Simultaneous assessment of regional distributions of atrophy across the neuraxis in MS patients
•We present a novel probabilistic brain and neck template to track atrophy.•It allows the simultaneous assessment of brain and spinal cord atrophy.•In MS patients, cervical cord atrophy is linked to impairment.•Our approach improves the utility of MRI to track disease evolution in trials. The abilit...
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Published in | NeuroImage clinical Vol. 34; p. 102985 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Inc
01.01.2022
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 2213-1582 2213-1582 |
DOI | 10.1016/j.nicl.2022.102985 |
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Abstract | •We present a novel probabilistic brain and neck template to track atrophy.•It allows the simultaneous assessment of brain and spinal cord atrophy.•In MS patients, cervical cord atrophy is linked to impairment.•Our approach improves the utility of MRI to track disease evolution in trials.
The ability to assess brain and cord atrophy simultaneously would improve the efficiency of MRI to track disease evolution.
To test a promising tool to simultaneously map the regional distribution of atrophy in multiple sclerosis (MS) patients across the brain and cord.
Voxel-based morphometry combined with a statistical parametric mapping probabilistic brain-spinal cord (SPM-BSC) template was applied to standard T1-weighted magnetic resonance imaging (MRI) scans covering the brain and cervical cord from 37 MS patients and 20 healthy controls (HC). We also measured the cord area at C2-C3 with a semi-automatic segmentation method using (i) the same T1-weighted acquisitions used for the new voxel-based analysis and (ii) dedicated spinal cord phase sensitive inversion recovery (PSIR) acquisitions. Cervical cord findings derived from the three approaches were compared to each other and the goodness to fit to clinical scores was assessed by regression analyses.
The SPM-BSC approach revealed a severity-dependent pattern of atrophy across the cervical cord and thalamus in MS patients when compared to HCs. The magnitude of cord atrophy was confirmed by the semi-automatic extraction approach at C2-C3 using both standard brain T1-weighted and advanced cord dedicated acquisitions. Associations between atrophy of cord and thalamus with disability and cognition were demonstrated.
Atrophy in the brain and cervical cord of MS patients can be identified simultaneously and rapidly at the voxel-level. The SPM-BSC approach yields similar results as available standard processing tools with the added advantage of performing the analysis simultaneously and faster. |
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AbstractList | Background: The ability to assess brain and cord atrophy simultaneously would improve the efficiency of MRI to track disease evolution. Objective: To test a promising tool to simultaneously map the regional distribution of atrophy in multiple sclerosis (MS) patients across the brain and cord. Methods: Voxel-based morphometry combined with a statistical parametric mapping probabilistic brain-spinal cord (SPM-BSC) template was applied to standard T1-weighted magnetic resonance imaging (MRI) scans covering the brain and cervical cord from 37 MS patients and 20 healthy controls (HC). We also measured the cord area at C2-C3 with a semi-automatic segmentation method using (i) the same T1-weighted acquisitions used for the new voxel-based analysis and (ii) dedicated spinal cord phase sensitive inversion recovery (PSIR) acquisitions. Cervical cord findings derived from the three approaches were compared to each other and the goodness to fit to clinical scores was assessed by regression analyses. Results: The SPM-BSC approach revealed a severity-dependent pattern of atrophy across the cervical cord and thalamus in MS patients when compared to HCs. The magnitude of cord atrophy was confirmed by the semi-automatic extraction approach at C2-C3 using both standard brain T1-weighted and advanced cord dedicated acquisitions. Associations between atrophy of cord and thalamus with disability and cognition were demonstrated. Conclusion: Atrophy in the brain and cervical cord of MS patients can be identified simultaneously and rapidly at the voxel-level. The SPM-BSC approach yields similar results as available standard processing tools with the added advantage of performing the analysis simultaneously and faster. The ability to assess brain and cord atrophy simultaneously would improve the efficiency of MRI to track disease evolution. To test a promising tool to simultaneously map the regional distribution of atrophy in multiple sclerosis (MS) patients across the brain and cord. Voxel-based morphometry combined with a statistical parametric mapping probabilistic brain-spinal cord (SPM-BSC) template was applied to standard T1-weighted magnetic resonance imaging (MRI) scans covering the brain and cervical cord from 37 MS patients and 20 healthy controls (HC). We also measured the cord area at C2-C3 with a semi-automatic segmentation method using (i) the same T1-weighted acquisitions used for the new voxel-based analysis and (ii) dedicated spinal cord phase sensitive