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巴尔的摩纵向衰老研究(BLSA)的神经病理学研究。

Neuropathologic studies of the Baltimore Longitudinal Study of Aging (BLSA).

机构信息

Department of Neurology, School of Medicine, Johns Hopkins University, Baltimore, MD 21224, USA.

出版信息

J Alzheimers Dis. 2009;18(3):665-75. doi: 10.3233/JAD-2009-1179.

Abstract

The Baltimore Longitudinal Study of Aging (BLSA) was established in 1958 and is one the oldest prospective studies of aging in the USA and the world. The BLSA is supported by the National Institute of Aging (NIA) and its mission is to learn what happens to people as they get old and how to sort out changes due to aging from those due to disease or other causes. In 1986, an autopsy program combined with comprehensive neurologic and cognitive evaluations was established in collaboration with the Johns Hopkins University Alzheimer's Disease Research Center (ADRC). Since then, 211 subjects have undergone autopsy. Here we review the key clinical neuropathological correlations from this autopsy series. The focus is on the morphological and biochemical changes that occur in normal aging, and the early neuropathological changes of neurodegenerative diseases, especially Alzheimer's disease (AD). We highlight the combined clinical, pathologic, morphometric, and biochemical evidence of asymptomatic AD, a state characterized by normal clinical evaluations in subjects with abundant AD pathology. We conclude that in some individuals, successful cognitive aging results from compensatory mechanisms that occur at the neuronal level (i.e., neuronal hypertrophy and synaptic plasticity) whereas a failure of compensation may culminate in disease.

摘要

巴尔的摩老龄化纵向研究(BLSA)成立于 1958 年,是美国和世界上最古老的前瞻性衰老研究之一。BLSA 得到了美国国家老龄化研究所(NIA)的支持,其使命是了解随着人们年龄的增长会发生什么,以及如何区分由于衰老引起的变化与由于疾病或其他原因引起的变化。1986 年,与约翰霍普金斯大学阿尔茨海默病研究中心(ADRC)合作,建立了尸检计划和全面的神经认知评估。从那时起,已有 211 名受试者接受了尸检。在这里,我们回顾了该尸检系列的关键临床神经病理学相关性。重点是正常衰老过程中发生的形态和生化变化,以及神经退行性疾病(尤其是阿尔茨海默病(AD))的早期神经病理学变化。我们强调了无症状 AD 的临床、病理、形态计量和生化证据的综合证据,无症状 AD 是指在具有大量 AD 病理学的受试者中,临床评估正常的一种状态。我们得出的结论是,在某些个体中,成功的认知衰老源自神经元水平的代偿机制(即神经元肥大和突触可塑性),而代偿机制的失败可能最终导致疾病。

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