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Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Development and validation of a simple and practical method for differentiating MS from other neuroinflammatory
1NYU MS Comprehensive Care Center, Department of Neurology, New York University Grossman School of Medicine, New York, NY, USA.
Abstract:
There is an unmet need to develop practical methods for differentiating multiple sclerosis (MS) from other neuroinflammatory disorders using standard brain MRI. To develop a practical approach for differentiating MS from neuromyelitis optica spectrum disorder (NMOSD) and MOG antibody-associated disorder (MOGAD) with brain MRI, we first identified lesion locations in the brain that are suggestive of MS-associated demyelination ("MS Lesion Checklist") and compared frequencies of brain lesions in the "MS Lesion Checklist" locations in a development sample of patients (n = 82) with clinically definite MS, NMOSD, and MOGAD. Patients with MS were more likely than patients with non-MS to have lesions in 3 locations only: anterior temporal horn (p < 0.0001), periventricular ("Dawson's finger") (p < 0.0001), and cerebellar hemisphere (p = 0.02). These three lesion locations were used as predictor variables in a multivariable regression model for discriminating MS from non-MS. The model had area under the curve (AUC) of 0.853 (95% confidence interval: 0.76-0.945), sensitivity of 87.1%, and specificity of 72.5%. We then used an independent validation sample with equal representation of MS and NMOSD/MOGAD cases (n = 97) to validate our prediction model. In the validation sample, the model was 76.3% accurate in discriminating MS from non-MS. Our simple method for predicting MS versus NMOSD/MOGAD only requires a neuroradiologist or clinician to ascertain the presence of lesions in three locations on conventional MRI sequences. It can therefore be readily applied in the real-world setting for training and clinical practice.
Insights
Differentiating multiple sclerosis (MS) from other neuroinflammatory disorders like neuromyelitis optica spectrum disorder (NMOSD) and MOG antibody-associated disorder (MOGAD) is crucial. A simple MRI checklist identifying lesions in three specific brain locations can effectively predict MS presence.
Area of Science:
- Neuroimaging
- Neurology
- Radiology
Background:
- Accurate differentiation of multiple sclerosis (MS) from other neuroinflammatory disorders is challenging using standard brain MRI.
- Existing diagnostic methods often require advanced techniques or invasive procedures.
Purpose of the Study:
- To develop and validate a practical MRI-based method for distinguishing MS from neuromyelitis optica spectrum disorder (NMOSD) and MOG antibody-associated disorder (MOGAD).
- To identify specific brain lesion locations indicative of MS.
Main Methods:
- Identification of "MS Lesion Checklist" locations suggestive of MS demyelination.
- Comparison of lesion frequencies in these locations between MS, NMOSD, and MOGAD patient groups (n=82).
- Development of a multivariable regression model using three key lesion locations (anterior temporal horn, periventricular, cerebellar hemisphere) to predict MS.
Main Results:
- Lesions in the anterior temporal horn, periventricular white matter (Dawson's fingers), and cerebellar hemispheres were significantly more frequent in MS patients.
- The prediction model achieved an Area Under the Curve (AUC) of 0.853 in the development sample.
- The model demonstrated 76.3% accuracy in an independent validation sample (n=97).
Conclusions:
- A simple MRI checklist focusing on three specific lesion locations can reliably differentiate MS from NMOSD and MOGAD.
- This method is practical for routine clinical use and training, enhancing diagnostic accuracy in neuroinflammatory conditions.
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