Biomarkers in small fiber neuropathy

Amanda C. Y. Chan, Kathleen Ong, J. J. Ong, V. Sharma, H. Wong, J. Vijayan
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Abstract

Small fiber neuropathy (SFN) is a relatively common, but largely understudied neurological syndrome which has affected the lives of many globally. The common symptoms of SFN include pain, dysesthesia, and autonomic dysfunction, which are caused by damage to small nerve fibers. Due to its heterogeneous nature, SFN causes a multitude of symptoms which makes the disease and its subtypes difficult to diagnose. Furthermore, as the pathophysiology of SFN remains largely enigmatic, no cause is found in around 50% of the cases and these are classified as idiopathic SFN (iSFN). The difficult task of diagnosing SFN, and the even more elusive feat of hunting for the underlying etiology, demands accurate, precise, preferably noninvasive, and affordable tools, or a combination of them. Accordingly, appropriate biomarkers for SFN are needed to stratify patients and develop cause-centered treatments in addition to symptomatic treatments. As peripheral axons grow and repair, identifying underlying causes of SFN and intervening early may spur axonal regeneration in young patients, which can greatly improve their symptoms and improve quality of life. This narrative review aims to objectively highlight functional, histological, and molecular biomarkers to aid clinicians in discerning the diagnostic tests they should use to diagnose, confirm and determine the etiology of SFN. The strengths and limitations of each potential biomarker will be discussed. Clearer diagnostic criteria, guidelines, and work-up for SFN are required for clinicians to better identify the disease in patients presenting with non-specific symptoms.
小纤维神经病的生物标志物
小纤维神经病(SFN)是一种相对常见,但在很大程度上尚未得到充分研究的神经系统综合征,它已经影响了全球许多人的生活。SFN的常见症状包括疼痛、感觉不良和自主神经功能障碍,这些都是由小神经纤维受损引起的。由于其异质性,SFN引起多种症状,这使得该疾病及其亚型难以诊断。此外,由于SFN的病理生理学仍然很大程度上是谜,大约50%的病例没有发现病因,这些病例被归类为特发性SFN (iSFN)。诊断SFN的困难任务,以及寻找潜在病因的更难以捉摸的壮举,需要准确、精确、最好是非侵入性的、负担得起的工具,或者它们的组合。因此,除了对症治疗外,还需要适当的SFN生物标志物来对患者进行分层,并制定以病因为中心的治疗方案。随着外周轴突的生长和修复,识别SFN的潜在原因并早期干预可能会刺激年轻患者的轴突再生,从而大大改善他们的症状并提高生活质量。这篇叙述性综述旨在客观地强调功能、组织学和分子生物标志物,以帮助临床医生识别诊断测试,他们应该用来诊断、确认和确定SFN的病因。每个潜在的生物标志物的优势和局限性将被讨论。临床医生需要更明确的SFN诊断标准、指南和检查,以便更好地在出现非特异性症状的患者中识别疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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