Hostname: page-component-78c5997874-t5tsf Total loading time: 0 Render date: 2024-11-18T08:49:45.153Z Has data issue: false hasContentIssue false
  • English
  • Français

Genetic Markers and Disordered Eating Amongst Adolescents- the Hunt Study

Published online by Cambridge University Press:  15 April 2020

F. Saeedzadeh Sardahaee ,
N. Micali ,
T. Lingaas Holmen  and
K. Kvaløy
F. Saeedzadeh Sardahaee
Affiliation:
HUNT research center, Institute of Public Health and general practice, Medical Faculty, NTNU Adult Psychiatry Department, Levanger Hospital, Levanger, Norway
N. Micali
Affiliation:
UCL Institute of Child Health, Behavioural and Brain Sciences Unit, London, United Kingdom
T. Lingaas Holmen
Affiliation:
HUNT research center, Institute of Public Health and general practice, Medical Faculty, NTNU
K. Kvaløy
Affiliation:
HUNT research center, Institute of Public Health and general practice, Medical Faculty, NTNU

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Introduction

Disordered eating has a strong genetic component which is not fully understood.

Objective

Possible associations between certain genetic markers and disordered eating at adolescence were tested in the Nord-Trøndelag Health Study (HUNT).

Methods

Logistic regression was employed to test for association with the gene variants rs6277 (DRD2), rs569356 (OPRD1), rs10195252 (GRB14), rs35683 (GHRL), rs4074134 (BDNF), rs10838738 (MTCH2), rs1121980 (FTO), rs17782313 (MC4R) and rs11084753 (KCTD15) in participants aged 13 to19. EAT-7, a shortened version of EAT-12 was used to identify cases as those scoring above cutoff on EAT-7(456 cases) and its anorexia (EAT-A, 259 cases) and bulimia subscale (EAT-B, 433 cases), compared against 5405 controls. A haplotype analysis was performed for markers within FTO, MC4R and BDNF genes. Associations were adjusted for gender, age and BMI.

Results

In males, rs6277 showed significant association with EAT-B (OR: 1.32, p = 0.03) after adjustments for age and BMI.

The A-allele of rs11084753 showed positive associations with EAT-A (OR: 1.25, p = 0.01) in the combined sample. In females, after adjusting for age and BMI, the C-allele of rs10195252 was positively associated with EAT-A (OR: 1.30, p = 0.01).

After adjustments for age and BMI in females, rs10195252 showed significant association with EAT-7(OR: 1.18, p: 0.02).

Haplotype analysis on FTO gene revealed a 'collective reinforced effect' of the GCT alleles from rs1121980, rs8050136 and rs9939609, respectively, compared to rs1121980 variant alone.

Conclusion

We found evidence in support of associations between DRD2, FTO, GRB14 and KCTD15 with disordered eating. Associations seem to vary based on gender.

Type
Article: 0359
Information
European Psychiatry , Volume 30 , Issue S1: Abstracts of the 23rd European Congress of Psychiatry , March 2015 , pp. 1
Copyright
Copyright © European Psychiatric Association 2015
Submit a response

Comments

No Comments have been published for this article.