inversion recovery (PSIR) acquisitions. Cervical cord findings derived from the three approaches were compared to each other and the goodness to fit to clinical scores was assessed by regression analyses. The SPM-BSC approach revealed a severity-dependent pattern of atrophy across the cervical cord and thalamus in MS patients when compared to HCs. The magnitude of cord atrophy was confirmed by the semi-automatic extraction approach at C2-C3 using both standard brain T1-weighted and advanced cord dedicated acquisitions. Associations between atrophy of cord and thalamus with disability and cognition were demonstrated. Atrophy in the brain and cervical cord of MS patients can be identified simultaneously and rapidly at the voxel-level. The SPM-BSC approach yields similar results as available standard processing tools with the added advantage of performing the analysis simultaneously and faster. Highlights•We present a novel probabilistic brain and neck template to track atrophy. •It allows the simultaneous assessment of brain and spinal cord atrophy. •In MS patients, cervical cord atrophy is linked to impairment. •Our approach improves the utility of MRI to track disease evolution in trials. •We present a novel probabilistic brain and neck template to track atrophy.•It allows the simultaneous assessment of brain and spinal cord atrophy.•In MS patients, cervical cord atrophy is linked to impairment.•Our approach improves the utility of MRI to track disease evolution in trials. The ability to assess brain and cord atrophy simultaneously would improve the efficiency of MRI to track disease evolution. To test a promising tool to simultaneously map the regional distribution of atrophy in multiple sclerosis (MS) patients across the brain and cord. Voxel-based morphometry combined with a statistical parametric mapping probabilistic brain-spinal cord (SPM-BSC) template was applied to standard T1-weighted magnetic resonance imaging (MRI) scans covering the brain and cervical cord from 37 MS patients and 20 healthy controls (HC). We also measured the cord area at C2-C3 with a semi-automatic segmentation method using (i) the same T1-weighted acquisitions used for the new voxel-based analysis and (ii) dedicated spinal cord phase sensitive inversion recovery (PSIR) acquisitions. Cervical cord findings derived from the three approaches were compared to each other and the goodness to fit to clinical scores was assessed by regression analyses. The SPM-BSC approach revealed a severity-dependent pattern of atrophy across the cervical cord and thalamus in MS patients when compared to HCs. The magnitude of cord atrophy was confirmed by the semi-automatic extraction approach at C2-C3 using both standard brain T1-weighted and advanced cord dedicated acquisitions. Associations between atrophy of cord and thalamus with disability and cognition were demonstrated. Atrophy in the brain and cervical cord of MS patients can be identified simultaneously and rapidly at the voxel-level. The SPM-BSC approach yields similar results as available standard processing tools with the added advantage of performing the analysis simultaneously and faster. The ability to assess brain and cord atrophy simultaneously would improve the efficiency of MRI to track disease evolution.BACKGROUNDThe ability to assess brain and cord atrophy simultaneously would improve the efficiency of MRI to track disease evolution.To test a promising tool to simultaneously map the regional distribution of atrophy in multiple sclerosis (MS) patients across the brain and cord.OBJECTIVETo test a promising tool to simultaneously map the regional distribution of atrophy in multiple sclerosis (MS) patients across the brain and cord.Voxel-based morphometry combined with a statistical parametric mapping probabilistic brain-spinal cord (SPM-BSC) template was applied to standard T1-weighted magnetic resonance imaging (MRI) scans covering the brain and cervical cord from 37 MS patients and 20 healthy controls (HC). We also measured the cord area at C2-C3 with a semi-automatic segmentation method using (i) the same T1-weighted acquisitions used for the new voxel-based analysis and (ii) dedicated spinal cord phase sensitive inversion recovery (PSIR) acquisitions. Cervical cord findings derived from the three approaches were compared to each other and the goodness to fit to clinical scores was assessed by regression analyses.METHODSVoxel-based morphometry combined with a statistical parametric mapping probabilistic brain-spinal cord (SPM-BSC) template was applied to standard T1-weighted magnetic resonance imaging (MRI) scans covering the brain and cervical cord from 37 MS patients and 20 healthy controls (HC). We also measured the cord area at C2-C3 with a semi-automatic segmentation method using (i) the same T1-weighted acquisitions used for the new voxel-based analysis and (ii) dedicated spinal cord phase sensitive inversion recovery (PSIR) acquisitions. Cervical cord findings derived from the three approaches were compared to each other and the goodness to fit to clinical scores was assessed by regression analyses.The SPM-BSC approach revealed a severity-dependent pattern of atrophy across the cervical cord and thalamus in MS patients when compared to HCs. The