Designing and implementing sample and data collection for an international genetics study: the Type 1 Diabetes Genetics Consortium (T1DGC)

Author:

Hilner Joan E1,Perdue Letitia H2,Sides Elizabeth G2,Pierce June J2,Wägner Ana M3,Aldrich Alan4,Loth Amanda5,Albret Lotte6,Wagenknecht Lynne E2,Nierras Concepcion7,Akolkar Beena8,

Affiliation:

1. Department of Biostatistics, School of Public Health, University of Alabama at Birmingham, Birmingham, AL, USA, jhilner@ms.soph.uab.edu

2. Division of Public Health Sciences, Wake Forest University Health Sciences, Winston Salem, NC, USA

3. Hagedorn Research Institute, Gentofte, Denmark, Department of Endocrinology, Hospital Universitario Insular de Gran Canaria, Las Palmas de Gran Canaria, Spain, Department of Medical and Surgical Science, Universidad de Las Palmas de Gran Canaria, Las Palmas de Gran Canaria, Spain

4. University of Alaska Anchorage College of Arts and Sciences, Integrated Sciences, Anchorage, AK, USA

5. Burnet Clinical Research Unit, Walter & Eliza Hall Institute of Medical Research, Melbourne, Australia

6. Hagedorn Research Institute, Gentofte, Denmark

7. Juvenile Diabetes Research Foundation International, New York, NY, USA

8. Division of Diabetes, Endocrinology and Metabolic Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA

Abstract

Background 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. Clinical Trials 2010; 7: S5—S32. http://ctj.sagepub.com

Publisher

SAGE Publications

Subject

Pharmacology,General Medicine

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