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Pathway-structured predictive modeling for multi-level drug response in multiple myeloma.
Zhang, Xinyan; Li, Bingzong; Han, Huiying; Song, Sha; Xu, Hongxia; Yi, Zixuan; Hong, Yating; Zhuang, Wenzhuo; Yi, Nengjun.
Afiliação
  • Zhang X; Department of Biostatistics, Jiann-Ping Hsu College of Public Health, Georgia Southern University, Statesboro, GA, USA.
  • Li B; Department of Hematology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
  • Han H; Department of Cell Biology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
  • Song S; Department of Cell Biology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
  • Xu H; Department of Cell Biology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
  • Yi Z; School of Medicine, Eastern Virginia Medical School, Norfork, VA, USA.
  • Hong Y; Department of Hematology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
  • Zhuang W; Department of Cell Biology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
  • Yi N; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.
Bioinformatics ; 34(21): 3609-3615, 2018 11 01.
Article em En | MEDLINE | ID: mdl-29850860
ABSTRACT
Motivation Molecular analyses suggest that myeloma is composed of distinct sub-types that have different molecular pathologies and various response rates to certain treatments. Drug responses in multiple myeloma (MM) are usually recorded as a multi-level ordinal outcome. One of the goals of drug response studies is to predict which response category any patients belong to with high probability based on their clinical and molecular features. However, as most of genes have small effects, gene-based models may provide limited predictive accuracy. In that case, methods for predicting multi-level ordinal drug responses by incorporating biological pathways are desired but have not been developed yet.

Results:

We propose a pathway-structured method for predicting multi-level ordinal responses using a two-stage approach. We first develop hierarchical ordinal logistic models and an efficient quasi-Newton algorithm for jointly analyzing numerous correlated variables. Our two-stage approach first obtains the linear predictor (called the pathway score) for each pathway by fitting all predictors within each pathway using the hierarchical ordinal logistic approach, and then combines the pathway scores as new predictors to build a predictive model. We applied the proposed method to two publicly available datasets for predicting multi-level ordinal drug responses in MM using large-scale gene expression data and pathway information. Our results show that our approach not only significantly improved the predictive performance compared with the corresponding gene-based model but also allowed us to identify biologically relevant pathways. Availability and implementation The proposed approach has been implemented in our R package BhGLM, which is freely available from the public GitHub repository https//github.com/abbyyan3/BhGLM.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenômenos Biológicos / Mieloma Múltiplo Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenômenos Biológicos / Mieloma Múltiplo Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article