Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population

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Abstract

Metabolomics-genome-wide association studies (mGWAS) have uncovered many metabolic quantitative trait loci (mQTLs) influencing human metabolic individuality, though predominantly in European cohorts. By combining whole-exome sequencing with a high-resolution metabolomics profiling for a highly consanguineous Middle Eastern population, we discover 21 common variant and 12 functional rare variant mQTLs, of which 45% are novel altogether. We fine-map 10 common variant mQTLs to new metabolite ratio associations, and 11 common variant mQTLs to putative protein-altering variants. This is the first work to report common and rare variant mQTLs linked to diseases and/or pharmacological targets in a consanguineous Arab cohort, with wide implications for precision medicine in the Middle East.

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Yousri, N. A., Fakhro, K. A., Robay, A., Rodriguez-Flores, J. L., Mohney, R. P., Zeriri, H., … Suhre, K. (2018). Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population. Nature Communications, 9(1). https://doi.org/10.1038/s41467-017-01972-9

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