Redondo-Rodriguez Rocío, Mena-Vázquez Natalia, Cabezas-Lucena Alba María, Manrique-Arija Sara, Mucientes Arkaitz, Fernández-Nebro Antonio
Instituto de Investigación Biomédica de Málaga (IBIMA), UGC de Reumatología, Hospital Regional Universitario de Málaga, 29010 Malaga, Spain.
Departamento de Medicina, Universidad de Málaga, 29016 Malaga, Spain.
J Clin Med. 2022 May 4;11(9):2573. doi: 10.3390/jcm11092573.
Objective: In this study, we aimed to evaluate the worldwide incidence and prevalence of ANCA-associated vasculitis (AAV). Methods: A systematic search of Medline and Embase was conducted until June 2020 for studies that analyzed the incidence and prevalence of patients aged >16 years diagnosed with AAV in different geographical areas. A meta-analysis was undertaken to estimate the pooled incidence per million person-years and prevalence per million persons in AAV overall and for each subtype of AAV: granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA). The 95% confidence interval (CI) and I2 for heterogeneity were calculated. Results: The meta-analysis included 25 studies that met the inclusion criteria and covered a total of 4547 patients with AAV. Frequency increased over time. The global pooled incidence (95% CI) was 17.2 per million person-years (13.3−21.6) and the global pooled prevalence (95% CI) was 198.0 per million persons (187.0−210.0). The pooled incidence per million person-years for each AAV subtype varied from highest to lowest, as follows: GPA, 9.0; MPA, 5.9; and EGPA, 1.7. The individual pooled prevalence per million persons was, as follows: GPA, 96.8; MPA, 39.2; and EGPA, 15.6. AAV was more predominant in the northern hemisphere. By continent, a higher incidence in America and pooled prevalence of AAV was observed in America and Europe. Conclusion: The pooled incidence and prevalence of AAV seem to be increasing over time and are higher in the case of GPA. AAV was generally more frequent (incidence and prevalence) in the northern hemisphere.
在本研究中,我们旨在评估抗中性粒细胞胞浆抗体相关性血管炎(AAV)在全球范围内的发病率和患病率。方法:对Medline和Embase进行系统检索,直至2020年6月,以查找分析不同地理区域中年龄大于16岁的AAV确诊患者发病率和患病率的研究。进行荟萃分析以估计AAV总体以及AAV各亚型(肉芽肿性多血管炎(GPA)、显微镜下多血管炎(MPA)和嗜酸性肉芽肿性多血管炎(EGPA))每百万人口年的合并发病率和每百万人口的患病率。计算95%置信区间(CI)和异质性的I²。结果:荟萃分析纳入了25项符合纳入标准的研究,共涵盖4547例AAV患者。发病率随时间增加。全球合并发病率(95%CI)为每百万人口年17.2例(13.3 - 21.6),全球合并患病率(95%CI)为每百万人口198.0例(187.0 - 210.0)。AAV各亚型每百万人口年的合并发病率从高到低依次为:GPA,9.0;MPA,5.9;EGPA,1.7。每百万人口的个体合并患病率依次为:GPA,96.8;MPA,39.2;EGPA,1