posted on 2018-01-26, 14:52authored byA. Mesut Erzurumluoglu, Denis Baird, Tom G. Richardson, Nicholas J. Timpson, Santiago Rodriguez
Y-chromosomal (Y-DNA) haplogroups are more widely used in population genetics than in genetic epidemiology, although associations between Y-DNA haplogroups and several traits, including cardiometabolic traits, have been reported. In apparently homogeneous populations defined by principal component analyses, there is still Y-DNA haplogroup variation which will result from population history. Therefore, hidden stratification and/or differential phenotypic effects by Y-DNA haplogroups could exist. To test this, we hypothesised that stratifying individuals according to their Y-DNA haplogroups before testing for associations between autosomal single nucleotide polymorphisms (SNPs) and phenotypes will yield difference in association. For proof of concept, we derived Y-DNA haplogroups from 6537 males from two epidemiological cohorts, Avon Longitudinal Study of Parents and Children (ALSPAC) (n = 5080; 816 Y-DNA SNPs) and the 1958 Birth Cohort (n = 1457; 1849 Y-DNA SNPs), and studied the robust associations between 32 SNPs and body mass index (BMI), including SNPs in or near Fat Mass and Obesity-associated protein (FTO) which yield the strongest effects. Overall, no association was replicated in both cohorts when Y-DNA haplogroups were considered and this suggests that, for BMI at least, there is little evidence of differences in phenotype or SNP association by Y-DNA structure. Further studies using other traits, phenome-wide association studies (PheWAS), other haplogroups and/or autosomal SNPs are required to test the generalisability and utility of this approach.
Funding
We are extremely grateful to all the parents and children who took part in this study,
the midwives for their help in recruiting them and the whole ALSPAC team, which includes interviewers,
computer and laboratory technicians, clerical workers, research scientists, volunteers, managers, receptionists and
nurses. The UK Medical Research Council and the Wellcome Trust (Grant ref: 102215/2/13/2) and the University
of Bristol provide core support for ALSPAC. ALSPAC is also part of the World Health Organisation initiated
European longitudinal study of parents and children. This study makes use of data generated by the Wellcome
Trust Case-Control Consortium and LabCorp (Laboratory Corporation of America) using support from 23andMe.
A full list of the investigators who contributed to the generation of the data is available from www.wtccc.org.uk.
Funding for the project was provided by the Wellcome Trust under award 076113 and 085475 and by a Medical
Research Council (MRC) grant awarded to Santiago Rodriguez (MR/K002767/1). A. Mesut Erzurumluoglu,
Denis Baird and Tom G. Richardson were Students funded by the Medical Research Council (MRC UK) when this
study was carried out. The Integrative Epidemiology Unit is supported by the MRC and the University of Bristol
(G0600705, MC_UU_12013/1-9).
History
Citation
Genes, 2018, 9 (1), 45
Author affiliation
/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Department of Health Sciences