Chang Thashi, Leite Maria Isabel, Senanayake Sunethra, Gunaratne Padma S, Gamage Ranjanie, Riffsy M T M, Jacobson Leslie W, Adhikari Madura, Perera Sanja, Vincent Angela
Department of Clinical Medicine, University of Colombo, Sri Lanka.
Department of Clinical Neurology, University of Oxford, United Kingdom.
J Neurol Sci. 2014 Aug 15;343(1-2):82-7. doi: 10.1016/j.jns.2014.05.037. Epub 2014 May 27.
Identification of autoantibodies has defined distinct clinico-immuno-pathological subtypes of myasthenia gravis (MG) such as AChR-antibody-positive-MG and MuSK-antibody-positive-MG. The use of more sensitive assays such as the cell-based assay (CBA) is expected to reduce the proportion of seronegative-MG. We studied the seroprevalence of AChR and MuSK antibodies using both radioimmunoprecipitation (RIA) and CBA amongst MG patients in Sri Lanka and related their antibody status to their clinical subtypes and severity.
113 patients with MG attending Neurology units in the district of Colombo were studied. Clinical data were obtained using an interviewer-administered questionnaire and medical records. The severity of MG was assessed according to MGFA clinical grading. RIA and CBA were used to detect serum AChR and MuSK antibodies. Patients with other neurological diseases were recruited as controls.
We detected either AChRAb (85%) or MuSKAb (6.2%) in 91.2% of MG patients. Complementing the RIA with the CBA improved the diagnostic power of detecting AChRAbs by 21% and MuSKAbs by 77%. The clinical characteristics and the occurrence of thymic pathology were similar to other populations except for a male preponderance (1.5:1). The AChRAb titer appeared to parallel the clinical severity. Seven of 11 (63.6%) patients with AChRAb-negative generalized MG had MuSK-MG.
Clinical characteristics of MG in Sri Lanka are similar to other populations. Complementing the RIA with CBA increases the diagnostic power of detecting pathogenic autoantibodies.
自身抗体的鉴定已明确了重症肌无力(MG)不同的临床免疫病理亚型,如乙酰胆碱受体(AChR)抗体阳性重症肌无力和肌肉特异性激酶(MuSK)抗体阳性重症肌无力。使用更敏感的检测方法,如基于细胞的检测法(CBA),有望降低血清阴性重症肌无力的比例。我们使用放射免疫沉淀法(RIA)和CBA检测了斯里兰卡重症肌无力患者中AChR和MuSK抗体的血清流行率,并将其抗体状态与临床亚型及严重程度相关联。
对科伦坡地区神经病学科室收治的113例重症肌无力患者进行了研究。通过访谈式问卷和病历获取临床数据。根据重症肌无力基金会(MGFA)临床分级评估重症肌无力的严重程度。使用RIA和CBA检测血清中的AChR和MuSK抗体。招募患有其他神经系统疾病的患者作为对照。
我们在91.2%的重症肌无力患者中检测到了AChR抗体(85%)或MuSK抗体(6.2%)。CBA与RIA相结合,将检测AChR抗体的诊断能力提高了21%,检测MuSK抗体的诊断能力提高了77%。除男性占优势(1.5:1)外,临床特征和胸腺病理情况与其他人群相似。AChR抗体滴度似乎与临床严重程度平行。11例AChR抗体阴性的全身型重症肌无力患者中有7例(63.6%)患有MuSK重症肌无力。
斯里兰卡重症肌无力的临床特征与其他人群相似。CBA与RIA相结合可提高检测致病性自身抗体的诊断能力。