Three-dimensional cardiovascular imaging-genetics: a mass univariate framework.

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Date
2018-01-01ICR Author
Author
Biffi, C
de Marvao, A
Attard, MI
Dawes, TJW
Whiffin, N
Bai, W
Shi, W
Francis, C
Meyer, H
Buchan, R
Cook, SA
Rueckert, D
O'Regan, DP
Type
Journal Article
Metadata
Show full item recordAbstract
MOTIVATION: Left ventricular (LV) hypertrophy is a strong predictor of cardiovascular outcomes, but its genetic regulation remains largely unexplained. Conventional phenotyping relies on manual calculation of LV mass and wall thickness, but advanced cardiac image analysis presents an opportunity for high-throughput mapping of genotype-phenotype associations in three dimensions (3D). RESULTS: High-resolution cardiac magnetic resonance images were automatically segmented in 1124 healthy volunteers to create a 3D shape model of the heart. Mass univariate regression was used to plot a 3D effect-size map for the association between wall thickness and a set of predictors at each vertex in the mesh. The vertices where a significant effect exists were determined by applying threshold-free cluster enhancement to boost areas of signal with spatial contiguity. Experiments on simulated phenotypic signals and SNP replication show that this approach offers a substantial gain in statistical power for cardiac genotype-phenotype associations while providing good control of the false discovery rate. This framework models the effects of genetic variation throughout the heart and can be automatically applied to large population cohorts. AVAILABILITY AND IMPLEMENTATION: The proposed approach has been coded in an R package freely available at https://doi.org/10.5281/zenodo.834610 together with the clinical data used in this work. CONTACT: [email protected]. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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Subject
Heart
Humans
Hypertrophy, Left Ventricular
Genetic Predisposition to Disease
Imaging, Three-Dimensional
Phenotype
Polymorphism, Single Nucleotide
Software
Female
Male
Genetic Association Studies
Research team
Molecular & Population Genetics
Language
eng
Date accepted
2017-09-01
License start date
2018-01
Citation
Bioinformatics (Oxford, England), 2018, 34 (1), pp. 97 - 103
Publisher
OXFORD UNIV PRESS