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Matrix decomposition for modeling lesion development processes in multiple sclerosis.
Hu, Menghan; Crainiceanu, Ciprian; Schindler, Matthew K; Dewey, Blake; Reich, Daniel S; Shinohara, Russell T; Eloyan, Ani.
Afiliación
  • Hu M; Department of Biostatistics, Brown University, Providence, RI 02903, USA.
  • Crainiceanu C; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
  • Schindler MK; Translational Neuroradiology Section, Division of Neuroimmunology and Neurovirology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
  • Dewey B; Translational Neuroradiology Section, Division of Neuroimmunology and Neurovirology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA and Department of Electrical and Computer Engineering, Johns Hopkins Whiting School of Engineering, Bal
  • Reich DS; Translational Neuroradiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
  • Shinohara RT; Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA and Department of Radiology, Center for Biomedical Image Computing and Analytics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
  • Eloyan A; Department of Biostatistics, Brown University, Providence, RI 02903, USA.
Biostatistics ; 23(1): 83-100, 2022 01 13.
Article en En | MEDLINE | ID: mdl-32318692
ABSTRACT
Our main goal is to study and quantify the evolution of multiple sclerosis lesions observed longitudinally over many years in multi-sequence structural magnetic resonance imaging (sMRI). To achieve that, we propose a class of functional models for capturing the temporal dynamics and spatial distribution of the voxel-specific intensity trajectories in all sMRI sequences. To accommodate the hierarchical data structure (observations nested within voxels, which are nested within lesions, which, in turn, are nested within study participants), we use structured functional principal component analysis. We propose and evaluate the finite sample properties of hypothesis tests of therapeutic intervention effects on lesion evolution while accounting for the multilevel structure of the data. Using this novel testing strategy, we found statistically significant differences in lesion evolution between treatment groups.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Múltiple Límite: Humans Idioma: En Revista: Biostatistics Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Múltiple Límite: Humans Idioma: En Revista: Biostatistics Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
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