Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.
Diabetes Unit, Department of Medical-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Rome, Italy.
Muscle Nerve. 2021 Jan;63(1):68-74. doi: 10.1002/mus.27080. Epub 2020 Oct 31.
We aimed at evaluating the differential involvement of large myelinated Aβ-, small myelinated Aδ-, and unmyelinated C-fibers in patients with diabetic polyneuropathy and how they contribute to neuropathic pain.
We collected clinical and diagnostic test variables in 133 consecutive patients with diabetic polyneuropathy. All patients underwent Aβ-fiber mediated nerve conduction study, Aδ-fiber mediated laser-evoked potentials and skin biopsy mainly assessing unmyelinated C-fibers.
Pure large-fiber and small-fiber polyneuropathy were relatively uncommon; conversely mixed-fiber polyneuropathy was the most common type of diabetic polyneuropathy (74%). The frequency of neuropathic pain was similar in the three different polyneuropathies. Ongoing burning pain and dynamic mechanical allodynia were similarly associated with specific small-fiber related variables.
Diabetic polyneuropathy mainly manifests as a mixed-fiber polyneuropathy, simultaneously involving Aβ-, Aδ-, and C-fibers. In most patients, neuropathic pain is distinctly associated with small-fiber damage. The evidence that the frequency of neuropathic pain does not differ across pure large-, pure small-, and mixed-fiber polyneuropathy, raises the possibility that in patients with pure large-fiber polyneuropathy nociceptive nerve terminal involvement might be undetected by standard diagnostic techniques.
我们旨在评估大髓鞘 Aβ 纤维、小髓鞘 Aδ 纤维和无髓鞘 C 纤维在糖尿病多发性神经病患者中的差异受累情况,以及它们如何导致神经性疼痛。
我们收集了 133 例连续的糖尿病多发性神经病患者的临床和诊断测试变量。所有患者均进行了 Aβ 纤维介导的神经传导研究、Aδ 纤维介导的激光诱发电位和皮肤活检,主要评估无髓鞘 C 纤维。
单纯大纤维和小纤维多发性神经病相对少见;相反,混合纤维多发性神经病是最常见的糖尿病多发性神经病类型(74%)。三种不同多发性神经病的神经性疼痛频率相似。持续的烧灼感和动态机械性感觉过敏与特定的小纤维相关变量相似相关。
糖尿病多发性神经病主要表现为混合纤维多发性神经病,同时累及 Aβ、Aδ 和 C 纤维。在大多数患者中,神经性疼痛与小纤维损伤明显相关。神经性疼痛的频率在纯大纤维、纯小纤维和混合纤维多发性神经病之间没有差异,这表明在纯大纤维多发性神经病患者中,疼痛性神经末梢受累可能无法通过标准诊断技术检测到。