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Heterogeneity of multiple sclerosis lesions in fast diffusional kurtosis imaging

BACKGROUND: Mean kurtosis (MK), one of the parameters derived from diffusion kurtosis imaging (DKI), has shown increased sensitivity to tissue microstructure damage in several neurological disorders. METHODS: Thirty-seven patients with relapsing-remitting MS and eleven healthy controls (HC) received...

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Detalles Bibliográficos
Autores principales: Thaler, Christian, Kyselyova, Anna A., Faizy, Tobias D., Nawka, Marie T., Jespersen, Sune, Hansen, Brian, Stellmann, Jan-Patrick, Heesen, Christoph, Stürner, Klarissa H., Stark, Maria, Fiehler, Jens, Bester, Maxim, Gellißen, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861404/
https://www.ncbi.nlm.nih.gov/pubmed/33539364
http://dx.doi.org/10.1371/journal.pone.0245844
Descripción
Sumario:BACKGROUND: Mean kurtosis (MK), one of the parameters derived from diffusion kurtosis imaging (DKI), has shown increased sensitivity to tissue microstructure damage in several neurological disorders. METHODS: Thirty-seven patients with relapsing-remitting MS and eleven healthy controls (HC) received brain imaging on a 3T MR scanner, including a fast DKI sequence. MK and mean diffusivity (MD) were measured in the white matter of HC, normal-appearing white matter (NAWM) of MS patients, contrast-enhancing lesions (CE-L), FLAIR lesions (FLAIR-L) and black holes (BH). RESULTS: Overall 1529 lesions were analyzed, including 30 CE-L, 832 FLAIR-L and 667 BH. Highest MK values were obtained in the white matter of HC (0.814 ± 0.129), followed by NAWM (0.724 ± 0.137), CE-L (0.619 ± 0.096), FLAIR-L (0.565 ± 0.123) and BH (0.549 ± 0.12). Lowest MD values were obtained in the white matter of HC (0.747 ± 0.068 10(−3)mm(2)/sec), followed by NAWM (0.808 ± 0.163 10(−3)mm(2)/sec), CE-L (0.853 ± 0.211 10(−3)mm(2)/sec), BH (0.957 ± 0.304 10(−3)mm(2)/sec) and FLAIR-L (0.976 ± 0.35 10(−3)mm(2)/sec). While MK differed significantly between CE-L and non-enhancing lesions, MD did not. CONCLUSION: MK adds predictive value to differentiate between MS lesions and might provide further information about diffuse white matter injury and lesion microstructure.