A longitudinal, epigenome-wide study of DNA methylation in anorexia nervosa: results in actively ill, partially weight-restored, long-term remitted and non-eating-disordered women

• Published in: Journal of psychiatry & neuroscience Vol. 44; no. 3; pp. 205 - 213
• Main Authors: Steiger, Howard, Booij, Linda, Kahan, `Esther, McGregor, Kevin, Thaler, Lea, Fletcher, Emilie, Labbe, Aurelie, Joober, Ridha, Israël, Mimi, Szyf, Moshe, Agellon, Luis B., Gauvin, Lise, St-Hilaire, Annie, Rossi, Erika
• Format: Journal Article
• Language: English
• Published: Canada Joule Inc 01.05.2019; CMA Impact, Inc
• Subjects: Adolescent; Adult; Age; Anorexia; Anorexia nervosa; Anorexia Nervosa - genetics; Anorexia Nervosa - physiopathology; Anorexia Nervosa - therapy; Body mass index; Brain research; Breast cancer; Chronic Disease; Deoxyribonucleic acid; DNA; DNA methylation; DNA Methylation - genetics; DNA probes; Dopamine; Eating disorders; EDTA; Epigenetic inheritance; Epigenetics; Epigenome - genetics; Female; Gene expression; Genes; Genetic aspects; Genetic research; Genomes; Genomics; Glucose; Glucose metabolism; Glutamate; Health aspects; Humans; Illnesses; Immune response; Inflammation; Insulin; Lipid metabolism; Lipids; Longitudinal Studies; Metabolism; Methylation; Middle Aged; Nutritional status; Olfaction; Phenols (Class of compounds); Psychological aspects; Remission; Remission Induction; Research Paper; Schizophrenia; Serotonin; Substance use; Women's health; Womens health; Young Adult
• ISSN: 1180-4882; 1488-2434; 1488-2434
• DOI: 10.1503/jpn.170242

This study explored state-related tendencies in DNA methylation in people with anorexia nervosa. We measured genome-wide DNA methylation in 75 women with active anorexia nervosa (active), 31 women showing stable remission of anorexia nervosa (remitted) and 41 women with no eating disorder (NED). We also obtained post-intervention methylation data from 52 of the women from the active group. Comparisons between members of the active and NED groups showed 58 differentially methylated sites (Q < 0.01) that corresponded to genes relevant to metabolic and nutritional status (lipid and glucose metabolism), psychiatric status (serotonin receptor activity) and immune function. Methylation levels in members of the remitted group differed from those in the active group on 265 probes that also involved sites associated with genes for serotonin and insulin activity, glucose metabolism and immunity. Intriguingly, the direction of methylation effects in remitted participants tended to be opposite to those seen in active participants. The chronicity of Illness correlated (usually inversely, at Q < 0.01) with methylation levels at 64 sites that mapped onto genes regulating glutamate and serotonin activity, insulin function and epigenetic age. In contrast, body mass index increases coincided (at Q < 0.05) with generally increased methylation-level changes at 73 probes associated with lipid and glucose metabolism, immune and inflammatory processes, and olfaction. Sample sizes were modest for this type of inquiry, and findings may have been subject to uncontrolled effects of medication and substance use. Findings point to the possibility of reversible epigenetic alterations in anorexia nervosa, and suggest that an adequate pathophysiological model would likely need to include psychiatric, metabolic and immune components.