Sneha Senthil, Ian Tagge, Dumitru Fetco, Cheng Hsun Hsieh, Haz-Edine Assemlal, Zahra Karimaghaloo, Emily Fetco, G R Wayne Moore, Douglas L Arnold, David A Rudko, Sridar Narayanan
Background: Recent studies suggest that disruptions of the blood-cerebrospinal fluid (CSF) barrier within the choroid plexus (ChP) may contribute to multiple sclerosis (MS) pathogenesis. We investigated the relationship between a quantitative marker of ChP enhancement and markers of focal and diffuse brain tissue injury in MS.
Methods: A group of 34 MS participants and 21 healthy participants underwent 7T MRI including magnetization prepared 2 rapid acquisition gradient echoes (MP2RAGE) and fluid attenuated inversion recovery (FLAIR) acquisitions. The MS group received contrast, and delta T1 (ΔT1) maps were computed to assess enhancement. ChP, white matter lesions (WML), normal-appearing white matter (NAWM), and gray matter (GM) were segmented. Pre-contrast quantitative T1 (qT1) values were compared between groups, and linear regression with mean ChP ΔT1 was performed for WML volume and pre-gadolinium (Gd) mean qT1 of WML, NAWM, and GM.
Results: Mean qT1 of ChP, NAWM, and GM, as well as ChP volume, were higher in MS compared to controls (p < 0.001). ChP ΔT1 was significantly associated with pre-Gd qT1 of NAWM (β = 0.20, R2 = 0.54, p < 0.001) and GM (β = 0.18, R2 = 0.49, p < 0.001), but not WML volume (p = 0.3) or WML qT1 (p = 0.05).
Conclusions: The association between ChP enhancement and diffuse tissue injury, together with elevated qT1 values and ChP volumes in MS, supports a mechanism of brain injury involving CSF-mediated toxicity distinct from classic lesion pathology in MS.
{"title":"Quantitative Choroid Plexus Gadolinium Enhancement Is Related to Diffuse Brain Tissue Injury in Multiple Sclerosis.","authors":"Sneha Senthil, Ian Tagge, Dumitru Fetco, Cheng Hsun Hsieh, Haz-Edine Assemlal, Zahra Karimaghaloo, Emily Fetco, G R Wayne Moore, Douglas L Arnold, David A Rudko, Sridar Narayanan","doi":"10.1111/jon.70132","DOIUrl":"10.1111/jon.70132","url":null,"abstract":"<p><strong>Background: </strong>Recent studies suggest that disruptions of the blood-cerebrospinal fluid (CSF) barrier within the choroid plexus (ChP) may contribute to multiple sclerosis (MS) pathogenesis. We investigated the relationship between a quantitative marker of ChP enhancement and markers of focal and diffuse brain tissue injury in MS.</p><p><strong>Methods: </strong>A group of 34 MS participants and 21 healthy participants underwent 7T MRI including magnetization prepared 2 rapid acquisition gradient echoes (MP2RAGE) and fluid attenuated inversion recovery (FLAIR) acquisitions. The MS group received contrast, and delta T1 (ΔT1) maps were computed to assess enhancement. ChP, white matter lesions (WML), normal-appearing white matter (NAWM), and gray matter (GM) were segmented. Pre-contrast quantitative T1 (qT1) values were compared between groups, and linear regression with mean ChP ΔT1 was performed for WML volume and pre-gadolinium (Gd) mean qT1 of WML, NAWM, and GM.