肌炎抗体在炎性肌病中的表达及意义

Expression and significance of myositis antibodies in inflammatory myopathy

  • 摘要:
      目的  探讨肌炎抗体在特发性炎性肌病(IIM)患者中的表达及意义。
      方法  收集2018年8月—2021年4月在安徽医科大学附属安庆医院住院的49例行肌炎抗体检测的IIM患者的临床资料,分析肌炎抗体与IIM患者的临床特征、实验室指标和预后的关系。
      结果  49例IIM患者中,肌炎抗体阳性者37例。肌炎特异性抗体(MSAs)中以抗氨基酰t-RNA合成酶(ARS)抗体(32.7%)和抗黑色素瘤分化相关基因5(MDA5)抗体(30.6%)阳性率最高;抗SSA/Ro抗体这种肌炎相关性抗体(MAA)亦有极高的阳性率(49.0%),多与MSAs合并出现。抗ARS抗体阳性者较少出现向阳性皮疹、"V"字征、披肩征、Gottron征,易出现技工手、肌痛、肺间质病变,淋巴细胞计数较阴性者高(P < 0.05);抗SSA/Ro抗体阳性者易出现肺间质病变,病死率较高(P < 0.05);抗Mi-2抗体阳性者易出现吞咽困难,天门冬氨酸氨基转移酶(AST)、肌酸激酶(CK)、乳酸脱氢酶(LDH)较阴性者高(P < 0.05);抗转录中介因子1γ(TIF1γ)抗体阳性者易合并肿瘤(P=0.015);抗MDA5抗体多见于皮肌炎(DM)和无肌病皮肌炎(ADM)患者,阳性者较阴性者易出现发热、向阳性皮疹、披肩征、Gottron征、关节痛、肺间质病变,病死率高,较少出现肌痛、肌无力,淋巴细胞计数、CK、LDH更低(P < 0.05)。Logistic回归分析发现抗ARS抗体是"V"字征、Gottron征的保护因素(P < 0.05);抗组氨酰tRNA合成酶(Jo-1)抗体是技工手的独立危险因素(OR=15.417,95% CI为2.641~90.000,P=0.002);抗Mi-2抗体是吞咽困难的独立危险因素(OR=21.000,95% CI为1.544~285.685,P=0.022);抗TIF1γ抗体是肿瘤的独立危险因素(OR=44.000,95% CI为2.709~714.585,P=0.008);抗MDA5抗体是发热、向阳性皮疹、关节痛、肺间质病变的独立危险因素,是肌痛、肌无力的保护因素(P < 0.05)。Cox回归分析发现抗MDA5抗体是IIM患者死亡的独立危险因素(HR=16.023,95% CI为1.944~135.066,P=0.010)。
      结论  肌炎抗体在IIM患者中阳性率高,其亚型与患者的临床特征、实验室指标及预后密切相关。检测肌炎抗体对指导IIM患者的诊治和预后判断具有重要意义。

     

    Abstract:
      Objective  To explore the expression and significance of myositis antibodies in patients with idiopathic inflammatory myopathy (IIM).
      Methods  The medical materials of 49 IIM hospitalized patients with myositis antibodies detection in Anqing Hospital Affiliated to Anhui Medical University from August 2018 to April 2021 were collected, and the correlations between myositis antibodies and clinical features, laboratory indexes and prognosis of IIM patients were analyzed.
      Results  Among 49 IIM patients, 37 cases were positive for myositis antibodies. The positive rates of anti ARS antibody (32.7%) and anti MDA5 antibody (30.6%) were the highest among the myositis specific autoantibodies (MSAs), and anti SSA/Ro antibody, a myositis associated antibody (MAA), also had a very high positive rate (49.0%), most of patients were combined with MSAs. Patients with positive anti-ARS antibodies were less likely to have heliotrope rash, V-shaped sign, shawl sign and Gottron sign, and were more likely to have mechanic's hand, myalgia and interstitial lung disease, and also had a high lymphocyte count than patients who were negative for anti-ARS (P < 0.05). Patients with anti-SSA/Ro-positive antibody were prone to occur interstitial lung disease and had a higher mortality (P < 0.05). Patients with positive anti-Mi-2 antibody had higher incidence rates of dysphagia and higher levels of aspartate transaminase (AST), creatine kinase (CK) and lactate dehydrogenase (LDH) than patients who were negative for anti-Mi-2 (P < 0.05). Patients with positive anti-transcription intermediary factor-1 γ(anti-TIF1γ) antibody were more likely to have tumors (P=0.0015). Anti-MDA5 antibody was more common in dermatomyositis (DM) and amyopathic dermatomyositis (ADM) patients. Compared with negative patients, positive patients were more likely to have fever, heliotrope rash, shawl sign, Gottron sign, arthralgia, interstitial lung disease, higher mortality, less myalgia and muscle weakness, lower levels of lymphocyte count, CK and LDH (P < 0.05). Logistic regression analysis identified anti-ARS-antibodies as a protective factor for V-shaped sign and Gottron sign (P < 0.05), aminoacyl-tRNA synthetase (Jo-1) antibody as an independent risk factor for the mechanic's hand (OR=15.417, 95%CI was 2.641 to 90.000, P=0.002), anti-Mi-2 antibody as independent risk factor for dysphagia (OR=21.000, 95%CI, 1.544 to 285.685, P=0.022), anti-TIF1γ antibody as an independent risk factor for tumors (OR=44.000, 95%CI, 2.709 to 714.585, P=0.008), anti-MDA5 antibody as an independent risk factor for fever, heliotrope rash, arthralgia, interstitial lung disease and a protective factor for myalgia, muscle weakness (P < 0.05). Cox regression analysis identified anti-MDA5 antibody as an independent risk factor for death in IIM patients (HR=16.023, 95%CI, 1.944 to 135.066, P=0.010).
      Conclusion  Myositis antibodies are highly positive in IIM patients, and their subtypes are closely related to clinical features, laboratory indexes and prognosis of patients. Detection of myositis antibodies has great significance in guiding the diagnosis, treatment and prognosis of IIM patients.

     

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