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Diagnostic Performance of Cortical Lesions and the Central Vein Sign in Multiple Sclerosis
Cagol, Alessandro (University of Genova (Gènova, Itàlia))
Cortese, Rosa (University College London Queen Square Institute of Neurology)
Barakovic, Muhamed (University Hospital Basel (Basilea, Suïssa))
Schaedelin, Sabine (University Hospital Basel (Basilea, Suïssa))
Ruberte, Esther (Medical Image Analysis Center (Basel, Suïssa))
Absinta, Martina (San Raffaele Scientific Institute (Milà, Itàlia))
Barkhof, Frederik (Multiple Sclerosis Center Amsterdam)
Calabrese, Massimiliano (University of Verona)
Castellaro, Marco (University of Padova)
Ciccarelli, Olga (University College London Hospitals)
Cocozza, Sirio (Università degli studi di Napoli Federico II)
De Stefano, Nicola (University of Siena. Department of Medicine, Surgery and Neuroscience)
Enzinger, Christian (Medical University of Graz)
Filippi, Massimo (Vita-Salute San Raffaele University (Milà, Itàlia))
Jurynczyk, Maciej (Polish Academy of Sciences (Warsaw, Polònia))
Maggi, Pietro (Université catholique de Louvain (Brusseles, Bèlgica))
Mahmoudi, Nima (Hannover Medical School)
Messina, Silvia (University of Oxford)
Montalban, Xavier (University of Toronto)
Palace, Jacqueline (University of Oxford)
Pontillo, Giuseppe (University of Naples Federico II)
Pröbstel, Anne-Katrin (Departments of Biomedicine and Clinical Research, University Hospital of Basel and University of Basel, Basel, Switzerland)
Rocca, Maria A. (Vita-Salute San Raffaele University (Milà, Itàlia))
Ropele, Stefan (Medical University Graz)
Rovira, Alex (Hospital Universitari Vall d'Hebron)
Schoonheim, Menno M. (Amsterdam UMC. University Medical Center)
Sowa, Piotr (Oslo University Hospital (Oslo, Noruega))
Strijbis, Eva (Multiple Sclerosis Center Amsterdam)
Wattjes, Mike P. (Hannover Medical School)
Sormani, Maria Pia (IRCCS Ospedale Policlinico San Martino (Gènova, Itàlia))
Kappos, Ludwig (University Hospital Basel (Basilea, Suïssa))
Granziera, Cristina (University Hospital Basel (Basilea, Suïssa))

Data: 2023
Resum: Can multiple sclerosis (MS) be differentiated from a wide range of non-MS conditions showing brain white matter lesions using solely imaging biomarkers for cortical lesions (CLs) and central vein sign (CVS)? In this cross-sectional study including 1051 participants, the presence of CLs had high specificity and low sensitivity, while application of the 40% CVS rule resulted in high specificity and moderate sensitivity for MS diagnosis. CVS and CLs outperformed the contribution of infratentorial, periventricular, and juxtacortical lesions in supporting the diagnosis of MS. The findings indicate that CVS and CLs may be valuable tools to increase the accuracy of MS diagnosis. This cross-sectional study evaluates the use of cortical lesions and central vein sign in distinguishing multiple sclerosis from other conditions. Multiple sclerosis (MS) misdiagnosis remains an important issue in clinical practice. To quantify the performance of cortical lesions (CLs) and central vein sign (CVS) in distinguishing MS from other conditions showing brain lesions on magnetic resonance imaging (MRI). This was a retrospective, cross-sectional multicenter study, with clinical and MRI data acquired between January 2010 and May 2020. Centralized MRI analysis was conducted between July 2020 and December 2022 by 2 raters blinded to participants' diagnosis. Participants were recruited from 14 European centers and from a multicenter pan-European cohort. Eligible participants had a diagnosis of MS, clinically isolated syndrome (CIS), or non-MS conditions; availability of a brain 3-T MRI scan with at least 1 sequence suitable for CL and CVS assessment; presence of T2-hyperintense white matter lesions (WMLs). A total of 1051 individuals were included with either MS/CIS (n = 599; 386 [64. 4%] female; mean [SD] age, 41. 5 [12. 3] years) or non-MS conditions (including other neuroinflammatory disorders, cerebrovascular disease, migraine, and incidental WMLs in healthy control individuals; n = 452; 302 [66. 8%] female; mean [SD] age, 49. 2 [14. 5] years). Five individuals were excluded due to missing clinical or demographic information (n = 3) or unclear diagnosis (n = 2). MS/CIS vs non-MS conditions. Area under the receiver operating characteristic curves (AUCs) were used to explore the diagnostic performance of CLs and the CVS in isolation and in combination; sensitivity, specificity, and accuracy were calculated for various cutoffs. The diagnostic importance of CLs and CVS compared to conventional MRI features (ie, presence of infratentorial, periventricular, and juxtacortical WMLs) was ranked with a random forest model. The presence of CLs and the previously proposed 40% CVS rule had a sensitivity, specificity, and accuracy for MS of 59. 0% (95% CI, 55. 1-62. 8), 93. 6% (95% CI, 91. 4-95. 6), and 73. 9% (95% CI, 71. 6-76. 3) and 78. 7% (95% CI, 75. 5-82. 0), 86. 0% (95% CI, 82. 1-89. 5), and 81. 5% (95% CI, 78. 9-83. 7), respectively. The diagnostic performance of the CVS (AUC, 0. 89 [95% CI, 0. 86-0. 91]) was superior to that of CLs (AUC, 0. 77 [95% CI, 0. 75-0. 80]; P < . 001), and was increased when combining the 2 imaging markers (AUC, 0. 92 [95% CI, 0. 90-0. 94]; P = . 04); in the random forest model, both CVS and CLs outperformed the presence of infratentorial, periventricular, and juxtacortical WMLs in supporting MS differential diagnosis. The findings in this study suggest that CVS and CLs may be valuable tools to increase the accuracy of MS diagnosis.
Drets: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Llengua: Anglès
Document: Article ; recerca ; Versió publicada
Publicat a: JAMA Neurology, Vol. 81 (december 2023) , p. 143-153, ISSN 2168-6157

DOI: 10.1001/jamaneurol.2023.4737
PMID: 38079177


11 p, 773.7 KB

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