A genome-wide significant linkage for severe depression on chromosome 3: the depression network study.

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Etat: Public
Version: de l'auteur
ID Serval
serval:BIB_398AF59E63AB
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
A genome-wide significant linkage for severe depression on chromosome 3: the depression network study.
Périodique
American Journal of Psychiatry
Auteur(s)
Breen G., Webb B.T., Butler A.W., van den Oord E.J., Tozzi F., Craddock N., Gill M., Korszun A., Maier W., Middleton L., Mors O., Owen M.J., Cohen-Woods S., Perry J., Galwey N.W., Upmanyu R., Craig I., Lewis C.M., Ng M., Brewster S., Preisig M., Rietschel M., Jones L., Knight J., Rice J., Muglia P., Farmer A.E., McGuffin P.
ISSN
1535-7228 (Electronic)
ISSN-L
0002-953X
Statut éditorial
Publié
Date de publication
2011
Peer-reviewed
Oui
Volume
168
Numéro
8
Pages
840-847
Langue
anglais
Résumé
Objective: The purpose of this study was to find loci for major depression via linkage analysis of a large sibling pair sample. Method: The authors conducted a genome-wide linkage analysis of 839 families consisting of 971 affected sibling pairs with severe recurrent major depression, comprising waves I and II of the Depression Network Study cohort. In addition to examining affected status, linkage analyses in the full data set were performed using diagnoses restricted by impairment severity, and association mapping of hits in a large case-control data set was attempted. Results: The authors identified genome-wide significant linkage to chromosome 3p25-26 when the diagnoses were restricted by severity, which was a maximum LOD score of 4.0 centered at the linkage marker D3S1515. The linkage signal identified was genome-wide significant after correction for the multiple phenotypes tested, although subsequent association mapping of the region in a genome-wide association study of a U.K. depression sample did not provide significant results. Conclusions: The authors report a genome-wide significant locus for depression that implicates genes that are highly plausible for involvement in the etiology of recurrent depression. Despite the fact that association mapping in the region was negative, the linkage finding was replicated by another group who found genome-wide-significant linkage for depression in the same region. This suggests that 3p25-26 is a new locus for severe recurrent depression. This represents the first report of a genome-wide significant locus for depression that also has an independent genome-wide significant replication.
Pubmed
Web of science
Création de la notice
22/08/2011 16:13
Dernière modification de la notice
20/08/2019 14:29
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