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GWAS Study

Exploring predictive biomarkers from clinical genome-wide association studies via multidimensional hierarchical mixture models.

Otani T, Noma H, Sugasawa S et al.

30202041 PubMed ID
GWAS Study Type
3289 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

OT
Otani T
NH
Noma H
SS
Sugasawa S
KA
Kuchiba A
GA
Goto A
YT
Yamaji T
KY
Kochi Y
IM
Iwasaki M
MS
Matsui S
TT
Tsunoda T
Chapter II

Abstract

Summary of the research findings

Although the detection of predictive biomarkers is of particular importance for the development of accurate molecular diagnostics, conventional statistical analyses based on gene-by-treatment interaction tests lack sufficient statistical power for this purpose, especially in large-scale clinical genome-wide studies that require an adjustment for multiplicity of a huge number of tests. Here we demonstrate an alternative efficient multi-subgroup screening method using multidimensional hierarchical mixture models developed to overcome this issue, with application to stroke and breast cancer randomized clinical trials with genomic data. We show that estimated effect size distributions of single nucleotide polymorphisms (SNPs) associated with outcomes, which could provide clues for exploring predictive biomarkers, optimizing individualized treatments, and understanding biological mechanisms of diseases. Furthermore, using this method we detected three new SNPs that are associated with blood homocysteine levels, which are strongly associated with the risk of stroke. We also detected six new SNPs that are associated with progression-free survival in breast cancer patients.

1,621 treated cases, 1,668 untreated cases

Chapter III

Study Statistics

Key metrics and study information

3289
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Germany
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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