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Published in: Diabetologia 6/2014

Open Access 01-06-2014 | Article

Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: rationale and design of the epidemiological studies within the IMI DIRECT Consortium

Authors: Robert W. Koivula, Alison Heggie, Anna Barnett, Henna Cederberg, Tue H. Hansen, Anitra D. Koopman, Martin Ridderstråle, Femke Rutters, Henrik Vestergaard, Ramneek Gupta, Sanna Herrgård, Martijn W. Heymans, Mandy H. Perry, Simone Rauh, Maritta Siloaho, Harriet J. A. Teare, Barbara Thorand, Jimmy Bell, Søren Brunak, Gary Frost, Bernd Jablonka, Andrea Mari, Tim J. McDonald, Jacqueline M. Dekker, Torben Hansen, Andrew Hattersley, Markku Laakso, Oluf Pedersen, Veikko Koivisto, Hartmut Ruetten, Mark Walker, Ewan Pearson, Paul W. Franks, for the DIRECT Consortium

Published in: Diabetologia | Issue 6/2014

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Abstract

Aims/hypothesis

The DIRECT (Diabetes Research on Patient Stratification) Study is part of a European Union Framework 7 Innovative Medicines Initiative project, a joint undertaking between four industry and 21 academic partners throughout Europe. The Consortium aims to discover and validate biomarkers that: (1) predict the rate of glycaemic deterioration before and after type 2 diabetes onset; (2) predict the response to diabetes therapies; and (3) help stratify type 2 diabetes into clearly definable disease subclasses that can be treated more effectively than without stratification. This paper describes two new prospective cohort studies conducted as part of DIRECT.

Methods

Prediabetic participants (target sample size 2,200–2,700) and patients with newly diagnosed type 2 diabetes (target sample size ~1,000) are undergoing detailed metabolic phenotyping at baseline and 18 months and 36 months later. Abdominal, pancreatic and liver fat is assessed using MRI. Insulin secretion and action are assessed using frequently sampled OGTTs in non-diabetic participants, and frequently sampled mixed-meal tolerance tests in patients with type 2 diabetes. Biosamples include venous blood, faeces, urine and nail clippings, which, among other biochemical analyses, will be characterised at genetic, transcriptomic, metabolomic, proteomic and metagenomic levels. Lifestyle is assessed using high-resolution triaxial accelerometry, 24 h diet record, and food habit questionnaires.

Conclusions/interpretation

DIRECT will yield an unprecedented array of biomaterials and data. This resource, available through managed access to scientists within and outside the Consortium, will facilitate the development of new treatments and therapeutic strategies for the prevention and management of type 2 diabetes.
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Metadata
Title
Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: rationale and design of the epidemiological studies within the IMI DIRECT Consortium
Authors
Robert W. Koivula
Alison Heggie
Anna Barnett
Henna Cederberg
Tue H. Hansen
Anitra D. Koopman
Martin Ridderstråle
Femke Rutters
Henrik Vestergaard
Ramneek Gupta
Sanna Herrgård
Martijn W. Heymans
Mandy H. Perry
Simone Rauh
Maritta Siloaho
Harriet J. A. Teare
Barbara Thorand
Jimmy Bell
Søren Brunak
Gary Frost
Bernd Jablonka
Andrea Mari
Tim J. McDonald
Jacqueline M. Dekker
Torben Hansen
Andrew Hattersley
Markku Laakso
Oluf Pedersen
Veikko Koivisto
Hartmut Ruetten
Mark Walker
Ewan Pearson
Paul W. Franks
for the DIRECT Consortium
Publication date
01-06-2014
Publisher
Springer Berlin Heidelberg
Published in
Diabetologia / Issue 6/2014
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-014-3216-x

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