Li Cathy Meng Fei, Nicolle Michael W, Sangam Kamala, Yang Liju, Budhram Adrian
Department of Clinical Neurological Sciences, Western University, London Health Sciences Centre, London, Ontario, Canada.
Department of Pathology and Laboratory Medicine, Western University, London Health Sciences Centre, London, Ontario, Canada.
Eur J Neurol. 2025 Mar;32(3):e70123. doi: 10.1111/ene.70123.
Fixed cell-based assays (CBAs) to detect acetylcholine receptor and muscle-specific tyrosine kinase antibodies (anti-AChR/MuSK) are now available, but evaluations of their diagnostic performance in clinical practice are lacking. We examined the positive predictive value (PPV) of anti-AChR/MuSK fixed CBA for myasthenia gravis (MG), following the implementation of this assay as first-line testing at our centre.
We identified all patients at our centre with positive anti-AChR/MuSK fixed CBA results between November 2021 and July 2024. Clinical information was reviewed to classify patients as having true positive or false positive antibody results. Patients with a clinical presentation compatible with MG and no more likely alternative diagnosis were classified as true positives, whereas all others were classified as false positives. Test PPV was calculated as the proportion of positives that were classified as true positives.
Of 770 patients who underwent anti-AChR/MuSK fixed CBA testing, 109 (14%) had positive antibody results (Anti-AChR, 105; Anti-MuSK, 4). Among them, one patient with anti-AChR positivity was classified as a false positive (suspected thymic hyperplasia without neurologic symptoms). The remaining 108 patients were classified as true positives, resulting in a calculated PPV of 99%.
We found that anti-AChR/MuSK fixed CBA had excellent PPV for MG. Anti-AChR positivity in one asymptomatic patient with suspected thymic hyperplasia was classified as a false positive result, although the possibility that it represents a true marker of thymic pathology in a patient who may later develop MG is challenging to exclude. The high PPV reported herein supports the use of anti-AChR/MuSK fixed CBA as first-line testing for suspected MG.
用于检测乙酰胆碱受体和肌肉特异性酪氨酸激酶抗体(抗AChR/MuSK)的固定细胞检测法(CBA)现已可用,但缺乏其在临床实践中诊断性能的评估。在我们中心将该检测法作为一线检测方法实施后,我们研究了抗AChR/MuSK固定CBA对重症肌无力(MG)的阳性预测值(PPV)。
我们确定了2021年11月至2024年7月期间在我们中心抗AChR/MuSK固定CBA检测结果为阳性的所有患者。回顾临床信息以将患者分类为抗体结果为真阳性或假阳性。临床表现与MG相符且无更可能的替代诊断的患者被分类为真阳性,而所有其他患者被分类为假阳性。检测PPV计算为被分类为真阳性的阳性比例。
在770例接受抗AChR/MuSK固定CBA检测的患者中,109例(14%)抗体结果为阳性(抗AChR,105例;抗MuSK,4例)。其中,1例抗AChR阳性患者被分类为假阳性(疑似胸腺增生但无神经症状)。其余108例患者被分类为真阳性,计算得出的PPV为99%。
我们发现抗AChR/MuSK固定CBA对MG具有出色的PPV。1例疑似胸腺增生的无症状患者的抗AChR阳性被分类为假阳性结果,尽管难以排除其可能代表后来可能发展为MG的患者胸腺病理的真实标志物。本文报道的高PPV支持将抗AChR/MuSK固定CBA用作疑似MG的一线检测方法。