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Predicting relapse in anti-neutrophil cytoplasmic antibody-associated vasculitis: a Systematic review and meta-analysis.
King, Catherine; Druce, Katie L; Nightingale, Peter; Kay, Ellen; Basu, Neil; Salama, Alan D; Harper, Lorraine.
Afiliação
  • King C; Centre for Translational Inflammation Research, University of Birmingham.
  • Druce KL; Department of Renal Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham.
  • Nightingale P; Centre for Epidemiology Versus Arthritis, University of Manchester.
  • Kay E; Manchester Academic Health Science Centre (MAHSC), University of Manchester, Manchester.
  • Basu N; Centre for Translational Inflammation Research, University of Birmingham.
  • Salama AD; Department of Renal Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham.
  • Harper L; Institution of Infection, Immunity and Inflammation, University of Glasgow, Glasgow.
Rheumatol Adv Pract ; 5(3): rkab018, 2021.
Article em En | MEDLINE | ID: mdl-34476335
ABSTRACT

OBJECTIVES:

Relapses affect 30-50% of patients with ANCA-associated vasculitis (AAV) over 5 years, necessitating long-term treatment. Although there have been studies looking at predictors of relapse in AAV, this research has yet to translate clinically into guidance on tailored therapy. The aim of this systematic review was to identify and meta-analyse existing risk factors from the literature and produce a model to calculate individualised patient risk of relapse.

METHOD:

A search strategy was developed to include all studies identifying predictors of AAV relapse using multivariate analysis. Individual risk factors were extracted and pooled hazard ratios (HRs) calculated. A model to predict the time to first relapse based on identified risk factors was tested retrospectively using a cohort of patients with AAV.

RESULTS:

The review of 2674 abstracts identified 117 papers for full text review, with 16 eligible for inclusion. Pooled HRs were calculated from significant risk factors, including anti-PR3 ANCA positivity [HR 1.69 (95% CI 1.46, 1.94)], cardiovascular involvement [HR 1.78 (95% CI 1.26, 2.53)], creatinine >200 µmol/l (relative to creatinine ≤100) [HR 0.39 (95% CI 0.22, 0.69)] and creatinine 101-200 µmol/l [HR 0.81 (95% CI 0.77, 0.85)]. Using data from 182 AAV patients to validate the model gave a C-statistic of 0.61.

CONCLUSION:

Anti-PR3 ANCA positivity, lower serum creatinine and cardiovascular system involvement are all associated with an increased risk of relapse, and a combination of these risk factors can be used to predict the individualised risk of relapse. In order to produce a clinically useful model to stratify risk, we need to identify more risk factors, with a focus on robust biomarkers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies / Systematic_reviews Idioma: En Revista: Rheumatol Adv Pract Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies / Systematic_reviews Idioma: En Revista: Rheumatol Adv Pract Ano de publicação: 2021 Tipo de documento: Article