Impact of chemerin, lipid profile, and insulin resistance on disease parameters in patients with multiple sclerosis

Neurol Sci. 2021 Jun;42(6):2471-2479. doi: 10.1007/s10072-020-04847-y. Epub 2020 Oct 24.

Abstract

Introduction: Plasma chemerin, which has chemotactic and adipogenic functions, is increased in several inflammatory diseases. However, its relationship with multiple sclerosis (MS) has not been explored yet. In this study, we aimed to determine chemerin levels and their possible role in MS.

Methods: Chemerin serum concentrations were evaluated by using ELISA kit in 91 clinically definite MS patients and 52 healthy controls. The mean serum chemerin, insulin, and cholesterol levels were compared. Patients were divided into two groups according to the body mass index (BMI), and the relationships between clinical and metabolic parameters were evaluated.

Results: Serum chemerin levels were 10.46 ± 1.65 ng/mL in MS patients and 10.26 ± 2.14 ng/mL in the control group. No significant difference was found between patients and controls (p = 0.55). We found no difference regarding age, gender, and BMI between two groups (p = 0.053, p = 0.54, p = 0.41). However, female patients with MS had higher chemerin levels than male patients. There were no associations between serum chemerin levels and EDSS score, annualized relapse rate, BMI, insulin resistance, and serum cholesterol levels in MS patients.

Conclusion: In this study, we aimed to determine serum chemerin levels in patients with MS. However, in our study, there was no significant difference between serum chemerin levels of MS patients and healthy controls'. Additionally, chemerin levels were not associated with other metabolic parameters, as well as cognitive dysfunction. Further studies are needed to evaluate the role of chemerin in MS patients.

Keywords: Chemerin; Disease activity; Multiple sclerosis; Obesity.

MeSH terms

  • Body Mass Index
  • Chemokines
  • Female
  • Humans
  • Insulin Resistance*
  • Intercellular Signaling Peptides and Proteins
  • Lipids
  • Male
  • Multiple Sclerosis*
  • Obesity

Substances

  • Chemokines
  • Intercellular Signaling Peptides and Proteins
  • Lipids
  • RARRES2 protein, human