# Eating disorder and bipolar mental illness through genome wide association studies

**Authors:** B. Abdelmoula, R. Rhaiem, A. Charfi, S. Kotti, I. Masmoudi, Y. Marsaoui, N. Bouayed Abdelmoula

PMC · DOI: 10.1192/j.eurpsy.2024.1153 · 2024-08-27

## TL;DR

This paper reviews genetic factors linking eating disorders and bipolar disorder, highlighting shared genetic variants and the need for further research.

## Contribution

The paper identifies specific genetic variants associated with eating disorders comorbid with bipolar disorder using GWAS data.

## Key findings

- 33 GWAS studies on eating disorders identified 324 genetic associations.
- 182 genetic associations were found in eating disorders within bipolar disorder comorbidity.
- Genetic variants include protein-coding, non-coding RNA, and pseudo-genes like CUBN and SOX2-OT.

## Abstract

Besides the role played by environmental factors and their epigenetic influences, scientific researchers showed that the susceptibility to develop an eating disorder among bipolar people is due to genetic factors.

To review the genetic factors behind eating disorders, highlight the role of genetics and epigenetics in the comorbidity of bipolar and eating disorders.

To delineate the role of genetics and epigenetics in eating disorders and bipolar disorders as two related mental illness, we comprehensively reviewed the scientific literature using GWAS (genome wide association studies) catalog databases to find genome-wide association studies carried out on patients with bipolar disorder EFO_0005203 and eating disorder comorbid condition (anorexia nervosa, binge eating, bulimia nervosa) EFO_0005203.

GWAS of eating disorders were found in 33 studies with 324 associations whereas those of bipolar disorder were found in 114 studies with 1469 associations. GWAS of eating disorders within bipolar disorders revealed 182 and 134 associations, as well as 10 and 8 publications respectively. Only anorexia nervosa and binge eating were studied in association with bipolar disorders. The genetic variants were protein coding genes (CUBN, FAM228B, FXR1, etc.), non-coding RNA genes (SOX2-OT, MMADHC-DT, etc.), and pseudo-genes (RNU1-23P, CACYBPP2, etc.).

About 300 genetic variants are associated with eating disorder as a comorbid condition of bipolar disorders. These variants may play a crucial role in the causes and mechanisms of eating disorders and should be more investigated towards more precise clinical and genetic entities.

None Declared

## Linked entities

- **Genes:** CUBN (cubilin) [NCBI Gene 8029], FAM228B (family with sequence similarity 228 member B) [NCBI Gene 375190], FXR1 (FMR1 autosomal homolog 1) [NCBI Gene 8087], SOX2-OT (SOX2 overlapping transcript) [NCBI Gene 347689], MMADHC-DT (MMADHC divergent transcript) [NCBI Gene 101929231], RNU1-23P (RNA, U1 small nuclear 23, pseudogene) [NCBI Gene 106478980], CACYBPP2 (calcyclin binding protein pseudogene 2) [NCBI Gene 644877]
- **Diseases:** eating disorder (MONDO:0005451), bipolar disorder (MONDO:0004985), anorexia nervosa (MONDO:0005351), binge eating (MONDO:0005582), bulimia nervosa (MONDO:0005452)

---
Source: https://tomesphere.com/paper/PMC11860012