Longitudinal Study of CSF Biomarkers in Patients with Alzheimer's Disease

被引:71
作者
Buchhave, Peder
Blennow, Kaj
Zetterberg, Henrik
Stomrud, Erik
Londos, Elisabet
Andreasen, Niels
Minthon, Lennart
Hansson, Oskar
机构
[1] Clinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund
[2] Neuropsychiatric Clinic, Malmö University Hospital, Malmö
[3] Institute of Neuroscience and Physiology, Department of Neurochemistry and Psychiatry, Göteborg University, Göteborg
[4] Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine, Göteborg University, Göteborg
[5] Karolinska Institutet, Department of Neurobiology, Caring Sciences and Society, Stockholm
关键词
CEREBROSPINAL-FLUID; TAU LEVELS; FOLLOW-UP; STABILITY; BETA-AMYLOID((1-42)); PROGRESSION; PREDICTION; DECLINE; RATIO;
D O I
10.1371/journal.pone.0006294
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The CSF biomarkers tau and A beta 42 can identify patients with AD, even during the preclinical stages. However, previous studies on longitudinal changes of tau and A beta 42 in individual patients with AD and elderly controls report somewhat inconsistent results. Methodology/Principal Findings: We investigated the levels of tau and A beta 42 at baseline and after 1 year in 100 patients with AD. In a second cohort of 45 AD patients we measured the CSF biomarkers at baseline and after 2 years. Moreover, in 34 healthy elderly controls the CSF biomarkers were followed for 4 years. The baseline levels of tau were increased with >60% in AD patients compared to controls (p<0.001), while baseline A beta 42 levels were decreased with >50% (p<0.001). In the AD group followed for 2 years, tau increased with 16% compared to the baseline levels (p<0.05). However, the levels of tau were stable over 4 years in the controls. The levels of A beta 42 did not change significantly over time in any of the groups. In the patients with AD, tau was moderately associated with worse cognitive performance already at baseline (p<0.05). Conclusions/Significance: Tau and A beta 42 in CSF seem to reflect the underlying disease state in both early and late stages of AD. The slight increase in tau over time observed in the patients with AD is modest when compared to the relatively large difference in absolute tau levels between AD patients and controls. Therefore, these markers maintain their usefulness as state markers over time and might serve as surrogate markers for treatment efficacy in clinical trials.
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页数:5
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