AI Article Synopsis

  • A meta-analysis was conducted to evaluate the serum levels of sclerostin and BMP-2 in ankylosing spondylitis (AS) patients, finding inconsistent results across various studies.
  • The analysis included 21 studies and revealed no significant difference in serum sclerostin levels between AS patients and controls, while BMP-2 levels were higher in AS patients, indicating a potential link to the condition.
  • Subgroup findings suggested geographic differences in sclerostin levels and that factors such as age, ESR, and BASFI scores affected sclerostin concentrations, while BMP-2 levels varied significantly among different populations.

Article Abstract

Various studies have investigated the serum sclerostin and bone morphogenetic protein-2 (BMP-2) levels in patients with ankylosing spondylitis (AS), but the results were inconsistent. The aim of this meta-analysis was to synthetically assess the associations of serum levels of sclerostin and BMP-2 with AS. Multiple electronic databases were searched to locate relevant articles published before November 2018. Pooled standard mean difference (SMD) with 95% confidence interval (CI) was calculated by the random-effect model. Totally, 21 studies were included. Meta-analysis results showed no significant difference between AS group and control group in serum sclerostin levels (SMD = 0.098, 95% CI - 0.395 to 0.591, p = 0.697). Nevertheless, serum BMP-2 levels in AS patients were higher than that in controls (SMD = 1.184, 95% CI 0.209 to 2.159, p = 0.017). Subgroup analysis demonstrated that European and South American AS patients had lower serum levels of sclerostin than controls. AS patients with age ≥ 40 years, erythrocyte sedimentation rate (ESR) ≤ 20 mm/h and Bath Ankylosing Spondylitis Functional Index (BASFI) < 4 had statistically significant lower serum sclerostin concentrations compared to controls. Chinese and Korean AS patients as well as patients with lower CRP had higher serum BMP-2 levels than controls, and country may be a source of heterogeneity across the studies. No publication bias existed and sensitivity analysis confirmed the stability of results. Serum BMP-2, but not sclerostin levels may be closely related to the development of AS.

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Source
http://dx.doi.org/10.1007/s00223-019-00542-zDOI Listing

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