Aug 2026· Nature Mental Health· Vol 4, pp. 1361 - 1377· 1 citation· 98 references
Medicine
TL;DR
A genomic meta-analysis of case–control studies of binge-eating behavior and analyses of anorexia nervosa and its subtypes, alongside analyses of AN, identified six BE-associated loci and eight areas that are associated with anorexia nervosa, in people of European ancestry.
Abstract
Eating disorders—including anorexia nervosa (AN), bulimia nervosa and binge-eating disorder—are clinically distinct but exhibit symptom overlap and diagnostic crossover. Genomic analyses have mostly examined AN. Here we conducted a genomic meta-analysis of case–control studies of binge-eating behavior (BE; 39,279 cases, 1,227,436 controls), alongside analyses of AN (24,223 cases, 1,243,971 controls) and its subtypes (all European ancestries). We identified six BE-associated loci, including loci associated with a higher body mass index and impulse-control behaviors. AN genome-wide association studies yielded eight loci, validating six loci. Subsequent polygenic risk score analysis demonstrated an association with AN in two East Asian ancestry studies. BE and AN exhibited similar positive genetic correlations with psychiatric disorders but opposing genetic correlations with anthropometric traits. Most of the genetic signal in BE and AN was not shared with body mass index. We have extended eating disorder genomics beyond AN; future work will incorporate multiple diagnoses and global ancestries. This research identified six areas in the genome that are associated with binge eating, and eight areas that are associated with anorexia nervosa, in people of European ancestry. Binge eating has both shared and distinct genetic features compared with anorexia nervosa.
A meta-GWAS with seven studies of European ancestry identified for the first time a robust chromosomal region associated with emotional eating in seven studies, supporting the hypothesis that shared genetic factors may influence both eating behavior traits and obesity risk.
M. Muntaner, K. Horn, B. de Lauzon-Guillain et al.· Molecular Psychiatry· 0 citations
Cross-disorder AN and PD research identified shared risk variants at chr3p21.31, genes and mechanisms linked to a shared endophenotype linked to a shared endophenotype.
Andrew W. Bergen, Carolina Makowski, Michael Garvin et al.· European eating disorders re...· 0 citations
Although both eating disorder phenotypes correlate genetically with other psychiatric conditions, binge eating also correlates with impulsivity, earlier age at first menstrual cycle and increased body mass, whereas anorexia nervosa shares genetics with metabolic traits.
Jonathan R. I. Coleman, H. Davies· Nature Mental Health· 0 citations
Findings support a multifactorial model of AN involving individual-specific influences and shared familial liability, and suggest that several clinical and phenotypic features may reflect familial liability for AN.
Hunna J. Watson, Elisabeth Welch, Elin Monell et al.· European eating disorders re...· 0 citations
Importance
Bulimia nervosa (BN) ranks second among eating disorders in both prevalence and disease burden, but its neurobiology is poorly understood. Progress has been limited by neuroimaging studies with inconsistent findings across small samples.
Objective
To identify reliable structural brain correlates of BN diag...
Laura A. Berner, Anusha Phadnis, M. Westwater et al.· JAMA psychiatry· 0 citations
Bipolar disorder’s genetic architecture appears hierarchical—a general liability resolving into dimensions of course and comorbidity, beyond subtypes, beyond subtypes.
Tracey van der Veen, M. Tesfaye, J. M. K. Yang et al.· Research Square· 0 citations
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