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外周血脑源性神经营养因子作为阿尔茨海默病的生物标志物:是否存在方法学偏倚?

Peripheral Blood Brain-Derived Neurotrophic Factor as a Biomarker of Alzheimer's Disease: Are There Methodological Biases?

机构信息

Center for Neurobiology of Aging, INRCA, Via Birarelli 8, 60121, Ancona, Italy.

Geriatrics Operative Unit, INRCA, Fermo, 63023, Italy.

出版信息

Mol Neurobiol. 2018 Aug;55(8):6661-6672. doi: 10.1007/s12035-017-0866-y. Epub 2018 Jan 13.

Abstract

Mounting evidence that alterations in brain-derived neurotrophic factor (BDNF) levels and signaling may be involved in the etiopathogenesis of Alzheimer's disease (AD) has suggested that its blood levels could be used as a biomarker of the disease. However, higher, lower, or unchanged circulating BDNF levels have all been described in AD patients compared to healthy controls. Although the reasons for such different findings are unclear, methodological issues are likely to be involved. The heterogeneity of participant recruitment criteria and the lack of control of variables that influence circulating BDNF levels regardless of dementia (depressive symptoms, medications, lifestyle, lack of overlap between serum and plasma, and experimental aspects) are likely to bias result and prevent study comparability. The present work reviews a broad panel of factors, whose close control could help reduce the inconsistency of study findings, and offers practical advice on their management. Research directed at elucidating the weight of each of these variables and at standardizing analytical methodologies is urgently needed.

摘要

越来越多的证据表明,脑源性神经营养因子(BDNF)水平和信号的改变可能与阿尔茨海默病(AD)的病因发病机制有关,这表明其血液水平可以作为该疾病的生物标志物。然而,与健康对照组相比,AD 患者的循环 BDNF 水平升高、降低或不变的情况都有描述。尽管造成这种不同发现的原因尚不清楚,但可能涉及到方法学问题。参与者招募标准的异质性以及缺乏控制变量的措施,这些变量会影响无论是否患有痴呆症(抑郁症状、药物、生活方式、血清和血浆之间缺乏重叠以及实验方面)的循环 BDNF 水平,这可能会使结果产生偏差并阻碍研究的可比性。目前这项工作综述了广泛的因素,密切控制这些因素有助于减少研究结果的不一致性,并就其管理提供了实用建议。迫切需要开展研究以阐明这些变量中的每一个变量的权重,并使分析方法标准化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b5/6061178/bdbd5831acf0/12035_2017_866_Fig1_HTML.jpg

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