TY - JOUR
T1 - Prognostic value of Alzheimer's biomarkers in mild cognitive impairment
T2 - the effect of age at onset
AU - Alzheimer’s Disease Neuroimaging Initiative
AU - Altomare, Daniele
AU - Ferrari, Clarissa
AU - Caroli, Anna
AU - Galluzzi, Samantha
AU - Prestia, Annapaola
AU - van der Flier, Wiesje M.
AU - Ossenkoppele, Rik
AU - van Berckel, Bart
AU - Barkhof, Frederik
AU - Teunissen, Charlotte E.
AU - Wall, Anders
AU - Carter, Stephen F.
AU - Schöll, Michael
AU - Choo, Il Han
AU - Grimmer, Timo
AU - Redolfi, Alberto
AU - Nordberg, Agneta
AU - Scheltens, Philip
AU - Drzezga, Alexander
AU - Frisoni, Giovanni B.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Objective: The aim of this study is to assess the impact of age at onset on the prognostic value of Alzheimer’s biomarkers in a large sample of patients with mild cognitive impairment (MCI). Methods: We measured Aβ42, t-tau, hippocampal volume on magnetic resonance imaging (MRI) and cortical metabolism on fluorodeoxyglucose–positron emission tomography (FDG-PET) in 188 MCI patients followed for at least 1 year. We categorised patients into earlier and later onset (EO/LO). Receiver operating characteristic curves and corresponding areas under the curve (AUCs) were performed to assess and compar the biomarker prognostic performances in EO and LO groups. Linear Model was adopted for estimating the time-to-progression in relation with earlier/later onset MCI groups and biomarkers. Results: In earlier onset patients, all the assessed biomarkers were able to predict cognitive decline (p < 0.05), with FDG-PET showing the best performance. In later onset patients, all biomarkers but t-tau predicted cognitive decline (p < 0.05). Moreover, FDG-PET alone in earlier onset patients showed a higher prognostic value than the one resulting from the combination of all the biomarkers in later onset patients (earlier onset AUC 0.935 vs later onset AUC 0.753, p < 0.001). Finally, FDG-PET showed a different prognostic value between earlier and later onset patients (p = 0.040) in time-to-progression allowing an estimate of the time free from disease. Discussion: FDG-PET may represent the most universal tool for the establishment of a prognosis in MCI patients and may be used for obtaining an onset-related estimate of the time free from disease.
AB - Objective: The aim of this study is to assess the impact of age at onset on the prognostic value of Alzheimer’s biomarkers in a large sample of patients with mild cognitive impairment (MCI). Methods: We measured Aβ42, t-tau, hippocampal volume on magnetic resonance imaging (MRI) and cortical metabolism on fluorodeoxyglucose–positron emission tomography (FDG-PET) in 188 MCI patients followed for at least 1 year. We categorised patients into earlier and later onset (EO/LO). Receiver operating characteristic curves and corresponding areas under the curve (AUCs) were performed to assess and compar the biomarker prognostic performances in EO and LO groups. Linear Model was adopted for estimating the time-to-progression in relation with earlier/later onset MCI groups and biomarkers. Results: In earlier onset patients, all the assessed biomarkers were able to predict cognitive decline (p < 0.05), with FDG-PET showing the best performance. In later onset patients, all biomarkers but t-tau predicted cognitive decline (p < 0.05). Moreover, FDG-PET alone in earlier onset patients showed a higher prognostic value than the one resulting from the combination of all the biomarkers in later onset patients (earlier onset AUC 0.935 vs later onset AUC 0.753, p < 0.001). Finally, FDG-PET showed a different prognostic value between earlier and later onset patients (p = 0.040) in time-to-progression allowing an estimate of the time free from disease. Discussion: FDG-PET may represent the most universal tool for the establishment of a prognosis in MCI patients and may be used for obtaining an onset-related estimate of the time free from disease.
KW - Alzheimer
KW - Biomarkers
KW - Cognition
KW - FDG-PET
KW - Imaging
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85068792506&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/31267207
U2 - https://doi.org/10.1007/s00415-019-09441-7
DO - https://doi.org/10.1007/s00415-019-09441-7
M3 - Article
C2 - 31267207
SN - 0340-5354
VL - 266
SP - 2535
EP - 2545
JO - Journal of neurology
JF - Journal of neurology
IS - 10
ER -