Assessing Global and Gene Specific DNA Methylation in Anorexia Nervosa: A Pilot Study

被引:22
作者
Saffrey, Richard [1 ,2 ]
Novakovic, Boris [1 ]
Wade, Tracey D. [3 ]
机构
[1] Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[2] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[3] Flinders Univ S Australia, Sch Psychol, Adelaide, SA 5001, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
anorexia nervosa; epigenetics; DNA methylation; EXPRESSION; EXPOSURE; PROMOTER; FEMALES; REVEALS; TWINS;
D O I
10.1002/eat.22200
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: At present there are no genome-wide methylation data available in anorexia nervosa (AN) and no studies have examined the potential dynamic nature of DNA methylation during treatment, so it is unclear whether epigenetic disruption established over long periods of malnourishment is reversible. The current study examined global levels of DNA methylation and methylation at a labile imprinted locus in women with AN. Method: Buccal swabs were collected from 10 women who were admitted to hospital for treatment of AN and 10 age-matched healthy controls DNA methylation of LINE-1 repetitive elements and the H19 imprinting control region was measured using previously validated assays using the Sequenom Mass Array platform. Results: No evidence for altered global or gene-specific DNA methylation was observed in association with AN. Discussion: Larger, genome-wide studies of epigenetic modifications, encompassing both DNA methylation and other epigenetic marks, are required to determine the degree to which AN is associated with specific epigenetic changes, potentially modifiable through appropriate treatments that improve nutrition. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:206 / 210
页数:5
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