Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga No. 15, Col. Sección XVI, Tlalpan, CP 14000, Mexico City, Mexico.
Department of Pathology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga No. 15, Col. Sección XVI, Tlalpan, CP 14000, Mexico City, Mexico.
Clin Rheumatol. 2019 Jan;38(1):97-106. doi: 10.1007/s10067-018-4212-1. Epub 2018 Jul 14.
We aimed to estimate the frequency of overlap of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) with systemic autoimmune diseases. Retrospective single-center study to identify patients with AAV diagnosis and concomitant autoimmune systemic diseases, simultaneously, before or after the diagnosis of AAV. Sociodemographic characteristics, such as comorbidities; follow-up time; type of AAV; disease duration; relapses; treatment and response; clinical, serological, and histological characteristics; disease activity and damage; prognosis; dialysis requirements, and death were assessed. Twenty-eight of two hundred and forty-seven patients (11.3%) with AAV had a concomitant diagnosis of autoimmune disease. The predominant AAV type was renal-limited vasculitis (39%), followed by granulomatosis with polyangiitis (29%), mycroscopic polyangiitis (25%), and eosinophilic granulomatosis with polyangiitis (7%). Mean age at AAV diagnosis was 50 ± 17 years and 24/28 were ANCA positive. The main clinical manifestations were renal (79%), otorhinolaryngologic (43%), and pulmonary and peripheral neuropathy (32%). Sixteen patients (57%) experienced partial or total remission at a median follow-up of 34 months, and four patients (14%) died. The most frequent autoimmune disease overlapped was rheumatoid arthritis (39%), followed by Sjögren's syndrome and systemic sclerosis (14%), mixed connective tissue disease (11%), systemic lupus erythematosus and juvenile idiopathic arthritis (7%), and ankylosing spondylitis and IgG4-related disease (4%). In nine patients (32%), both diagnoses were simultaneous; in the rest, median time elapsed between the autoimmune disease and AAV diagnosis was 173 months. The prevalence of overlap AAV with other autoimmune diseases was low. The most common AAV phenotype was renal-limited vasculitis, and the most frequent overlap disease was rheumatoid arthritis.
我们旨在评估抗中性粒细胞胞浆抗体(ANCA)相关性血管炎(AAV)与系统性自身免疫性疾病重叠的频率。这是一项回顾性单中心研究,旨在确定同时诊断为 AAV 及其他系统性自身免疫性疾病的患者,这些疾病可与 AAV 同时诊断,也可在 AAV 之前或之后诊断。评估的社会人口学特征包括合并症;随访时间;AAV 类型;疾病持续时间;复发;治疗和反应;临床、血清学和组织学特征;疾病活动度和损伤;预后;透析需求和死亡。在 247 例 AAV 患者中,有 28 例(11.3%)同时诊断为自身免疫性疾病。主要的 AAV 类型是肾血管炎(39%),其次是肉芽肿性多血管炎(29%)、显微镜下多血管炎(25%)和嗜酸性肉芽肿性多血管炎(7%)。AAV 诊断时的平均年龄为 50±17 岁,24/28 例为 ANCA 阳性。主要的临床表现为肾(79%)、耳鼻喉(43%)和肺及周围神经病(32%)。在中位随访 34 个月时,16 例患者(57%)部分或完全缓解,4 例患者(14%)死亡。重叠的最常见自身免疫性疾病是类风湿关节炎(39%),其次是干燥综合征和系统性硬化症(14%)、混合性结缔组织病(11%)、系统性红斑狼疮和幼年特发性关节炎(7%)、和强直性脊柱炎和 IgG4 相关疾病(4%)。在 9 例患者(32%)中,两种诊断同时存在;在其余患者中,自身免疫性疾病与 AAV 诊断之间的中位时间间隔为 173 个月。重叠 AAV 与其他自身免疫性疾病的患病率较低。最常见的 AAV 表型是肾血管炎,最常见的重叠疾病是类风湿关节炎。