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Soluble CD163 as a Potential Biomarker in Systemic Sclerosis.
Frantz, Camelia; Pezet, Sonia; Avouac, Jerome; Allanore, Yannick.
Affiliation
  • Frantz C; Inserm U1016, UMR8104, Rheumatology A Department, Cochin Hospital, Paris Descartes University, Paris, France.
  • Pezet S; Inserm U1016, UMR8104, Rheumatology A Department, Cochin Hospital, Paris Descartes University, Paris, France.
  • Avouac J; Inserm U1016, UMR8104, Rheumatology A Department, Cochin Hospital, Paris Descartes University, Paris, France.
  • Allanore Y; Inserm U1016, UMR8104, Rheumatology A Department, Cochin Hospital, Paris Descartes University, Paris, France.
Dis Markers ; 2018: 8509583, 2018.
Article in En | MEDLINE | ID: mdl-29805720
ABSTRACT

OBJECTIVE:

To evaluate the performance of serum and urinary sCD163 concentrations as possible biomarker in systemic sclerosis (SSc).

METHODS:

Urine and serum samples were obtained from SSc patients and age- and sex-matched controls. Serum and urinary sCD163 concentrations were measured by commercially available ELISA kit. SSc patients were assessed following international guidelines. Cross-sectional analyses were performed.

RESULTS:

Two hundred and three SSc patients were included. The control group consisted of 47 age- and sex-matched patients having noninflammatory diseases, mainly osteoporosis. Serum sCD163 levels were significantly higher in SSc patients compared with controls (mean ± SD 529 ± 251 versus 385 ± 153 ng/mL; p < 0.001). Urinary sCD163 concentrations were higher in SSc patients than controls, but this did not reach significance (236 ± 498 versus 176 ± 173 ng/mg uCr; p = 0.580). The sCD163 concentrations were not associated with clinical, laboratory, and instrumental characteristics of SSc patients.

CONCLUSION:

To our knowledge, this is the first evaluation of both serum and urinary sCD163 levels in SSc. Our results show a significant difference for sera values that should be prioritized for further studies as compared to urinary measurements. Our results further support that the M2 macrophages/CD163 signaling system may play a role in the pathogenesis of SSc, although we could not identify a subset of SSc patients with higher concentrations.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Scleroderma, Systemic / Antigens, Differentiation, Myelomonocytic / Antigens, CD / Receptors, Cell Surface Type of study: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Dis Markers Journal subject: BIOQUIMICA Year: 2018 Document type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Scleroderma, Systemic / Antigens, Differentiation, Myelomonocytic / Antigens, CD / Receptors, Cell Surface Type of study: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Dis Markers Journal subject: BIOQUIMICA Year: 2018 Document type: Article Affiliation country: France