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在自然主义的临床环境中,脑脊液中的载脂蛋白A1不足以区分阿尔茨海默病与其他痴呆症。

Apolipoprotein A1 in Cerebrospinal Fluid Is Insufficient to Distinguish Alzheimer's Disease from Other Dementias in a Naturalistic, Clinical Setting.

作者信息

Stoye Nicolai Maximilian, Jung Patrick, Guilherme Malena Dos Santos, Lotz Johannes, Fellgiebel Andreas, Endres Kristina

机构信息

Department of Psychiatry and Psychotherapy, University Medical Center Johannes Gutenberg University, Mainz, Germany.

Institute for Clinical Chemistry and Laboratory Medicine, University Medical Center Johannes Gutenberg University, Mainz, Germany.

出版信息

J Alzheimers Dis Rep. 2020 Feb 4;4(1):15-19. doi: 10.3233/ADR-190165.

Abstract

Apolipoprotein A1 (ApoA1) is the major protein component of the high-density lipoprotein and involved in cholesterol transport. Disruption of cholesterol homeostasis has been identified as a contributing factor for Alzheimer's disease (AD). Moreover, polymorphisms of ApoA1 have been associated with higher risk of disease onset and cognitive decline. Therefore, ApoA1 has been suggested as a biomarker in AD. Here, we tested a small cohort of AD and non-AD dementia patients and measured levels of ApoA1 in cerebrospinal fluid. Our results indicate that ApoA1 might not be applicable to distinguish AD from other forms of dementia.

摘要

载脂蛋白A1(ApoA1)是高密度脂蛋白的主要蛋白质成分,参与胆固醇转运。胆固醇稳态的破坏已被确定为阿尔茨海默病(AD)的一个促成因素。此外,ApoA1的多态性与疾病发作和认知衰退的较高风险相关。因此,ApoA1被认为是AD的一种生物标志物。在此,我们检测了一小群AD和非AD痴呆患者,并测量了脑脊液中ApoA1的水平。我们的结果表明,ApoA1可能不适用于区分AD与其他形式的痴呆。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7eb/7081088/04ec5685a47d/adr-4-adr190165-g001.jpg

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