NTAD: A longitudinal neuroimaging dataset of Alzheimer's disease pathology
- 1University of Cambridge
Abstract
We introduce the New Therapeutics in Alzheimer's Disease (NTAD) dataset, a multi-modal and longitudinal imaging dataset from 70 biomarker-positive people with early dementia or Mild Cognitive Impairment (MCI) due to Alzheimer's Disease (AD), assessed over 2.5 years, and 35 healthy controls assessed at baseline. The data include simultaneous magneto- and electro-encephalography (M/EEG), 3-Tesla structural and functional magnetic resonance imaging (MRI), Amyloid-beta; positron emission tomography (PET), fluid proteomic biomarkers in cerebrospinal fluid and blood, and a battery of clinical and neuropsychological assessments. 11C UCB-J PET was undertaken for a subset of participants. For people with AD, assessments were repeated at approximately three weeks, 15 months, and 28 months after baseline. The data can be accessed through the Dementias Platform UK (DPUK), including pre-processed M/EEG and T1 MRI in pseudonymised BIDS format. With the pressing need to develop treatments for slowing, reversing, and preventing AD, these data provide an opportunity for identifying and validating novel biomarkers of Alzheimer's disease neurophysiology, as well as understanding its treatable pathology.
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BibTeX
@misc{es2026ntad,
title = {{NTAD: A longitudinal neuroimaging dataset of Alzheimer's disease pathology}},
author = {M. W. J. van Es and M. N. Perquin and A. J. Quinn and J. Pitt and A. Krugliak and T. Thayanandan and J. Lanskey and E. Kocagoncu and M. Karadag and C. Alcock and M. Naessens and S. Lowe and H. Fye and V. Raymont and K. D. Singh and R. N. Henson and A. C. Nobre and M. W. Woolrich and J. Rowe and the NTAD study group},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.30.763020},
url = {https://www.biorxiv.org/content/10.64898/2026.10.30.763020v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - NTAD: A longitudinal neuroimaging dataset of Alzheimer's disease pathology
AU - M. W. J. van Es
AU - M. N. Perquin
AU - A. J. Quinn
AU - J. Pitt
AU - A. Krugliak
AU - T. Thayanandan
AU - J. Lanskey
AU - E. Kocagoncu
AU - M. Karadag
AU - C. Alcock
AU - M. Naessens
AU - S. Lowe
AU - H. Fye
AU - V. Raymont
AU - K. D. Singh
AU - R. N. Henson
AU - A. C. Nobre
AU - M. W. Woolrich
AU - J. Rowe
AU - the NTAD study group
PY - 2026
DA - 2026/10/30
PB - bioRxiv
DO - 10.64898/2026.10.30.763020
UR - https://www.biorxiv.org/content/10.64898/2026.10.30.763020v1
AB - We introduce the New Therapeutics in Alzheimer's Disease (NTAD) dataset, a multi-modal and longitudinal imaging dataset from 70 biomarker-positive people with early dementia or Mild Cognitive Impairment (MCI) due to Alzheimer's Disease (AD), assessed over 2.5 years, and 35 healthy controls assessed at baseline. The data include simultaneous magneto- and electro-encephalography (M/EEG), 3-Tesla structural and functional magnetic resonance imaging (MRI), Amyloid-beta; positron emission tomography (PET), fluid proteomic biomarkers in cerebrospinal fluid and blood, and a battery of clinical and neuropsychological assessments. 11C UCB-J PET was undertaken for a subset of participants. For people with AD, assessments were repeated at approximately three weeks, 15 months, and 28 months after baseline. The data can be accessed through the Dementias Platform UK (DPUK), including pre-processed M/EEG and T1 MRI in pseudonymised BIDS format. With the pressing need to develop treatments for slowing, reversing, and preventing AD, these data provide an opportunity for identifying and validating novel biomarkers of Alzheimer's disease neurophysiology, as well as understanding its treatable pathology.
ER -