</p><p><strong>Results: </strong>Mean qT1 of ChP, NAWM, and GM, as well as ChP volume, were higher in MS compared to controls (p < 0.001). ChP ΔT1 was significantly associated with pre-Gd qT1 of NAWM (β = 0.20, R<sup>2</sup> = 0.54, p < 0.001) and GM (β = 0.18, R<sup>2</sup> = 0.49, p < 0.001), but not WML volume (p = 0.3) or WML qT1 (p = 0.05).</p><p><strong>Conclusions: </strong>The association between ChP enhancement and diffuse tissue injury, together with elevated qT1 values and ChP volumes in MS, supports a mechanism of brain injury involving CSF-mediated toxicity distinct from classic lesion pathology in MS.</p>","PeriodicalId":16399,"journal":{"name":"Journal of Neuroimaging","volume":"36 2","pages":"e70132"},"PeriodicalIF":2.3,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12972605/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147390300","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ngoc Mai Le, Joseph Samaha, Ananya S Iyyangar, Javier Gomez-Farias, Bruna Kfoury, Ritesh Bajaj, Connor Nguyen, Syed Shams, Camille Neal-Harris, Emmanuel Ebirim, Hussain Azeem, Anjan N Ballekere, Saagar Dhanjani, Eunyoung Lee, Luca Giancardo, Sunil A Sheth
Background and purpose: We evaluated agreement and performance of non-contrast head-computerized tomography (NCHCT) and CT-perfusion (CTP) in identifying large core infarct in acute ischemic stroke (AIS) due to large vessel occlusion (LVO) undergoing endovascular therapy (EVT), using MRI as reference.
Methods: From our prospective multicenter registry, we identified patients with LVO-AIS due to internal carotid artery or middle cerebral artery M1occlusions who underwent EVT between 2017 and 2024. Final infarct volume (FIV) was defined using 24-48 h post-EVT diffusion-weighted imaging magnetic resonance imaging (MRI-FIV). To limit infarct growth bias, only patients with CTP-to-EVT start time <3 h were included. Large core infarct was defined at FIV thresholds: 50, 70, and 100 mL. The primary outcome was agreement between NCHCT and CTP in identifying large core infarct using kappa-statistics. Large core was considered if NCHCT-ASPECTS<6 or rCBF<30% volume>70 mL on CTP (RAPID/Viz.AI). Secondary outcomes included classification accuracy of each modality relative to MRI-FIV using the area under the receiver operating characteristic curve (AUC-ROC). Sensitivity analyses were performed in subgroups with TICI 2c-3 and cases processed by RAPID.
Results: Among 241 EVT-treated LVO-AIS patients, median NIHSS was 15 [IQR: 10-20], MRI-FIV 13.8 Ml [IQR: 5-41.0], ASPECTS 8 [IQR: 7-10], and CTP-predicted core 8 mL [IQR: 0-31.0]. CTP and NCHCT showed slight agreement in identifying large core (κ = 0.192) and weak-to-acceptable discrimination for identifying large core infarcts (AUC-ROC: 0.61-0.72 across MRI-FIV thresholds). Both modalities showed limited predictive ability for 90-day functional independence (AUC-ROC: 0.63-0.65). Similar findings were observed in sensitivity analyses.
Conclusions: Among LVO-AIS EVT-treated patients, NCHCT and CTP demonstrated slight agreement in classifying small versus large core, and neither technique was effective at predicting FIV or clinical outcomes.
