Value of 7T MRI and post‐processing in patients with nonlesional 3T MRI undergoing epilepsy presurgical evaluation

Objective Ultra‐high‐field 7‐Tesla (7T) magnetic resonance imaging (MRI) offers increased signal‐to‐noise and contrast‐to‐noise ratios, which may improve visualization of cortical malformations. We aim to assess the clinical value of in vivo structural 7T MRI and its post‐processing for the noninvas...

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Published inEpilepsia (Copenhagen) Vol. 61; no. 11; pp. 2509 - 2520
Main Authors Wang, Irene, Oh, Sehong, Blümcke, Ingmar, Coras, Roland, Krishnan, Balu, Kim, Sanghoon, McBride, Aaron, Grinenko, Olesya, Lin, Yicong, Overmyer, Margit, Aung, Tin Tun, Lowe, Mark, Larvie, Mykol, Alexopoulos, Andreas V., Bingaman, William, Gonzalez‐Martinez, Jorge A., Najm, Imad, Jones, Stephen E.
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.11.2020
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Abstract Objective Ultra‐high‐field 7‐Tesla (7T) magnetic resonance imaging (MRI) offers increased signal‐to‐noise and contrast‐to‐noise ratios, which may improve visualization of cortical malformations. We aim to assess the clinical value of in vivo structural 7T MRI and its post‐processing for the noninvasive identification of epileptic brain lesions in patients with pharmacoresistant epilepsy and nonlesional 3T MRI who are undergoing presurgical evaluation. Methods Sixty‐seven patients were included who had nonlesional 3T MRI by official radiology report. Epilepsy protocols were used for the 3T and 7T acquisitions. Post‐processing of the 7T T1‐weighted magnetization‐prepared two rapid acquisition gradient echoes sequence was performed using the morphometric analysis program (MAP) with comparison to a normal database consisting of 50 healthy controls. Review of 7T was performed by an experienced board‐certified neuroradiologist and at the multimodal patient management conference. The clinical significance of 7T findings was assessed based on intracranial electroencephalography (ICEEG) ictal onset, surgery, postoperative seizure outcomes, and histopathology. Results Unaided visual review of 7T detected previously unappreciated subtle lesions in 22% (15/67). When aided by 7T MAP, the total yield increased to 43% (29/67). The location of the 7T‐identified lesion was identical to or contained within the ICEEG ictal onset in 13 of 16 (81%). Complete resection of the 7T‐identified lesion was associated with seizure freedom (P = .03). Histopathology of the 7T‐identified lesions encountered mainly focal cortical dysplasia (FCD). 7T MAP yielded 25% more lesions (6/24) than 3T MAP, and showed improved conspicuity in 46% (11/24). Significance Our data suggest a major benefit of 7T with post‐processing for detecting subtle FCD lesions for patients with pharmacoresistant epilepsy and nonlesional 3T MRI.
AbstractList Objective Ultra‐high‐field 7‐Tesla (7T) magnetic resonance imaging (MRI) offers increased signal‐to‐noise and contrast‐to‐noise ratios, which may improve visualization of cortical malformations. We aim to assess the clinical value of in vivo structural 7T MRI and its post‐processing for the noninvasive identification of epileptic brain lesions in patients with pharmacoresistant epilepsy and nonlesional 3T MRI who are undergoing presurgical evaluation. Methods Sixty‐seven patients were included who had nonlesional 3T MRI by official radiology report. Epilepsy protocols were used for the 3T and 7T acquisitions. Post‐processing of the 7T T1‐weighted magnetization‐prepared two rapid acquisition gradient echoes sequence was performed using the morphometric analysis program (MAP) with comparison to a normal database consisting of 50 healthy controls. Review of 7T was performed by an experienced board‐certified neuroradiologist and at the multimodal patient management conference. The clinical significance of 7T findings was assessed based on intracranial electroencephalography (ICEEG) ictal onset, surgery, postoperative seizure outcomes, and histopathology. Results Unaided visual review of 7T detected previously unappreciated subtle lesions in 22% (15/67). When aided by 7T MAP, the total yield increased to 43% (29/67). The location of the 7T‐identified lesion was identical to or contained within the ICEEG ictal onset in 13 of 16 (81%). Complete resection of the 7T‐identified lesion was associated with seizure freedom (P = .03). Histopathology of the 7T‐identified lesions encountered mainly focal cortical dysplasia (FCD). 7T MAP yielded 25% more lesions (6/24) than 3T MAP, and showed improved conspicuity in 46% (11/24). Significance Our data suggest a major benefit of 7T with post‐processing for detecting subtle FCD lesions for patients with pharmacoresistant epilepsy and nonlesional 3T MRI.
