Risk Factors for Relapse and/or Prolonged Glucocorticoid Therapy in Polymyalgia Rheumatica

Author:

Vinicki Juan Pablo1,Gut Oscar2,Maliandi María del Rosario3,Velasco Zamora Jose Luis4,Linarez Miguel5,Cusa Maria Alejandra6,Got Julio7,Spinetto Maria Andrea2,Estevez Adrian Jorge8,Brigante Alejandro9,Curti Ana Carolina10,Costi Ana Carolina11,Cavallasca Javier12

Affiliation:

1. Sección Reumatología, Hospital de Quilmes

2. Centro Médico Privado, Buenos Aires

3. Unidad de Reumatología, Sanatorio Garay, Santa Fe

4. Instituto de Investigaciones Clínicas, Quilmes

5. Obra Social del Personal Maritimo

6. Medicina Reumatológica, Centro Médico Privado, Buenos Aires

7. Unidad de Reumatología, Instituto Médico Humanitas, Chaco

8. Unidad de Inmunoreumatología, Hospital El Cruce

9. Sección Reumatológica, Sanatorio Güemes, Buenos Aires

10. Centro Médico Privado, Mendoza

11. Servicio de Reumatología, HIGA San Martín de La Plata, Buenos Aires

12. Sección Reumatología, Hospital José Bernardo Iturraspe, Santa Fe, Argentina.

Abstract

Background In polymyalgia rheumatica (PMR) relapses and long-term GC dependency are common. We assessed risk factors for higher relapse rate and/or prolonged glucocorticoid therapy in PMR patients. Methods A multicenter and observational study (chart review) of PMR patients seen between 2006 and 2021 who had at least a 3-month follow-up period after starting GCs was performed. Results were expressed as median and interquartile range 25th–75th or mean ± standard deviation for numerical variables and percentage for categorical ones. Relapse versus nonrelapse groups were compared using Cox proportional analysis. Hazards ratios (HRs) with 95% confidence intervals (CIs) are reported. In all cases, a p value <0.05 was considered to indicate statistical significance. Results We included 185 patients (69.1% female). The median follow-up time was 17.1 months (interquartile range, 6.8–34.7). Incidence of relapses was 1.2 per 100 persons/month. In univariate analysis, PMR patients with a previous history of dyslipidemia had a lower risk of relapse (HR, 0.55; 95% CI, 0.33–0.94; p = 0.03); high-dose GC (HR, 2.35; 95% CI, 1.42–3.87; p = 0.001) and faster GC dose reduction had higher risk of relapse (HR, 3.04; 95% CI, 1.77–5.21; p = 0.001). In multivariate analysis, a previous history of dyslipidemia had a lower risk of relapse (HR, 0.54; 95% CI, 0.32–0.92; p = 0.023), and high dose of GC (HR, 2.46; 95% CI, 1.49–4.08; p = 0.001) remained the only risk factors for relapse. Conclusions Lower doses of corticosteroids and a slow rate of reduction are critical to avoid relapse in PMR. Risk factors for higher relapse rate rely on therapy more than clinical characteristics of the patients at the time of diagnosis of PMR.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Rheumatology

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