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


Journal

Journal of Alzheimer's disease : JAD
ISSN: 1875-8908
Titre abrégé: J Alzheimers Dis
Pays: Netherlands
ID NLM: 9814863

Informations de publication

Date de publication:
2021
Historique:
pubmed: 3 8 2021
medline: 15 12 2021
entrez: 2 8 2021
Statut: ppublish

Résumé

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. 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. 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. 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%). 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.

Sections du résumé

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.

Identifiants

pubmed: 34334402
pii: JAD210450
doi: 10.3233/JAD-210450
pmc: PMC8543261
doi:

Types de publication

Comparative Study Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

623-639

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Auteurs

Mandy Melissa Jane Wittens (MMJ)

Reference Center for Biological Markers of Dementia (BIODEM), Laboratory of Neurochemistry and Behavior, University of Antwerp, Antwerp, Belgium.
Center for Neurosciences (C4N), Vrije Universiteit Brussel (VUB), Brussels, Belgium.

Diana Maria Sima (DM)

icometrix, Leuven, Belgium.

Ruben Houbrechts (R)

icometrix, Leuven, Belgium.

Annemie Ribbens (A)

icometrix, Leuven, Belgium.

Ellis Niemantsverdriet (E)

Reference Center for Biological Markers of Dementia (BIODEM), Laboratory of Neurochemistry and Behavior, University of Antwerp, Antwerp, Belgium.

Erik Fransen (E)

StatUa Center for Statistics, University of Antwerp, Belgium.

Christine Bastin (C)

GIGA Cyclotron Research Centre in vivo Imaging, University of Liège, Liège, Belgium.

Florence Benoit (F)

Department of Geriatrics, Centre Hospitalier Universitaire (CHU) Brugmann, Brussels, Belgium.

Bruno Bergmans (B)

Department of Neurology and Center for Cognitive Disorders, Brugge, Belgium.

Jean-Christophe Bier (JC)

Department of Neurology, Erasme Hospital - ULB, Brussels, Belgium.

Peter Paul De Deyn (PP)

Reference Center for Biological Markers of Dementia (BIODEM), Laboratory of Neurochemistry and Behavior, University of Antwerp, Antwerp, Belgium.
Department of Neurology and Memory Clinic, Hospital Network Antwerp (ZNA), Antwerp, Belgium.

Olivier Deryck (O)

Department of Neurology and Center for Cognitive Disorders, Brugge, Belgium.

Bernard Hanseeuw (B)

Department of Neurology, Cliniques Universitaires St Luc and Institute of Neuroscience, Université catholique de Louvain, Woluwe-Saint-Lambert (Brussels), Belgium.

Adrian Ivanoiu (A)

Department of Neurology, Cliniques Universitaires St Luc and Institute of Neuroscience, Université catholique de Louvain, Woluwe-Saint-Lambert (Brussels), Belgium.

Jean-Claude Lemper (JC)

Department of Geriatrics, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel, Brussels, Belgium.
Silva medical Scheutbos, Molenbeek-Saint-Jean (Brussels), Belgium.

Eric Mormont (E)

UCLouvain, CHU UCL Namur, service de Neurologie, Yvoir, Belgium.
UCLouvain, Institute of NeuroScience, Louvain-la-Neuve, Belgium.

Gaëtane Picard (G)

Department of Neurology, Clinique Saint-Pierre, Ottignies, Belgium.

Ezequiel de la Rosa (E)

icometrix, Leuven, Belgium.

Eric Salmon (E)

GIGA Cyclotron Research Centre in vivo Imaging, University of Liège, Liège, Belgium.
Department of Neurology, Memory Clinic, Centre Hospitalier Universitaire (CHU) Liège, Liège, Belgium.

Kurt Segers (K)

Department of Neurology, Centre Hospitalier Universitaire (CHU) Brugmann, Brussels, Belgium.

Anne Sieben (A)

Department of Neurology, University Hospital Ghent, Ghent University, Ghent, Belgium.

Dirk Smeets (D)

icometrix, Leuven, Belgium.

Hanne Struyfs (H)

Reference Center for Biological Markers of Dementia (BIODEM), Laboratory of Neurochemistry and Behavior, University of Antwerp, Antwerp, Belgium.

Evert Thiery (E)

Department of Neurology, University Hospital Ghent, Ghent University, Ghent, Belgium.

Jos Tournoy (J)

Geriatric Medicine and Memory Clinic, University Hospitals Leuven & Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, Belgium.

Eric Triau (E)

Neurologie Consult, Leuven, Belgium.

Anne-Marie Vanbinst (AM)

Department of Radiology, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.

Jan Versijpt (J)

Department of Neurology, Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.
Center for Neurosciences (C4N), Vrije Universiteit Brussel (VUB), Brussels, Belgium.

Maria Bjerke (M)

Reference Center for Biological Markers of Dementia (BIODEM), Laboratory of Neurochemistry and Behavior, University of Antwerp, Antwerp, Belgium.
Center for Neurosciences (C4N), Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Laboratory of Neurochemistry, Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.

Sebastiaan Engelborghs (S)

Reference Center for Biological Markers of Dementia (BIODEM), Laboratory of Neurochemistry and Behavior, University of Antwerp, Antwerp, Belgium.
Department of Neurology, Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.
Center for Neurosciences (C4N), Vrije Universiteit Brussel (VUB), Brussels, Belgium.

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