Gene-metabolite annotation with shortest reactional distance enhances metabolite genome-wide association studies results
Cantin Baron,
Sarah Cherkaoui,
Sandra Therrien-Laperriere,
Yann Ilboudo,
Raphaël Poujol,
Pamela Mehanna,
Melanie E. Garrett,
Marilyn J. Telen,
Allison E. Ashley-Koch,
Pablo Bartolucci,
John D. Rioux,
Guillaume Lettre,
Christine Des Rosiers,
Matthieu Ruiz,
Julie G. Hussin
Affiliations
Cantin Baron
Département de Biochimie et de Médecine Moléculaire, Université de Montréal, Montréal, QC, Canada; Montreal Heart Institute, Montréal, QC, Canada
Sarah Cherkaoui
Montreal Heart Institute, Montréal, QC, Canada; Division of Oncology and Children’s Research Center, University Children’s Hospital Zurich, University of Zurich, Zurich, Switzerland; Department of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Center, Université Paris-Saclay, Villejuif, France
Sandra Therrien-Laperriere
Montreal Heart Institute, Montréal, QC, Canada
Yann Ilboudo
Département de Biochimie et de Médecine Moléculaire, Université de Montréal, Montréal, QC, Canada; Montreal Heart Institute, Montréal, QC, Canada
Raphaël Poujol
Montreal Heart Institute, Montréal, QC, Canada
Pamela Mehanna
Montreal Heart Institute, Montréal, QC, Canada
Melanie E. Garrett
Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC, USA
Marilyn J. Telen
Division of Hematology, Department of Medicine, Duke University Medical Center, Durham, NC, USA
Allison E. Ashley-Koch
Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC, USA
Pablo Bartolucci
Université Paris Est Créteil, Hôpitaux Universitaires Henri Mondor, APHP, Sickle cell referral center – UMGGR, Créteil, France; Université Paris Est Créteil, IMRB, Laboratory of excellence LABEX, Créteil, France
John D. Rioux
Département de Biochimie et de Médecine Moléculaire, Université de Montréal, Montréal, QC, Canada; Montreal Heart Institute, Montréal, QC, Canada; Département de Médecine, Université de Montréal, Montréal, QC, Canada
Guillaume Lettre
Montreal Heart Institute, Montréal, QC, Canada; Département de Médecine, Université de Montréal, Montréal, QC, Canada
Christine Des Rosiers
Département de Biochimie et de Médecine Moléculaire, Université de Montréal, Montréal, QC, Canada; Montreal Heart Institute, Montréal, QC, Canada; Département de Nutrition, Université de Montréal, Montréal, QC, Canada
Matthieu Ruiz
Montreal Heart Institute, Montréal, QC, Canada; Département de Nutrition, Université de Montréal, Montréal, QC, Canada
Julie G. Hussin
Montreal Heart Institute, Montréal, QC, Canada; Département de Médecine, Université de Montréal, Montréal, QC, Canada; Corresponding author
Summary: Metabolite genome-wide association studies (mGWAS) have advanced our understanding of the genetic control of metabolite levels. However, interpreting these associations remains challenging due to a lack of tools to annotate gene-metabolite pairs beyond the use of conservative statistical significance threshold. Here, we introduce the shortest reactional distance (SRD) metric, drawing from the comprehensive KEGG database, to enhance the biological interpretation of mGWAS results. We applied this approach to three independent mGWAS, including a case study on sickle cell disease patients. Our analysis reveals an enrichment of small SRD values in reported mGWAS pairs, with SRD values significantly correlating with mGWAS p values, even beyond the standard conservative thresholds. We demonstrate the utility of SRD annotation in identifying potential false negatives and inaccuracies within current metabolic pathway databases. Our findings highlight the SRD metric as an objective, quantitative and easy-to-compute annotation for gene-metabolite pairs, suitable to integrate statistical evidence to biological networks.