Cerebrospinal fluid tau/beta-amyloid(42) ratio as a prediction of cognitive decline in nondemented older adults - PubMed (original) (raw)
Cerebrospinal fluid tau/beta-amyloid(42) ratio as a prediction of cognitive decline in nondemented older adults
Anne M Fagan et al. Arch Neurol. 2007 Mar.
Abstract
Objectives: To investigate the ability of cerebrospinal fluid (CSF) and plasma measures to discriminate early-stage Alzheimer disease (AD) (defined by clinical criteria and presence/absence of brain amyloid) from nondemented aging and to assess whether these biomarkers can predict future dementia in cognitively normal individuals.
Design: Evaluation of CSF beta-amyloid(40) (Abeta(40)), Abeta(42), tau, phosphorylated tau(181), and plasma Abeta(40) and Abeta(42) and longitudinal clinical follow-up (from 1 to 8 years).
Setting: Longitudinal studies of healthy aging and dementia through an AD research center.
Participants: Community-dwelling volunteers (n = 139) aged 60 to 91 years and clinically judged as cognitively normal (Clinical Dementia Rating [CDR], 0) or having very mild (CDR, 0.5) or mild (CDR, 1) AD dementia.
Results: Individuals with very mild or mild AD have reduced mean levels of CSF Abeta(42) and increased levels of CSF tau and phosphorylated tau(181). Cerebrospinal fluid Abeta(42) level completely corresponds with the presence or absence of brain amyloid (imaged with Pittsburgh Compound B) in demented and nondemented individuals. The CSF tau/Abeta(42) ratio (adjusted hazard ratio, 5.21; 95% confidence interval, 1.58-17.22) and phosphorylated tau(181)/Abeta(42) ratio (adjusted hazard ratio, 4.39; 95% confidence interval, 1.62-11.86) predict conversion from a CDR of 0 to a CDR greater than 0.
Conclusions: The very mildest symptomatic stage of AD exhibits the same CSF biomarker phenotype as more advanced AD. In addition, levels of CSF Abeta(42), when combined with amyloid imaging, augment clinical methods for identifying in individuals with brain amyloid deposits whether dementia is present or not. Importantly, CSF tau/Abeta(42) ratios show strong promise as antecedent (preclinical) biomarkers that predict future dementia in cognitively normal older adults.
Comment in
- Biomarkers in dementia.
Vanacore N, Galeotti F, Maggini M, Raschetti R. Vanacore N, et al. Arch Neurol. 2007 Sep;64(9):1356; author reply 1357-9. doi: 10.1001/archneur.64.9.1356. Arch Neurol. 2007. PMID: 17846281 No abstract available. - Medication use as a confounding factor in the use of the cerebrospinal fluid tau/beta-amyloid42 ratio.
Wong V. Wong V. Arch Neurol. 2007 Sep;64(9):1357; author reply 1357-9. doi: 10.1001/archneur.64.9.1357-a. Arch Neurol. 2007. PMID: 17846282 No abstract available.
Similar articles
- Correlation of longitudinal cerebrospinal fluid biomarkers with cognitive decline in healthy older adults.
Stomrud E, Hansson O, Zetterberg H, Blennow K, Minthon L, Londos E. Stomrud E, et al. Arch Neurol. 2010 Feb;67(2):217-23. doi: 10.1001/archneurol.2009.316. Arch Neurol. 2010. PMID: 20142530 - Cerebrospinal fluid {beta}-amyloid 42 and tau proteins as biomarkers of Alzheimer-type pathologic changes in the brain.
Tapiola T, Alafuzoff I, Herukka SK, Parkkinen L, Hartikainen P, Soininen H, Pirttilä T. Tapiola T, et al. Arch Neurol. 2009 Mar;66(3):382-9. doi: 10.1001/archneurol.2008.596. Arch Neurol. 2009. PMID: 19273758 - CSF tau/Abeta42 ratio for increased risk of mild cognitive impairment: a follow-up study.
Li G, Sokal I, Quinn JF, Leverenz JB, Brodey M, Schellenberg GD, Kaye JA, Raskind MA, Zhang J, Peskind ER, Montine TJ. Li G, et al. Neurology. 2007 Aug 14;69(7):631-9. doi: 10.1212/01.wnl.0000267428.62582.aa. Neurology. 2007. PMID: 17698783 - Biomarkers as predictors for conversion from mild cognitive impairment to Alzheimer-type dementia: implications for trial design.
van Rossum IA, Vos S, Handels R, Visser PJ. van Rossum IA, et al. J Alzheimers Dis. 2010;20(3):881-91. doi: 10.3233/JAD-2010-091606. J Alzheimers Dis. 2010. PMID: 20413876 Review. - CSF biomarkers for mild cognitive impairment.
Blennow K. Blennow K. J Intern Med. 2004 Sep;256(3):224-34. doi: 10.1111/j.1365-2796.2004.01368.x. J Intern Med. 2004. PMID: 15324365 Review.
Cited by
- Amyloid β-mediated Zn2+ influx into dentate granule cells transiently induces a short-term cognitive deficit.
Takeda A, Nakamura M, Fujii H, Uematsu C, Minamino T, Adlard PA, Bush AI, Tamano H. Takeda A, et al. PLoS One. 2014 Dec 23;9(12):e115923. doi: 10.1371/journal.pone.0115923. eCollection 2014. PLoS One. 2014. PMID: 25536033 Free PMC article. - Multicolor time-stamp reveals the dynamics and toxicity of amyloid deposition.
Condello C, Schain A, Grutzendler J. Condello C, et al. Sci Rep. 2011;1:19. doi: 10.1038/srep00019. Epub 2011 Jun 21. Sci Rep. 2011. PMID: 22355538 Free PMC article. - Biomarkers for the Early Detection and Progression of Alzheimer's Disease.
Counts SE, Ikonomovic MD, Mercado N, Vega IE, Mufson EJ. Counts SE, et al. Neurotherapeutics. 2017 Jan;14(1):35-53. doi: 10.1007/s13311-016-0481-z. Neurotherapeutics. 2017. PMID: 27738903 Free PMC article. Review. - The impact of cerebrospinal fluid biomarkers on the diagnosis of Alzheimer's disease.
Engelborghs S, Le Bastard N. Engelborghs S, et al. Mol Diagn Ther. 2012 Jun 1;16(3):135-41. doi: 10.1007/BF03262201. Mol Diagn Ther. 2012. PMID: 22646065 - The impacts of sex and the 5xFAD model of Alzheimer's disease on the sleep and spatial learning responses to feeding time.
Campbell KJ, Jiang P, Olker C, Lin X, Kim SY, Lee CJ, Song EJ, Turek FW, Vitaterna MH. Campbell KJ, et al. Front Neurol. 2024 Jul 31;15:1430989. doi: 10.3389/fneur.2024.1430989. eCollection 2024. Front Neurol. 2024. PMID: 39144714 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical