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An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Multivariable Models to Predict a Diagnosis of Giant Cell Arteritis: Systematic Review and Metaanalysis.
Mats L Junek1, Iva Okaj2, Sagar Patel2
1M.L. Junek, MD, MSc, N. Khalidi, MD, St. Joseph's Healthcare, and McMaster University, Division of Rheumatology, Department of Medicine, Hamilton, Ontario; junekm@mcmaster.ca.
Predictive models for giant cell arteritis (GCA) show consistent predictors like jaw claudication and elevated CRP. However, these models often suffer from poor methodological quality, necessitating more rigorous development for accurate GCA diagnosis.
Area of Science:
- Rheumatology
- Clinical Epidemiology
- Diagnostic Accuracy Studies
Background:
- Giant cell arteritis (GCA) is a systemic vasculitis requiring timely diagnosis.
- Numerous multivariable models have been developed to aid clinicians in diagnosing GCA.
- The performance and variables of these predictive models require systematic evaluation.
Purpose of the Study:
- To conduct a systematic review and meta-analysis of variables used in GCA diagnostic models.
- To assess the performance and risk of bias of existing GCA predictive models.
Main Methods:
- Systematic search of PubMed, Embase, and Cochrane Library (1990-2024).
- Inclusion of studies using multivariable models for GCA diagnosis.
- Meta-analysis of individual signs/symptoms and assessment of predictor certainty using GRADE.
- Risk of bias assessment using the Prediction Model Risk of Bias Assessment Tool (PROBAST).
Main Results:
- 44 studies including 15,409 patients and 4340 GCA diagnoses were analyzed.
- Predictors with high certainty and large effect size: jaw claudication, elevated C-reactive protein (>24.5 mg/L), thrombocytosis (>400 × 10^9/L), positive temporal artery ultrasound, and synovitis (predictive of non-GCA).
- Classical GCA symptoms (vision loss, polymyalgia rheumatica, headache) had lower certainty of effect.
- Most models exhibited a high risk of bias.
Conclusions:
- Key predictors for GCA diagnosis are consistent across models.
- Existing GCA predictive models are generally of poor methodological quality.
- Future development of GCA diagnostic models requires enhanced methodological rigor.
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