Maria A Rocca1, Laura Parisi, Elisabetta Pagani, Massimiliano Copetti, Mariaemma Rodegher, Bruno Colombo, Giancarlo Comi, Andrea Falini, Massimo Filippi. 1. From the Neuroimaging Research Unit (M.A.R., L.P., E.P., M.F.), Department of Neurology, Institute of Experimental Neurology, Division of Neuroscience (M.A.R., M.R., B.C., G.C., M.F.), and Department of Neuroradiology (A.F.), CERMAC, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Via Olgettina 60, Milan 20132, Italy; and Biostatistics Unit, IRCCS-Ospedale Casa Sollievo della Sofferenza, San Giovanni Rotondo, Foggia, Italy (M.C.).
Abstract
PURPOSE: To use magnetic resonance (MR) imaging and advanced analysis to assess the role of lesions in normal-appearing white matter ( NAWM normal-appearing white matter ) and gray matter ( GM gray matter ) damage, global versus regional damage, and atrophy versus microstructural abnormalities in the pathogenesis of fatigue in multiple sclerosis ( MS multiple sclerosis ). MATERIALS AND METHODS: Local ethics committee approval and written informed consent were obtained. Dual-echo, double inversion-recovery, high-resolution T1-weighted and diffusion-tensor ( DT diffusion tensor ) MR was performed in 31 fatigued patients, 32 nonfatigued patients, and 35 control subjects. Global and regional atrophy and DT diffusion tensor MR measures of damage to lesions, NAWM normal-appearing white matter , and GM gray matter were compared (analysis of variance). RESULTS: Lesional, atrophy, and DT diffusion tensor MR measures of global damage to brain, white matter ( WM white matter ), and GM gray matter did not differ between fatigued and nonfatigued patients. Compared with nonfatigued patients and control subjects, fatigued patients experienced atrophy of the right side of the accumbens (mean volume ± standard deviation, 0.37 mL ± 0.09 in control subjects; 0.39 mL ± 0.1 in nonfatigued patients; and 0.33 mL ± 0.09 in fatigued patients), right inferior temporal gyrus ( ITG inferior temporal gyrus ) (Montreal Neurological Institute [ MNI Montreal Neurological Institute ] coordinates: 51, -51, -11; t value, 4.83), left superior frontal gyrus ( MNI Montreal Neurological Institute coordinates: -10, 49, 24; t value, 3.40), and forceps major ( MNI Montreal Neurological Institute coordinates: 11, -91, 18; t value, 3.37). They also had lower fractional anisotropy ( FA fractional anisotropy ) of forceps major ( MNI Montreal Neurological Institute coordinates: -17, -78, 6), left inferior fronto-occipital fasciculus ( MNI Montreal Neurological Institute coordinates: -25, 2, -11), and right anterior thalamic radiation ( ATR anterior thalamic radiation ) ( MNI Montreal Neurological Institute coordinates: 11, 2, -6) (P < .05, corrected). More lesions were found at T2-weighted imaging in fatigued patients. Multivariable model was used to identify right ITG inferior temporal gyrus atrophy (odds ratio, 0.83; 95% confidence interval [ CI confidence interval ]: 0.82, 0.97; P = .009) and right ATR anterior thalamic radiation FA fractional anisotropy (odds ratio, 0.74; 95% CI confidence interval : 0.61, 0.90; P = .003) as covariates independently associated with fatigue (C statistic, 0.85). CONCLUSION: Damage to strategic brain WM white matter and GM gray matter regions, in terms of microstructural abnormalities and atrophy, contributes to pathogenesis of fatigue in MS multiple sclerosis , whereas global lesional, WM white matter , and GM gray matter damage does not seem to have a role.
PURPOSE: To use magnetic resonance (MR) imaging and advanced analysis to assess the role of lesions in normal-appearing white matter ( NAWM normal-appearing white matter ) and gray matter ( GM gray matter ) damage, global versus regional damage, and atrophy versus microstructural abnormalities in the pathogenesis of fatigue in multiple sclerosis ( MS multiple sclerosis ). MATERIALS AND METHODS: Local ethics committee approval and written informed consent were obtained. Dual-echo, double inversion-recovery, high-resolution T1-weighted and diffusion-tensor ( DT diffusion tensor ) MR was performed in 31 fatigued patients, 32 nonfatigued patients, and 35 control subjects. Global and regional atrophy and DT diffusion tensor MR measures of damage to lesions, NAWM normal-appearing white matter , and GM gray matter were compared (analysis of variance). RESULTS: Lesional, atrophy, and DT diffusion tensor MR measures of global damage to brain, white matter ( WM white matter ), and GM gray matter did not differ between fatigued and nonfatigued patients. Compared with nonfatigued patients and control subjects, fatigued patients experienced atrophy of the right side of the accumbens (mean volume ± standard deviation, 0.37 mL ± 0.09 in control subjects; 0.39 mL ± 0.1 in nonfatigued patients; and 0.33 mL ± 0.09 in fatigued patients), right inferior temporal gyrus ( ITG inferior temporal gyrus ) (Montreal Neurological Institute [ MNI Montreal Neurological Institute ] coordinates: 51, -51, -11; t value, 4.83), left superior frontal gyrus ( MNI Montreal Neurological Institute coordinates: -10, 49, 24; t value, 3.40), and forceps major ( MNI Montreal Neurological Institute coordinates: 11, -91, 18; t value, 3.37). They also had lower fractional anisotropy ( FA fractional anisotropy ) of forceps major ( MNI Montreal Neurological Institute coordinates: -17, -78, 6), left inferior fronto-occipital fasciculus ( MNI Montreal Neurological Institute coordinates: -25, 2, -11), and right anterior thalamic radiation ( ATR anterior thalamic radiation ) ( MNI Montreal Neurological Institute coordinates: 11, 2, -6) (P < .05, corrected). More lesions were found at T2-weighted imaging in fatigued patients. Multivariable model was used to identify right ITG inferior temporal gyrus atrophy (odds ratio, 0.83; 95% confidence interval [ CI confidence interval ]: 0.82, 0.97; P = .009) and right ATR anterior thalamic radiation FA fractional anisotropy (odds ratio, 0.74; 95% CI confidence interval : 0.61, 0.90; P = .003) as covariates independently associated with fatigue (C statistic, 0.85). CONCLUSION: Damage to strategic brain WM white matter and GM gray matter regions, in terms of microstructural abnormalities and atrophy, contributes to pathogenesis of fatigue in MS multiple sclerosis , whereas global lesional, WM white matter , and GM gray matter damage does not seem to have a role.
Authors: F Pache; H Zimmermann; C Finke; A Lacheta; S Papazoglou; J Kuchling; J Wuerfel; B Hamm; K Ruprecht; F Paul; A U Brandt; M Scheel Journal: Eur Radiol Date: 2016-03-24 Impact factor: 5.315
Authors: Emily Wasson; Andrea L Rosso; Adam J Santanasto; Caterina Rosano; Meryl A Butters; W Jack Rejeski; Robert M Boudreau; Howard Aizenstein; Theresa Gmelin; Nancy W Glynn Journal: Exp Gerontol Date: 2018-12-04 Impact factor: 4.032
Authors: Martin Weygandt; Lil Meyer-Arndt; Janina Ruth Behrens; Katharina Wakonig; Judith Bellmann-Strobl; Kerstin Ritter; Michael Scheel; Alexander U Brandt; Christian Labadie; Stefan Hetzer; Stefan M Gold; Friedemann Paul; John-Dylan Haynes Journal: Proc Natl Acad Sci U S A Date: 2016-11-07 Impact factor: 11.205