Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, USA.
Department of Pathology, Rush University Medical Center, Chicago, USA.
Acta Neuropathol. 2017 Aug;134(2):171-186. doi: 10.1007/s00401-017-1717-7. Epub 2017 May 9.
Longitudinal clinical-pathological studies have increasingly recognized the importance of mixed pathologies (the coexistence of one or more neurodegenerative and cerebrovascular disease pathologies) as important factors in the development of Alzheimer's disease (AD) and other forms of dementia. Older persons with AD pathology, often have concomitant cerebrovascular disease pathologies (macroinfarcts, microinfarcts, atherosclerosis, arteriolosclerosis, cerebral amyloid angiopathy) as well as other concomitant neurodegenerative disease pathologies (Lewy bodies, TDP-43, hippocampal sclerosis). These additional pathologies lower the threshold for clinical diagnosis of AD. Many of these findings from pathologic studies, especially for CVD, have been confirmed using sophisticated neuroimaging technologies. In vivo biomarker studies are necessary to provide an understanding of specific pathologic contributions and time course relationships along the spectrum of accumulating pathologies. In this review, we provide a clinical-pathological perspective on the role of multiple brain pathologies in dementia followed by a review of the available clinical and biomarker data on some of the mixed pathologies.
纵向临床病理学研究越来越认识到混合病理学(一种或多种神经退行性疾病和脑血管疾病病理学共存)作为阿尔茨海默病(AD)和其他形式痴呆发展的重要因素的重要性。AD 病理学患者年龄较大,通常伴有脑血管疾病病理学(大梗塞、小梗塞、动脉粥样硬化、小动脉硬化、脑淀粉样血管病)以及其他伴随的神经退行性疾病病理学(路易体、TDP-43、海马硬化)。这些额外的病理学降低了 AD 的临床诊断阈值。这些病理学研究的许多发现,尤其是对于 CVD,已经使用复杂的神经影像学技术得到了证实。体内生物标志物研究对于了解积累病理学谱中特定病理学的贡献和时间关系是必要的。在这篇综述中,我们从临床病理学的角度提供了对多种脑病理学在痴呆中的作用的看法,然后回顾了一些混合病理学的现有临床和生物标志物数据。