Weight loss reduces serum monocyte chemoattractant protein-1 concentrations in association with improvements in renal injury in obese men with metabolic syndrome

Clin Chem Lab Med. 2015 Mar;53(4):623-9. doi: 10.1515/cclm-2014-0468.

Abstract

Background: Monocyte chemoattractant protein-1 (MCP-1) is involved in obesity-related renal injury. The aim of the present study was to examine the effects of weight loss on changes in MCP-1 and markers of renal injury, specifically serum cystatin C (S-CysC) and urinary N-acetyl glucosaminidase (UNAG), in obese people.

Methods: In this prospective study, 40 obese men with metabolic syndrome (MetS) participated in a 3-month dietary and exercise intervention. Twenty-eight subjects completed the study with a ≥5% weight loss. Circulating MCP-1, S-CysC and UNAG to creatinine ratio (UNCR) were determined before and after the weight loss program.

Results: Obesity-associated components of MetS demonstrated significant improvements after the weight loss program. In addition, at baseline, circulating MCP-1 concentrations were positively correlated with UNCR and S-CysC levels. After weight loss, blood MCP-1 and UNCR levels were significantly decreased, but S-CysC was not affected. Using multiple linear regression analysis, there was a significant relationship between changes in UNCR and MCP-1 after adjusting for other potential confounding factors.

Conclusions: Weight loss may improve renal tubular injury by ameliorating obesity-related inflammation in obese men with MetS.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylglucosaminidase / urine
  • Adult
  • Chemokine CCL2 / blood*
  • Cystatin C / blood
  • Diet
  • Exercise
  • Humans
  • Kidney / injuries*
  • Kidney / physiopathology*
  • Male
  • Metabolic Syndrome / complications*
  • Obesity / blood
  • Obesity / complications*
  • Obesity / physiopathology*
  • Obesity / urine
  • Weight Loss*

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • Cystatin C
  • alpha-N-acetyl-D-glucosaminidase
  • Acetylglucosaminidase