Ultra-high-field 7-Tesla (7T) magnetic resonance imaging (MRI) offers increased signal-to-noise and contrast-to-noise ratios, which may improve visualization of cortical malformations. We aim to assess the clinical value of in vivo structural 7T MRI and its post-processing for the noninvasive identification of epileptic brain lesions in patients with pharmacoresistant epilepsy and nonlesional 3T MRI who are undergoing presurgical evaluation. Sixty-seven patients were included who had nonlesional 3T MRI by official radiology report. Epilepsy protocols were used for the 3T and 7T acquisitions. Post-processing of the 7T T1-weighted magnetization-prepared two rapid acquisition gradient echoes sequence was performed using the morphometric analysis program (MAP) with comparison to a normal database consisting of 50 healthy controls. Review of 7T was performed by an experienced board-certified neuroradiologist and at the multimodal patient management conference. The clinical significance of 7T findings was assessed based on intracranial electroencephalography (ICEEG) ictal onset, surgery, postoperative seizure outcomes, and histopathology. Unaided visual review of 7T detected previously unappreciated subtle lesions in 22% (15/67). When aided by 7T MAP, the total yield increased to 43% (29/67). The location of the 7T-identified lesion was identical to or contained within the ICEEG ictal onset in 13 of 16 (81%). Complete resection of the 7T-identified lesion was associated with seizure freedom (P = .03). Histopathology of the 7T-identified lesions encountered mainly focal cortical dysplasia (FCD). 7T MAP yielded 25% more lesions (6/24) than 3T MAP, and showed improved conspicuity in 46% (11/24). Our data suggest a major benefit of 7T with post-processing for detecting subtle FCD lesions for patients with pharmacoresistant epilepsy and nonlesional 3T MRI.
ObjectiveUltra‐high‐field 7‐Tesla (7T) magnetic resonance imaging (MRI) offers increased signal‐to‐noise and contrast‐to‐noise ratios, which may improve visualization of cortical malformations. We aim to assess the clinical value of in vivo structural 7T MRI and its post‐processing for the noninvasive identification of epileptic brain lesions in patients with pharmacoresistant epilepsy and nonlesional 3T MRI who are undergoing presurgical evaluation.MethodsSixty‐seven patients were included who had nonlesional 3T MRI by official radiology report. Epilepsy protocols were used for the 3T and 7T acquisitions. Post‐processing of the 7T T1‐weighted magnetization‐prepared two rapid acquisition gradient echoes sequence was performed using the morphometric analysis program (MAP) with comparison to a normal database consisting of 50 healthy controls. Review of 7T was performed by an experienced board‐certified neuroradiologist and at the multimodal patient management conference. The clinical significance of 7T findings was assessed based on intracranial electroencephalography (ICEEG) ictal onset, surgery, postoperative seizure outcomes, and histopathology.ResultsUnaided visual review of 7T detected previously unappreciated subtle lesions in 22% (15/67). When aided by 7T MAP, the total yield increased to 43% (29/67). The location of the 7T‐identified lesion was identical to or contained within the ICEEG ictal onset in 13 of 16 (81%). Complete resection of the 7T‐identified lesion was associated with seizure freedom (P = .03). Histopathology of the 7T‐identified lesions encountered mainly focal cortical dysplasia (FCD). 7T MAP yielded 25% more lesions (6/24) than 3T MAP, and showed improved conspicuity in 46% (11/24).SignificanceOur data suggest a major benefit of 7T with post‐processing for detecting subtle FCD lesions for patients with pharmacoresistant epilepsy and nonlesional 3T MRI.
Abstract Objective Ultra‐high‐field 7‐Tesla (7T) magnetic resonance imaging (MRI) offers increased signal‐to‐noise and contrast‐to‐noise ratios, which may improve visualization of cortical malformations. We aim to assess the clinical value of in vivo structural 7T MRI and its post‐processing for the noninvasive identification of epileptic brain lesions in patients with pharmacoresistant epilepsy and nonlesional 3T MRI who are undergoing presurgical evaluation. Methods Sixty‐seven patients were included who had nonlesional 3T MRI by official radiology report. Epilepsy protocols were used for the 3T and 7T acquisitions. Post‐processing of the 7T T1‐weighted magnetization‐prepared two rapid acquisition gradient echoes sequence was performed using the morphometric analysis program (MAP) with comparison to a normal database consisting of 50 healthy controls. Review of 7T was performed by an experienced board‐certified neuroradiologist and at the multimodal patient management conference. The clinical significance of 7T findings was assessed based on intracranial electroencephalography (ICEEG) ictal onset, surgery, postoperative seizure outcomes, and histopathology. Results Unaided visual review of 7T detected previously unappreciated subtle lesions in 22% (15/67). When aided by 7T MAP, the total yield increased to 43% (29/67). The location of the 7T‐identified lesion was identical to or contained within the ICEEG ictal onset in 13 of 16 (81%). Complete resection of the 7T‐identified lesion was associated with seizure freedom ( P  = .03). Histopathology of the 7T‐identified lesions encountered mainly focal cortical dysplasia (FCD). 7T MAP yielded 25% more lesions (6/24) than 3T MAP, and showed improved conspicuity in 46% (11/24). Significance Our data suggest a major benefit of 7T with post‐processing for detecting subtle FCD lesions for patients with pharmacoresistant epilepsy and nonlesional 3T MRI.
