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慢性炎症性脱髓鞘性多发性神经病各亚型感觉神经受累的不同模式。

Different patterns of sensory nerve involvement in chronic inflammatory demyelinating polyneuropathy subtypes.

机构信息

Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.

出版信息

Muscle Nerve. 2022 Aug;66(2):131-135. doi: 10.1002/mus.27530. Epub 2022 Apr 2.

Abstract

INTRODUCTION/AIMS: Among subtypes of chronic inflammatory demyelinating polyneuropathy (CIDP), different immune pathophysiologies have been proposed. In this study, sensory nerve conduction studies were compared among clinical subtypes to attempt to better understand the underlying pathophysiology.

METHODS

A total of 138 patients with CIDP was classified into clinical subtypes: typical CIDP (N = 68), multifocal CIDP (N = 27), or other (N = 2). Patients with immunoglobulin M (IgM) neuropathy anti-myelin-associated glycoprotein neuropathy (MAG; N = 19) were also included as disease controls. Sensory nerve action potentials (SNAPs) were recorded in the median, ulnar, and superficial radial and sural nerves.

RESULTS

SNAP amplitudes (P < .05) and conduction velocities (P < .01) in the median nerve and conduction velocities (P < .05) in the ulnar nerve were lower in typical CIDP than in multifocal CIDP, whereas those in the radial and sural nerves were comparable in each group. Low median and normal sural SNAP amplitudes were more common in typical CIDP (P < .005) than in multifocal CIDP, suggesting predominant involvement at terminal portions of the nerves.

DISCUSSION

Terminal portions of sensory nerves are preferentially affected in typical CIDP compared with multifocal CIDP. These findings might be partially explained by the hypothesis of antibody-mediated demyelination in typical CIDP at the regions where the blood-nerve barrier is anatomically deficient, whereas multifocal CIDP predominantly affects the nerve trunks, largely due to cell-mediated demyelination, with disruption of the blood-nerve barrier.

摘要

介绍/目的:在慢性炎症性脱髓鞘性多发性神经病(CIDP)的亚型中,已经提出了不同的免疫病理生理学。在这项研究中,我们比较了临床亚型之间的感觉神经传导研究,试图更好地理解潜在的病理生理学。

方法

共 138 例 CIDP 患者分为临床亚型:典型 CIDP(N=68)、多灶性 CIDP(N=27)或其他(N=2)。免疫球蛋白 M(IgM)神经病抗髓鞘相关糖蛋白神经病(MAG;N=19)患者也被包括作为疾病对照。记录正中神经、尺神经、浅桡神经和腓肠神经的感觉神经动作电位(SNAP)。

结果

与多灶性 CIDP 相比,典型 CIDP 患者的正中神经 SNAP 振幅(P<.05)和传导速度(P<.01)以及尺神经传导速度(P<.05)较低,而桡神经和腓肠神经在各组之间则相当。典型 CIDP 中更常见的是正中神经和正常的腓肠神经 SNAP 振幅低(P<.005),提示神经末端的主要受累。

讨论

与多灶性 CIDP 相比,典型 CIDP 患者的感觉神经末端更易受影响。这些发现部分可以用典型 CIDP 中抗体介导的脱髓鞘的假说来解释,在这些区域,血-神经屏障在解剖上是不足的,而多灶性 CIDP 主要影响神经干,主要是由于细胞介导的脱髓鞘,血-神经屏障被破坏。

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