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格林-巴利综合征急性炎性脱髓鞘性多神经根神经病变异型中脑脊液蛋白水平与电生理异常的关系。

Relationship between cerebrospinal fluid protein level and electrophysiologic abnormalities in the acute inflammatory demyelinating polyradiculoneuropathy variant of Guillain-Barré syndrome.

机构信息

Department of Neurology, Dr. Ruth K. M. Pfau Civil Hospital Karachi & Dow University of Health Sciences, Karachi, Pakistan.

Department of Medicine & Allied, Jinnah Medical College Hospital Korangi, Karachi, Pakistan.

出版信息

Ger Med Sci. 2021 Sep 1;19:Doc12. doi: 10.3205/000299. eCollection 2021.

DOI:10.3205/000299
PMID:34539302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8422794/
Abstract

Guillain-Barré syndrome (GBS) is an autoimmune disease characterized by weakness in limbs or cranial nerve innervated muscles. Acute inflammatory demyelinating polyradiculoneuropathy (AIDP) is the most common variant. Electrophysiologic abnormalities and elevated cerebrospinal fluid (CSF) protein are frequently present in AIDP, but the relationship between these two parameters is not well known. We aimed to fill this gap by studying this relationship. This was a prospective cross-sectional study conducted for two years in the Department of Neurology, Dr. Ruth K. M. Pfau Civil Hospital, Karachi, Pakistan. All 90 adult patients with the AIDP variant of GBS were selected. Nerve conduction studies were performed to determine the degree of demyelination through the four electrophysiologic demyelination criteria. The CSF sample was sent to lab immediately after lumbar puncture. SPSS version 20.0 was used. The CSF protein level was measured with mean ±SD. Demyelination criteria were measured in frequency and percentages. Chi-square test was applied to a number of demyelination criteria and T-test/ANOVA was applied on mean CSF protein level. We found a mean CSF protein of 37.41 mg/dl (±3.69) with one demyelination criterion, 81.87 mg/dl (±17.39) with two demyelination criteria, 119.75 mg/dl (±31.42) with three demyelination criteria, and 134.00 mg/dl (±42.87) with four demyelination criteria (P-value <0.001). This study demonstrates a significant relationship between CSF protein levels and degree of demyelination in the AIDP variant of GBS. This is an under-researched area in GBS and this study adds favorably to limited data in this regard.

摘要

格林-巴利综合征(GBS)是一种以四肢或颅神经支配的肌肉无力为特征的自身免疫性疾病。急性炎症性脱髓鞘性多发性神经病(AIDP)是最常见的变异型。AIDP 常伴有电生理异常和升高的脑脊液(CSF)蛋白,但这两个参数之间的关系尚不清楚。我们旨在通过研究这种关系来填补这一空白。

这是一项为期两年的前瞻性横断面研究,在巴基斯坦卡拉奇的 Ruth K. M. Pfau 民事医院神经病学系进行。所有 90 名成人 AIDP 变异型 GBS 患者均入选。通过四项电生理脱髓鞘标准进行神经传导研究,以确定脱髓鞘程度。腰椎穿刺后立即将 CSF 样本送到实验室。使用 SPSS 版本 20.0。CSF 蛋白水平用平均值±标准差表示。脱髓鞘标准以频率和百分比表示。应用卡方检验对多项脱髓鞘标准进行检验,对平均 CSF 蛋白水平进行 T 检验/方差分析。

我们发现平均 CSF 蛋白为 37.41mg/dl(±3.69),有一个脱髓鞘标准;81.87mg/dl(±17.39),有两个脱髓鞘标准;119.75mg/dl(±31.42),有三个脱髓鞘标准;134.00mg/dl(±42.87),有四个脱髓鞘标准(P 值<0.001)。

本研究表明,AIDP 变异型 GBS 中 CSF 蛋白水平与脱髓鞘程度之间存在显著关系。这是 GBS 中一个研究较少的领域,本研究为此类研究提供了有利的数据支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/ce26b9206ac3/GMS-19-12-g-004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/32c10acc444a/GMS-19-12-t-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/600cf0270fe1/GMS-19-12-t-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/77b5e93b7500/GMS-19-12-t-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/b126ea665894/GMS-19-12-g-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/8a47fab74ac4/GMS-19-12-g-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/caca148dfe46/GMS-19-12-g-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/ce26b9206ac3/GMS-19-12-g-004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/32c10acc444a/GMS-19-12-t-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/600cf0270fe1/GMS-19-12-t-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/77b5e93b7500/GMS-19-12-t-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/b126ea665894/GMS-19-12-g-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/8a47fab74ac4/GMS-19-12-g-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/caca148dfe46/GMS-19-12-g-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da84/8422794/ce26b9206ac3/GMS-19-12-g-004.jpg

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