Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Lange, Catharinaa; b | Suppa, Pera; c | Pietrzyk, Uweb; d | Makowski, Marcus R.e | Spies, Lotharc | Peters, Oliverf | Buchert, Ralpha; g; * | for the Alzheimer’s Disease Neuroimaging Initiative1
Affiliations: [a] Department of Nuclear Medicine, Charité – Universitätsmedizin Berlin, Berlin, Germany | [b] School of Mathematics and Natural Science, University of Wuppertal, Wuppertal, Germany | [c] jung diagnostics GmbH, Hamburg, Germany | [d] Institute of Neuroscience and Medicine, Forschungszentrum Jülich, Jülich, Germany | [e] Department of Radiology, Charité – Universitätsmedizin Berlin, Berlin, Germany | [f] Department of Psychiatry and Psychotherapy, Charité – Universitätsmedizin Berlin, Berlin, Germany | [g] Department of Diagnostic and Interventional Radiology and Nuclear Medicine, Center for Radiology and Endoscopy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Correspondence: [*] Correspondence to: Ralph Buchert, Department of Diagnostic and Interventional Radiology and Nuclear Medicine, Center for Radiology and Endoscopy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Tel.: +49 40 7410 54347; Fax: +49 40 7410 40265; E-mail: r.buchert@uke.de.
Note: [1] Data used in preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (http://adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at: http://adni.loni.usc.edu/wp-content/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf
Abstract: The aim of this study was to evaluate the incremental benefit of biomarkers for prediction of Alzheimer’s disease dementia (ADD) in patients with mild cognitive impairment (MCI) when added stepwise in the order of their collection in clinical routine. The model started with cognitive status characterized by the ADAS-13 score. Hippocampus volume (HV), cerebrospinal fluid (CSF) phospho-tau (pTau), and the FDG t-sum score in an AD meta-region-of-interest were compared as neurodegeneration markers. CSF-Aβ1-42 was used as amyloidosis marker. The incremental prognostic benefit from these markers was assessed by stepwise Kaplan-Meier survival analysis in 402 ADNI MCI subjects. Predefined cutoffs were used to dichotomize patients as ‘negative’ or ‘positive’ for AD characteristic alteration with respect to each marker. Among the neurodegeneration markers, CSF-pTau provided the best incremental risk stratification when added to ADAS-13. FDG PET outperformed HV only in MCI subjects with relatively preserved cognition. Adding CSF-Aβ provided further risk stratification in pTau-positive subjects, independent of their cognitive status. Stepwise integration of biomarkers allows stepwise refinement of risk estimates for MCI-to-ADD progression. Incremental benefit strongly depends on the patient’s status according to the preceding diagnostic steps. The stepwise Kaplan-Meier curves might be useful to optimize diagnostic workflow in individual patients.
Keywords: Alzheimer’s disease, biomarker, cerebrospinal fluid, FDG, magnetic resonance imaging, mild cognitive impairment, neuropsychological testing, positron emission tomography, prediction, white matter hyperintensities
DOI: 10.3233/JAD-170705
Journal: Journal of Alzheimer's Disease, vol. 61, no. 1, pp. 373-388, 2018
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
sales@iospress.com
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
info@iospress.nl
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office info@iospress.nl
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
china@iospress.cn
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
如果您在出版方面需要帮助或有任何建, 件至: editorial@iospress.nl