Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans. Issue 1 (December 2017)
- Record Type:
- Journal Article
- Title:
- Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans. Issue 1 (December 2017)
- Main Title:
- Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans
- Authors:
- Gottlieb, Assaf
Daneshjou, Roxana
DeGorter, Marianne
Bourgeois, Stephane
Svensson, Peter
Wadelius, Mia
Deloukas, Panos
Montgomery, Stephen
Altman, Russ - Abstract:
- Abstract Background Genome-wide association studies are useful for discovering genotype–phenotype associations but are limited because they require large cohorts to identify a signal, which can be population-specific. Mapping genetic variation to genes improves power and allows the effects of both protein-coding variation as well as variation in expression to be combined into "gene level" effects. Methods Previous work has shown that warfarin dose can be predicted using information from genetic variation that affects protein-coding regions. Here, we introduce a method that improves dose prediction by integrating tissue-specific gene expression. In particular, we use drug pathways and expression quantitative trait loci knowledge to impute gene expression—on the assumption that differential expression of key pathway genes may impact dose requirement. We focus on 116 genes from the pharmacokinetic and pharmacodynamic pathways of warfarin within training and validation sets comprising both European and African-descent individuals. Results We build gene-tissue signatures associated with warfarin dose in a cohort-specific manner and identify a signature of 11 gene-tissue pairs that significantly augments the International Warfarin Pharmacogenetics Consortium dosage-prediction algorithm in both populations. Conclusions Our results demonstrate that imputed expression can improve dose prediction and bridge population-specific compositions. MATLAB code is availableAbstract Background Genome-wide association studies are useful for discovering genotype–phenotype associations but are limited because they require large cohorts to identify a signal, which can be population-specific. Mapping genetic variation to genes improves power and allows the effects of both protein-coding variation as well as variation in expression to be combined into "gene level" effects. Methods Previous work has shown that warfarin dose can be predicted using information from genetic variation that affects protein-coding regions. Here, we introduce a method that improves dose prediction by integrating tissue-specific gene expression. In particular, we use drug pathways and expression quantitative trait loci knowledge to impute gene expression—on the assumption that differential expression of key pathway genes may impact dose requirement. We focus on 116 genes from the pharmacokinetic and pharmacodynamic pathways of warfarin within training and validation sets comprising both European and African-descent individuals. Results We build gene-tissue signatures associated with warfarin dose in a cohort-specific manner and identify a signature of 11 gene-tissue pairs that significantly augments the International Warfarin Pharmacogenetics Consortium dosage-prediction algorithm in both populations. Conclusions Our results demonstrate that imputed expression can improve dose prediction and bridge population-specific compositions. MATLAB code is available athttps://github.com/assafgo/warfarin-cohort … (more)
- Is Part Of:
- Genome medicine. Volume 9:Issue 1(2017)
- Journal:
- Genome medicine
- Issue:
- Volume 9:Issue 1(2017)
- Issue Display:
- Volume 9, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 9
- Issue:
- 1
- Issue Sort Value:
- 2017-0009-0001-0000
- Page Start:
- 1
- Page End:
- 9
- Publication Date:
- 2017-12
- Subjects:
- Pharmacogenomics -- Warfarin dose -- International Warfarin Pharmacogenetics Consortium -- African Americans
Genomics -- Periodicals
Medical genetics -- Periodicals
616.042 - Journal URLs:
- http://www.genomemedicine.com ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=863&action=archive ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s13073-017-0495-0 ↗
- Languages:
- English
- ISSNs:
- 1756-994X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11157.xml