Earley Christopher J, Connor James, Garcia-Borreguero Diego, Jenner Peter, Winkelman John, Zee Phyllis C, Allen Richard
Department of Neurology, The Johns Hopkins Bayview Medical Center, Baltimore, MD, USA.
Department of Neurosurgery, Pennsylvania State University College of Medicine, Hershey, PA, USA.
Sleep Med. 2014 Nov;15(11):1288-301. doi: 10.1016/j.sleep.2014.05.009. Epub 2014 Jun 16.
Restless legs syndrome (RLS), also known as Willis-Ekbom Disease (WED), is a sensorimotor disorder for which the exact pathophysiology remains unclear. Brain iron insufficiency and altered dopaminergic function appear to play important roles in the etiology of the disorder. This concept is based partly on extensive research studies using cerebrospinal fluid (CSF), autopsy material, and brain imaging indicating reduced regional brain iron and on the clinical efficacy of dopamine receptor agonists for alleviating RLS symptoms. Finding causal relations, linking low brain iron to altered dopaminergic function in RLS, has required however the use of animal models. These models have provided insights into how alterations in brain iron homeostasis and dopaminergic system may be involved in RLS. The results of animal models of RLS and biochemical, postmortem, and imaging studies in patients with the disease suggest that disruptions in brain iron trafficking lead to disturbances in striatal dopamine neurotransmission for at least some patients with RLS. This review examines the data supporting an iron deficiency-dopamine metabolic theory of RLS by relating the results from animal model investigations of the influence of brain iron deficiency on dopaminergic systems to data from clinical studies in patients with RLS.
不宁腿综合征(RLS),也称为威利斯-埃克博姆病(WED),是一种感觉运动障碍,其确切的病理生理学仍不清楚。脑铁缺乏和多巴胺能功能改变似乎在该疾病的病因中起重要作用。这一概念部分基于使用脑脊液(CSF)、尸检材料和脑成像的广泛研究,这些研究表明脑局部铁含量降低,以及多巴胺受体激动剂缓解RLS症状的临床疗效。然而,要找到将低脑铁与RLS中多巴胺能功能改变联系起来的因果关系,需要使用动物模型。这些模型提供了关于脑铁稳态和多巴胺能系统改变如何可能与RLS相关的见解。RLS动物模型以及该疾病患者的生化、尸检和成像研究结果表明,至少对于一些RLS患者来说,脑铁转运的破坏会导致纹状体多巴胺神经传递紊乱。本综述通过将脑铁缺乏对多巴胺能系统影响的动物模型研究结果与RLS患者临床研究数据相关联,来审视支持RLS铁缺乏-多巴胺代谢理论的数据。