Department of Neurosurgery, Pennsylvania State University College of Medicine, Milton S. Hershey Medical Center, Hershey, PA 17033-0850, USA.
Sleep Med. 2011 Jun;12(6):614-9. doi: 10.1016/j.sleep.2010.10.009. Epub 2011 May 12.
Restless legs syndrome (RLS) is a neurological disorder characterized by a strong urge to move the legs and has been shown in many studies with abnormally low brain iron. Iron deficiency is associated with hypomyelination in brains of animals. Therefore we hypothesized that a myelin deficit should be present in the brains of patients with RLS.
We performed Western blot analysis on myelin isolated from RLS (n=11) and control (n=11) brain tissue obtained at autopsy for the expression of the integral myelin proteins, myelin basic protein (MBP), and proteolipid protein (PLP) and the oligodendrocyte specific enzyme 3'5'-cyclic nucleotide phosphohydrolase (CNPase). To expand the postmortem findings to in vivo, we analyzed the brains of RLS patients (n=23) and controls (n=23) using voxel-based morphometry (VBM).
The expression of MBP, PLP and CNPase in the myelin from RLS was decreased by approximately 25% (p<0.05) compared to controls. The amounts of transferrin (Tf) and H-ferritin (H-Frt) in the myelin fraction were also significantly decreased in RLS compared to controls. The imaging analysis revealed significant small decreases in white matter volume in RLS patients compared to controls in the corpus callosum, anterior cingulum and precentral gyrus.
A decrease in myelin similar to that reported in animal models of iron deficiency was found in the brains of individuals with RLS. The evidence for less myelin and loss of myelin integrity in RLS brains, coupled with decreased ferritin and transferrin in the myelin fractions, is a compelling argument for brain iron insufficiency in RLS. These data also indicate the need to look beyond the sensorimotor symptoms that typically define the syndrome and its assumed relation to the dopaminergic system. Understanding the full range of RLS pathology may help us better understand the complex, intermittent nature and diversity of the clinical features of RLS and expand our consideration of treatment options for RLS.
不宁腿综合征(RLS)是一种以强烈的腿部移动欲望为特征的神经系统疾病,许多研究表明其脑内铁含量异常低。铁缺乏与动物大脑中的少突胶质细胞脱髓鞘有关。因此,我们假设 RLS 患者的大脑中应该存在髓鞘缺陷。
我们对尸检获得的 RLS(n=11)和对照组(n=11)脑组织中的髓鞘进行 Western blot 分析,以检测完整髓鞘蛋白髓鞘碱性蛋白(MBP)和少突胶质细胞特异性酶 3'5'-环核苷酸磷酸二酯酶(CNPase)的表达。为了将尸检结果扩展到体内,我们使用基于体素的形态计量学(VBM)分析了 RLS 患者(n=23)和对照组(n=23)的大脑。
与对照组相比,RLS 患者的髓鞘中 MBP、PLP 和 CNPase 的表达降低了约 25%(p<0.05)。髓鞘中转铁蛋白(Tf)和 H 铁蛋白(H-Frt)的含量也明显低于对照组。成像分析显示,与对照组相比,RLS 患者的胼胝体、前扣带回和中央前回的白质体积有明显的小幅度减少。
在 RLS 患者的大脑中发现了与动物缺铁模型中报道的类似的髓鞘减少。RLS 大脑中少突胶质细胞数量减少和髓鞘完整性丧失的证据,以及髓鞘中 ferritin 和 transferrin 的减少,有力地证明了 RLS 中脑铁不足。这些数据还表明,我们需要超越通常定义该综合征及其与多巴胺能系统假定关系的感觉运动症状,全面了解 RLS 病理。了解 RLS 病理的全貌可能有助于我们更好地理解 RLS 复杂、间歇性和多样性的临床特征,并扩大我们对 RLS 治疗选择的考虑。