比较 FGFR-3 和 TS-HDS 血清阳性小纤维神经病:独特的患者特征、症状、实验室和神经传导研究结果。

Q3 Medicine
Peyton J Murin, Farid Khasiyev, Jasmina Profirovic, Margarita Fedorova, Jafar Kafaie
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引用次数: 0

摘要

目的:小纤维神经病是诊断和治疗方面的一大难题。为了解决这一难题,人们一直在努力确定与这种疾病相关的自身抗体。以往的文献通常将三硫化肝素二糖(TS-HDS)和成纤维细胞生长因子受体 3(FGFR3)视为单一的血清阳性组,并且/或者主要关注症状相关性:根据 TS-HDS 血清阳性反应、FGFR-3 血清阳性反应和血清阴性对照组,挑选了 172 名华盛顿大学感觉神经病小组的小纤维神经病患者。收集了每个亚组的人口统计学、症状和实验室概况数据:结果:各组间的女性百分比(P = 0.0043)、神经病理性疼痛症状频率(P = 0.0074)、红细胞沉降率(P = 0.0293)、维生素 D(P < 0.0001)和维生素 B12(P = 0.0033)均有差异。FGFR-3组和TS-HDS组中,皮肤活检正常的比例更高(P = 0.0253):结论:TS-HDS 和 FGFR-3 显示出与对照组和其他组不同的表型。针对 FGFR-3 的免疫球蛋白 M (IgM) 和针对 TS-HDS 的免疫球蛋白 M (IgM) 可能是形成不同临床表型的有价值的个体标记物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparing FGFR-3 and TS-HDS Seropositive Small Fiber Neuropathy: Unique Patient Features, Symptoms, Laboratory, and Nerve Conduction Study Findings.

Objectives: Small fiber neuropathy presents a significant diagnostic and therapeutic challenge. To solve this challenge, efforts have been made to identify autoantibodies associated with this condition. Previous literature has often considered tri-sulfated heparin disaccharide (TS-HDS) and fibroblast growth factor receptor 3 (FGFR3) as a singular seropositive group and/or focused primarily on symptomatic associations.

Methods: One hundred seventy-two small fiber neuropathy patients with a Washington University Sensory Neuropathy panel were selected for TS-HDS seropositivity, FGFR-3 seropositivity, and seronegative controls. Data were collected to on the demographic, symptomatic, and laboratory profiles of each subgroup.

Results: Percent female (P = 0.0043), frequency of neuropathic pain symptoms (P = 0.0074), and erythrocyte sedimentation rate (P = 0.0293), vitamin D (P < 0.0001), and vitamin B12 (P = 0.0033) differed between the groups. Skin biopsy was more frequently normal within both the FGFR-3 and the TS-HDS cohort (P = 0.0253).

Conclusions: TS-HDS and FGFR-3 display a distinct phenotype from both controls and one another. Immunoglobulin M (IgM) against FGFR-3 and IgM against TS-HDS may be individually valuable markers for the development of distinct clinical phenotypes.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
64
期刊介绍: Journal of Clinical Neuromuscular Disease provides original articles of interest to physicians who treat patients with neuromuscular diseases, including disorders of the motor neuron, peripheral nerves, neuromuscular junction, muscle, and autonomic nervous system. Each issue highlights the most advanced and successful approaches to diagnosis, functional assessment, surgical intervention, pharmacologic treatment, rehabilitation, and more.
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