Abstract

BackgroundAxial spondyloarthritis including ankylosing spondylitis (AS) is characterized by chronic inflammation and new bone formation in the axial skeleton. On the other hand, bone loss, osteoporosis and an increased risk of vertebral fractures is known to frequently occur in AS. In the MEASURE 1 study, the clinically efficacious interleukin-17A inhibitor secukinumab was shown to have limited radiographic progression through 4 years in patients with active AS. Here we present a post hoc analysis to evaluate the effect of secukinumab on bone mineral density (BMD) and bone turnover biomarkers over 2 years in this study.MethodsBMD was measured by dual-energy X-ray absorptiometry at the lumbar spine, total hip, and femoral neck. Spinal radiographs performed at baseline and Week 104 were assessed by modified Stoke Ankylosing Spondylitis Spinal Score (mSASSS) and analyzed in relation to BMD change, considering baseline syndesmophytes. Bone turnover biomarkers were assessed at baseline and at Weeks 52 or 104.ResultsAmong 104 patients included in this analysis, 66% were male, with a mean (SD) age of 40.4 (12.3) years. In postmenopausal women and men ≥50 years of age (T-score), the proportion of patients having normal BMD at baseline and Week 104 were 54.5%/54.5% (lumbar spine), 31.6%/55.6% (total hip), and 42.1%/44.4% (femoral neck). Similarly, at baseline, the proportion of patients with osteopenia/osteoporosis was 31.8%/13.6% (lumbar spine), 57.9%/10.5% (total hip), 42.1%/15.8% (femoral neck), and 36.4%/9.1% (lumbar spine), 44.4%/0% (total hip) and 55.6%/0% (femoral neck) at Week 104, respectively. In premenopausal women and men < 50 years of age (Z-score), the proportion of patients having BMD below the expected range for age at baseline and Week 104 were 25.0%/21.2% (lumbar spine), 11.3%/17.8% (total hip), and 9.9%/8.9% (femoral neck). In relation to mSASSS change scores ≥2 over 2 years, the increase in lumbar spine BMD was not related to radiographic progression and syndesmophyte formation. No significant changes were observed in the bone turnover markers over time.ConclusionThe high proportion of AS patients with diminished BMD was confirmed in this study. An increase of BMD in the lumbar spine after 2 years of secukinumab treatment in patients with AS was found that was probably unrelated to radiographic progression. No relevant effects of secukinumab on bone turnover biomarkers were documented.Trial registrationMEASURE 1 (post hoc analysis) Clinicaltrials.gov, NCT01358175; Registered, 23 May 2011.

Highlights

  • Axial spondyloarthritis including ankylosing spondylitis (AS) is characterized by chronic inflammation and new bone formation in the axial skeleton

  • Patients (n = 78) with a non-missing baseline bone mineral density (BMD) value and at least one post-baseline lumbar spine BMD value at Weeks 52 or 104 from the full analysis set were considered for further analysis of normal BMD, osteopenia, and osteoporosis

  • To the best of our knowledge, this post hoc analysis in secukinumab 150 mg (IV → 150 mg) group is the first study assessing the effects of an IL-17 inhibitor on BMD at different sites and in relation to radiographic progression, in combination with the evaluation of bone turnover markers

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Summary

Introduction

Axial spondyloarthritis including ankylosing spondylitis (AS) is characterized by chronic inflammation and new bone formation in the axial skeleton. Ankylosing spondylitis (AS) or radiographic axial spondyloarthritis (axSpA), is a chronic inflammatory disease that primarily affects the axial skeleton, including the sacroiliac joints and the vertebral column [1]. It is often characterized by inflammatory back pain and spinal stiffness leading to impaired physical function [2]. In addition to BMD assessment using dual-energy X-ray absorptiometry (DXA), biochemical markers of bone metabolism, known as bone turnover biomarkers, including markers of bone formation (growth), bone resorption (loss) and bone turnover regulators, can be useful diagnostic tools for the assessment of fracture risk in patients with AS [16, 17]

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