The relationships between serum sclerostin, bone mineral density, and vascular calcification in rheumatoid arthritis

J Clin Endocrinol Metab. 2014 Dec;99(12):4740-8. doi: 10.1210/jc.2014-2327.

Abstract

Context: Recent data indicate that the secreted glycoprotein sclerostin may be involved in vascular calcification (VC).

Objective: The objective of the study was to establish whether serum sclerostin levels are associated with VC in patients with rheumatoid arthritis (RA).

Design: This was a cross-sectional study.

Setting: The study was conducted with ambulatory care.

Patients: We compared 75 RA patients with 75 age- and gender-matched control participants.

Intervention: Coronary artery calcification (CAC) and abdominal aortic calcification (AAC) scores were evaluated by computed tomography.

Main outcome measure: Serum sclerostin levels (determined with an ELISA) were assessed. A statistical analysis was performed to identify the determinants of serum sclerostin and VC.

Results: AAC and CAC were more prevalent and more severe in patients with RA than in controls. Higher levels of AAC (P = .02) and a higher lumbar bone mineral density (BMD; P = .03) were identified as independent determinants of higher serum sclerostin levels in RA patients, whereas male gender (P = .03), higher lumbar BMD (P < .0001), and low estimated glomerular rate (P < .001) were identified as determinants in controls. In RA patients, a multivariate logistic regression analysis indicated that older age [P < .01, with an odds ratio (OR) per year 1.10] and male gender (P = .02, OR 6.79) were independent determinants of CAC and that older age (P < .001, OR 1.16) were independent determinants of AAC. In controls, the independent determinants were older age (P < .01, OR 1.19), hypertension (P < .01, OR 7.31), and lumbar BMD (P = .03, OR per 30 mg/cm(2) increment of 1.14) for CAC and older age (P = .01, OR 1.11) for AAC.

Conclusions: Serum sclerostin levels were significantly and independently associated with AAC in RA patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Absorptiometry, Photon
  • Adaptor Proteins, Signal Transducing
  • Aged
  • Arthritis, Rheumatoid / blood*
  • Arthritis, Rheumatoid / complications
  • Arthritis, Rheumatoid / pathology*
  • Bone Density*
  • Bone Morphogenetic Proteins / blood*
  • Cardiovascular Diseases / epidemiology
  • Cross-Sectional Studies
  • Female
  • Genetic Markers
  • Humans
  • Male
  • Middle Aged
  • Prevalence
  • Risk Factors
  • Vascular Calcification / etiology
  • Vascular Calcification / pathology*

Substances

  • Adaptor Proteins, Signal Transducing
  • Bone Morphogenetic Proteins
  • Genetic Markers
  • SOST protein, human