Evaluation of a deep learning segmentation tool to help detect spinal cord lesions from combined T2 and STIR acquisitions in people with multiple sclerosis

被引:0
作者
Lode, Baptiste [1 ,2 ]
Hussein, Burhan Rashid [2 ]
Meuree, Cedric [2 ]
Walsh, Ricky [2 ]
Gaubert, Malo [2 ]
Lassalle, Nicolas [3 ]
Courbon, Guilhem [4 ]
Martin, Agathe [4 ]
Le Bars, Jeanne [4 ]
Durand-Dubief, Francoise [5 ,6 ]
Bourre, Bertrand [7 ]
Maarouf, Adil [8 ,9 ]
Outteryck, Olivier [10 ]
Mehier, Clement [3 ]
Poulin, Alexandre [3 ]
Cathelineau, Camille [3 ]
Hong, Jeremy [3 ]
Criton, Guillaume [11 ,12 ,13 ]
Motillon-Alonso, Sophie [3 ]
Lecler, Augustin [14 ,15 ]
Charbonneau, Frederique [14 ]
Duron, Loic [14 ]
Bani-Sadr, Alexandre [12 ,13 ,16 ]
Delpierre, Celine [17 ]
Ferre, Jean-Christophe [3 ]
Edan, Gilles [4 ,18 ]
Cotton, Francois [12 ,13 ,19 ]
Casey, Romain [20 ]
Galassi, Francesca [2 ]
Combes, Benoit [2 ]
Kerbrat, Anne [2 ,4 ]
机构
[1] Rennes Univ Hosp, Dept Neuroradiol, Rennes, France
[2] Rennes Univ, EMPENN Res Team, IRISA, CNRS,INSERM,INRIA, Rennes, France
[3] Rennes Univ Hosp, Dept Radiol, Rennes, France
[4] Rennes Univ Hosp, Neurol Dept, Rennes, France
[5] Univ Lyon 1, Hop Neurol Pierre Wertheimer, Neurol A, Hosp Civils Lyon, Lyon, France
[6] Univ Claude Bernard Lyon 1, Creatis LRMN, Inserm U630, CNRS,UMR 5220, Lyon, France
[7] CHU Rouen, Dept Neurol, Rouen, France
[8] Aix Marseille Univ, CRMBM, CNRS, Marseille, France
[9] Hop La Timone, APHM, Marseille, France
[10] Univ Lille, Dept Neuroradiol, INSERM, CHU Lille, Lille, France
[11] Lyon Univ Hosp, Dept Radiol, Lyon, France
[12] Univ Claude Bernard Lyon 1, CREATIS, CNRS, UMR 5220, Lyon, France
[13] Univ Claude Bernard Lyon 1, INSERM U1044, Lyon, France
[14] Fdn Adolphe Rothschild Hosp, Dept Neuroradiol, Paris, France
[15] Paris Cite Univ, Paris, France
[16] Hosp Civils Lyon, East Grp Hosp, Dept Neuroradiol, Bron, France
[17] Rouen Univ Hosp, Dept Neuroradiol, Rouen, France
[18] Univ Hosp Rennes, CIC P 1414 INSERM, Rennes, France
[19] Hosp Civils Lyon, Lyon Sud Hosp, Dept Radiol, Lyon, France
[20] Univ Claude Bernard Lyon 1, Univ Lyon, Ctr Rech Neurosci Lyon, Hosp Civils Lyon,Fdn EDMUS,OFSEP, Lyon, France
关键词
Spinal cord; MRI; Multiple sclerosis; Deep learning-based tool; STIR sequence; MRI;
D O I
10.1007/s00330-025-11541-0
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
ObjectiveTo develop a deep learning (DL) model for the detection of spinal cord (SC) multiple sclerosis (MS) lesions from both sagittal T2 and short tau inversion recovery (STIR) sequences and to investigate whether such a model could improve the performance of clinicians in detecting SC lesions. Materials and methodsA DL tool was developed based on SC sagittal T2 and STIR acquisitions from the imaging database of the French MS registry (OFSEP), including retrospective data from 40 different scanners. A multi-reader study based on retrospective data was performed between December 2023 and June 2024 to compare the performance of 20 clinicians in interpreting upper and lower SC acquisitions with and without the use of the tool. A ground truth was established by three experts. Sensitivity, precision, and inter-reader variability were evaluated. ResultsWe included 50 patients (39 females, median age: 41 years [range: 15-67]) with SC MRI acquired between February 2017 and December 2022. When reading with the tool, the clinicians' mean sensitivity to detect SC lesions improved (from 74.3% [95% CI = 67.8-80.6%] to 79.2% [95% CI: 73.5-85.0%]; p < 0.0001), with no evidence of difference in the mean precision: (69.0% [95% CI: 62.8-75.2%] vs 70.1% [95% CI: 64.3-75.9%]; p = 0.08). Inter-reader variability in lesion detection was slightly improved with the tool (Light's kappa = 0.55 vs 0.60), but without statistical difference (p = 0.056). ConclusionThe use of an automatic tool can help clinicians detect SC lesions in pwMS by increasing their sensitivity. Key PointsQuestionNo tool to help detect MS SC lesions is used in clinical practice despite their frequency and prognostic value.FindingsThis DL-based tool led to improvement in clinicians' sensitivity in detecting SC lesions from both sagittal T2 and STIR sequences, without decreasing precision.Clinical relevanceOur study indicated the potential of a DL-based tool to assist clinicians in the challenging task of detecting SC lesions in people with MS on a combination of sequences commonly acquired in clinical practice. Key PointsQuestionNo tool to help detect MS SC lesions is used in clinical practice despite their frequency and prognostic value.FindingsThis DL-based tool led to improvement in clinicians' sensitivity in detecting SC lesions from both sagittal T2 and STIR sequences, without decreasing precision.Clinical relevanceOur study indicated the potential of a DL-based tool to assist clinicians in the challenging task of detecting SC lesions in people with MS on a combination of sequences commonly acquired in clinical practice. Key PointsQuestionNo tool to help detect MS SC lesions is used in clinical practice despite their frequency and prognostic value.FindingsThis DL-based tool led to improvement in clinicians' sensitivity in detecting SC lesions from both sagittal T2 and STIR sequences, without decreasing precision.Clinical relevanceOur study indicated the potential of a DL-based tool to assist clinicians in the challenging task of detecting SC lesions in people with MS on a combination of sequences commonly acquired in clinical practice.
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