A genome-wide association study of anorexia nervosa
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
U24 CA074783
NCI NIH HHS - United States
R01 MH066122
NIMH NIH HHS - United States
R01 AA009203
NIAAA NIH HHS - United States
K01 MH100435
NIMH NIH HHS - United States
K05 AA000145
NIAAA NIH HHS - United States
UM1 CA167551
NCI NIH HHS - United States
MH0662
NIMH NIH HHS - United States
R37 AA012502
NIAAA NIH HHS - United States
K02AA018755
NIAAA NIH HHS - United States
MH066117
NIMH NIH HHS - United States
F32 NS010045
NINDS NIH HHS - United States
MH066146
NIMH NIH HHS - United States
5R01ES011740
NIEHS NIH HHS - United States
R01 MH078075
NIMH NIH HHS - United States
UL1TR000083
NCATS NIH HHS - United States
MH066288
NIMH NIH HHS - United States
088827
Wellcome Trust - United Kingdom
R01 CA133996
NCI NIH HHS - United States
R01 MH066287
NIMH NIH HHS - United States
P50 CA097007
NCI NIH HHS - United States
WT088984
Wellcome Trust - United Kingdom
3P50CA093459
NCI NIH HHS - United States
R01 MH066193
NIMH NIH HHS - United States
MH066193
NIMH NIH HHS - United States
5P50CA097007
NCI NIH HHS - United States
R01 ES011740
NIEHS NIH HHS - United States
MH066145
NIMH NIH HHS - United States
AA-09203
NIAAA NIH HHS - United States
MR/J006742/1
Medical Research Council - United Kingdom
MR/K500999/1
Medical Research Council - United Kingdom
AA-00145
NIAAA NIH HHS - United States
R01 MH066296
NIMH NIH HHS - United States
AA15416
NIAAA NIH HHS - United States
MH066296
NIMH NIH HHS - United States
U54 RR0252204-01
NCRR NIH HHS - United States
R01 MH066147
NIMH NIH HHS - United States
R01 MH066146
NIMH NIH HHS - United States
5R01CA133996
NCI NIH HHS - United States
K02 AA018755
NIAAA NIH HHS - United States
090532
Wellcome Trust - United Kingdom
R01 MH066288
NIMH NIH HHS - United States
T32 MH076694
NIMH NIH HHS - United States
MH066122
NIMH NIH HHS - United States
AA-12502
NIAAA NIH HHS - United States
R01 AA012502
NIAAA NIH HHS - United States
K12HD001441
NICHD NIH HHS - United States
R01 AA015416
NIAAA NIH HHS - United States
R01 MH066117
NIMH NIH HHS - United States
MH066287
NIMH NIH HHS - United States
HSRU1
Chief Scientist Office - United Kingdom
R01 MH066145
NIMH NIH HHS - United States
U01 CA074783
NCI NIH HHS - United States
WT088827/Z/09
Wellcome Trust - United Kingdom
P50 CA093459
NCI NIH HHS - United States
K12 HD001441
NICHD NIH HHS - United States
001
World Health Organization - International
MH066147
NIMH NIH HHS - United States
PubMed
24514567
PubMed Central
PMC4325090
DOI
10.1038/mp.2013.187
PII: mp2013187
Knihovny.cz E-zdroje
- MeSH
- Asijci genetika MeSH
- běloši genetika MeSH
- celogenomová asociační studie MeSH
- jaderné proteiny genetika MeSH
- jednonukleotidový polymorfismus MeSH
- kalcineurin genetika MeSH
- kulinové proteiny genetika MeSH
- lidé MeSH
- mentální anorexie genetika MeSH
- metaanalýza jako téma MeSH
- studie případů a kontrol MeSH
- transportní proteiny genetika MeSH
- výměnné faktory guaninnukleotidů genetika MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Geografické názvy
- Japonsko MeSH
- Názvy látek
- CUL3 protein, human MeSH Prohlížeč
- FAM124B protein, human MeSH Prohlížeč
- jaderné proteiny MeSH
- kalcineurin MeSH
- kulinové proteiny MeSH
- PPP3CA protein, human MeSH Prohlížeč
- SPATA13 protein, human MeSH Prohlížeč
- transportní proteiny MeSH
- výměnné faktory guaninnukleotidů MeSH
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 2907 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 data sets. Seventy-six (72 independent) single nucleotide polymorphisms were taken forward for in silico (two data sets) or de novo (13 data sets) replication genotyping in 2677 independent AN cases and 8629 European ancestry controls along with 458 AN cases and 421 controls from Japan. The final global meta-analysis across discovery and replication data sets comprised 5551 AN cases and 21 080 controls. AN subtype analyses (1606 AN restricting; 1445 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 with 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 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.
