Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/175455
Title: Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort
Author: Galván Femenía, Iván
Obón Santacana, Mireia
Piñeyro, David
Guindo Martínez, Marta
Duran, Xavier
Carreras, Anna
Pluvinet, Raquel
Velasco, Juan
Ramos, Laia
Aussó, Susanna
Mercader, J.M.
Puig, Lluis
Perucho, Manuel
Torrents Arenales, David
Moreno Aguado, Víctor
Sumoy, Lauro
Cid, Rafael de
Keywords: Fenotip
Malalties hereditàries
Factors de risc en les malalties
Phenotype
Genetic diseases
Risk factors in diseases
Issue Date: 1-Nov-2018
Publisher: BMJ Publishing Group
Abstract: BACKGROUND: Heritability estimates have revealed an important contribution of SNP variants for most common traits; however, SNP analysis by single-trait genome-wide association studies (GWAS) has failed to uncover their impact. In this study, we applied a multitrait GWAS approach to discover additional factor of the missing heritability of human anthropometric variation. METHODS: We analysed 205 traits, including diseases identified at baseline in the GCAT cohort (Genomes For Life- Cohort study of the Genomes of Catalonia) (n=4988), a Mediterranean adult population-based cohort study from the south of Europe. We estimated SNP heritability contribution and single-trait GWAS for all traits from 15 million SNP variants. Then, we applied a multitrait-related approach to study genome-wide association to anthropometric measures in a two-stage meta-analysis with the UK Biobank cohort (n=336 107). RESULTS: Heritability estimates (eg, skin colour, alcohol consumption, smoking habit, body mass index, educational level or height) revealed an important contribution of SNP variants, ranging from 18% to 77%. Single-trait analysis identified 1785 SNPs with genome-wide significance threshold. From these, several previously reported single-trait hits were confirmed in our sample with LINC01432 (p=1.9×10-9) variants associated with male baldness, LDLR variants with hyperlipidaemia (ICD-9:272) (p=9.4×10-10) and variants in IRF4 (p=2.8×10-57), SLC45A2 (p=2.2×10-130), HERC2 (p=2.8×10-176), OCA2 (p=2.4×10-121) and MC1R (p=7.7×10-22) associated with hair, eye and skin colour, freckling, tanning capacity and sun burning sensitivity and the Fitzpatrick phototype score, all highly correlated cross-phenotypes. Multitrait meta-analysis of anthropometric variation validated 27 loci in a two-stage meta-analysis with a large British ancestry cohort, six of which are newly reported here (p value threshold <5×10-9) at ZRANB2-AS2, PIK3R1, EPHA7, MAD1L1, CACUL1 and MAP3K9. CONCLUSION: Considering multiple-related genetic phenotypes improve associated genome signal detection. These results indicate the potential value of data-driven multivariate phenotyping for genetic studies in large population-based cohorts to contribute to knowledge of complex traits.
Note: Reproducció del document publicat a: https://doi.org/10.1136/jmedgenet-2018-105437
It is part of: Journal of Medical Genetics, 2018, vol. 55, num. 11, p. 765-778
URI: http://hdl.handle.net/2445/175455
Related resource: https://doi.org/10.1136/jmedgenet-2018-105437
ISSN: 0022-2593
Appears in Collections:Articles publicats en revistes (Ciències Clíniques)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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