About: Evolution of cortical and thalamus atrophy and disability progression in early relapsing-remitting MS during 5 years     Goto   Sponge   NotDistinct   Permalink

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  • BACKGROUND AND PURPOSE: Pathologic changes inGMhave an important role in MS.Weinvestigated the association between SDGM and cortical volume changes and disability progression in early RRMS. MATERIALS AND METHODS: One hundred eighty patients with RRMS had clinical assessment during 5 years and were divided into those with or without SDP at 5 years by the usual definition in treatment trials. The number of available MR imaging scans at various time points was the following: at baseline, 178; and at 6 months, 172; at 12 months, 175; at 24 months, 155; at 36 months, 160; at 48 months, 158; and at 60 months, 162, respectively. Longitudinal changes in cortical, GM, and WM volume were calculated by using the direct method. RESULTS: At 5 years, 90 patients with RRMS experienced SDP and 90 had stable disease. At baseline, patients with SDP had longer disease duration, greater T2-lesion volume, and smaller whole-brain, WM, cortical, and SDGM volume (P < .01). At 5 years, patients with SDP had significantly greater percentage decreases from baseline compared with those without SDP in the volume of the whole brain (P < .0001), cortex (P = .001), GM (P = .003), and thalamus (P = .01). In patients who developed SDP at 5 years and those who did not, mixed-effect models, adjusted for age, disease duration, and change of the treatment status, showed significant interactions between SDP status at 5 years and changes with time in whole-brain, cortical, lateral ventricle (all P<.001), thalamus (P=.006), and total SDGM (P=.0095) volume. CONCLUSIONS: SDP is associated with progression of cortical, central, and thalamic atrophy in early RRMS during 5 years.
  • BACKGROUND AND PURPOSE: Pathologic changes inGMhave an important role in MS.Weinvestigated the association between SDGM and cortical volume changes and disability progression in early RRMS. MATERIALS AND METHODS: One hundred eighty patients with RRMS had clinical assessment during 5 years and were divided into those with or without SDP at 5 years by the usual definition in treatment trials. The number of available MR imaging scans at various time points was the following: at baseline, 178; and at 6 months, 172; at 12 months, 175; at 24 months, 155; at 36 months, 160; at 48 months, 158; and at 60 months, 162, respectively. Longitudinal changes in cortical, GM, and WM volume were calculated by using the direct method. RESULTS: At 5 years, 90 patients with RRMS experienced SDP and 90 had stable disease. At baseline, patients with SDP had longer disease duration, greater T2-lesion volume, and smaller whole-brain, WM, cortical, and SDGM volume (P < .01). At 5 years, patients with SDP had significantly greater percentage decreases from baseline compared with those without SDP in the volume of the whole brain (P < .0001), cortex (P = .001), GM (P = .003), and thalamus (P = .01). In patients who developed SDP at 5 years and those who did not, mixed-effect models, adjusted for age, disease duration, and change of the treatment status, showed significant interactions between SDP status at 5 years and changes with time in whole-brain, cortical, lateral ventricle (all P<.001), thalamus (P=.006), and total SDGM (P=.0095) volume. CONCLUSIONS: SDP is associated with progression of cortical, central, and thalamic atrophy in early RRMS during 5 years. (en)
Title
  • Evolution of cortical and thalamus atrophy and disability progression in early relapsing-remitting MS during 5 years
  • Evolution of cortical and thalamus atrophy and disability progression in early relapsing-remitting MS during 5 years (en)
skos:prefLabel
  • Evolution of cortical and thalamus atrophy and disability progression in early relapsing-remitting MS during 5 years
  • Evolution of cortical and thalamus atrophy and disability progression in early relapsing-remitting MS during 5 years (en)
skos:notation
  • RIV/00064165:_____/13:10193029!RIV14-MZ0-00064165
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I, P(NT13237), Z(MSM0021620849)
http://linked.open...iv/cisloPeriodika
  • 10
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 73793
http://linked.open...ai/riv/idVysledku
  • RIV/00064165:_____/13:10193029
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • thalamus; neuroimaging; multiple sclerosis; male; major clinical study; lateral brain ventricle; human; gray matter; female; disease duration; disability; controlled study; brain size; brain cortex; brain atrophy; Adult (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [02546A9FD379]
http://linked.open...i/riv/nazevZdroje
  • American Journal of Neuroradiology
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 34
http://linked.open...iv/tvurceVysledku
  • Havrdová, Eva
  • Seidl, Zdeněk
  • Vaněčková, Manuela
  • Horáková, Dana
  • Krásenský, Jan
  • Zivadinov, Robert
  • Doležal, Ondřej
  • Kalinčík, Tomáš
  • Bergsland, N.
  • Dwyer, M. G.
  • Hussein, S.
  • Potts, J. A
http://linked.open...ain/vavai/riv/wos
  • 000330539400016
http://linked.open...n/vavai/riv/zamer
issn
  • 0195-6108
number of pages
http://bibframe.org/vocab/doi
  • 10.3174/ajnr.A3503
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