Institute for Clinical Diabetology, German Diabetes Center, Leibniz Center for Diabetes Research, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
German Center for Diabetes Research, Munich-Neuherberg, Neuherberg, Partner Düsseldorf, Düsseldorf, Germany.
Endocr Rev. 2019 Feb 1;40(1):153-192. doi: 10.1210/er.2018-00107.
Diabetic neuropathy, with its major clinical sequels, notably neuropathic pain, foot ulcers, and autonomic dysfunction, is associated with substantial morbidity, increased risk of mortality, and reduced quality of life. Despite its major clinical impact, diabetic neuropathy remains underdiagnosed and undertreated. Moreover, the evidence supporting a benefit for causal treatment is weak at least in patients with type 2 diabetes, and current pharmacotherapy is largely limited to symptomatic treatment options. Thus, a better understanding of the underlying pathophysiology is mandatory for translation into new diagnostic and treatment approaches. Improved knowledge about pathogenic pathways implicated in the development of diabetic neuropathy could lead to novel diagnostic techniques that have the potential of improving the early detection of neuropathy in diabetes and prediabetes to eventually embark on new treatment strategies. In this review, we first provide an overview on the current clinical aspects and illustrate the pathogenetic concepts of (pre)diabetic neuropathy. We then describe the biomarkers emerging from these concepts and novel diagnostic tools and appraise their utility in the early detection and prediction of predominantly distal sensorimotor polyneuropathy. Finally, we discuss the evidence for and limitations of the current and novel therapy options with particular emphasis on lifestyle modification and pathogenesis-derived treatment approaches. Altogether, recent years have brought forth a multitude of emerging biomarkers reflecting different pathogenic pathways such as oxidative stress and inflammation and diagnostic tools for an early detection and prediction of (pre)diabetic neuropathy. Ultimately, these insights should culminate in improving our therapeutic armamentarium against this common and debilitating or even life-threatening condition.
糖尿病神经病变,其主要的临床后果包括神经病理性疼痛、足部溃疡和自主神经功能障碍,与较高的发病率、死亡率增加和生活质量降低有关。尽管其具有重要的临床影响,但糖尿病神经病变仍未得到充分诊断和治疗。此外,至少在 2 型糖尿病患者中,支持因果治疗益处的证据是薄弱的,而且目前的药物治疗主要限于对症治疗方案。因此,为了转化为新的诊断和治疗方法,必须更好地了解潜在的病理生理学。对糖尿病神经病变发展中涉及的致病途径的认识的提高,可以导致新的诊断技术,这些技术有可能改善糖尿病和糖尿病前期患者神经病变的早期检测,最终可以采用新的治疗策略。在这篇综述中,我们首先概述了目前的临床方面,并说明了(前)糖尿病神经病变的发病机制概念。然后,我们描述了这些概念和新的诊断工具中出现的生物标志物,并评估了它们在主要为远端感觉运动多发性神经病的早期检测和预测中的实用性。最后,我们讨论了当前和新型治疗选择的证据和局限性,特别强调了生活方式的改变和发病机制治疗方法。总的来说,近年来出现了许多反映不同发病途径的新兴生物标志物,如氧化应激和炎症,以及用于早期检测和预测(前)糖尿病神经病变的诊断工具。最终,这些研究结果应该会改善我们针对这种常见且使人衰弱甚至危及生命的疾病的治疗手段。