Protocol for the EMPHASIS study; epigenetic mechanisms linking maternal pre-conceptional nutrition and children’s health in India and Sub-Saharan Africa
Giriraj R. Chandak,
Matt J. Silver,
Ayden Saffari,
Karen A. Lillycrop,
Smeeta Shrestha,
Sirazul Ameen Sahariah,
Chiara Di Gravio,
Gail Goldberg,
Ashutosh Singh Tomar,
Modupeh Betts,
Sara Sajjadi,
Lena Acolatse,
Philip James,
Prachand Issarapu,
Kalyanaraman Kumaran,
Ramesh D. Potdar,
Andrew M. Prentice,
Caroline H. D. Fall,
the EMPHASIS study group,
Lena Acolatse,
Meraj Ahmed,
Modupeh Betts,
Giriraj R. Chandak,
Harsha Chopra,
Cyrus Cooper,
Momodou K. Darboe,
Chiara Di Gravio,
Caroline H. D. Fall,
Meera Gandhi,
Gail R. Goldberg,
Prachand Issarapu,
Philip James,
Ramatoulie Janha,
Landing M. A. Jarjou,
Lovejeet Kaur,
Sarah H. Kehoe,
Kalyanaraman Kumaran,
Karen A. Lillycrop,
Mohammed Ngum,
Suraj S. Nongmaithem,
Stephen Owens,
Ramesh D. Potdar,
Andrew M. Prentice,
Ann Prentice,
Tallapragada Divya Sri Priyanka,
Ayden Saffari,
Sirazul Ameen Sahariah,
Sara Sajjadi,
Harshad Sane,
Smeeta Shrestha,
Matt J. Silver,
Ashutosh Singh Tomar,
Kate A. Ward,
Dilip Kumar Yadav,
Chittaranjan S. Yajnik
Affiliations
Giriraj R. Chandak
CSIR-Centre for Cellular and Molecular Biology
Matt J. Silver
MRC Unit The Gambia and MRC International Nutrition Group, London School of Hygiene and Tropical Medicine
Ayden Saffari
MRC Unit The Gambia and MRC International Nutrition Group, London School of Hygiene and Tropical Medicine
Karen A. Lillycrop
University of Southampton
Smeeta Shrestha
CSIR-Centre for Cellular and Molecular Biology
Sirazul Ameen Sahariah
Centre for the Study of Social Change
Chiara Di Gravio
MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton General Hospital
Gail Goldberg
MRC Elsie Widdowson Laboratory
Ashutosh Singh Tomar
CSIR-Centre for Cellular and Molecular Biology
Modupeh Betts
MRC Unit, The Gambia
Sara Sajjadi
CSIR-Centre for Cellular and Molecular Biology
Lena Acolatse
MRC Unit, The Gambia
Philip James
MRC Unit The Gambia and MRC International Nutrition Group, London School of Hygiene and Tropical Medicine
Prachand Issarapu
CSIR-Centre for Cellular and Molecular Biology
Kalyanaraman Kumaran
MRC Lifecourse Epidemiology Unit, University of Southampton, UK and CSI Holdsworth Memorial Hospital
Ramesh D. Potdar
Centre for the Study of Social Change
Andrew M. Prentice
MRC Unit, The Gambia and MRC International Nutrition Group, London School of Hygiene and Tropical Medicine
Caroline H. D. Fall
MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton General Hospital
Abstract Background Animal studies have shown that nutritional exposures during pregnancy can modify epigenetic marks regulating fetal development and susceptibility to later disease, providing a plausible mechanism to explain the developmental origins of health and disease. Human observational studies have shown that maternal peri-conceptional diet predicts DNA methylation in offspring. However, a causal pathway from maternal diet, through changes in DNA methylation, to later health outcomes has yet to be established. The EMPHASIS study (Epigenetic Mechanisms linking Pre-conceptional nutrition and Health Assessed in India and Sub-Saharan Africa, ISRCTN14266771) will investigate epigenetically mediated links between peri-conceptional nutrition and health-related outcomes in children whose mothers participated in two randomized controlled trials of micronutrient supplementation before and during pregnancy. Methods The original trials were the Mumbai Maternal Nutrition Project (MMNP, ISRCTN62811278) in which Indian women were offered a daily snack made from micronutrient-rich foods or low-micronutrient foods (controls), and the Peri-conceptional Multiple Micronutrient Supplementation Trial (PMMST, ISRCTN13687662) in rural Gambia, in which women were offered a daily multiple micronutrient (UNIMMAP) tablet or placebo. In the EMPHASIS study, DNA methylation will be analysed in the children of these women (~1100 children aged 5–7 y in MMNP and 298 children aged 7–9 y in PMMST). Cohort-specific and cross-cohort effects will be explored. Differences in DNA methylation between allocation groups will be identified using the Illumina Infinium MethylationEPIC array, and by pyrosequencing top hits and selected candidate loci. Associations will be analysed between DNA methylation and health-related phenotypic outcomes, including size at birth, and children’s post-natal growth, body composition, skeletal development, cardio-metabolic risk markers (blood pressure, serum lipids, plasma glucose and insulin) and cognitive function. Pathways analysis will be used to test for enrichment of nutrition-sensitive loci in biological pathways. Causal mechanisms for nutrition-methylation-phenotype associations will be explored using Mendelian Randomization. Associations between methylation unrelated to supplementation and phenotypes will also be analysed. Conclusion The study will increase understanding of the epigenetic mechanisms underpinning the long-term impact of maternal nutrition on offspring health. It will potentially lead to better nutritional interventions for mothers preparing for pregnancy, and to identification of early life biomarkers of later disease risk.