In 2015, a genome-wide association study described 59 independent signals that showed strong associations with 85 fasting metabolite concentrations as measured by the Biocrates AbsoluteIDQ p150 kit. However, the human body resides in a nonfasting state for the greater part of the day, and the genetic basis of postprandial metabolite concentrations remains largely unknown. We systematically examined these previously identified genetic associations in postprandial metabolite concentrations after a mixed meal. Of these 85 metabolites, 23 were identified with significant changes after the meal, for which 38 gene-metabolite associations were analyzed. Of these 38 associations, 31 gene-metabolite associations were replicated with postprandial metabolite concentrations. These data indicate that the genetics of fasting and postprandial metabolite levels are significantly overlapping.
Ruifang Li‐Gao, Renée de Mutsert, Patrick C.N. Rensen, Jan B. van Klinken, Cornelia Prehn, Jerzy Adamski, Astrid van Hylckama Vlieg, Martin den Heijer, Saskia le Cessie, Frits R. Rosendaal, Ko Willems van Dijk, Dennis O. Mook‐Kanamori
Ruifang Li‐Gao, David A. Hughes, Saskia le Cessie, Renée de Mutsert, Martin den Heijer, Frits R. Rosendaal, Ko Willems van Dijk, Nicholas J. Timpson, Dennis O. Mook‐Kanamori
Dorina Ibi, Raymond Noordam, Jan B. van Klinken, Ruifang Li‐Gao, Renée de Mutsert, Stella Trompet, Tim Christen, Lisanne L. Blauw, Diana van Heemst, Dennis O. Mook‐Kanamori, Frits R. Rosendaal, J. Wouter Jukema, Martijn E.T. Dollé, Patrick C.N. Rensen, Ko Willems van Dijk
David A. Hughes, Ruifang Li‐Gao, Caroline J. Bull, Renée de Mutsert, Frits R. Rosendaal, Dennis O. Mook‐Kanamori, Ko Willems van Dijk, Nicholas J. Timpson
David A. Hughes, Ruifang Li‐Gao, Caroline J. Bull, Renée de Mutsert, Frits R. Rosendaal, Dennis O. Mook‐Kanamori, Ko Willems van Dijk, Nicholas J. Timpson
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