Serum levels of TWEAK and scavenger receptor CD163 in type 1 diabetes mellitus: relationship with cardiovascular risk factors. a case-control study

PLoS One. 2012;7(8):e43919. doi: 10.1371/journal.pone.0043919. Epub 2012 Aug 24.

Abstract

Objective: To test the usefulness of serum concentrations of tumor necrosis factor-like weak inducer of apoptosis (sTWEAK) and soluble scavenger receptor CD163 (sCD163) as markers of subtle inflammation in patients with type 1 diabetes mellitus (T1DM) without clinical cardiovascular (CV) disease and to evaluate their relationship with arterial stiffness (AS).

Methods: Sixty-eight patients with T1DM and 68 age and sex-matched, healthy subjects were evaluated. Anthropometrical variables and CV risk factors were recorded. Serum concentrations of sTWEAK and sCD163 were measured. AS was assessed by aortic pulse wave velocity (aPWV). All statistical analyses were stratified by gender.

Results: T1DM patients showed lower serum concentrations of sTWEAK (Men: 1636.5 (1146.3-3754.8) pg/mL vs. 765.9 (650.4-1097.1) pg/mL; p<0.001. Women: 1401.0 (788.0-2422.2) pg/mL vs. 830.1 (562.6-1175.9) pg/mL; p = 0.011) compared with their respective controls. Additionally, T1DM men had higher serum concentrations of sCD163 (285.0 (247.7-357.1) ng/mL vs. 224.8 (193.3-296.5) ng/mL; p = 0.012) compared with their respective controls. sTWEAK correlated negatively with aPWV in men (r = -0.443; p<0.001). However, this association disappeared after adjusting for potential confounders. In men, the best multiple linear regression model showed that the independent predictors of sTWEAK were T1DM and WHR (R(2) = 0.640; p<0.001). In women, T1DM and SBP were the independent predictors for sTWEAK (R(2) = 0.231; p = 0.001).

Conclusion: sTWEAK is decreased in T1DM patients compared with age and sex-matched healthy subjects after adjusting for classic CV risk factors, although sTWEAK levels may be partially influenced by some of them. Additionally, T1DM men have higher serum concentrations of sCD163. These results point out an association between the inflammatory system and CV risk in T1DM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antigens, CD / blood*
  • Antigens, Differentiation, Myelomonocytic / blood*
  • Aorta / physiopathology
  • Biomarkers / blood
  • Case-Control Studies
  • Cytokine TWEAK
  • Diabetes Mellitus, Type 1 / blood*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Pulse Wave Analysis
  • Receptors, Cell Surface / blood*
  • Risk Factors
  • Tumor Necrosis Factors / blood*
  • Vascular Stiffness / physiology*

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Biomarkers
  • CD163 antigen
  • Cytokine TWEAK
  • Receptors, Cell Surface
  • TNFSF12 protein, human
  • Tumor Necrosis Factors

Grants and funding

Financial support was provided by: 1) Fundació la Marató de TV3-2008 (Project N° 081410); 2) FIS PS09/01360 (Instituto de Salud Carlos III, Ministerio de Sanidad y Consumo, Spain); 3) PI08/0733 (Instituto de Salud Carlos III, Ministerio de Sanidad y Consumo, Spain); 4) PI11/00049 (Instituto de Salud Carlos III, Ministerio de Sanidad y Consumo, Spain); and 5) Matilde R. Chacón is supported by a fellowship from the Fondo de Investigación Sanitaria (FIS) CP06/00119. CP06/00119 PI08/0733 and PI11/00049 are co-financed by the European Regional Development Fund (ERDF). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.