Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, United Kingdom.
Histology and Pathology Department, Lille University Hospital, University Lille Nord de France, Lille, France.
Brain Pathol. 2020 Jan;30(1):191-202. doi: 10.1111/bpa.12769. Epub 2019 Aug 16.
We performed a clinicopathological study to assess the burden of small vessel disease (SVD) type of pathological changes in elderly demented subjects, who had clinical evidence of autonomic dysfunction, either carotid sinus hypersensitivity or orthostatic hypotension or both or had exhibited unexpected repeated falls. Clinical and neuropathological diagnoses in 112 demented subjects comprised dementia with Lewy bodies (DLB), Parkinson's disease with dementia (PDD), Alzheimer's disease (AD), Mixed dementia (mostly AD-DLB) and vascular dementia (VaD). Of these, 12 DLB subjects had no recorded unexpected falls in life and therefore no evidence of concomitant autonomic dysfunction. A further 17 subjects were assessed as aging controls without significant pathology or signs of autonomic dysfunction. We quantified brain vascular pathological changes and determined severities of neurodegenerative lesions including α-synuclein pathology. We found moderate-severe vascular changes and high-vascular pathology scores (P < 0.01) in all neurodegenerative dementias and as expected in VaD compared to similar age controls. Arteriolosclerosis, perivascular spacing and microinfarcts were frequent in the basal ganglia and frontal white matter (WM) across all dementias, whereas small infarcts (<5 mm) were restricted to VaD. In a sub-set of demented subjects, we found that vascular pathology scores were correlated with WM hyperintensity volumes determined by MRI in life (P < 0.02). Sclerotic index values were increased by ~50% in both the WM and neocortex in all dementias compared to similar age controls. We found no evidence for increased α-synuclein deposition in subjects with autonomic dysfunction. Our findings suggest greater SVD pathological changes occur in the elderly diagnosed with neurodegenerative dementias including DLB and who develop autonomic dysfunction. SVD changes may not necessarily manifest in clinically overt symptoms but they likely confound motor or cognitive dysfunction. We propose dysautonomia promotes chronic cerebral hypoperfusion to impact upon aging-related neurodegenerative disorders and characterize their end-stage clinical syndromes.
我们进行了一项临床病理研究,以评估有临床自主神经功能障碍证据的老年痴呆患者(颈动脉窦过敏、直立性低血压或两者兼有,或有意外反复跌倒)的小血管疾病(SVD)类型的病理改变负担。112 名痴呆患者的临床和神经病理学诊断包括路易体痴呆(DLB)、帕金森病伴痴呆(PDD)、阿尔茨海默病(AD)、混合性痴呆(主要为 AD-DLB)和血管性痴呆(VaD)。其中,12 名 DLB 患者在生活中没有记录到意外跌倒,因此没有合并自主神经功能障碍的证据。另外 17 名患者被评估为年龄匹配的对照组,没有明显的病理学或自主神经功能障碍的迹象。我们量化了脑血管病理变化,并确定了神经退行性病变的严重程度,包括α-突触核蛋白病理学。我们发现,所有神经退行性痴呆症患者都有中重度血管变化和高血管病理评分(P<0.01),与年龄匹配的对照组相比,VaD 更是如此。在所有痴呆症中,纹状体和额白质(WM)中常见的小动脉粥样硬化、血管周围间隙和微梗死,而小梗死(<5mm)则仅限于 VaD。在一组痴呆症患者中,我们发现血管病理评分与生活中 MRI 确定的 WM 高信号体积相关(P<0.02)。与年龄匹配的对照组相比,WM 和新皮质的硬化指数值在所有痴呆症中都增加了约 50%。我们没有发现自主神经功能障碍患者α-突触核蛋白沉积增加的证据。我们的研究结果表明,在被诊断为神经退行性痴呆症(包括 DLB)且发生自主神经功能障碍的老年患者中,SVD 病理变化更为严重。SVD 变化可能不会表现出明显的临床症状,但它们可能会使运动或认知功能障碍复杂化。我们提出自主神经功能障碍会促进慢性脑灌注不足,从而影响与衰老相关的神经退行性疾病,并描述其终末期临床综合征。