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Tumor radiogenomics in gliomas with Bayesian layered variable selection.
Mohammed, Shariq; Kurtek, Sebastian; Bharath, Karthik; Rao, Arvind; Baladandayuthapani, Veerabhadran.
Affiliation
  • Mohammed S; Department of Biostatistics, Boston University, 801 Massachusetts Ave, Boston, MA 02118, United States; Department of Biostatistics, University of Michigan, 1415 Washington Heights, Ann Arbor, MI 48103, United States; Department of Computational Medicine and Bioinformatics, University of Michigan, 1
  • Kurtek S; Department of Statistics, The Ohio State University, 1958 Neil Avenue, Columbus, OH 43210, United States.
  • Bharath K; School of Mathematical Sciences, University Park, Nottingham, NG7 2RD, United Kingdom.
  • Rao A; Department of Biostatistics, University of Michigan, 1415 Washington Heights, Ann Arbor, MI 48103, United States; Department of Computational Medicine and Bioinformatics, University of Michigan, 100 Washtenaw Avenue, Ann Arbor, MI 48109, United States; Department of Radiation Oncology, University of
  • Baladandayuthapani V; Department of Biostatistics, University of Michigan, 1415 Washington Heights, Ann Arbor, MI 48103, United States.
Med Image Anal ; 90: 102964, 2023 12.
Article in En | MEDLINE | ID: mdl-37797481
ABSTRACT
We propose a statistical framework to analyze radiological magnetic resonance imaging (MRI) and genomic data to identify the underlying radiogenomic associations in lower grade gliomas (LGG). We devise a novel imaging phenotype by dividing the tumor region into concentric spherical layers that mimics the tumor evolution process. MRI data within each layer is represented by voxel-intensity-based probability density functions which capture the complete information about tumor heterogeneity. Under a Riemannian-geometric framework these densities are mapped to a vector of principal component scores which act as imaging phenotypes. Subsequently, we build Bayesian variable selection models for each layer with the imaging phenotypes as the response and the genomic markers as predictors. Our novel hierarchical prior formulation incorporates the interior-to-exterior structure of the layers, and the correlation between the genomic markers. We employ a computationally-efficient Expectation-Maximization-based strategy for estimation. Simulation studies demonstrate the superior performance of our approach compared to other approaches. With a focus on the cancer driver genes in LGG, we discuss some biologically relevant findings. Genes implicated with survival and oncogenesis are identified as being associated with the spherical layers, which could potentially serve as early-stage diagnostic markers for disease monitoring, prior to routine invasive approaches. We provide a R package that can be used to deploy our framework to identify radiogenomic associations.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glioma Type of study: Prognostic_studies Limits: Humans Language: En Journal: Med Image Anal Journal subject: DIAGNOSTICO POR IMAGEM Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glioma Type of study: Prognostic_studies Limits: Humans Language: En Journal: Med Image Anal Journal subject: DIAGNOSTICO POR IMAGEM Year: 2023 Document type: Article