Camille Parent , Louis-Simon Rousseau , David Predovan , Simon Duchesne , Carol Hudon
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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 <em>p</em>-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.</p></div>","PeriodicalId":72131,"journal":{"name":"Aging brain","volume":"3 ","pages":"Article 100074"},"PeriodicalIF":1.7000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/76/38/main.PMC10173297.pdf","citationCount":"0","resultStr":"{\"title\":\"Longitudinal association between ß-amyloid accumulation and cognitive decline in cognitively healthy older adults: A systematic review\",\"authors\":\"Camille Parent , Louis-Simon Rousseau , David Predovan , Simon Duchesne , Carol Hudon\",\"doi\":\"10.1016/j.nbas.2023.100074\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>This systematic review examined the longitudinal association between amyloid-β (Aβ) accumulation and cognitive decline in cognitively healthy adults. 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引用次数: 0
摘要
这项系统综述研究了认知健康成年人淀粉样蛋白-β(Aβ)积累与认知能力下降之间的纵向关联。它使用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。总之,本综述包括17项纵向临床研究。少数(17项研究中有7项)报告称,通过正电子发射断层扫描(PET;n=6)和腰椎穿刺(n=1)测量,认知能力下降与Aβ变化之间存在统计学上显著的关联或预测,认知能力的平均随访时间为3.17年,Aβ的平均随访期为2.99年。报告PET显著结果的研究发现,额叶、后扣带回、侧顶叶和全脑(全脑)皮质以及楔前叶存在差异。情节记忆(n=6)和整体认知(n=1)之间存在显著关联。在使用综合认知评分的七项研究中,有五项发现了显著的结果。质量评估揭示了广泛的方法偏差,如未能报告或解释随访和数据缺失的损失,以及未能报告p值和非显著结果的影响大小。总体而言,Aβ积累与临床前阿尔茨海默病认知能力下降之间的纵向关联尚不清楚。研究之间结果的差异部分可以解释为用于测量Aβ变化的神经成像技术的选择、纵向研究的持续时间、健康临床前人群的异质性,重要的是,使用复合评分来捕捉敏感度增加的认知变化。需要更多具有更大样本量的纵向研究来阐明这种关系。
Longitudinal association between ß-amyloid accumulation and cognitive decline in cognitively healthy older adults: A systematic review
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 p-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.