Overview of biomarkers in myasthenia gravis

Fatemeh Afrashteh, Rayan Rajabi
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Abstract

Myasthenia gravis (MG) is a rare auto-immune neuromuscular junction (NMJ) disorder which is caused by formation of autoantibodies and destruction of NMJ components. The MG diagnosis is based on the symptoms, autoantibodies detection and paraclinical tests. Given that MG patients have so many differential diagnosis and various medication responses, choosing an accurate diagnosis and the therapy plan in MG is challenging. According to the studies, there are the immunologic, genetic, microRNAs, gut microbiome, and other established or newly proposed biomarkers for diagnosis and prognosis of MG. More studies are needed to provide better collection of biomarkers in MG patients and evaluate their role in MG pathology.
重症肌无力生物标志物综述
重症肌无力(MG)是一种罕见的自身免疫神经肌肉接头(NMJ)疾病,它是由自身抗体的形成和NMJ组分的破坏引起的。MG的诊断是基于症状、自身抗体检测和临床旁检查。MG患者鉴别诊断多,药物反应多样,因此选择准确的诊断和治疗方案是一项挑战。根据研究,有免疫学、遗传学、microrna、肠道微生物组和其他已建立或新提出的生物标志物用于MG的诊断和预后。需要更多的研究来更好地收集MG患者的生物标志物,并评估它们在MG病理中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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