肠易激综合征中的小纤维神经病。

Q3 Medicine
Pouria Motaghi, Iman Adibi, Peyman Adibi, Majid Ghasemi
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引用次数: 0

摘要

目的:本研究旨在评估肠易激综合征(IBS)患者小纤维神经病变的发生率:背景:小纤维神经病(SFN)是一种感觉神经病,由小 Aδ纤维和无髓鞘 C 纤维变性引起。SFN 表现为刺痛、烧灼感、刺痒和疼痛等阳性症状,以及麻木、紧绷和冰冷等阴性症状。以往的研究曾报道 SFN 与其他合并症(如纤维肌痛、炎症性肠病、乳糜泻)同时存在:我们进行了一项横断面研究,以评估 SFN 与肠易激综合征并存的情况。我们要求 42 名 IBS 患者和 43 名健康人填写密歇根神经病变筛查工具(MNSI)问卷。结果大于 3(>3)即为阳性。根据犹他州早期神经病变量表(UENS)检查,对 MNSI 问卷结果呈阳性的参与者进行了神经病变体征检查。对问卷和检查结果均为阳性的参与者进行了腓肠肌和腓浅神经传导检查(NCS)。正常的 NCS 代表完整的大纤维和 SFN 诊断:10 名参与者(肠易激综合征组 7 人(16.7%),健康组 3 人(6.9%))的问卷调查结果呈阳性。有四名参与者的检查结果呈阳性,但其 NCS 正常,被归类为 SFN 阳性。这四位 SFN 患者均来自肠易激综合征组。健康组中没有人被诊断为 SFN。我们发现了明显的统计学差异(pConclusion):SFN 和肠易激综合征的并发表明,可能存在以广泛神经元损伤为特征的全身神经病综合征。因此,肠易激综合征患者的任何周围神经病变症状(也可能是其他慢性疼痛疾病)都应进行 SFN 评估,因为及时诊断和适当治疗可提高患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Small fiber neuropathy in irritable bowel syndrome.

Aim: In this study, we intend to evaluate the occurrence of small fiber neuropathy in patients with irritable bowel syndrome (IBS).

Background: Small fiber neuropathy (SFN) is a sensory neuropathy that results from the degeneration of small Aδ and unmyelinated C fibers. SFN manifests positive symptoms, such as tingling, burning, prickling, and aching, and negative symptoms, including numbness, tightness, and coldness. The SFN coexistence with other comorbidities (e.g., fibromyalgia, inflammatory bowel disease, celiac disease) has been reported in previous studies.

Methods: We conducted a cross-sectional study to assess the coexistence of SFN and IBS. Forty-two IBS patients and forty-three healthy individuals were asked to complete the Michigan Neuropathy Screening Instrument (MNSI) questionnaire. Results greater than three (>3) were considered positive. Participants with positive MNSI questionnaire results were examined for any neuropathy signs according to the Utah Early Neuropathy Scale (UENS) examination. The participants with positive results for the questionnaire and examination were checked for the sural and the superficial peroneal nerve conduction study (NCS). Normal NCS represented intact large fibers and the diagnosis of SFN.

Results: Ten participants, 7 (16.7 %) in the IBS group and 3 (6.9 %) in the healthy group, had positive results for the questionnaire. Four participants were positive for the examination, with normal NCS, and were classified as SFN-positive. All four SFN diagnoses were from the IBS group. No one in the healthy group was diagnosed with SFN. We could find a significant statistical difference (p<0.05) between the IBS and healthy groups regarding the prevalence of SFN diagnosis.

Conclusion: The co-occurrence of SFN and IBS suggests the possibility of a generalized neuropathy syndrome characterized by widespread neuronal impairment. Thus, any peripheral neuropathy symptom in IBS patients (and potentially other chronic pain disorders) should be evaluated for SFN since timely diagnosis and proper treatment result in a better quality of life for the patients.

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CiteScore
2.30
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