Biomarker-based prognosis for people with mild cognitive impairment (ABIDE): a modelling study

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift


Background: Biomarker-based risk predictions of dementia in people with mild cognitive impairment are highly relevant for care planning and to select patients for treatment when disease-modifying drugs become available. We aimed to establish robust prediction models of disease progression in people at risk of dementia. Methods: In this modelling study, we included people with mild cognitive impairment (MCI) from single-centre and multicentre cohorts in Europe and North America: the European Medical Information Framework for Alzheimer's Disease (EMIF-AD; n=883), Alzheimer's Disease Neuroimaging Initiative (ADNI; n=829), Amsterdam Dementia Cohort (ADC; n=666), and the Swedish BioFINDER study (n=233). Inclusion criteria were a baseline diagnosis of MCI, at least 6 months of follow-up, and availability of a baseline Mini-Mental State Examination (MMSE) and MRI or CSF biomarker assessment. The primary endpoint was clinical progression to any type of dementia. We evaluated performance of previously developed risk prediction models—a demographics model, a hippocampal volume model, and a CSF biomarkers model—by evaluating them across cohorts, incorporating different biomarker measurement methods, and determining prognostic performance with Harrell's C statistic. We then updated the models by re-estimating parameters with and without centre-specific effects and evaluated model calibration by comparing observed and expected survival. Finally, we constructed a model combining markers for amyloid deposition, tauopathy, and neurodegeneration (ATN), in accordance with the National Institute on Aging and Alzheimer's Association research framework. Findings: We included all 2611 individuals with MCI in the four cohorts, 1007 (39%) of whom progressed to dementia. The validated demographics model (Harrell's C 0·62, 95% CI 0·59–0·65), validated hippocampal volume model (0·67, 0·62–0·72), and updated CSF biomarkers model (0·72, 0·68–0·74) had adequate prognostic performance across cohorts and were well calibrated. The newly constructed ATN model had the highest performance (0·74, 0·71–0·76). Interpretation: We generated risk models that are robust across cohorts, which adds to their potential clinical applicability. The models could aid clinicians in the interpretation of CSF biomarker and hippocampal volume results in individuals with MCI, and help research and clinical settings to prepare for a future of precision medicine in Alzheimer's disease. Future research should focus on the clinical utility of the models, particularly if their use affects participants' understanding, emotional wellbeing, and behaviour. Funding: ZonMW-Memorabel.


  • Ingrid S. van Maurik
  • Stephanie J. Vos
  • Isabelle Bos
  • Femke H. Bouwman
  • Charlotte E. Teunissen
  • Philip Scheltens
  • Frederik Barkhof
  • Lutz Frolich
  • Johannes Kornhuber
  • Jens Wiltfang
  • Wolfgang Maier
  • Oliver Peters
  • Eckart Rüther
  • Flavio Nobili
  • Giovanni B. Frisoni
  • Luiza Spiru
  • Yvonne Freund-Levi
  • Asa K. Wallin
  • Harald Hampel
  • Hilkka Soininen
  • Magda Tsolaki
  • Frans Verhey
  • Iwona Kłoszewska
  • Patrizia Mecocci
  • Bruno Vellas
  • Simon Lovestone
  • Samantha Galluzzi
  • Sanna Kaisa Herukka
  • Isabel Santana
  • Ines Baldeiras
  • Alexandre de Mendonça
  • Dina Silva
  • Gael Chetelat
  • Stephanie Egret
  • Sebastian Palmqvist
  • Oskar Hansson
  • Pieter Jelle Visser
  • Johannes Berkhof
  • Wiesje M. van der Flier
  • Alzheimer's Disease Neuroimaging Initiative
Enheter & grupper
Externa organisationer
  • Maastricht University
  • University College London
  • Friedrich-Alexander University Erlangen-Nürnberg
  • University Medical Center Göttingen
  • German Center for Neurodegenerative Diseases
  • University of Aveiro
  • University of Bonn
  • Charité Universitätsmedizin Berlin
  • University of Göttingen
  • University of Genoa
  • Azienda Ospedaliera Universitaria San Martino IST
  • University of Geneva
  • Carol Davila University of Medicine and Pharmacy
  • Ana Aslan International Foundation
  • Örebro University
  • Karolinska Institute
  • King's College London
  • Pitié Salpetriere University Paris
  • Eisai Inc.
  • University of Eastern Finland
  • Aristotle University of Thessaloniki
  • Medical University of Lodz
  • University of Perugia
  • Toulouse University Hospital
  • University of Oxford
  • Centro San Giovanni di Dio Fatebenefratelli
  • University of Coimbra
  • University Hospital of Coimbra
  • University of Lisbon
  • University of Algarve, Portugal
  • University of Caen Normandy
  • Skåne University Hospital
  • Vrije Universiteit Amsterdam
  • VU University Medical Center
  • Heidelberg University
  • Humboldt University of Berlin
  • Paris-Sorbonne University
  • Kuopio University Hospital

Ämnesklassifikation (UKÄ) – OBLIGATORISK

  • Neurologi
Sidor (från-till)1034-1044
Antal sidor11
TidskriftThe Lancet Neurology
Utgåva nummer11
StatusPublished - 2019
Peer review utfördJa