Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/64142
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dc.contributor.authorHilner, Joan E.en
dc.contributor.authorPerdue, Letitia H.en
dc.contributor.authorSides, Elizabeth G.en
dc.contributor.authorPierce, June J.en
dc.contributor.authorWagner, Ana M.en
dc.contributor.authorAldrich, Alanen
dc.contributor.authorLoth, Amandaen
dc.contributor.authorAlbret, Lotteen
dc.contributor.authorWagenknecht, Lynne E.en
dc.contributor.authorNierras, Concepcionen
dc.contributor.authorAkolkar, Beenaen
dc.contributor.authorType 1 Diabetes Genetics Consortiumen
dc.date.issued2010en
dc.identifier.citationClinical Trials, 2010;7(1 Suppl):S5-S32en
dc.identifier.issn1740-7745en
dc.identifier.urihttp://hdl.handle.net/2440/64142-
dc.description.abstractBackground and Purpose The Type 1 Diabetes Genetics Consortium (T1DGC) is an international project whose primary aims are to: (a) discover genes that modify type 1 diabetes risk; and (b) expand upon the existing genetic resources for type 1 diabetes research. The initial goal was to collect 2500 affected sibling pair (ASP) families worldwide. Methods T1DGC was organized into four regional networks (Asia-Pacific, Europe, North America, and the United Kingdom) and a Coordinating Center. A Steering Committee, with representatives from each network, the Coordinating Center, and the funding organizations, was responsible for T1DGC operations. The Coordinating Center, with regional network representatives, developed study documents and data systems. Each network established laboratories for: DNA extraction and cell line production; human leukocyte antigen genotyping; and autoantibody measurement. Samples were tracked from the point of collection, processed at network laboratories and stored for deposit at National Institute for Diabetes and Digestive and Kidney Diseases (NIDDK) Central Repositories. Phenotypic data were collected and entered into the study database maintained by the Coordinating Center. Results T1DGC achieved its original ASP recruitment goal. In response to research design changes, the T1DGC infrastructure also recruited trios, cases, and controls. Results of genetic analyses have identified many novel regions that affect susceptibility to type 1 diabetes. T1DGC created a resource of data and samples that is accessible to the research community. Limitations Participation in T1DGC was declined by some countries due to study requirements for the processing of samples at network laboratories and/or final deposition of samples in NIDDK Central Repositories. Re-contact of participants was not included in informed consent templates, preventing collection of additional samples for functional studies. Conclusions T1DGC implemented a distributed, regional network structure to reach ASP recruitment targets. The infrastructure proved robust and flexible enough to accommodate additional recruitment. T1DGC has established significant resources that provide a basis for future discovery in the study of type 1 diabetes genetics.en
dc.description.statementofresponsibilityJoan E Hilner, Letitia H Perdue, Elizabeth G Sides, June J Pierce, Ana M Wägner, Alan Aldrich, Amanda Loth, Lotte Albret, Lynne E Wagenknecht, Concepcion Nierras, Beena Akolkar and the T1DGCen
dc.language.isoenen
dc.publisherSage Publications Ltd.en
dc.rights(c) 2010 The Authors. Sage Publications Ltd.en
dc.rights.urihttp://www.sagepub.co.uk/journalsPermissions.naven
dc.titleDesigning and implementing sample and data collection for an international genetics study: the Type 1 Diabetes Genetics Consortiumen
dc.typeJournal articleen
dc.contributor.schoolSchool of Paediatrics and Reproductive Health : Paediatricsen
dc.identifier.doi10.1177/1740774510373497en
Appears in Collections:Paediatrics publications

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