» Articles » PMID: 19260027

Decreased Cerebrospinal Fluid Abeta(42) Correlates with Brain Atrophy in Cognitively Normal Elderly

Overview
Journal Ann Neurol
Specialty Neurology
Date 2009 Mar 5
PMID 19260027
Citations 180
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: For therapies for Alzheimer's disease (AD) to have the greatest impact, it will likely be necessary to treat individuals in the "preclinical" (presymptomatic) stage. Fluid and neuroimaging measures are being explored as possible biomarkers of AD pathology that could aid in identifying individuals in this stage to target them for clinical trials and to direct and monitor therapy. The objective of this study was to determine whether cerebrospinal fluid (CSF) biomarkers for AD suggest the presence of brain damage in the preclinical stage of AD.

Methods: We investigated the relation between structural neuroimaging measures (whole-brain volume) and levels of CSF amyloid-beta (Abeta)(40), Abeta(42), tau, and phosphorylated tau(181) (ptau(181)), and plasma Abeta(40) and Abeta(42) in well-characterized research subjects with very mild and mild dementia of the Alzheimer type (n = 29) and age-matched, cognitively normal control subjects (n = 69).

Results: Levels of CSF tau and ptau(181), but not Abeta(42), correlated inversely with whole-brain volume in very mild and mild dementia of the Alzheimer type, whereas levels of CSF Abeta(42), but not tau or ptau(181), were positively correlated with whole-brain volume in nondemented control subjects.

Interpretation: Reduction in CSF Abeta(42), likely reflecting Abeta aggregation in the brain, is associated with brain atrophy in the preclinical phase of AD. This suggests that there is toxicity associated with Abeta aggregation before the onset of clinically detectable disease. Increases in CSF tau (and ptau(181)) are later events that correlate with further structural damage and occur with clinical onset and progression.

Citing Articles

Hippocampal Subfield Volume in Relation to Cerebrospinal Fluid Amyloid-ß in Early Alzheimer's Disease: Diagnostic Utility of 7T MRI.

Adeyemi O, Gowland P, Bowtell R, Mougin O, Hosseini A Eur J Neurol. 2025; 32(2):e70076.

PMID: 39921301 PMC: 11806197. DOI: 10.1111/ene.70076.


Elevated locus coeruleus metabolism provides resilience against cognitive decline in preclinical Alzheimer's disease.

Koops E, Dutta J, Hanseeuw B, Becker J, Van Egroo M, Prokopiou P Alzheimers Dement. 2024; 21(1):e14385.

PMID: 39588792 PMC: 11772725. DOI: 10.1002/alz.14385.


Effect of Treatment of the Cholinergic Precursor Choline Alphoscerate in Mild Cognitive Dysfunction: A Randomized Controlled Trial.

Carotenuto A, Andreone V, Amenta F, Traini E Medicina (Kaunas). 2024; 60(6).

PMID: 38929542 PMC: 11205363. DOI: 10.3390/medicina60060925.


CSF biomarkers of immune activation and Alzheimer's disease for predicting cognitive impairment risk in the elderly.

Shue F, White L, Hendrix R, Ulrich J, Henson R, Knight W Sci Adv. 2024; 10(14):eadk3674.

PMID: 38569027 PMC: 10990276. DOI: 10.1126/sciadv.adk3674.


Correlational analyses of biomarkers that are harmonized through a bridging study due to measurement errors.

Xiong C, Schindler S, Henson R, Wolk D, Shaw L, Agboola F Stat Methods Med Res. 2023; 33(2):185-202.

PMID: 37994004 PMC: 10939855. DOI: 10.1177/09622802231215810.


References
1.
Silbert L, Quinn J, Moore M, Corbridge E, Ball M, Murdoch G . Changes in premorbid brain volume predict Alzheimer's disease pathology. Neurology. 2003; 61(4):487-92. DOI: 10.1212/01.wnl.0000079053.77227.14. View

2.
Fagan A, Mintun M, Mach R, Lee S, Dence C, Shah A . Inverse relation between in vivo amyloid imaging load and cerebrospinal fluid Abeta42 in humans. Ann Neurol. 2005; 59(3):512-9. DOI: 10.1002/ana.20730. View

3.
Zhang Y, Brady M, Smith S . Segmentation of brain MR images through a hidden Markov random field model and the expectation-maximization algorithm. IEEE Trans Med Imaging. 2001; 20(1):45-57. DOI: 10.1109/42.906424. View

4.
Kanai M, Matsubara E, ISOE K, Urakami K, Nakashima K, Arai H . Longitudinal study of cerebrospinal fluid levels of tau, A beta1-40, and A beta1-42(43) in Alzheimer's disease: a study in Japan. Ann Neurol. 1998; 44(1):17-26. DOI: 10.1002/ana.410440108. View

5.
Andreasen N, Vanmechelen E, Van de Voorde A, Davidsson P, Hesse C, Tarvonen S . Cerebrospinal fluid tau protein as a biochemical marker for Alzheimer's disease: a community based follow up study. J Neurol Neurosurg Psychiatry. 1998; 64(3):298-305. PMC: 2170016. DOI: 10.1136/jnnp.64.3.298. View