Pamuk Ömer Nuri, Dönmez Salim, Calayır Gökçe Büşra, Pamuk Gülsüm Emel
Department of Rheumatology, Trakya University Medical Faculty, Eski Yildiz Cad. Park Apt. No:22 Daire: 18, 34349, Besiktas-Istanbul, Edirne, Turkey.
Department of Internal Medicine, Trakya University Medical Faculty, Edirne, Turkey.
Clin Rheumatol. 2016 Aug;35(8):2063-2071. doi: 10.1007/s10067-016-3232-y. Epub 2016 Mar 18.
Epidemiological data about antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is very limited. Until now, there has been no study about the epidemiology of AAV in Turkey. In this study, we evaluated the frequency of AAV in the northeastern part of Turkey. The general clinical features of patients diagnosed with AAV at our center within the last 10 years (2004-2014) were retrospectively recorded down. The incidence rates and the prevalence per 1,000,000 population aged ≥16 years were calculated. In addition, we evaluated the clinical features and survival rates of AAV patients. There were 30 patients with granulomatous polyangiitis (GPA), 15 with microscopic polyangiitis (MPA), and 5 with eosinophilic polyangiitis (EGPA). The overall prevalence of AAV in our region was 69.3/1,000,000 in individuals ≥16 years. Males had a similar prevalence (73.2/1,000,000) with females (65.4/1,000,000). The mean annual incidence rate was 8.1/million for all AAV. The annual incidence of AAV in females was 6.9/million; in males, it was 9.2/million. The annual incidence for GPA was calculated as 4.8/1,000,000, the incidence for MPA was 2.4/1,000,000, and the incidence for CSS was 0.8/1,000,000. Ten-year survival of patients with AAV was 65.3 %. The only independent poor prognostic factor in Cox's multivariate analysis was advanced age at the time of diagnosis (OR 7.5, 95 % CI 10.6-526, p = 0.043). The frequency of all AAV in northwestern Turkey was similar to that in southern Europe; however, it was lower than the frequency in Northern Europe.
关于抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)的流行病学数据非常有限。到目前为止,土耳其尚未有关于AAV流行病学的研究。在本研究中,我们评估了土耳其东北部地区AAV的发病率。回顾性记录了过去10年(2004 - 2014年)在我们中心诊断为AAV的患者的一般临床特征。计算了≥16岁人群每100万人口的发病率和患病率。此外,我们评估了AAV患者的临床特征和生存率。有30例肉芽肿性多血管炎(GPA)患者、15例显微镜下多血管炎(MPA)患者和5例嗜酸性肉芽肿性多血管炎(EGPA)患者。在我们地区,≥16岁个体中AAV的总体患病率为69.3/100万。男性患病率(73.2/100万)与女性(65.4/100万)相似。所有AAV的年平均发病率为8.1/百万。女性AAV的年发病率为6.9/百万;男性为9.2/百万。GPA的年发病率计算为4.8/100万,MPA的发病率为2.4/100万,CSS的发病率为0.8/100万。AAV患者的10年生存率为65.3%。Cox多变量分析中唯一独立的不良预后因素是诊断时年龄较大(比值比7.5,95%可信区间10.6 - 526,p = 0.043)。土耳其西北部所有AAV的发病率与南欧相似;然而,低于北欧的发病率。