Guo Shiyi, Huang Jinsha, Jiang Haiyang, Han Chao, Li Jie, Xu Xiaoyun, Zhang Guoxin, Lin Zhicheng, Xiong Nian, Wang Tao
Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyWuhan, China.
Department of Psychiatry, Harvard Medical School, BelmontMA, United States.
Front Aging Neurosci. 2017 Jun 2;9:171. doi: 10.3389/fnagi.2017.00171. eCollection 2017.
Restless legs syndrome (RLS), a common neurological sensorimotor disorder in western countries, has gained more and more attention in Asian countries. The prevalence of RLS is higher in older people and females. RLS is most commonly related to iron deficiency, pregnancy and uremia. The RLS symptoms show a significant circadian rhythm and a close relationship to periodic limb movements (PLMs) in clinical observations, while the pathophysiological pathways are still unknown. The diagnostic criteria have been revised in 2012 to improve the validity of RLS diagnosis. Recent studies have suggested an important role of iron decrease of brain in RLS pathophysiology. Dopaminergic (DA) system dysfunction in A11 cell groups has been recognized long ago from clinical treatment and autopsy. Nowadays, it is believed that iron dysfunction can affect DA system from different pathways and opioids have a protective effect on DA system. Several susceptible single nucleotide polymorphisms such as BTBD9 and MEIS1, which are thought to be involved in embryonic neuronal development, have been reported to be associated with RLS. Several pharmacological and non-pharmacological treatment are discussed in this review. First-line treatments of RLS include DA agents and α2δ agonists. Augmentation is very common in long-term treatment of RLS which makes prevention and management of augmentation very important for RLS patients. A combination of different types of medication is effective in preventing and treating augmentation. The knowledge on RLS is still limited, the pathophysiology and better management of RLS remain to be discovered.
不安腿综合征(RLS)是西方国家常见的神经感觉运动障碍,在亚洲国家也越来越受到关注。RLS在老年人和女性中的患病率较高。RLS最常与缺铁、妊娠和尿毒症有关。临床观察中,RLS症状呈现明显的昼夜节律,且与周期性肢体运动(PLMs)密切相关,但其病理生理途径仍不清楚。2012年对诊断标准进行了修订,以提高RLS诊断的有效性。最近的研究表明,脑铁减少在RLS病理生理学中起重要作用。从临床治疗和尸检中早就认识到A11细胞群中的多巴胺能(DA)系统功能障碍。如今,人们认为铁功能障碍可通过不同途径影响DA系统,且阿片类药物对DA系统有保护作用。据报道,一些易感单核苷酸多态性,如BTBD9和MEIS1,被认为与胚胎神经元发育有关,也与RLS相关。本文综述了几种药物和非药物治疗方法。RLS的一线治疗包括DA药物和α2δ激动剂。在RLS的长期治疗中,症状加重很常见,因此对RLS患者来说,预防和处理症状加重非常重要。联合使用不同类型的药物对预防和治疗症状加重有效。关于RLS的知识仍然有限,其病理生理学和更好的治疗方法仍有待发现。