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 inJournal of neurology Vol. 271; no. 10; pp. 6935 - 6943
Main Authors Callen, Alexis M., Zurawski, Jonathan, Chu, Renxin, Tie, Yanmei, Tauhid, Shahamat, Quattrucci, Molly, Healy, Brian C., Bakshi, Rohit
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg 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
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Keywords Atrophy
Disability
Thalamus
Multiple sclerosis
7 T
MRI
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PublicationTitle Journal of neurology
PublicationTitleAbbrev J Neurol
PublicationTitleAlternate J Neurol
PublicationYear 2024
Publisher Springer Berlin Heidelberg
Springer Nature B.V
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Snippet Background 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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StartPage 6935
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
URI https://link.springer.com/article/10.1007/s00415-024-12656-y
https://www.ncbi.nlm.nih.gov/pubmed/39240345
https://www.proquest.com/docview/3112267613
https://www.proquest.com/docview/3101240306
Volume 271
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