Boeve B F, Silber M H, Parisi J E, Dickson D W, Ferman T J, Benarroch E E, Schmeichel A M, Smith G E, Petersen R C, Ahlskog J E, Matsumoto J Y, Knopman D S, Schenck C H, Mahowald M W
Department of Neurology, Mayo Clinic, Rochester, Minneapolis, MN 55905, USA.
Neurology. 2003 Jul 8;61(1):40-5. doi: 10.1212/01.wnl.0000073619.94467.b0.
To determine if synucleinopathy pathology is related to REM sleep behavior disorder (RBD) plus dementia or parkinsonism.
The clinical and neuropathologic findings were analyzed on all autopsied cases evaluated at Mayo Clinic Rochester from January 1990 to April 2002 who were diagnosed with RBD and a neurodegenerative disorder. Ubiquitin and/or alpha-synuclein immunocytochemistry was used in all cases. The clinical and neuropathologic diagnoses were based on published criteria.
Fifteen cases were identified (14 men). All had clear histories of dream enactment behavior, and 10 had RBD confirmed by polysomnography. RBD preceded dementia or parkinsonism in 10 (66.7%) patients by a median of 10 (range 2 to 29) years. The clinical diagnoses included dementia with Lewy bodies (DLB) (n = 6); multiple-system atrophy (MSA) (n = 2); combined DLB, AD, and vascular dementia (n = 1); dementia (n = 1); dementia with parkinsonism (n = 1); PD (n = 1); PD with dementia (n = 1); dementia/parkinsonism/motor neuron disease (n = 1); and AD/Binswanger's disease (n = 1). The neuropathologic diagnoses were Lewy body disease (LBD) in 12 (neocortical in 11 and limbic in 1) and MSA in 3. Three also had argyrophilic grain pathology. In the LBD cases, concomitant AD pathology was present in six (one also with Binswanger's pathology, and one also with multiple subcortical infarcts).
In the setting of degenerative dementia or parkinsonism, RBD often reflects an underlying synucleinopathy.
确定突触核蛋白病病理是否与快速眼动睡眠行为障碍(RBD)合并痴呆或帕金森综合征相关。
分析1990年1月至2002年4月在罗切斯特梅奥诊所接受尸检的所有被诊断为RBD和神经退行性疾病的病例的临床和神经病理学发现。所有病例均采用泛素和/或α-突触核蛋白免疫细胞化学方法。临床和神经病理学诊断基于已发表的标准。
共识别出15例(14名男性)。所有患者均有明确的梦呓行为史,其中10例经多导睡眠图证实为RBD。10例(66.7%)患者的RBD先于痴呆或帕金森综合征出现,中位时间为10年(范围2至29年)。临床诊断包括路易体痴呆(DLB)(n = 6);多系统萎缩(MSA)(n = 2);合并DLB、AD和血管性痴呆(n = 1);痴呆(n = 1);帕金森综合征伴痴呆(n = 1);帕金森病(PD)(n = 1);帕金森病伴痴呆(n = 1);痴呆/帕金森综合征/运动神经元病(n = 1);以及AD/宾斯旺格病(n = 1)。神经病理学诊断为路易体病(LBD)12例(11例为新皮质型,1例为边缘型),MSA 3例。3例还伴有嗜银颗粒病理改变。在LBD病例中,6例同时存在AD病理改变(1例还伴有宾斯旺格病理改变,1例还伴有多发性皮质下梗死)。
在退行性痴呆或帕金森综合征的情况下,RBD通常反映潜在的突触核蛋白病。