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Hippocampal sclerosis of aging is a key Alzheimers disease mimic: clinical-pathologic correlations and comparisons with both Alzheimers disease and non-tauopathic frontotemporal lobar degeneration

机译:海马硬化的衰老是阿尔茨海默氏病的关键模仿:与阿尔茨海默氏病和非taopathic额颞叶变性的临床病理相关性和比较

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摘要

Hippocampal sclerosis of aging (HS-Aging) neuropathology was observed in more than 15% of aged individuals in prior studies. However, much remains unknown about the clinical correlates of HS-Aging pathology or the association(s) between HS-Aging, Alzheimer's disease (AD), and frontotemporal lobar degeneration (FTLD) pathology. Clinical and comorbid pathological features linked to HS-Aging pathology were analyzed using National Alzheimer's Coordinating Center (NACC) data. From autopsy data extending back to 1990 (N=9,817 participants), the neuropathologic diagnoses were evaluated from American AD Centers (ADCs). Among participants who died between 2005-2012 (N=1,422), additional analyses identified clinical and pathological features associated with HS-Aging pathology. We also compared cognitive testing and longevity outcomes between HS-Aging cases and a subsample with non-tauopathy FTLD (N=210). Reporting of HS pathology increased dramatically among ADCs in recent years, to nearly 20% of autopsies in 2012. Participants with relatively “pure” HS-Aging pathology were often diagnosed clinically as having probable (68%) or possible (15%) AD. However, the co-occurrence of HS-Aging pathology and AD neuropathology (AD-NP) did not indicate any pattern of correlation between the two pathologies. Compared other pathologies, participants with HS-Aging pathology had higher overall cognitive/functional ability (versus AD-NP) and verbal fluency (versus both AD-NP and FTLD) but similar episodic memory impairment at one clinic visit 2 -5 years prior to death. Patients with HS-Aging live considerably longer than patients with non-tauopathy FTLD. We conclude that the manifestations of HS-Aging, increasingly recognized in recent years, probably indicate a separate disease process of direct relevance to patient care, dementia research, and clinical trials.
机译:在先前的研究中,在超过15%的老年人中观察到了海马硬化性衰老(HS-Aging)神经病理学。然而,关于HS-衰老病理学的临床相关性或HS-衰老,阿尔茨海默氏病(AD)和额颞叶变性(FTLD)病理之间的关联尚不清楚。使用国家阿尔茨海默氏症协调中心(NACC)的数据分析了与HS衰老病理相关的临床和共病病理特征。从可追溯至1990年的尸检数据(N = 9,817名参与者),通过美国AD中心(ADC)对神经病理学诊断进行了评估。在2005年至2012年之间死亡的参与者(N = 1,422)中,进一步的分析确定了与HS衰老病理相关的临床和病理特征。我们还比较了HS衰老病例与非手足病FTLD(N = 210)的子样本之间的认知测试和长寿结果。近年来,ADC中HS病理学的报告急剧增加,到2012年占尸检的近20%。具有相对“纯正” HS-Aging病理学的参与者通常在临床上被诊断为可能(68%)或可能(15%)AD。但是,HS衰老病理学与AD神经病理学(AD-NP)的并发并没有表明两种病理学之间的任何相关模式。与其他病理相比,HS-Aging病理的参与者具有更高的整体认知/功能能力(相对于AD-NP)和口语流利性(相对于AD-NP和FTLD),但是在2到5年之前的一次门诊就诊时存在类似的发作性记忆障碍死亡。 HS-Aging患者的寿命比非tauopathy FTLD患者更长。我们得出的结论是,近年来逐渐被认可的HS-Aging表现可能表明与患者护理,痴呆研究和临床试验直接相关的独立疾病过程。

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