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双相情感障碍患者与健康对照者的认知表现及神经退行性变的脑脊液生物标志物:一项研究

Cognitive performance and cerebrospinal fluid biomarkers of neurodegeneration: a study of patients with bipolar disorder and healthy controls.

作者信息

Rolstad Sindre, Jakobsson Joel, Sellgren Carl, Ekman Carl-Johan, Blennow Kaj, Zetterberg Henrik, Pålsson Erik, Landén Mikael

机构信息

Institute of neuroscience and physiology, the Sahlgrenska Academy at the Gothenburg University, Gothenburg, Sweden.

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

出版信息

PLoS One. 2015 May 8;10(5):e0127100. doi: 10.1371/journal.pone.0127100. eCollection 2015.

Abstract

The purpose of the present study was to investigate if cerebrospinal fluid (CSF) biomarkers of neurodegeneration are associated with cognition in bipolar disorder and healthy controls, respectively. CSF concentrations of total and phosphorylated tau, amyloid beta (Aβ)1-42, ratios of Aβ42/40 and Aβ42/38, soluble amyloid precursor protein α and β, and neurofilament light chain protein were analyzed in relation to neuropsychological performance in 82 euthymic bipolar disorder patients and 71 healthy controls. Linear regression models were applied to account for performance in five cognitive domains using the CSF biomarkers. In patients, the CSF biomarkers explained a significant proportion of the variance (15-36%, p=.002 - <.0005) in all cognitive domains independently of age, medication, disease status, and bipolar subtype I or II. However, the CSF biomarkers specifically mirroring Alzheimer-type brain changes, i.e., P-tau and Aβ1-42, did not contribute significantly. In healthy controls, CSF biomarkers did not explain the variance in cognitive performance. Selected CSF biomarkers of neurodegenerative processes accounted for cognitive performance in persons with bipolar disorder, but not for healthy controls. Specifically, the ratios of Aβ42/40 and Aβ42/38 were consistently associated with altered cognitive performance.

摘要

本研究的目的是分别调查神经退行性变的脑脊液(CSF)生物标志物与双相情感障碍患者及健康对照者认知功能之间是否存在关联。分析了82例心境正常的双相情感障碍患者和71名健康对照者的脑脊液中总tau蛋白和磷酸化tau蛋白、淀粉样β蛋白(Aβ)1-42、Aβ42/40和Aβ42/38的比值、可溶性淀粉样前体蛋白α和β以及神经丝轻链蛋白的浓度,并将其与神经心理学表现进行关联分析。应用线性回归模型,以脑脊液生物标志物来解释五个认知领域的表现。在患者中,脑脊液生物标志物独立于年龄、用药情况、疾病状态以及双相I型或II型,解释了所有认知领域中显著比例的变异(15%-36%,p = 0.002 - <0.0005)。然而,特异性反映阿尔茨海默型脑改变的脑脊液生物标志物,即磷酸化tau蛋白和Aβ1-42,并未作出显著贡献。在健康对照者中,脑脊液生物标志物无法解释认知表现的变异。神经退行性变过程中选定的脑脊液生物标志物可解释双相情感障碍患者的认知表现,但无法解释健康对照者的认知表现。具体而言,Aβ42/40和Aβ42/38的比值始终与认知表现改变相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c34c/4425506/751865762ac7/pone.0127100.g001.jpg

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