Author Krishnan, Balu
Aung, Tin Tun
Larvie, Mykol
Lowe, Mark
Coras, Roland
Lin, Yicong
Wang, Irene
Oh, Sehong
Kim, Sanghoon
Bingaman, William
Overmyer, Margit
Gonzalez‐Martinez, Jorge A.
Grinenko, Olesya
Jones, Stephen E.
Alexopoulos, Andreas V.
Blümcke, Ingmar
McBride, Aaron
Najm, Imad
AuthorAffiliation 8. Department of Neurosurgery, Cleveland Clinic, Cleveland, OH
6. Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China
1. Epilepsy Center, Cleveland Clinic, Cleveland, OH, USA
3. Imaging Institute, Cleveland Clinic, Cleveland, OH, USA
7. Department of Neurology, Helsinki University Hospital, Helsinki, Finland
4. Institute of Neuropathology, University Hospitals Erlangen, Erlangen, Germany
5. Cleveland Clinic Lerner College of Medicine, Cleveland Clinic, Cleveland, OH, USA
2. Division of Biomedical Engineering, Hankuk University of Foreign Studies, Yongin, Republic of Korea
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– name: 2. Division of Biomedical Engineering, Hankuk University of Foreign Studies, Yongin, Republic of Korea
– name: 3. Imaging Institute, Cleveland Clinic, Cleveland, OH, USA
– name: 6. Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China
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2020 International League Against Epilepsy.
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Issue 11
Keywords focal cortical dysplasia
presurgical evaluation
MRI
ultra-high field
7T
nonlesional
Language English
License 2020 International League Against Epilepsy.
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PublicationCentury 2000
PublicationDate November 2020
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PublicationTitle Epilepsia (Copenhagen)
PublicationTitleAlternate Epilepsia
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Publisher Wiley Subscription Services, Inc
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References 2015; 79
2008; 191
2018; 28
2010; 75
2017; 2
2018; 140
2006; 32
2017; 27
2015; 77
2019; 14
2013; 106
1995; 118
2011; 52
1996
2005; 65
2016; 51
2001; 49
2016; 18
2018; 44
2017; 377
2014; 83
2011; 134
2005; 67
2016; 57
2011; 7
2012; 53
2001; 42
2010; 49
2016; 3
2019; 21
2008; 49
2006; 47
2019; 26
2002; 43
2017; 12
2018; 91
2016; 139
2016; 116
2020; 22
2018; 54
2017; 168
2018; 59
2019; 175
2014; 75
33033406 - Nat Rev Neurol. 2020 Dec;16(12):654
33236772 - Epilepsia. 2021 Jan;62(1):281
33236780 - Epilepsia. 2021 Jan;62(1):279-280
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Snippet Objective Ultra‐high‐field 7‐Tesla (7T) magnetic resonance imaging (MRI) offers increased signal‐to‐noise and contrast‐to‐noise ratios, which may improve...
Ultra-high-field 7-Tesla (7T) magnetic resonance imaging (MRI) offers increased signal-to-noise and contrast-to-noise ratios, which may improve visualization...
Abstract Objective Ultra‐high‐field 7‐Tesla (7T) magnetic resonance imaging (MRI) offers increased signal‐to‐noise and contrast‐to‐noise ratios, which may...
ObjectiveUltra‐high‐field 7‐Tesla (7T) magnetic resonance imaging (MRI) offers increased signal‐to‐noise and contrast‐to‐noise ratios, which may improve...
OBJECTIVEUltra-high-field 7-Tesla (7T) magnetic resonance imaging (MRI) offers increased signal-to-noise and contrast-to-noise ratios, which may improve...
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SubjectTerms Adolescent
Adult
Child
Clinical significance
Cohort Studies
Convulsions & seizures
Drug Resistant Epilepsy - diagnostic imaging
Drug Resistant Epilepsy - physiopathology
Drug Resistant Epilepsy - surgery
Dysplasia
EEG
Electroencephalography - methods
Electroencephalography - standards
Epilepsy
Female
focal cortical dysplasia
Histopathology
Humans
Lesions
Magnetic resonance imaging
Magnetic Resonance Imaging - methods
Magnetic Resonance Imaging - standards
Male
Middle Aged
Morphometry
MRI
Neuroimaging
nonlesional
Patients
Preoperative Care - methods
Preoperative Care - standards
presurgical evaluation
Prospective Studies
Seizures
Surgery
ultra‐high field
Young Adult
Title Value of 7T MRI and post‐processing in patients with nonlesional 3T MRI undergoing epilepsy presurgical evaluation
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fepi.16682
https://www.ncbi.nlm.nih.gov/pubmed/32949471
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https://pubmed.ncbi.nlm.nih.gov/PMC7722133
Volume 61
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