Participation in a lifestyle intervention programme resulted in a significant reduction in sCD163. Our data support the utility of sCD163 as a biomarker for monitoring the efficacy of therapeutic interventions in NAFLD.
DOI: 10.1080/00365513.2017.1346823