Sudoscan检测硼替佐米引起的疼痛性神经病变的诊断效用:对18例多发性骨髓瘤患者的研究

A. Allegra, V. Rizzo, V. Innao, A. Alibrandi, A. Mazzeo, R. Leanza, C. Terranova, L. Gentile, P. Girlanda, A. G. Allegra, A. Alonci, C. Musolino
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引用次数: 4

摘要

在过去的几年里,多发性骨髓瘤的治疗经历了一个深刻的变化,使用新的治疗方法包括蛋白酶体抑制剂。硼替佐米是治疗多发性骨髓瘤的一线药物。周围神经病变的发作是药物剂量限制的附带效应。这种神经病变是一种远端对称神经病变,影响大纤维和小纤维。神经传导研究(NCS)可用于诊断硼替佐米神经病,但该技术显示大神经纤维的改变。Sudoscan是一种用于评估sudomotor功能的新技术。本研究的主要目的是比较Sudoscan在硼替佐米治疗后神经传导研究中的敏感性和诊断特异性。材料与方法对18例多发性骨髓瘤患者进行研究,其中男性10例(55.5%),女性8例(44.5%)。患者在基线和用硼替佐米治疗6个月后进行分析。使用Sudoscan装置对受试者进行神经传导研究和皮肤电导评价。患者还接受了疼痛和神经病变的临床测量。结果基线NCS显示只有3例(16.7%)患者的平均脑脊液SAP振幅低于正常的2SD下限,同时我们发现2例(11.1%)患者的Sudoscan谱发生改变。治疗6个月后,13例(72.2%)患者的NCS谱发生改变,11例(61.1%)患者的Sudoscan谱发生改变。结论我们的研究结果表明,Sudoscan可用于硼替佐米诱发的神经病变的诊断。它是客观的,可重复的,而且肯定比传统的神经传导研究更容易。Sudoscan可能有助于管理多发性骨髓瘤的治疗干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic utility of Sudoscan for detecting bortezomib-induced painful neuropathy: a study on 18 patients with multiple myeloma
Introduction In the past few years, treatment of multiple myeloma has undergone a deep change for the employment of novel treatment comprising proteasome inhibitors. Bortezomib is a first-line drug in therapy of multiple myeloma. The onset of peripheral neuropathy is a dose-limiting collateral effect of the drug. This neuropathy is a distal symmetric neuropathy that affects both large and small fibers. Nerve conduction study (NCS) can be used for the diagnosis of bortezomib neuropathy, but this technique demonstrates alterations of the large nerve fibers. Sudoscan is a novel technique utilized to offer an evaluation of sudomotor function. The main objective of this study was to compare the sensitivity and diagnostic specificity of Sudoscan with respect to the nerve conduction study after bortezomib treatment. Material and methods A total of 18 multiple myeloma patients were studied, 10 (55.5%) men and 8 (44.5%) women. Patients were analyzed at baseline and after 6 months of treatment with bortezomib. Subjects were submitted to nerve conduction study and electrochemical skin conductance evaluation with the Sudoscan device. Patients were also submitted to a clinical measure of pain and neuropathy. Results At baseline NCS showed that only the mean sural SAP amplitude was below the 2SD lower limit of normal in 3 (16.7%) patients, while at same time we found an alteration of Sudoscan profiles in 2 (11.1%) patients. After 6 months of treatment, the NCS profiles were altered in 13 (72.2%) patients, and the Sudoscan profiles were modified in 11 (61.1%) subjects. Conclusions Our results suggest that Sudoscan can be considered for the diagnosis of bortezomib-induced neuropathy. It is objective, reproducible, and surely easier than the traditional nerve conduction study. Sudoscan may be a useful help to manage the therapeutic interventions in multiple myeloma.
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