Department of Neurology, Copenhagen University Hospital (Rigshospitalet), Copenhagen, Denmark.
Department of Clinical Neurophysiology, Rigshospitalet, Copenhagen, Denmark.
Eur J Neurol. 2024 Jul;31(7):e16305. doi: 10.1111/ene.16305. Epub 2024 Apr 23.
To evaluate whether ongoing axonal loss can be prevented in multifocal motor neuropathy (MMN) treated with immunoglobulin G (IgG), a group of patients with a median disease duration of 15.7 years (range: 8.3-37.8), treated with titrated dosages of immunoglobulins, was studied electrophysiologically at time of diagnosis and at follow-up.
At follow-up, the Z-score of the compound motor action potential amplitude of the median, fibular, and tibial nerves and the neurological performances were determined. In seven patients with a treatment-free period of 0.3 years (0.2-0.4), there was no progression of axonal loss (p = 0.2), whereas a trend toward further axonal loss by 1.3 Z-scores (0.9-17.0, p = 0.06) was observed in five patients with a treatment-free period of 4.0 years (0.9-9.0). The axonal loss in the group with a short treatment delay was significantly smaller than in the group with a longer treatment delay (p = 0.02). Also, there was an association between treatment delay and ongoing axonal loss (p = 0.004). The electrophysiological findings at follow-up were associated with the isokinetic strength performance, the neurological impairment score, and the disability, supporting the clinical relevance of the electrophysiological estimate of axonal loss.
Swift initiation of an immediately titrated IgG dosage can prevent further axonal loss and disability in continuously treated MMN patients.
为了评估在接受免疫球蛋白 G(IgG)治疗的多灶性运动神经病(MMN)中是否可以防止持续的轴突丢失,对一组中位病程为 15.7 年(范围:8.3-37.8 年)的患者进行了研究,这些患者接受了滴定剂量的免疫球蛋白治疗,并在诊断时和随访时进行了电生理研究。
在随访时,测定了正中神经、腓总神经和胫神经的复合运动动作电位幅度的 Z 评分和神经功能表现。在 7 名治疗无间隔期为 0.3 年(0.2-0.4 年)的患者中,没有观察到轴突丢失的进展(p=0.2),而在 5 名治疗无间隔期为 4.0 年(0.9-9.0 年)的患者中,轴突丢失有进一步增加 1.3 Z 评分(0.9-17.0,p=0.06)的趋势。治疗延迟时间较短的组的轴突丢失明显小于治疗延迟时间较长的组(p=0.02)。此外,治疗延迟与持续的轴突丢失之间存在关联(p=0.004)。随访时的电生理发现与等速肌力表现、神经损伤评分和残疾有关,支持电生理估计轴突丢失的临床相关性。
立即开始滴定 IgG 剂量可以防止连续治疗的 MMN 患者进一步的轴突丢失和残疾。