@article{Ma2020, abstract = { Background: DNA methylation patterns associated with habitual diet have not been well studied. Methods: Diet quality was characterized using a Mediterranean-style diet score and the Alternative Healthy Eating Index score. We conducted ethnicity-specific and trans-ethnic epigenome-wide association analyses for diet quality and leukocyte-derived DNA methylation at over 400 000 CpGs (cytosine-guanine dinucleotides) in 5 population-based cohorts including 6662 European ancestry, 2702 African ancestry, and 360 Hispanic ancestry participants. For diet-associated CpGs identified in epigenome-wide analyses, we conducted Mendelian randomization (MR) analysis to examine their relations to cardiovascular disease risk factors and examined their longitudinal associations with all-cause mortality. Results: We identified 30 CpGs associated with either Mediterranean-style diet score or Alternative Healthy Eating Index, or both, in European ancestry participants. Among these CpGs, 12 CpGs were significantly associated with all-cause mortality (Bonferroni corrected P <1.6×10 −3 ). Hypermethylation of cg18181703 ( SOCS3 ) was associated with higher scores of both Mediterranean-style diet score and Alternative Healthy Eating Index and lower risk for all-cause mortality ( P =5.7×10 −15 ). Ten additional diet-associated CpGs were nominally associated with all-cause mortality ( P <0.05). MR analysis revealed 8 putatively causal associations for 6 CpGs with 4 cardiovascular disease risk factors (body mass index, triglycerides, high-density lipoprotein cholesterol concentrations, and type 2 diabetes mellitus; Bonferroni corrected MR P <4.5×10 −4 ). For example, hypermethylation of cg11250194 ( FADS2 ) was associated with lower triglyceride concentrations (MR, P =1.5×10 −14 ).and hypermethylation of cg02079413 ( SNORA54 ; NAP1L4 ) was associated with body mass index (corrected MR, P =1×10 −6 ). Conclusions: Habitual diet quality was associated with differential peripheral leukocyte DNA methylation levels of 30 CpGs, most of which were also associated with multiple health outcomes, in European ancestry individuals. These findings demonstrate that integrative genomic analysis of dietary information may reveal molecular targets for disease prevention and treatment. }, author = {Ma, Jiantao and Rebholz, Casey M. and Braun, Kim V. E. and Reynolds, Lindsay M. and Aslibekyan, Stella and Xia, Rui and Biligowda, Niranjan G. and Huan, Tianxiao and Liu, Chunyu and Mendelson, Michael M. and Joehanes, Roby and Hu, Emily A. and Vitolins, Mara Z. and Wood, Alexis C. and Lohman, Kurt and Ochoa-Rosales, Carolina and van Meurs, Joyce and Uitterlinden, André and Liu, Yongmei and Elhadad, Mohamed A. and Heier, Margit and Waldenberger, Melanie and Peters, Annette and Colicino, Elena and Whitsel, Eric A. and Baldassari, Antoine and Gharib, Sina A. and Sotoodehnia, Nona and Brody, Jennifer A. and Sitlani, Colleen M. and Tanaka, Toshiko and Hill, W. David and Corley, Janie and Deary, Ian J. and Zhang, Yan and Schöttker, Ben and Brenner, Hermann and Walker, Maura E. and Ye, Shumao and Nguyen, Steve and Pankow, Jim and Demerath, Ellen W. and Zheng, Yinan and Hou, Lifang and Liang, Liming and Lichtenstein, Alice H. and Hu, Frank B. and Fornage, Myriam and Voortman, Trudy and Levy, Daniel}, doi = {10.1161/circgen.119.002766}, journal = {Circulation: Genomic and Precision Medicine}, month = {jun}, title = {Whole Blood DNA Methylation Signatures of Diet Are Associated with Cardiovascular Disease Risk Factors and All-cause Mortality}, url = {https://oadoi.org/10.1161/circgen.119.002766}, volume = {13}, year = {2020} }