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Correlation between magnetic resonance imaging (MRI) findings and the new bone formation factor Dkk-1 in patients
Zheng Zhao1, Gang Wang1, Yanyan Wang1
1Department of Rheumatology, PLA General Hospital, 28# Fuxing Road, Beijing, China.
Abstract:
In recent years, MRI has been regarded as a major diagnostic tool for spondyloarthritis (SpA), and anti-TNF therapy has been widely confirmed as an effective treatment strategy. This study was designed to investigate the correlation between the secreted protein dickkopf-1 (Dkk-1) and abnormal findings on magnetic resonance imaging (MRI) through a prospective study of 30 cases of SpA. Thirty patients with active SpA were included, all treated with recombinant human tumor necrosis factor (TNF) receptor-antibody fusion protein (YiSaiPu) injection at 50 mg/week for 6 months. All patients were also examined for their clinical, serological, and imaging manifestations of the condition before and after treatment. In patients receiving TNF inhibitor treatment, the erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and clinical activity indices BASDAI, BASFI, BASMI, ASDAS-CRP were significantly decreased (p < 0.01). Serum Dkk-1 concentration was also significantly decreased (p < 0.05), as were the scores of bone marrow edema of the sacroiliac joints and the spine (p < 0.05). The score of sacroiliac joint backfill was significantly increased (p < 0.05), and the baseline and changes in the serum Dkk-1 concentration were significantly correlated with the baseline and changes in spinal bone marrow edema levels. Inhibition of the level of serum Dkk-1 by TNF inhibitors may be the molecular basis for inhibiting the formation of new bone in SpA patients. In addition, spinal marrow edema may have significance for predicting new bone formation.
Insights
Anti-TNF therapy effectively treats spondyloarthritis (SpA), reducing inflammation and bone edema. This study links decreased Dickkopf-1 (Dkk-1) levels to treatment response and reduced new bone formation in SpA patients.
Area of Science:
- Rheumatology
- Immunology
- Radiology
Background:
- Spondyloarthritis (SpA) diagnosis increasingly relies on MRI.
- Anti-tumor necrosis factor (TNF) therapy is an established treatment for SpA.
- The role of Dickkopf-1 (Dkk-1) in SpA pathogenesis and treatment response requires further elucidation.
Purpose of the Study:
- To investigate the correlation between serum Dkk-1 levels and MRI findings in SpA patients undergoing anti-TNF therapy.
- To assess the impact of anti-TNF therapy on clinical, serological, and imaging markers of SpA activity.
- To explore the potential role of Dkk-1 as a biomarker for treatment response and new bone formation in SpA.
Main Methods:
- Prospective study of 30 active SpA patients treated with anti-TNF therapy (recombinant human TNF receptor-antibody fusion protein) for 6 months.
- Clinical, serological (ESR, CRP), and imaging (MRI of sacroiliac joints and spine) assessments were performed before and after treatment.
- Serum Dkk-1 concentrations were measured and correlated with clinical and imaging outcomes.
Main Results:
- Anti-TNF treatment significantly reduced inflammatory markers (ESR, CRP) and clinical indices (BASDAI, BASFI, ASDAS-CRP).
- Serum Dkk-1 levels, bone marrow edema scores in sacroiliac joints and spine significantly decreased post-treatment.
- Increased sacroiliac joint backfill scores were observed, and baseline/changes in serum Dkk-1 correlated with spinal bone marrow edema.
- Spinal bone marrow edema may predict new bone formation.
Conclusions:
- TNF inhibitors may reduce new bone formation in SpA by inhibiting serum Dkk-1 levels.
- Decreased Dkk-1 levels are associated with successful anti-TNF therapy in SpA.
- Spinal bone marrow edema on MRI is a potential predictor of new bone formation in SpA patients.
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