背景和目的:我们以MRI为参考,评估了非对比头部计算机断层扫描(NCHCT)和ct灌注(CTP)在识别血管内治疗(EVT)大血管闭塞(LVO)引起的急性缺血性卒中(AIS)大核心梗死的一致性和性能。方法:从我们的前瞻性多中心注册表中,我们确定了2017年至2024年间因颈内动脉或大脑中动脉m1闭塞而接受EVT的LVO-AIS患者。最终梗死体积(FIV)采用evt后24-48小时弥散加权成像磁共振成像(MRI-FIV)确定。为了限制梗死生长偏倚,只有CTP- To - evt开始时间为70 mL的患者使用CTP (RAPID/Viz.AI)。次要结果包括使用受试者工作特征曲线(AUC-ROC)下的面积相对于MRI-FIV的每种模式的分类准确性。对TICI 2c-3亚组和RAPID处理病例进行敏感性分析。结果:241例evt治疗的LVO-AIS患者中位NIHSS为15 [IQR: 10-20], MRI-FIV为13.8 Ml [IQR: 5-41.0], ASPECTS为8 [IQR: 7-10], ctp预测的core为8 Ml [IQR: 0-31.0]。CTP和NCHCT在识别大核心梗死方面表现出轻微的一致性(κ = 0.192),而在识别大核心梗死方面表现出弱至可接受的区别(AUC-ROC: 0.61-0.72, MRI-FIV阈值)。两种方法对90天功能独立的预测能力有限(AUC-ROC: 0.63-0.65)。在敏感性分析中也观察到类似的结果。结论:在LVO-AIS evt治疗的患者中,NCHCT和CTP对小核和大核的分类略有一致,两种技术都不能有效预测FIV或临床结果。
{"title":"Defining Large Core Infarction: Comparing the Accuracy of Non-Contrast CT ASPECTS Versus CT Perfusion Core Volume.","authors":"Ngoc Mai Le, Joseph Samaha, Ananya S Iyyangar, Javier Gomez-Farias, Bruna Kfoury, Ritesh Bajaj, Connor Nguyen, Syed Shams, Camille Neal-Harris, Emmanuel Ebirim, Hussain Azeem, Anjan N Ballekere, Saagar Dhanjani, Eunyoung Lee, Luca Giancardo, Sunil A Sheth","doi":"10.1111/jon.70130","DOIUrl":"10.1111/jon.70130","url":null,"abstract":"<p><strong>Background and purpose: </strong>We evaluated agreement and performance of non-contrast head-computerized tomography (NCHCT) and CT-perfusion (CTP) in identifying large core infarct in acute ischemic stroke (AIS) due to large vessel occlusion (LVO) undergoing endovascular therapy (EVT), using MRI as reference.</p><p><strong>Methods: </strong>From our prospective multicenter registry, we identified patients with LVO-AIS due to internal carotid artery or middle cerebral artery M1occlusions who underwent EVT between 2017 and 2024. Final infarct volume (FIV) was defined using 24-48 h post-EVT diffusion-weighted imaging magnetic resonance imaging (MRI-FIV). To limit infarct growth bias, only patients with CTP-to-EVT start time <3 h were included. Large core infarct was defined at FIV thresholds: 50, 70, and 100 mL. The primary outcome was agreement between NCHCT and CTP in identifying large core infarct using kappa-statistics. Large core was considered if NCHCT-ASPECTS<6 or rCBF<30% volume>70 mL on CTP (RAPID/Viz.AI). Secondary outcomes included classification accuracy of each modality relative to MRI-FIV using the area under the receiver operating characteristic curve (AUC-ROC). Sensitivity analyses were performed in subgroups with TICI 2c-3 and cases processed by RAPID.</p><p><strong>Results: </strong>Among 241 EVT-treated LVO-AIS patients, median NIHSS was 15 [IQR: 10-20], MRI-FIV 13.8 Ml [IQR: 5-41.0], ASPECTS 8 [IQR: 7-10], and CTP-predicted core 8 mL [IQR: 0-31.0]. CTP and NCHCT showed slight agreement in identifying large core (κ = 0.192) and weak-to-acceptable discrimination for identifying large core infarcts (AUC-ROC: 0.61-0.72 across MRI-FIV thresholds). Both modalities showed limited predictive ability for 90-day functional independence (AUC-ROC: 0.63-0.65). Similar findings were observed in sensitivity analyses.</p><p><strong>Conclusions: </strong>Among LVO-AIS EVT-treated patients, NCHCT and CTP demonstrated slight agreement in classifying small versus large core, and neither technique was effective at predicting FIV or clinical outcomes.</p>","PeriodicalId":16399,"journal":{"name":"Journal of Neuroimaging","volume":"36 2","pages":"e70130"},"PeriodicalIF":2.3,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12937044/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147290117","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yunjia Ni, Shawn M Stevens, Trenton House, Ashton Huppert Steed, Alma Jukic, Parvathy Hareesh, Anthony M Asher, Kaith K Almefty, Kris A Smith, Randall W Porter, Michael T Lawton, Richard D Dortch
Background: Facial nerve (CN VII) diffusion MR tractography is considered as a useful adjunct in pre-operative planning prior to vestibular schwannoma (VS) resection, especially in larger (Koos Grade III/IV) tumors. Since 2016, several systematic reviews have investigated the clinical value of CN VII tractography in VS, and all reported a "success rate" of at least 87% for predicting the pre-operative CN VII position. Yet in clinical practice, CN VII tractography has not yet been widely adopted into routine clinical practice. We suspected that underlying methodology and reporting metrics for existing tractography algorithms may be overestimating success rate. This motivated us to revisit the literature from a different perspective to unravel the caveats and nuances behind this technology.
