The role of 7 T MRI to assess atrophy of the subcortical deep gray matter in relapsing–remitting multiple sclerosis
Background Deep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS). Objective To optimize automated segmentation for 7 T DGM volumetrics and assess sensitivity to atrophy and relationship to DGM lesions and disability in relapsing–remitting (RR) MS. Methods 30 RRMS subjects [...
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Published in | Journal of neurology Vol. 271; no. 10; pp. 6935 - 6943 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Springer Berlin Heidelberg
01.10.2024
Springer Nature B.V |
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Abstract | Background
Deep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS).
Objective
To optimize automated segmentation for 7 T DGM volumetrics and assess sensitivity to atrophy and relationship to DGM lesions and disability in relapsing–remitting (RR) MS.
Methods
30 RRMS subjects [mean age 44.0 years, median Expanded Disability Status Scale (EDSS) score 2] and 14 healthy controls underwent 7 T MRI with 3D magnetization-prepared 2 rapid gradient-echoes (MP2RAGE) and fluid-attenuated inversion recovery. Customizing an automated pipeline to assess DGM structure volumes required pre-processing combining two MP2RAGE inversion times and uniform T1 images, and noise-suppressed reconstruction. DGM volumes were normalized. Brain DGM lesions and white matter T2 lesion volume (T2LV) were expert-quantified. Spearman correlations and Wilcoxon rank-sum tests were assessed.
Results
DGM lesions were found in 77% (
n
= 23) of MS subjects and no controls, with thalamic lesions most prevalent (73%). An average of 3.6 DGM lesions was found per person with MS. Total DGM volumes were lower in MS vs. controls (
p
= 0.034), varying by region, most pronounced in the caudate (
p
= 0.008). DGM volumes inversely correlated with EDSS (total DGM:
r
= – 0.45,
p
= 0.014; globus pallidus:
r
= – 0.42,
p
= 0.023; putamen:
r
= – 0.44,
p
= 0.016; caudate:
r
= – 0.37,
p
= 0.047) and T2LV (total DGM:
r
= – 0.53,
p
= 0.003; putamen:
r
= – 0.40,
p
= 0.030; thalamus:
r
= – 0.63,
p
< 0.001). DGM atrophy was most closely linked to disability among all MRI measures. Thalamic lesion volume correlated inversely with thalamic volume (
r
= – 0.38,
p
= 0.045).
Conclusion
7 T MRI shows a link between DGM atrophy and both white matter lesions and physical disability in RRMS. Thalamic lesions are associated with thalamic atrophy. |
---|---|
AbstractList | Deep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS).
To optimize automated segmentation for 7 T DGM volumetrics and assess sensitivity to atrophy and relationship to DGM lesions and disability in relapsing-remitting (RR) MS.
30 RRMS subjects [mean age 44.0 years, median Expanded Disability Status Scale (EDSS) score 2] and 14 healthy controls underwent 7 T MRI with 3D magnetization-prepared 2 rapid gradient-echoes (MP2RAGE) and fluid-attenuated inversion recovery. Customizing an automated pipeline to assess DGM structure volumes required pre-processing combining two MP2RAGE inversion times and uniform T1 images, and noise-suppressed reconstruction. DGM volumes were normalized. Brain DGM lesions and white matter T2 lesion volume (T2LV) were expert-quantified. Spearman correlations and Wilcoxon rank-sum tests were assessed.
DGM lesions were found in 77% (n = 23) of MS subjects and no controls, with thalamic lesions most prevalent (73%). An average of 3.6 DGM lesions was found per person with MS. Total DGM volumes were lower in MS vs. controls (p = 0.034), varying by region, most pronounced in the caudate (p = 0.008). DGM volumes inversely correlated with EDSS (total DGM: r = - 0.45, p = 0.014; globus pallidus: r = - 0.42, p = 0.023; putamen: r = - 0.44, p = 0.016; caudate: r = - 0.37, p = 0.047) and T2LV (total DGM: r = - 0.53, p = 0.003; putamen: r = - 0.40, p = 0.030; thalamus: r = - 0.63, p < 0.001). DGM atrophy was most closely linked to disability among all MRI measures. Thalamic lesion volume correlated inversely with thalamic volume (r = - 0.38, p = 0.045).
