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重新审视痛性糖尿病周围神经病。

A new look at painful diabetic neuropathy.

机构信息

Diabetes Research Unit, Sheffield Teaching Hospitals NHS Foundation Trust & Academic Unit of Radiology, University of Sheffield, Sheffield, United Kingdom.

Department of Endocrinology, Xiangya Hospital, Central South University, Changsha, Hunan, China.

出版信息

Diabetes Res Clin Pract. 2018 Oct;144:177-191. doi: 10.1016/j.diabres.2018.08.020. Epub 2018 Sep 7.

Abstract

The prevalence of diabetes mellitus and its chronic complications continue to increase alarmingly. Consequently, the massive expenditure on diabetic distal symmetrical polyneuropathy (DSPN) and its sequelae, will also likely rise. Up to 50% of patients with diabetes develop DSPN, and about 20% develop neuropathic pain (painful-DSPN). Painful-DSPN can cast a huge burden on sufferers' lives with increased rates of unemployment, mental health disorders and physical co-morbidities. Unfortunately, due to limited understanding of the mechanisms leading to painful-DSPN, current treatments remain inadequate. Recent studies examining the pathophysiology of painful-DSPN have identified maladaptive alterations at the level of both the peripheral and central nervous systems. Additionally, genetic studies have suggested that patients with variants of voltage gated sodium channels may be more at risk of developing neuropathic pain in the presence of a disease trigger such as diabetes. We review the recent advances in genetics, skin biopsy immunohistochemistry and neuro-imaging, which have the potential to further our understanding of the condition, and identify targets for new mechanism based therapies.

摘要

糖尿病的患病率及其慢性并发症仍在惊人地增加。因此,用于治疗糖尿病远端对称性多发性神经病(DSPN)及其后遗症的巨额支出也可能会上升。多达 50%的糖尿病患者会发展为 DSPN,约 20%会发展为神经性疼痛(痛性 DSPN)。痛性 DSPN 会给患者的生活带来巨大负担,导致失业率、精神健康障碍和身体合并症的发生率增加。不幸的是,由于对导致痛性 DSPN 的机制的了解有限,目前的治疗方法仍然不足。最近对痛性 DSPN 的病理生理学的研究已经在周围和中枢神经系统的水平上确定了适应性的改变。此外,遗传研究表明,在存在疾病触发因素(如糖尿病)的情况下,电压门控钠离子通道的变体可能会使患者更容易患上神经性疼痛。我们回顾了遗传学、皮肤活检免疫组织化学和神经影像学方面的最新进展,这些进展有可能进一步了解这种疾病,并确定新的基于机制的治疗方法的靶点。

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