Department of Neurology, University of Michigan, Ann Arbor, MI.
Ann Neurol. 2013 Sep;74(3):397-403. doi: 10.1002/ana.23986.
The metabolic syndrome and neuropathy are common conditions, especially in the elderly, that are associated with significant morbidity. Furthermore, the metabolic syndrome is reaching epidemic proportions across the world. Current evidence supports the association of the metabolic syndrome and its individual components with neuropathy. Several clinical trials have demonstrated that treating hyperglycemia, a component of the metabolic syndrome, has a significant effect on reducing the incidence of neuropathy in those with type 1 diabetes. However, glucose control has only a marginal effect on preventing neuropathy in those with type 2 diabetes, suggesting that other factors may be driving nerve injury in these patients. Emerging evidence supports the metabolic syndrome as including risk factors for neuropathy. Interventions exist for treatment of all of the metabolic syndrome components, but only glucose control has strong evidence to support its use and is widely employed. Our understanding of the biology of metabolic nerve injury has rapidly expanded over the past several years. Mechanisms of injury include fatty deposition in nerves, extracellular protein glycation, mitochondrial dysfunction, and oxidative stress. Additionally, the activation of counter-regulatory signaling pathways leads to chronic metabolic inflammation. Medications that target these signaling pathways are being used for a variety of diseases and are intriguing therapeutic agents for future neuropathy clinical trials. As we move forward, we need to expand our understanding of the association between the metabolic syndrome and neuropathy by addressing limitations of previous studies. Just as importantly, we must continue to investigate the pathophysiology of metabolically induced nerve injury.
代谢综合征和神经病变是常见的病症,尤其是在老年人中,它们与显著的发病率相关。此外,代谢综合征在全球范围内呈流行趋势。目前的证据支持代谢综合征及其各个组成部分与神经病变之间的关联。几项临床试验表明,治疗代谢综合征的组成部分之一——高血糖,对降低 1 型糖尿病患者神经病变的发生率有显著影响。然而,血糖控制对预防 2 型糖尿病患者的神经病变只有微小的作用,这表明其他因素可能导致这些患者的神经损伤。新出现的证据支持代谢综合征包括神经病变的危险因素。虽然有针对所有代谢综合征组成部分的治疗干预措施,但只有血糖控制具有强有力的证据支持其使用,并被广泛应用。在过去的几年中,我们对代谢性神经损伤的生物学理解迅速扩展。损伤机制包括神经内脂肪沉积、细胞外蛋白糖化、线粒体功能障碍和氧化应激。此外,代偿性信号通路的激活导致慢性代谢性炎症。针对这些信号通路的药物被用于多种疾病,它们是未来神经病变临床试验中很有前途的治疗药物。在我们向前推进的过程中,我们需要通过解决以前研究的局限性来扩大我们对代谢综合征和神经病变之间关联的理解。同样重要的是,我们必须继续研究代谢引起的神经损伤的病理生理学。