7 T MRI shows a link between DGM atrophy and both white matter lesions and physical disability in RRMS. Thalamic lesions are associated with thalamic atrophy. Background Deep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS). Objective To optimize automated segmentation for 7 T DGM volumetrics and assess sensitivity to atrophy and relationship to DGM lesions and disability in relapsing–remitting (RR) MS. Methods 30 RRMS subjects [mean age 44.0 years, median Expanded Disability Status Scale (EDSS) score 2] and 14 healthy controls underwent 7 T MRI with 3D magnetization-prepared 2 rapid gradient-echoes (MP2RAGE) and fluid-attenuated inversion recovery. Customizing an automated pipeline to assess DGM structure volumes required pre-processing combining two MP2RAGE inversion times and uniform T1 images, and noise-suppressed reconstruction. DGM volumes were normalized. Brain DGM lesions and white matter T2 lesion volume (T2LV) were expert-quantified. Spearman correlations and Wilcoxon rank-sum tests were assessed. Results DGM lesions were found in 77% ( n = 23) of MS subjects and no controls, with thalamic lesions most prevalent (73%). An average of 3.6 DGM lesions was found per person with MS. Total DGM volumes were lower in MS vs. controls ( p = 0.034), varying by region, most pronounced in the caudate ( p = 0.008). DGM volumes inversely correlated with EDSS (total DGM: r = – 0.45, p = 0.014; globus pallidus: r = – 0.42, p = 0.023; putamen: r = – 0.44, p = 0.016; caudate: r = – 0.37, p = 0.047) and T2LV (total DGM: r = – 0.53, p = 0.003; putamen: r = – 0.40, p = 0.030; thalamus: r = – 0.63, p < 0.001). DGM atrophy was most closely linked to disability among all MRI measures. Thalamic lesion volume correlated inversely with thalamic volume ( r = – 0.38, p = 0.045). Conclusion 7 T MRI shows a link between DGM atrophy and both white matter lesions and physical disability in RRMS. Thalamic lesions are associated with thalamic atrophy. Deep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS).BACKGROUNDDeep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS).To optimize automated segmentation for 7 T DGM volumetrics and assess sensitivity to atrophy and relationship to DGM lesions and disability in relapsing-remitting (RR) MS.OBJECTIVETo optimize automated segmentation for 7 T DGM volumetrics and assess sensitivity to atrophy and relationship to DGM lesions and disability in relapsing-remitting (RR) MS.30 RRMS subjects [mean age 44.0 years, median Expanded Disability Status Scale (EDSS) score 2] and 14 healthy controls underwent 7 T MRI with 3D magnetization-prepared 2 rapid gradient-echoes (MP2RAGE) and fluid-attenuated inversion recovery. Customizing an automated pipeline to assess DGM structure volumes required pre-processing combining two MP2RAGE inversion times and uniform T1 images, and noise-suppressed reconstruction. DGM volumes were normalized. Brain DGM lesions and white matter T2 lesion volume (T2LV) were expert-quantified. Spearman correlations and Wilcoxon rank-sum tests were assessed.METHODS30 RRMS subjects [mean age 44.0 years, median Expanded Disability Status Scale (EDSS) score 2] and 14 healthy controls underwent 7 T MRI with 3D magnetization-prepared 2 rapid gradient-echoes (MP2RAGE) and fluid-attenuated inversion recovery. Customizing an automated pipeline to assess DGM structure volumes required pre-processing combining two MP2RAGE inversion times and uniform T1 images, and noise-suppressed reconstruction. DGM volumes were normalized. Brain DGM lesions and white matter T2 lesion volume (T2LV) were expert-quantified. Spearman correlations and Wilcoxon rank-sum tests were assessed.DGM lesions were found in 77% (n = 23) of MS subjects and no controls, with thalamic lesions most prevalent (73%). An average of 3.6 DGM lesions was found per person with MS. Total DGM volumes were lower in MS vs. controls (p = 0.034), varying by region, most pronounced in the caudate (p = 0.008). DGM volumes inversely correlated with EDSS (total DGM: r = - 0.45, p = 0.014; globus pallidus: r = - 0.42, p = 0.023; putamen: r = - 0.44, p = 0.016; caudate: r = - 0.37, p = 0.047) and T2LV (total DGM: r = - 0.53, p = 0.003; putamen: r = - 0.40, p = 0.030; thalamus: r = - 0.63, p < 0.001). DGM atrophy was most closely linked to disability among all MRI measures. Thalamic lesion volume correlated inversely with thalamic volume (r = - 0.38, p = 0.045).RESULTSDGM lesions were found in 77% (n = 23) of MS subjects and no controls, with thalamic lesions most prevalent (73%). An average of 3.6 DGM lesions was found per person with MS. Total DGM volumes were lower in MS vs. controls (p = 0.034), varying by region, most pronounced in the caudate (p = 0.008). DGM volumes inversely correlated with EDSS (total DGM: r = - 0.45, p = 0.014; globus pallidus: r = - 0.42, p = 0.023; putamen: r = - 0.44, p = 0.016; caudate: r = - 0.37, p = 0.047) and T2LV (total DGM: r = - 0.53, p = 0.003; putamen: r = - 0.40, p = 0.030; thalamus: r = - 0.63, p < 0.001). DGM atrophy was most closely linked to disability among all MRI measures. Thalamic lesion volume correlated inversely with thalamic volume (r = - 0.38, p = 0.045).7 T MRI shows a link between DGM atrophy and both white matter lesions and physical disability in RRMS. Thalamic lesions are associated with thalamic atrophy.CONCLUSION7 T MRI shows a link between DGM atrophy and both white matter lesions