Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/220074
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dc.contributor.authorNaval Baudin, Pablo-
dc.contributor.authorPons Escoda, Albert-
dc.contributor.authorCamins, Àngels-
dc.contributor.authorArroyo Pereiro, Pablo-
dc.contributor.authorViveros, Mildred-
dc.contributor.authorCastell Aulet, Josep-
dc.contributor.authorCos Domingo, Mònica-
dc.contributor.authorMartínez‑Yélamos, Antonio-
dc.contributor.authorMartínez‑Yélamos, Sergio-
dc.contributor.authorMajós Torró, Carlos-
dc.date.accessioned2025-03-27T19:13:04Z-
dc.date.available2025-03-27T19:13:04Z-
dc.date.issued2023-06-06-
dc.identifier.issn0938-7994-
dc.identifier.urihttps://hdl.handle.net/2445/220074-
dc.description.abstractObjectives: The development of new drugs for the treatment of progressive multiple sclerosis (MS) highlights the need for new prognostic biomarkers. Phase-rim lesions (PRLs) have been proposed as markers of progressive disease but are difficult to identify and quantify. Previous studies have identified T1-hypointensity in PRLs. The aim of this study was to compare the intensity profiles of PRLs and non-PRL white-matter lesions (nPR-WMLs) on three-dimensional T1-weighted turbo field echo (3DT1TFE) MRI. We then evaluated the performance of a derived metric as a surrogate for PRLs as potential markers for risk of disease progression. Methods: This study enrolled a cohort of relapsing-remitting (n = 10) and secondary progressive MS (n = 10) patients for whom 3 T MRI was available. PRLs and nPR-WMLs were segmented, and voxel-wise normalized T1-intensity histograms were analyzed. The lesions were divided equally into training and test datasets, and the fifth-percentile (p5)-normalized T1-intensity of each lesion was compared between groups and used for classification prediction. Results: Voxel-wise histogram analysis showed a unimodal histogram for nPR-WMLs and a bimodal histogram for PRLs with a large peak in the hypointense limit. Lesion-wise analysis included 1075 nPR-WMLs and 39 PRLs. The p5 intensity of PRLs was significantly lower than that of nPR-WMLs. The T1 intensity-based PRL classifier had a sensitivity of 0.526 and specificity of 0.959. Conclusions: Profound hypointensity on 3DT1TFE MRI is characteristic of PRLs and rare in other white-matter lesions. Given the widespread availability of T1-weighted imaging, this feature might serve as a surrogate biomarker for smoldering inflammation. Clinical relevance statement: Quantitative analysis of 3DT1TFE may detect deeply hypointense voxels in multiple sclerosis lesions, which are highly specific to PRLs. This could serve as a specific indicator of smoldering inflammation in MS, aiding in early detection of disease progression. Key points: • Phase-rim lesions (PRLs) in multiple sclerosis present a characteristic T1-hypointensity on 3DT1TFE MRI. • Intensity-normalized 3DT1TFE can be used to systematically identify and quantify these deeply hypointense foci. • Deep T1-hypointensity may act as an easily detectable, surrogate marker for PRLs.-
dc.format.extent9 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Verlag-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1007/s00330-023-09784-w-
dc.relation.ispartofEuropean Radiology, 2023, vol. 34, p. 1337-1345-
dc.relation.urihttps://doi.org/10.1007/s00330-023-09784-w-
dc.rightscc by (c) Naval Baudin, Pablo et al., 2023-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.sourceArticles publicats en revistes (Ciències Clíniques)-
dc.subject.classificationImatges per ressonància magnètica-
dc.subject.classificationInflamació-
dc.subject.classificationCervell-
dc.subject.otherMagnetic resonance imaging-
dc.subject.otherInflammation-
dc.subject.otherBrain-
dc.titleDeeply 3D‑T1‑TFE hypointense voxels are characteristic of phase‑rim lesions in multiple sclerosis-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec744276-
dc.date.updated2025-03-27T19:13:04Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid37278854-
Appears in Collections:Articles publicats en revistes (Ciències Clíniques)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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