Methods: We screened all published works on PubMed related to pre-operative CN VII tractography in VS. Twenty-two studies were reviewed in detail.
Results: We observed a strikingly high heterogeneity in tractography protocols in all domains of the tractography acquisition and analysis pipeline across studies.
Conclusions: These findings suggest that the reliability and reproducibility of CN VII tractography in large VS has been overestimated. We believe that employing standardized reporting metrics, including sensitivity, true predictive value, and false discovery rate, would increase the transparency of benchmarking over other commonly reported metrics ("success rate" or "concordance rate"). In addition, ongoing research should aim to systematically investigate and improve each step in the acquisition and analysis pipeline for CN VII tractography in VS.
{"title":"Facial Nerve Tractography of Vestibular Schwannomas: A Systematic Review of MR Acquisition and Analysis Pipelines.","authors":"Yunjia Ni, Shawn M Stevens, Trenton House, Ashton Huppert Steed, Alma Jukic, Parvathy Hareesh, Anthony M Asher, Kaith K Almefty, Kris A Smith, Randall W Porter, Michael T Lawton, Richard D Dortch","doi":"10.1111/jon.70131","DOIUrl":"https://doi.org/10.1111/jon.70131","url":null,"abstract":"<p><strong>Background: </strong>Facial nerve (CN VII) diffusion MR tractography is considered as a useful adjunct in pre-operative planning prior to vestibular schwannoma (VS) resection, especially in larger (Koos Grade III/IV) tumors. Since 2016, several systematic reviews have investigated the clinical value of CN VII tractography in VS, and all reported a \"success rate\" of at least 87% for predicting the pre-operative CN VII position. Yet in clinical practice, CN VII tractography has not yet been widely adopted into routine clinical practice. We suspected that underlying methodology and reporting metrics for existing tractography algorithms may be overestimating success rate. This motivated us to revisit the literature from a different perspective to unravel the caveats and nuances behind this technology.</p><p><strong>Methods: </strong>We screened all published works on PubMed related to pre-operative CN VII tractography in VS. Twenty-two studies were reviewed in detail.</p><p><strong>Results: </strong>We observed a strikingly high heterogeneity in tractography protocols in all domains of the tractography acquisition and analysis pipeline across studies.</p><p><strong>Conclusions: </strong>These findings suggest that the reliability and reproducibility of CN VII tractography in large VS has been overestimated. We believe that employing standardized reporting metrics, including sensitivity, true predictive value, and false discovery rate, would increase the transparency of benchmarking over other commonly reported metrics (\"success rate\" or \"concordance rate\"). In addition, ongoing research should aim to systematically investigate and improve each step in the acquisition and analysis pipeline for CN VII tractography in VS.</p>","PeriodicalId":16399,"journal":{"name":"Journal of Neuroimaging","volume":"36 2","pages":"e70131"},"PeriodicalIF":2.3,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147503933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}