TY - JOUR
T1 - A real-world clinical validation for AI-based MRI monitoring in multiple sclerosis
AU - Barnett, Michael
AU - Wang, Dongang
AU - Beadnall, Heidi
AU - Bischof, Antje
AU - Brunacci, David
AU - Butzkueven, Helmut
AU - Brown, J. William L.
AU - Cabezas, Mariano
AU - Das, Tilak
AU - Dugal, Tej
AU - Guilfoyle, Daniel
AU - Klistorner, Alexander
AU - Krieger, Stephen
AU - Kyle, Kain
AU - Ly, Linda
AU - Masters, Lynette
AU - Shieh, Andy
AU - Tang, Zihao
AU - van der Walt, Anneke
AU - Ward, Kayla
AU - Wiendl, Heinz
AU - Zhan, Geng
AU - Zivadinov, Robert
AU - Barnett, Yael
AU - Wang, Chenyu
N1 - Copyright the Author(s) 2023. Version archived for private and non-commercial use with the permission of the author/s and according to publisher conditions. For further rights please contact the publisher.
PY - 2023/12
Y1 - 2023/12
N2 - Modern management of MS targets No Evidence of Disease Activity (NEDA): no clinical relapses, no magnetic resonance imaging (MRI) disease activity and no disability worsening. While MRI is the principal tool available to neurologists for monitoring clinically silent MS disease activity and, where appropriate, escalating treatment, standard radiology reports are qualitative and may be insensitive to the development of new or enlarging lesions. Existing quantitative neuroimaging tools lack adequate clinical validation. In 397 multi-center MRI scan pairs acquired in routine practice, we demonstrate superior case-level sensitivity of a clinically integrated AI-based tool over standard radiology reports (93.3% vs 58.3%), relative to a consensus ground truth, with minimal loss of specificity. We also demonstrate equivalence of the AI-tool with a core clinical trial imaging lab for lesion activity and quantitative brain volumetric measures, including percentage brain volume loss (PBVC), an accepted biomarker of neurodegeneration in MS (mean PBVC −0.32% vs −0.36%, respectively), whereas even severe atrophy (>0.8% loss) was not appreciated in radiology reports. Finally, the AI-tool additionally embeds a clinically meaningful, experiential comparator that returns a relevant MS patient centile for lesion burden, revealing, in our cohort, inconsistencies in qualitative descriptors used in radiology reports. AI-based image quantitation enhances the accuracy of, and value-adds to, qualitative radiology reporting. Scaled deployment of these tools will open a path to precision management for patients with MS.
AB - Modern management of MS targets No Evidence of Disease Activity (NEDA): no clinical relapses, no magnetic resonance imaging (MRI) disease activity and no disability worsening. While MRI is the principal tool available to neurologists for monitoring clinically silent MS disease activity and, where appropriate, escalating treatment, standard radiology reports are qualitative and may be insensitive to the development of new or enlarging lesions. Existing quantitative neuroimaging tools lack adequate clinical validation. In 397 multi-center MRI scan pairs acquired in routine practice, we demonstrate superior case-level sensitivity of a clinically integrated AI-based tool over standard radiology reports (93.3% vs 58.3%), relative to a consensus ground truth, with minimal loss of specificity. We also demonstrate equivalence of the AI-tool with a core clinical trial imaging lab for lesion activity and quantitative brain volumetric measures, including percentage brain volume loss (PBVC), an accepted biomarker of neurodegeneration in MS (mean PBVC −0.32% vs −0.36%, respectively), whereas even severe atrophy (>0.8% loss) was not appreciated in radiology reports. Finally, the AI-tool additionally embeds a clinically meaningful, experiential comparator that returns a relevant MS patient centile for lesion burden, revealing, in our cohort, inconsistencies in qualitative descriptors used in radiology reports. AI-based image quantitation enhances the accuracy of, and value-adds to, qualitative radiology reporting. Scaled deployment of these tools will open a path to precision management for patients with MS.
UR - http://www.scopus.com/inward/record.url?scp=85174534623&partnerID=8YFLogxK
U2 - 10.1038/s41746-023-00940-6
DO - 10.1038/s41746-023-00940-6
M3 - Article
C2 - 37857813
SN - 2398-6352
VL - 6
SP - 1
EP - 9
JO - npj Digital Medicine
JF - npj Digital Medicine
IS - 1
M1 - 196
ER -