magnitude of cord atrophy was confirmed by the semi-automatic extraction approach at C2-C3 using both standard brain T1-weighted and advanced cord dedicated acquisitions. Associations between atrophy of cord and thalamus with disability and cognition were demonstrated.RESULTSThe SPM-BSC approach revealed a severity-dependent pattern of atrophy across the cervical cord and thalamus in MS patients when compared to HCs. The magnitude of cord atrophy was confirmed by the semi-automatic extraction approach at C2-C3 using both standard brain T1-weighted and advanced cord dedicated acquisitions. Associations between atrophy of cord and thalamus with disability and cognition were demonstrated.Atrophy in the brain and cervical cord of MS patients can be identified simultaneously and rapidly at the voxel-level. The SPM-BSC approach yields similar results as available standard processing tools with the added advantage of performing the analysis simultaneously and faster.CONCLUSIONAtrophy in the brain and cervical cord of MS patients can be identified simultaneously and rapidly at the voxel-level. The SPM-BSC approach yields similar results as available standard processing tools with the added advantage of performing the analysis simultaneously and faster. • We present a novel probabilistic brain and neck template to track atrophy. • It allows the simultaneous assessment of brain and spinal cord atrophy. • In MS patients, cervical cord atrophy is linked to impairment. • Our approach improves the utility of MRI to track disease evolution in trials. |
ArticleNumber | 102985 |
Author | Hauser, Stephen L. Henry, Roland G. Papinutto, Nico Azzarito, Michela Kirkish, Gina Ashburner, John Thompson, Alan Freund, Patrick Bischof, Antje |
Author_xml | – sequence: 1 givenname: Patrick surname: Freund fullname: Freund, Patrick email: patrick.freund@balgrist.ch organization: Spinal Cord Injury Center Balgrist, University Hospital Zurich, University of Zurich, Zurich, Switzerland – sequence: 2 givenname: Nico surname: Papinutto fullname: Papinutto, Nico organization: UCSF Weill Institute for Neurosciences, Department of Neurology, University of California San Francisco, San Francisco, CA, USA – sequence: 3 givenname: Antje surname: Bischof fullname: Bischof, Antje organization: UCSF Weill Institute for Neurosciences, Department of Neurology, University of California San Francisco, San Francisco, CA, USA – sequence: 4 givenname: Michela surname: Azzarito fullname: Azzarito, Michela organization: Spinal Cord Injury Center Balgrist, University Hospital Zurich, University of Zurich, Zurich, Switzerland – sequence: 5 givenname: Gina surname: Kirkish fullname: Kirkish, Gina organization: UCSF Weill Institute for Neurosciences, Department of Neurology, University of California San Francisco, San Francisco, CA, USA – sequence: 6 givenname: John surname: Ashburner fullname: Ashburner, John organization: Wellcome Centre for Human Neuroimaging, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom – sequence: 7 givenname: Alan surname: Thompson fullname: Thompson, Alan organization: Departments of Neuroinflammation, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom – sequence: 8 givenname: Stephen L. surname: Hauser fullname: Hauser, Stephen L. organization: UCSF Weill Institute for Neurosciences, Department of Neurology, University of California San Francisco, San Francisco, CA, USA – sequence: 9 givenname: Roland G. surname: Henry fullname: Henry, Roland G. organization: UCSF Weill Institute for Neurosciences, Department of Neurology, University of California San Francisco, San Francisco, CA, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35316667$$D View this record in MEDLINE/PubMed |
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Snippet | •We present a novel probabilistic brain and neck template to track atrophy.•It allows the simultaneous assessment of brain and spinal cord atrophy.•In MS... Highlights•We present a novel probabilistic brain and neck template to track atrophy. •It allows the simultaneous assessment of brain and spinal cord atrophy.... The ability to assess brain and cord atrophy simultaneously would improve the efficiency of MRI to track disease evolution. To test a promising tool to... The ability to assess brain and cord atrophy simultaneously would improve the efficiency of MRI to track disease evolution.BACKGROUNDThe ability to assess... • We present a novel probabilistic brain and neck template to track atrophy. • It allows the simultaneous assessment of brain and spinal cord atrophy. • In MS... Background: The ability to assess brain and cord atrophy simultaneously would improve the efficiency of MRI to track disease evolution. Objective: To test a... |
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SubjectTerms | Atrophy - pathology Cervical Cord - diagnostic imaging Cervical Cord - pathology Humans Magnetic Resonance Imaging - methods Multiple Sclerosis - diagnostic imaging Multiple Sclerosis - pathology Radiology Regular Spinal Cord - pathology |
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Title | Simultaneous assessment of regional distributions of atrophy across the neuraxis in MS patients |
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