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Cholesterol, 24-Hydroxycholesterol, and 27-Hydroxycholesterol as Surrogate Biomarkers in Cerebrospinal Fluid in Mild Cognitive Impairment and Alzheimer's Disease: A Meta-Analysis.

Authors :
Hua-Long Wang
Yan-Yong Wang
Xin-Gang Liu
Sheng-Han Kuo
Na Liu
Qiao-Yun Song
Ming-Wei Wang
Wang, Hua-Long
Wang, Yan-Yong
Liu, Xin-Gang
Kuo, Sheng-Han
Liu, Na
Song, Qiao-Yun
Wang, Ming-Wei
Source :
Journal of Alzheimer's Disease; 2016, Vol. 51 Issue 1, p45-55, 11p
Publication Year :
2016

Abstract

Abnormal cholesterol metabolism is an established feature of Alzheimer's disease (AD). Cerebrospinal fluid (CSF) is the fluid surrounding the central nervous system, and the protein and lipid content alterations in the CSF could be biomarkers for degenerative changes in the brain. The laboratory diagnosis of AD is limited to the analysis of three biomarkers in CSF: Aβ42, total tau, and phospho-tau. The purpose of this analysis is to systematically analyze the available data describing the biomarkers of cholesterol and its metabolites in the CSF of subjects with AD. MEDLINE, EMBASE, and the Cochrane Central database were systematically queried to collect studies that have evaluated the markers of cholesterol and its metabolites in the CSF of subjects with mild cognitive impairment (MCI) or AD and age-matched controls. Analysis of the published data shows that the levels of cholesterol are increased in MCI subjects; 24-hydroxycholesterol and 27-hydroxycholesterol are elevated in AD and MCI subjects compared to controls. There is a significant dysfunction of cholesterol metabolism in the CSF of AD subjects. This analysis indicates that in addition to the available biomarkers in the CSF, such as Aβ42, total tau, and phospho-tau, 24-hydroxycholesterol, 27-hydroxycholesterol, and cholesterol appear to be sensitive biomarkers for the evaluation of MCI and AD. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13872877
Volume :
51
Issue :
1
Database :
Complementary Index
Journal :
Journal of Alzheimer's Disease
Publication Type :
Academic Journal
Accession number :
113473768
Full Text :
https://doi.org/10.3233/JAD-150734