] Genomics and Disease Group Centre for Genomic Regulation Barcelona Spain
1st Department of Psychiatry Athens University Medical School Athens Greece
Altrecht Eating Disorders Rintveld Zeist The Netherlands
Centre de Psychiatrie et Neurosciences Inserm U894 Paris France
Clinical Genetics Unit Department of Woman and Child Health University of Padova Padova Italy
CNRS 8090 Institute of Biology Pasteur Institute Lille France
Department of Cancer Epidemiology and Genetics Masaryk Memorial Cancer Institute Brno Czech Republic
Department of Child and Adolescent Psychiatry Institute of Psychiatry and Neurology Warsaw Poland
Department of Epidemiology Institute of Occupational Medicine Department of Epidemiology Lodz Poland
Department of Genetics The University of North Carolina at Chapel Hill Chapel Hill NC USA
Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden
Department of Medical Genetics University Medical Center Utrecht Utrecht The Netherlands
Department of Molecular Life Sciences Tokai University School of Medicine Kanagawa Japan
Department of Neurosciences University of Padova Padova Italy
Department of Nutrition and Dietetics Harokopio University Athens Greece
Department of Pediatrics 1st Faculty of Medicine Charles University Prague Czech Republic
Department of Psychiatry 1st Faculty of Medicine Charles University Prague Czech Republic
Department of Psychiatry and Psychotherapy Medical University of Vienna Vienna Austria
Department of Psychiatry McLean Hospital Harvard Medical School Belmont MA USA
Department of Psychiatry Poznan University of Medical Sciences Poznan Poland
Department of Psychiatry University of Naples SUN Naples Italy
Department of Psychiatry University of North Carolina at Chapel Hill Chapel Hill NC USA
Department of Psychiatry University of Pennsylvania Philadelphia PA USA
Department of Psychology Michigan State University East Lansing MI USA
Department of Psychology University of Oslo Oslo Norway
Department of Psychosomatic Research National Institute of Mental Health NCNP Tokyo Japan
Departments of Psychosocial and Internal Medicine Heidelberg University Heidelberg Germany
Eating Disorders Unit 1st Department of Psychiatry Athens University Medical School Athens Greece
Estonian Genome Center University of Tartu Tartu Estonia
Genetic Epidemiology Group International Agency for Research on Cancer Lyon France
Health Services Research Unit University of Aberdeen Aberdeen UK
Hjelt Institute University of Helsinki Helsinki Finland
INSERM U894 Centre of Psychiatry and Neuroscience Paris France
Institute of Clinical Molecular Biology University of Kiel Kiel Germany
Kartini Clinic Portland OR USA
Klinikum der Medizinischen Fakultät Martin Luther Universität Halle Wittenberg Halle Saale Germany
M Sklodowska Curie Cancer Center and Institute of Oncology Warsaw Poland
McGill University and Genome Quebec Innovation Centre Montreal QC Canada
Palacky University Olomouc Czech Republic
Parklandklinik Bad Wildungen Germany
Rheumatology Unit Department of Medicine at the Karolinska University Hospital Solna Sweden
Seattle University College of Nursing Seattle WA USA
Section of Eating Disorders Institute of Psychiatry King's College London London UK
The Center for Applied Genomics The Children's Hospital of Philadelphia Philadelphia PA USA
The Institute of Environmental Medicine Karolinska Institutet Stockholm Sweden
Wellcome Trust Sanger Institute Wellcome Trust Genome Campus Hinxton Cambridge UK
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