A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling
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Boraska, V, et al. A Genome-wide Association Study of Anorexia Nervosa Suggests a Risk Locus Implicated In Dysregulated Leptin Signaling. 2014. https://doi.org/10.17615/1j9k-h794APA
Boraska, V., Franklin, C., Floyd, J., Thornton, L., Huckins, L., Southam, L., Rayner, N., Tachmazidou, I., Klump, K., Treasure, J., Lewis, C., Schmidt, U., Tozzi, F., Kiezebrink, K., Hebebrand, J., Gorwood, P., Adan, R., Kas, M., Favaro, A., Santonastaso, P., Fernández Aranda, F., Gratacos, M., Rybakowski, F., Dmitrzak Weglarz, M., Kaprio, J., Keski Rahkonen, A., Raevuori, A., Van Furth, E., Slof Op 'T Landt, M., Hudson, J., Reichborn Kjennerud, T., & Knudsen, G. (2014). A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling. https://doi.org/10.17615/1j9k-h794Chicago
Boraska, V, C S Franklin, J A B Floyd, L M Thornton, L M Huckins, L Southam, N W Rayner et al. 2014. A Genome-Wide Association Study of Anorexia Nervosa Suggests a Risk Locus Implicated In Dysregulated Leptin Signaling. https://doi.org/10.17615/1j9k-h794- Creator
- Boraska, V
- Franklin, C S
- Floyd, J A B
- Thornton, L M
- Huckins, L M
- Southam, L
- Rayner, N W
- Tachmazidou, I
- Klump, K L
- Treasure, J
- Lewis, C M
- Schmidt, U
- Tozzi, F
- Kiezebrink, K
- Hebebrand, J
- Gorwood, P
- Adan, R A H
- Kas, M J H
- Favaro, A
- Santonastaso, P
- Fernández-Aranda, F
- Gratacos, M
- Rybakowski, F
- Dmitrzak-Weglarz, M
- Kaprio, J
- Keski-Rahkonen, A
- Raevuori, A
- Van Furth, E F
- Slof-Op 't Landt, M C T
- Hudson, J I
- Reichborn-Kjennerud, T
- Knudsen, G P S
- Abstract
- Anorexia nervosa (AN) is a complex and heritable eating disorder characterized by dangerously low body weight. Neither candidate gene studies nor an initial genome wide association study (GWAS) have yielded significant and replicated results. We performed a GWAS in 2,907 cases with AN from 14 countries (15 sites) and 14,860 ancestrally matched controls as part of the Genetic Consortium for AN (GCAN) and the Wellcome Trust Case Control Consortium 3 (WTCCC3). Individual association analyses were conducted in each stratum and meta-analyzed across all 15 discovery datasets. Seventy-six (72 independent) SNPs were taken forward for in silico (two datasets) or de novo (13 datasets) replication genotyping in 2,677 independent AN cases and 8,629 European ancestry controls along with 458 AN cases and 421 controls from Japan. The final global meta-analysis across discovery and replication datasets comprised 5,551 AN cases and 21,080 controls. AN subtype analyses (1,606 AN restricting; 1,445 AN binge-purge) were performed. No findings reached genome-wide significance. Two intronic variants were suggestively associated: rs9839776 (P=3.01×10-7) in SOX2OT and rs17030795 (P=5.84×10-6) in PPP3CA. Two additional signals were specific to Europeans: rs1523921 (P=5.76×10-6) between CUL3 and FAM124B and rs1886797 (P=8.05×10-6) near SPATA13. Comparing discovery to replication results, 76% of the effects were in the same direction, an observation highly unlikely to be due to chance (P=4×10-6), strongly suggesting that true findings exist but that our sample, the largest yet reported, was underpowered for their detection. The accrual of large genotyped AN case-control samples should be an immediate priority for the field.
- Date of publication
- 2014
- Keyword
- metabolic
- eating disorders
- OF-THE-LITERATURE
- POPULATION-BASED TWIN
- Neurosciences
- ANXIETY DISORDERS
- Science & Technology
- genome-wide association study
- Biochemistry & Molecular Biology
- GWAS
- body mass index
- LINKAGE ANALYSIS
- MEDICAL COMPLICATIONS
- anorexia nervosa
- BODY-MASS INDEX
- Neurosciences & Neurology
- Psychiatry
- CONTROLLED FAMILY
- BULIMIA-NERVOSA
- Life Sciences & Biomedicine
- EATING-DISORDERS
- RISK-FACTORS
- DOI
- Identifier
- PMCID: PMC4325090
- PMID: 24514567
- Publisher DOI: https://doi.org/10.1038/mp.2013.187
- Onescience id: f45bd8238d782bc997ad8c69de06427782f33770
- Resource type
- Article
- Rights statement
- In Copyright
- Journal title
- Molecular Psychiatry
- Journal volume
- 19
- Journal issue
- 10
- Language
- English
- ISSN
- 1476-5578
- 1359-4184
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