Diagnostic Performance of Automated MRI Volumetry by icobrain dm for Alzheimer's Disease in a Clinical Setting: A REMEMBER Study

Mandy Melissa Jane Wittens, Diana Maria Sima, Ruben Houbrechts, Annemie Ribbens, Ellis Niemantsverdriet, Erik Fransen, Christine Bastin, Florence Benoit, Bruno Bergmans, Jean-Christophe Bier, Peter Paul De Deyn, Olivier Deryck, Bernard Hanseeuw, Adrian Ivanoiu, Jean-Claude Lemper, Eric Mormont, Gaëtane Picard, Ezequiel de la Rosa, Eric Salmon, Kurt SegersAnne Sieben, Dirk Smeets, Hanne Struyfs, Evert Thiery, Jos Tournoy, Eric Triau, Anne-Marie Vanbinst, Jan Versijpt, Maria Bjerke, Sebastiaan Engelborghs

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

Abstract

BACKGROUND: Magnetic resonance imaging (MRI) has become important in the diagnostic work-up of neurodegenerative diseases. icobrain dm, a CE-labeled and FDA-cleared automated brain volumetry software, has shown potential in differentiating cognitively healthy controls (HC) from Alzheimer's disease (AD) dementia (ADD) patients in selected research cohorts.

OBJECTIVE: This study examines the diagnostic value of icobrain dm for AD in routine clinical practice, including a comparison to the widely used FreeSurfer software, and investigates if combined brain volumes contribute to establish an AD diagnosis.

METHODS: The study population included HC (n = 90), subjective cognitive decline (SCD, n = 93), mild cognitive impairment (MCI, n = 357), and ADD (n = 280) patients. Through automated volumetric analyses of global, cortical, and subcortical brain structures on clinical brain MRI T1w (n = 820) images from a retrospective, multi-center study (REMEMBER), icobrain dm's (v.4.4.0) ability to differentiate disease stages via ROC analysis was compared to FreeSurfer (v.6.0). Stepwise backward regression models were constructed to investigate if combined brain volumes can differentiate between AD stages.

RESULTS: icobrain dm outperformed FreeSurfer in processing time (15-30 min versus 9-32 h), robustness (0 versus 67 failures), and diagnostic performance for whole brain, hippocampal volumes, and lateral ventricles between HC and ADD patients. Stepwise backward regression showed improved diagnostic accuracy for pairwise group differentiations, with highest performance obtained for distinguishing HC from ADD (AUC = 0.914; Specificity 83.0%; Sensitivity 86.3%).

CONCLUSION: Automated volumetry has a diagnostic value for ADD diagnosis in routine clinical practice. Our findings indicate that combined brain volumes improve diagnostic accuracy, using real-world imaging data from a clinical setting.

Original languageEnglish
Pages (from-to)623-639
Number of pages17
JournalJournal of Alzheimer's Disease
Volume83
Issue number2
DOIs
Publication statusPublished - 2021

Bibliographical note

Funding Information:
This research was in part supported by the agency of Flanders Innovation & Intrepreneurship (VLAIO), the Flemish Agency for Innovation by Science and Technology (IWT 140262), the Interreg V programme Flanders-The Netherlands of the European Regional Development Fund (ERDF) (Herinner-ingen/Memories project), the European Union’s Horizon 2020 research and innovation programme under grant agreement numbers 666992 (EURO-POND) and 765148 (TRABIT). For the University of Liège center, this work was supported by a French Speaking Community Concerted Research Action (ARC-06/11-340) and a Belgian InterUniversity Attraction Pole (P6/29). We acknowledge the contribution of Sebastiaan Mariën and Roxanne Bladt.

Funding Information:
The study was approved by the ethics committee of the University of Antwerp / Universitair Ziekenhuis Antwerp (N-16/2/18), Antwerp and by the ethics committees of Algemeen Ziekenhuis Sint-Jan Brugge-Oostende, Bruges (N-1992); Centre Hospitalier Universitaire Brugmann (CHU Brugmann), Brussels (N-2016/84); Centre Hospitalier Universitaire Liege (CHU Liege), Liege (N-2012/274); Cliniques Universitaires de Bruxelles (ULB), Hopital Erasme, Brussels (N-P2016/187); Cliniques Universitaires Saint-Luc (UCL), Brussels (N-2016/07jui/261); Clinique St-Pierre Ottignies, Ottignies (N-OM045); Universitair Ziekenhuis Brussel, Brussels (N-2016/183); and Ziekenhuis Netwerk Antwerp (ZNA), Antwerp (N-4730).

Publisher Copyright:
© 2021 - The authors.

Copyright:
Copyright 2022 Elsevier B.V., All rights reserved.

Keywords

  • Alzheimer’s disease
  • automated volumetry
  • biomarkers
  • magnetic resonance imaging
  • mild cognitive impairment

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