Survival analysis of longitudinal microarrays

Bioinformatics. 2006 Nov 1;22(21):2643-9. doi: 10.1093/bioinformatics/btl450. Epub 2006 Oct 10.

Abstract

Motivation: The development of methods for linking gene expressions to various clinical and phenotypic characteristics is an active area of genomic research. Scientists hope that such analysis may, for example, describe relationships between gene function and clinical events such as death or recovery. Methods are available for relating gene expression to measurements that are categorized or continuous, but there is less work in relating expressions to an observed event time such as time to death, response or relapse. When gene expressions are measured over time, there are methods for differentiating temporal patterns. However, methods have not yet been proposed for the survival analysis of longitudinally collected microarrays.

Results: We describe an approach for the survival analysis of longitudinal gene expression data. We construct a measure of association between the time to an event and gene expressions collected over time. Statistical significance is addressed using permutations and control of the false discovery rate. Our proposed method is illustrated on a dataset from a multi-center research study of inflammation and response to injury that aims to uncover the biological reasons why patients can have dramatically different outcomes after suffering a traumatic injury (www.gluegrant.org).

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Algorithms
  • Biomarkers / analysis
  • Diagnosis, Computer-Assisted / methods
  • Gene Expression Profiling / methods
  • Inflammation / diagnosis
  • Inflammation / metabolism*
  • Inflammation / mortality*
  • Longitudinal Studies
  • Oligonucleotide Array Sequence Analysis / methods*
  • Proteins / analysis
  • Risk Assessment / methods*
  • Risk Factors
  • Survival Analysis*
  • Survival Rate
  • Time Factors
  • Wounds and Injuries / diagnosis
  • Wounds and Injuries / metabolism*
  • Wounds and Injuries / mortality*

Substances

  • Biomarkers
  • Proteins