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Inflammatory Myopathies With Anti-Ku Antibodies: A Prognosis Dependent on Associated Lung Disease

机译:抗-Ku抗体引起的炎症性肌病:预后取决于相关的肺病

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Anti-Ku antibodies have been reported in a wide spectrum of autoimmune diseases, sometimes in association with inflammatory myopathies (IM). We studied the clinical, laboratory, and muscle histologic features of all anti-Ku-positive patients detected in our hospital during the last 10 years, as well as their treatment and outcomes. Anti-Ku antibodies were found in 34 patients (0.46% of 20,600 sera positive for antinuclear antibodies), and complete data were available for 30 patients; 86.7% were female, mean age was 49 years (range, 20–73 yr). The most frequent clinical manifestations were arthralgia (77%) and Raynaud phenomenon (53%). Eleven (37%) patients had IM, 8 of them as part of an overlap syndrome defined as IM associated with connective autoimmune disease (5 systemic sclerosis [SSc], 2 Sj?gren syndrome (SS), and 1 systemic lupus erythematosus [SLE]). Of 21 patients without IM, 19 had autoimmune diseases (including 6 SLE, 2 SSc, 2 SS, and 2 rheumatoid arthritis), 1 had bronchial neoplasia, and 1 had nephroangiosclerosis. Clinical features of the 9 patients with IM were myalgia (91%), proximal muscle weakness (89%), and dysphagia (36%). All had increased creatine kinase (median, 2210 U/L; range, 194–4073 U/L). Muscle biopsy showed necrosis, inflammation, and positive HLA class I immunostaining. Interstitial lung disease (ILD) was detected on computed tomography (CT) scan in 11 patients (37%) and was significantly more frequent in patients with IM (82% vs. 10.5%, p Anti-Ku antibodies remain rarely detected, but their presence can be frequently associated with corticosensitive IM and severe, corticoresistant ILD. Abbreviations: ANA = antinuclear antibodies CT = computed tomography ENA = extractable nuclear antigen IBM = inclusion body myositis ILD = interstitial lung disease IM = inflammatory myopathies NSIP = nonspecific interstitial pneumonia SLE = systemic lupus erythematosus SS = Sj?gren syndrome SSc = systemic sclerosis UIP = usual interstitial pneumonia.
机译:在各种自身免疫疾病中,有时与炎症性肌病(IM)有关的抗Ku抗体的报道。我们研究了过去10年在我们医院发现的所有抗Kuu阳性患者的临床,实验室和肌肉组织学特征,以及他们的治疗方法和结果。在34例患者中发现了抗Ku抗体(20,600份血清中抗核抗体阳性的比例为0.46%),并且有30例患者的完整数据。女性占86.7%,平均年龄为49岁(20-73岁)。最常见的临床表现是关节痛(77%)和雷诺现象(53%)。 11例(37%)患者患有IM,其中8例是重叠综合征的一部分,重叠综合征被定义为与结缔性自身免疫病相关的IM(5全身性硬化症[SSc],2 Sj?gren综合征(SS)和1全身性红斑狼疮[SLE ])。 21例无IM的患者中,有19例患有自身免疫性疾病(包括6例SLE,2例SSc,2例SS和2例类风湿性关节炎),1例患有支气管肿瘤,1例患有肾血管硬化。 9例IM患者的临床特征为肌痛(91%),近端肌无力(89%)和吞咽困难(36%)。所有患者的肌酸激酶均升高(中位数为2210 U / L;范围为194–4073 U / L)。肌肉活检显示坏死,炎症和HLA I类免疫染色阳性。在11例(37%)的计算机断层扫描(CT)扫描中发现了间质性肺病(ILD),而在IM患者中则更为频繁(82%vs. 10.5%,p Anti-Ku抗体仍然很少被检测到,但是缩写通常为:ANA =抗核抗体CT =计算机断层扫描ENA =可提取核抗原IBM =包涵体肌炎ILD =间质性肺病IM =炎症性肌病NSIP =非特异性间质性肺炎SLE =系统性红斑狼疮SS =干燥综合征SSc =全身性硬化症UIP =常见的间质性肺炎。

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