血管负担和淀粉样蛋白异常对记忆门诊病人认知能力下降的影响

IF 2.8 Q2 NEUROSCIENCES Journal of Alzheimer's disease reports Pub Date : 2023-11-30 eCollection Date: 2023-01-01 DOI:10.3233/ADR-230040
Veerle van Gils, Inez Ramakers, Willemijn J Jansen, Leonie Banning, Domantė Kučikienė, Ana Sofia Costa, Jörg B Schulz, Pieter Jelle Visser, Frans Verhey, Kathrin Reetz, Stephanie J B Vos
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引用次数: 0

摘要

背景:阿尔茨海默病的病理和血管负担在老年人中非常普遍,而且经常同时发生。目前仍不清楚两者与认知能力下降的关系:目的:研究淀粉样蛋白异常和血管负担是否会协同导致记忆力下降:我们纳入了来自马斯特里赫特和亚琛记忆诊所的 227 名患者。淀粉样蛋白异常(A+)由 CSF Aβ42 定义,采用数据驱动的临界值。血管负担(V+)的定义是磁共振成像上出现中度至重度白质高密度,或任何微出血、大出血或梗塞。通过线性混合模型分析了A-V-组、A-V+组、A+V-组、A+V+组在整体认知、记忆、处理速度、执行功能和语言流畅性方面的纵向变化。此外,个别核磁共振成像测量、血管风险和血管疾病也被用作 V 的定义:基线时,A+V+组在整体认知和言语流畅性方面的得分比所有其他组差,记忆力也比A-V+组和A-V-组差。随着时间的推移(平均 2.7+ - 1.5 年),A+V+ 组和 A+V- 组的整体认知能力下降速度快于 A-V+ 组和 A-V- 组。只有 A+V- 组的记忆力和语言流畅性有所下降。A-V+ 组与 A-V- 组没有差异。个别磁共振成像血管测量结果仅显示微出血与执行功能下降有独立关联。结论:我们的研究表明,淀粉样蛋白病变会导致执行功能下降:我们的研究表明,在记忆门诊人群中,淀粉样蛋白异常可预测认知功能下降,与血管负担无关。血管负担对这些患者认知能力下降的影响较小。这对预后具有重要意义。
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Contributions of Vascular Burden and Amyloid Abnormality to Cognitive Decline in Memory Clinic Patients.

Background: Alzheimer's disease pathology and vascular burden are highly prevalent and often co-occur in elderly. It remains unclear how both relate to cognitive decline.

Objective: To investigate whether amyloid abnormality and vascular burden synergistically contribute to cognitive decline in a memory clinic population.

Methods: We included 227 patients from Maastricht and Aachen memory clinics. Amyloid abnormality (A+) was defined by CSF Aβ42 using data-driven cut-offs. Vascular burden (V+) was defined as having moderate to severe white matter hyperintensities, or any microbleeds, macrohemorrhage or infarcts on MRI. Longitudinal change in global cognition, memory, processing speed, executive functioning, and verbal fluency was analysed across the A-V-, A-V+, A+V-, A+V+ groups by linear mixed models. Additionally, individual MRI measures, vascular risk and vascular disease were used as V definitions.

Results: At baseline, the A+V+ group scored worse on global cognition and verbal fluency compared to all other groups, and showed worse memory compared to A-V+ and A-V- groups. Over time (mean 2.7+ - 1.5 years), A+V+ and A+V- groups showed faster global cognition decline than A-V+ and A-V- groups. Only the A+V- group showed decline on memory and verbal fluency. The A-V+ group did not differ from the A-V- group. Individual MRI vascular measures only indicated an independent association of microbleeds with executive functioning decline. Findings were similar using other V definitions.

Conclusions: Our study demonstrates that amyloid abnormality predicts cognitive decline independent from vascular burden in a memory clinic population. Vascular burden shows a minor contribution to cognitive decline in these patients. This has important prognostic implications.

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