早期阿尔茨海默病中焦虑症的患病率、风险因素和影响:对尸检确认队列的回顾性研究

Palak Patel, Mark A. Bernard, Arjun V. Masurkar
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摘要

焦虑是阿尔茨海默病(AD)患者的一种神经精神症状(NPS),主要通过对临床诊断的阿尔茨海默病进行前瞻性和回顾性研究来研究。然而,这可能会受到其他原发病因的干扰。此外,对尸检证实的 AD 病例中主观认知能力下降 (SCD)、轻度认知障碍 (MCI) 和痴呆阶段的焦虑尚未进行过全面研究。我们对 212 名经尸检证实的 AD 患者进行了回顾性纵向分析,这些患者于 1986 年至 2013 年期间在纽约大学阿尔茨海默病研究中心接受了随访,通过全球恶化量表进行分期,并通过 BEHAVE-AD 评估 NPS。我们发现,焦虑随阶段的不同而变化,是SCD和MCI中最常见的NPS(35-40%的患病率)。载脂蛋白E4携带者仅在轻度痴呆时焦虑率较高。SCD患者的焦虑症与脑淀粉样血管病变和脑尸检动脉硬化有关,但与MCI和轻度痴呆症的伴随神经病理学没有关联。焦虑与 SCD 到 MCI/痴呆阶段的进展率增加(约 2.5 倍)有关,但与 MCI 到痴呆阶段的进展率增加无关。这些结果表明,焦虑与注意力缺失症之间存在重要关系,尤其是在临床前阶段。因此,有必要对焦虑这一可能影响疾病经历和病程的可调节因素进行进一步研究。
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Prevalence, risk factors, and impact of anxiety in early Alzheimer disease: a retrospective study of an autopsy-confirmed cohort
Anxiety is a neuropsychiatric symptom (NPS) of Alzheimer disease (AD) patients which has been studied primarily in prospective and retrospective studies of clinically diagnosed AD. However, this can be confounded by other primary etiologies. Moreover, anxiety has not been comprehensively studied in autopsy-confirmed AD cases across subjective cognitive decline (SCD), mild cognitive impairment (MCI), and dementia stages. We conducted a retrospective longitudinal analysis of 212 participants with autopsy-confirmed AD, followed from 1986-2013 at the NYU Alzheimer Disease Research Center with staging via the Global Deterioration Scale and NPS assessed via BEHAVE-AD. We found that anxiety varied uniquely with stage and was the most common NPS in SCD and MCI (35-40% prevalence). ApoE4 carriage associated with a higher rate of anxiety only at mild dementia. Anxiety in SCD associated with cerebral amyloid angiopathy and arteriosclerosis on brain autopsy, but there were no such associations with concomitant neuropathology at MCI and mild dementia. Anxiety associated with increased progression rate (~2.5-fold) from SCD to MCI/dementia stages, but not from MCI to dementia. These results suggest an important relationship between anxiety and AD, especially at the preclinical stage. This warrants further study of anxiety as a possible modifiable factor of disease experience and course.
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