and physical disability in RRMS. Thalamic lesions are associated with thalamic atrophy. BackgroundDeep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS).ObjectiveTo optimize automated segmentation for 7 T DGM volumetrics and assess sensitivity to atrophy and relationship to DGM lesions and disability in relapsing–remitting (RR) MS.Methods30 RRMS subjects [mean age 44.0 years, median Expanded Disability Status Scale (EDSS) score 2] and 14 healthy controls underwent 7 T MRI with 3D magnetization-prepared 2 rapid gradient-echoes (MP2RAGE) and fluid-attenuated inversion recovery. Customizing an automated pipeline to assess DGM structure volumes required pre-processing combining two MP2RAGE inversion times and uniform T1 images, and noise-suppressed reconstruction. DGM volumes were normalized. Brain DGM lesions and white matter T2 lesion volume (T2LV) were expert-quantified. Spearman correlations and Wilcoxon rank-sum tests were assessed.ResultsDGM lesions were found in 77% (n = 23) of MS subjects and no controls, with thalamic lesions most prevalent (73%). An average of 3.6 DGM lesions was found per person with MS. Total DGM volumes were lower in MS vs. controls (p = 0.034), varying by region, most pronounced in the caudate (p = 0.008). DGM volumes inversely correlated with EDSS (total DGM: r = – 0.45, p = 0.014; globus pallidus: r = – 0.42, p = 0.023; putamen: r = – 0.44, p = 0.016; caudate: r = – 0.37, p = 0.047) and T2LV (total DGM: r = – 0.53, p = 0.003; putamen: r = – 0.40, p = 0.030; thalamus: r = – 0.63, p < 0.001). DGM atrophy was most closely linked to disability among all MRI measures. Thalamic lesion volume correlated inversely with thalamic volume (r = – 0.38, p = 0.045).Conclusion7 T MRI shows a link between DGM atrophy and both white matter lesions and physical disability in RRMS. Thalamic lesions are associated with thalamic atrophy. |
Author | Zurawski, Jonathan Tie, Yanmei Bakshi, Rohit Tauhid, Shahamat Chu, Renxin Healy, Brian C. Callen, Alexis M. Quattrucci, Molly |
Author_xml | – sequence: 1 givenname: Alexis M. surname: Callen fullname: Callen, Alexis M. organization: Department of Neurology, Brigham Multiple Sclerosis Center, Brigham and Women’s Hospital, Harvard Medical School – sequence: 2 givenname: Jonathan surname: Zurawski fullname: Zurawski, Jonathan organization: Department of Neurology, Brigham Multiple Sclerosis Center, Brigham and Women’s Hospital, Harvard Medical School – sequence: 3 givenname: Renxin surname: Chu fullname: Chu, Renxin organization: Department of Neurology, Brigham Multiple Sclerosis Center, Brigham and Women’s Hospital, Harvard Medical School – sequence: 4 givenname: Yanmei surname: Tie fullname: Tie, Yanmei organization: Department of Neurosurgery, Brigham and Women’s Hospital, Harvard Medical School – sequence: 5 givenname: Shahamat surname: Tauhid fullname: Tauhid, Shahamat organization: Department of Neurology, Brigham Multiple Sclerosis Center, Brigham and Women’s Hospital, Harvard Medical School – sequence: 6 givenname: Molly surname: Quattrucci fullname: Quattrucci, Molly organization: Department of Neurology, Brigham Multiple Sclerosis Center, Brigham and Women’s Hospital, Harvard Medical School – sequence: 7 givenname: Brian C. surname: Healy fullname: Healy, Brian C. organization: Department of Neurology, Brigham Multiple Sclerosis Center, Brigham and Women’s Hospital, Harvard Medical School – sequence: 8 givenname: Rohit orcidid: 0000-0001-8601-5534 surname: Bakshi fullname: Bakshi, Rohit email: rbakshi@post.harvard.edu organization: Department of Neurology, Brigham Multiple Sclerosis Center, Brigham and Women’s Hospital, Harvard Medical School, Department of Radiology, Brigham and Women’s Hospital, Harvard Medical School |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39240345$$D View this record in MEDLINE/PubMed |
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Keywords | Atrophy Disability Thalamus Multiple sclerosis 7 T MRI |
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Deep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS).
Objective
To optimize automated segmentation for 7 T DGM... Deep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS). To optimize automated segmentation for 7 T DGM volumetrics and assess... BackgroundDeep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS).ObjectiveTo optimize automated segmentation for 7 T DGM volumetrics... Deep gray matter (DGM) atrophy and lesions are found in multiple sclerosis (MS).BACKGROUNDDeep gray matter (DGM) atrophy and lesions are found in multiple... |
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SubjectTerms | Adult Atrophy Atrophy - pathology Automation Brain - diagnostic imaging Brain - pathology Disability Evaluation Female Globus pallidus Gray Matter - diagnostic imaging Gray Matter - pathology Humans Image processing Image Processing, Computer-Assisted Lesions Magnetic Resonance Imaging Male Medicine Medicine & Public Health Middle Aged Multiple sclerosis Multiple Sclerosis, Relapsing-Remitting - diagnostic imaging Multiple Sclerosis, Relapsing-Remitting - pathology Neurology Neuroradiology Neurosciences Original Communication Putamen Substantia alba Substantia grisea Thalamus |
Title | The role of 7 T MRI to assess atrophy of the subcortical deep gray matter in relapsing–remitting multiple sclerosis |
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