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ARS Home » Northeast Area » Boston, Massachusetts » Jean Mayer Human Nutrition Research Center On Aging » Research » Publications at this Location » Publication #395950

Research Project: Personalized Nutrition and Healthy Aging

Location: Jean Mayer Human Nutrition Research Center On Aging

Title: A gene-diet interaction-based score predicts response to dietary fat in the Women's Health Initiative

Author
item WESTERMAN, KENNETH - Jean Mayer Human Nutrition Research Center On Aging At Tufts University
item LIU, QING - Brown University
item LIU, SIMIN - Boston University
item Parnell, Laurence
item SEBASTIANI, PAOLI - Boston University
item JACQUES, PAUL - Jean Mayer Human Nutrition Research Center On Aging At Tufts University
item DEMEO, DAWN - Brigham & Women'S Hospital
item ORDOVAS, JOSE - Jean Mayer Human Nutrition Research Center On Aging At Tufts University

Submitted to: The American Journal of Clinical Nutrition
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 2/14/2020
Publication Date: 3/5/2020
Citation: Westerman, K., Liu, Q., Liu, S., Parnell, L.D., Sebastiani, P., Jacques, P.F., Demeo, D.L., Ordovas, J. 2020. A gene-diet interaction-based score predicts response to dietary fat in the Women's Health Initiative. American Journal of Clinical Nutrition. 111(4):893-902. https://doi.org/10.1093/ajcn/nqaa037.
DOI: https://doi.org/10.1093/ajcn/nqaa037

Interpretive Summary: Response to diet is highly variable among individuals. Part of that variability is due to genetic factors. However, till now, the search for genes implicated in dietary response has been carried piecemeal, and little investigation has gone into the development of diet response scores integrating the whole genome. Scientists at the HNRCA in Boston, in collaboration with researchers at Harvard, Boston University, and Brown, developed such genomic-wide scores for the response of 6 cardiovascular risk factors (body mass index, systolic blood pressure, LDL cholesterol, HDL cholesterol, triglycerides, and fasting glucose) to dietary fat using a large intervention study. One of the scores identified, including 1760 genetic variants, explained a significant amount of the variability in one-year blood cholesterol changes to dietary intervention. These results lay the foundation for future research in diet response prediction for use in personalized nutrition.

Technical Abstract: BACKGROUND: Although diet response prediction for cardiometabolic risk factors (CRFs) has been demonstrated using single genetic variants and main-effect genetic risk scores, little investigation has gone into the development of genome-wide diet response scores. OBJECTIVE: We sought to leverage the multistudy setup of the Women's Health Initiative cohort to generate and test genetic scores for the response of 6 CRFs (BMI, systolic blood pressure, LDL cholesterol, HDL cholesterol, triglycerides, and fasting glucose) to dietary fat. METHODS: A genome-wide interaction study was undertaken for each CRF in women (n ~ 9000) not participating in the dietary modification (DM) trial, which focused on the reduction of dietary fat. Genetic scores based on these analyses were developed using a pruning-and-thresholding approach and tested for the prediction of 1-y CRF changes as well as long-term chronic disease development in DM trial participants (n ~ 5000). RESULTS: Only 1 of these genetic scores, for LDL cholesterol, predicted changes in the associated CRF. This 1760-variant score explained 3.7% (95% CI: 0.09, 11.9) of the variance in 1-y LDL cholesterol changes in the intervention arm but was unassociated with changes in the control arm. In contrast, a main-effect genetic risk score for LDL cholesterol was not useful for predicting dietary fat response. Further investigation of this score with respect to downstream disease outcomes revealed suggestive differential associations across DM trial arms, especially with respect to coronary heart disease and stroke subtypes. CONCLUSIONS: These results lay the foundation for the combination of many genome-wide gene-diet interactions for diet response prediction while highlighting the need for further research and larger samples in order to achieve robust biomarkers for use in personalized nutrition.