Prevalence of overlap of antineutrophil cytoplasmic antibody associated vasculitis with systemic autoimmune diseases: an unrecognized example of poliautoimmunity

被引:26
作者
Martin-Nares, Eduardo [1 ]
Zuniga-Tamayo, Diego [2 ]
Hinojosa-Azaola, Andrea [1 ]
机构
[1] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Immunol & Rheumatol, Vasco de Quiroga 15,Col Secc 16, Mexico City 14000, DF, Mexico
[2] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Pathol, Vasco de Quiroga 15,Col Secc 16, Mexico City 14000, DF, Mexico
关键词
ANCA; Autoimmune diseases; Overlap syndromes; Vasculitis; ANCA-ASSOCIATED VASCULITIS; CONNECTIVE-TISSUE DISEASE; PRIMARY SJOGRENS-SYNDROME; RHEUMATOID-ARTHRITIS; CRESCENTIC GLOMERULONEPHRITIS; GRANULOMATOSIS; POLYANGIITIS; AUTOANTIBODIES; POLYMORPHISM; SCLEROSIS;
D O I
10.1007/s10067-018-4212-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 +/- 17years 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 34months, and four patients (14%) died. The most frequent autoimmune disease overlapped was rheumatoid arthritis (39%), followed by Sjogren'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 173months. 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.
引用
收藏
页码:97 / 106
页数:10
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