Methylome-wide association study of central adiposity implicates genes involved in immune and endocrine systems

Anne E Justice, Geetha Chittoor, Rahul Gondalia, Phillip E Melton, Elise Lim, Megan L Grove, Eric A Whitsel, Ching-Ti Liu, L Adrienne Cupples, Lindsay Fernandez-Rhodes, Weihua Guan, Jan Bressler, Myriam Fornage, Eric Boerwinkle, Yun Li, Ellen Demerath, Nancy Heard-Costa, Dan Levy, James D Stewart, Andrea BaccarelliLifang Hou, Karen Conneely, Trevor A Mori, Lawrence J Beilin, Rae-Chi Huang, Penny Gordon-Larsen, Annie Green Howard, Kari E North

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Aim:We conducted a methylome-wide association study to examine associations between DNA methylation in whole blood and central adiposity and body fat distribution, measured as waist circumference, waist-to-hip ratio and waist-to-height ratio adjusted for body mass index, in 2684 African-American adults in the Atherosclerosis Risk in Communities study.Materials & methods:We validated significantly associated cytosine-phosphate-guanine methylation sites (CpGs) among adults using the Women's Health Initiative and Framingham Heart Study participants (combined n = 5743) and generalized associations in adolescents from The Raine Study (n = 820).Results & conclusion:We identified 11 CpGs that were robustly associated with one or more central adiposity trait in adults and two in adolescents, including CpG site associations nearTXNIP,ADCY7,SREBF1andRAP1GAP2that had not previously been associated with obesity-related traits.

Original languageEnglish
Pages (from-to) 1483-1499
Number of pages18
JournalEpigenomics
Volume12
Issue number17
DOIs
Publication statusPublished - Sep 2020

Fingerprint Dive into the research topics of 'Methylome-wide association study of central adiposity implicates genes involved in immune and endocrine systems'. Together they form a unique fingerprint.

Cite this