Parent Camille, Rousseau Louis-Simon, Predovan David, Duchesne Simon, Hudon Carol
École de psychologie, Université Laval, Québec, QC, Canada.
Centre de recherche CERVO, Institut universitaire de santé mentale de Québec, Québec, QC, Canada.
Aging Brain. 2023 Apr 28;3:100074. doi: 10.1016/j.nbas.2023.100074. eCollection 2023.
This systematic review examined the longitudinal association between amyloid-β (Aβ) accumulation and cognitive decline in cognitively healthy adults. It was conducted using the PubMed, Embase, PsycInfo, and Web of Science databases. The methodological quality of the selected articles was assessed. In fine, seventeen longitudinal clinical studies were included in this review. A minority (seven out of 17) of studies reported a statistically significant association or prediction of cognitive decline with Aβ change, measured by positron emission tomography (PET; n = 6) and lumbar puncture (n = 1), with a mean follow-up duration of 3.17 years for cognition and 2.99 years for Aβ. The studies reporting significant results with PET found differences in the frontal, posterior cingular, lateral parietal and global (whole brain) cortices as well as in the precuneus. Significant associations were found with episodic memory (n = 6) and global cognition (n = 1). Five of the seven studies using a composite cognitive score found significant results. A quality assessment revealed widespread methodological biases, such as failure to report or account for loss-to follow up and missing data, and failure to report -values and effect sizes of non-significant results. Overall, the longitudinal association between Aβ accumulation and cognitive decline in preclinical Alzheimer's disease remains unclear. The discrepancy in results between studies may be explained in part by the choice of neuroimaging technique used to measure Aβ change, the duration of longitudinal studies, the heterogeneity of the healthy preclinical population, and importantly, the use of a composite score to capture cognitive changes with increased sensitivity. More longitudinal studies with larger sample sizes are needed to elucidate this relationship.
本系统评价考察了认知健康成年人中淀粉样蛋白β(Aβ)积累与认知衰退之间的纵向关联。研究通过PubMed、Embase、PsycInfo和Web of Science数据库进行。对所选文章的方法学质量进行了评估。最终,本评价纳入了17项纵向临床研究。少数研究(17项中的7项)报告了认知衰退与Aβ变化之间具有统计学意义的关联或预测,Aβ变化通过正电子发射断层扫描(PET;n = 6)和腰椎穿刺(n = 1)测量,认知的平均随访时间为3.17年,Aβ的平均随访时间为2.99年。报告PET有显著结果的研究发现,额叶、后扣带回、外侧顶叶和全脑皮质以及楔前叶存在差异。发现与情景记忆(n = 6)和整体认知(n = 1)存在显著关联。使用综合认知评分的7项研究中有5项发现了显著结果。质量评估显示存在广泛的方法学偏差,如未报告或未说明失访和缺失数据情况,以及未报告非显著结果的P值和效应量。总体而言,临床前阿尔茨海默病中Aβ积累与认知衰退之间的纵向关联仍不明确。研究结果的差异可能部分归因于用于测量Aβ变化的神经影像学技术的选择、纵向研究的持续时间、健康临床前人群的异质性,重要的是,使用综合评分以更高的敏感性捕捉认知变化。需要更多样本量更大的纵向研究来阐明这种关系。