Department of Neurology, Mayo Clinic, Rochester, MN, United States.
Neurobiol Aging. 2011 May;32(5):857-63. doi: 10.1016/j.neurobiolaging.2009.05.019. Epub 2009 Jun 26.
Lewy pathology occurs in 8-17% of neurologically normal people age >60, termed incidental Lewy body disease (iLBD). It is often assumed to represent preclinical Parkinson disease (PD). However, some iLBD cases have diffuse pathology inconsistent with preclinical PD. We analyzed iLBD cases (α-synuclein immunohistochemistry) using the Braak PD staging scheme and determined if some had a neuropathological pattern suggestive of preclinical dementia with Lewy bodies (DLB). Of the 235 brains examined, 34 had iLBD (14.5%) and all but one could be assigned a Braak PD stage. The distribution of α-synuclein pathology in the 33 cases fell into three patterns: (1) diffuse cortical and subcortical α-synuclein pathology; (2) no cortical α-synuclein pathology, but a caudal-to-rostral ascending pattern, primarily involving brainstem; and (3) intermediate between these two categories. Also, 6/33 cases failed to follow the pattern of contiguous spread proposed by Braak. These findings suggest dichotomy in the distribution of iLBD: some cases fit the Braak ascending scheme, conceptually consistent with preclinical PD, whereas others displayed prominent cortical involvement that might represent preclinical DLB.
路易体病理发生于 8-17%的 60 岁以上无神经学异常的人群中,被称为偶发路易体病(iLBD)。它通常被认为代表临床前帕金森病(PD)。然而,一些 iLBD 病例的弥漫性病理表现与临床前 PD 不一致。我们使用 Braak PD 分期方案分析了 iLBD 病例(α-突触核蛋白免疫组化),并确定了一些病例是否具有提示临床前路易体痴呆(DLB)的神经病理学模式。在检查的 235 例大脑中,有 34 例存在 iLBD(14.5%),除 1 例外,其余均可被分配到 Braak PD 分期。33 例病例的α-突触核蛋白病理分布分为三种模式:(1)弥漫性皮质和皮质下α-突触核蛋白病理;(2)无皮质α-突触核蛋白病理,但存在从尾到头上升的模式,主要涉及脑干;(3)介于这两种类型之间。此外,有 6/33 例病例未能遵循 Braak 提出的连续扩散模式。这些发现提示 iLBD 的分布存在二分法:一些病例符合 Braak 的上升方案,与临床前 PD 概念上一致,而另一些病例则表现出明显的皮质受累,可能代表临床前 DLB。