Imperial College London

ProfessorPhilippeFroguel

Faculty of MedicineDepartment of Metabolism, Digestion and Reproduction

Chair in Genomic Medicine
 
 
 
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Contact

 

+44 (0)20 7594 6520p.froguel

 
 
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Assistant

 

Mrs Patricia Murphy +44 (0)20 7594 1603

 
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Location

 

E306Burlington DanesHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Koivula:2019:10.1007/s00125-019-4906-1,
author = {Koivula, RW and Forgie, IM and Kurbasic, A and Viñuela, A and Heggie, A and Giordano, GN and Hansen, TH and Hudson, M and Koopman, ADM and Rutters, F and Siloaho, M and Allin, KH and Brage, S and Brorsson, CA and Dawed, AY and De, Masi F and Groves, CJ and Kokkola, T and Mahajan, A and Perry, MH and Rauh, SP and Ridderstråle, M and Teare, HJA and Thomas, EL and Tura, A and Vestergaard, H and White, T and Adamski, J and Bell, JD and Beulens, JW and Brunak, S and Dermitzakis, ET and Froguel, P and Frost, G and Gupta, R and Hansen, T and Hattersley, A and Jablonka, B and Kaye, J and Laakso, M and McDonald, TJ and Pedersen, O and Schwenk, JM and Pavo, I and Mari, A and McCarthy, MI and Ruetten, H and Walker, M and Pearson, E and Franks, PW and IMI, DIRECT Consortium},
doi = {10.1007/s00125-019-4906-1},
journal = {Diabetologia},
pages = {1601--1615},
title = {Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: descriptive characteristics of the epidemiological studies within the IMI DIRECT Consortium.},
url = {http://dx.doi.org/10.1007/s00125-019-4906-1},
volume = {62},
year = {2019}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - AIMS/HYPOTHESIS: Here, we describe the characteristics of the Innovative Medicines Initiative (IMI) Diabetes Research on Patient Stratification (DIRECT) epidemiological cohorts at baseline and follow-up examinations (18, 36 and 48 months of follow-up). METHODS: From a sampling frame of 24,682 adults of European ancestry enrolled in population-based cohorts across Europe, participants at varying risk of glycaemic deterioration were identified using a risk prediction algorithm (based on age, BMI, waist circumference, use of antihypertensive medication, smoking status and parental history of type 2 diabetes) and enrolled into a prospective cohort study (n = 2127) (cohort 1, prediabetes risk). We also recruited people from clinical registries with type 2 diabetes diagnosed 6-24 months previously (n = 789) into a second cohort study (cohort 2, diabetes). Follow-up examinations took place at ~18 months (both cohorts) and at ~48 months (cohort 1) or ~36 months (cohort 2) after baseline examinations. The cohorts were studied in parallel using matched protocols across seven clinical centres in northern Europe. RESULTS: Using ADA 2011 glycaemic categories, 33% (n = 693) of cohort 1 (prediabetes risk) had normal glucose regulation and 67% (n = 1419) had impaired glucose regulation. Seventy-six per cent of participants in cohort 1 was male. Cohort 1 participants had the following characteristics (mean ± SD) at baseline: age 62 (6.2) years; BMI 27.9 (4.0) kg/m2; fasting glucose 5.7 (0.6) mmol/l; 2 h glucose 5.9 (1.6) mmol/l. At the final follow-up examination the participants' clinical characteristics were as follows: fasting glucose 6.0 (0.6) mmol/l; 2 h OGTT glucose 6.5 (2.0) mmol/l. In cohort 2 (diabetes), 66% (n = 517) were treated by lifestyle modification and 34% (n = 272) were treated with metformin plus lifestyle modification at enro
AU - Koivula,RW
AU - Forgie,IM
AU - Kurbasic,A
AU - Viñuela,A
AU - Heggie,A
AU - Giordano,GN
AU - Hansen,TH
AU - Hudson,M
AU - Koopman,ADM
AU - Rutters,F
AU - Siloaho,M
AU - Allin,KH
AU - Brage,S
AU - Brorsson,CA
AU - Dawed,AY
AU - De,Masi F
AU - Groves,CJ
AU - Kokkola,T
AU - Mahajan,A
AU - Perry,MH
AU - Rauh,SP
AU - Ridderstråle,M
AU - Teare,HJA
AU - Thomas,EL
AU - Tura,A
AU - Vestergaard,H
AU - White,T
AU - Adamski,J
AU - Bell,JD
AU - Beulens,JW
AU - Brunak,S
AU - Dermitzakis,ET
AU - Froguel,P
AU - Frost,G
AU - Gupta,R
AU - Hansen,T
AU - Hattersley,A
AU - Jablonka,B
AU - Kaye,J
AU - Laakso,M
AU - McDonald,TJ
AU - Pedersen,O
AU - Schwenk,JM
AU - Pavo,I
AU - Mari,A
AU - McCarthy,MI
AU - Ruetten,H
AU - Walker,M
AU - Pearson,E
AU - Franks,PW
AU - IMI,DIRECT Consortium
DO - 10.1007/s00125-019-4906-1
EP - 1615
PY - 2019///
SN - 0012-186X
SP - 1601
TI - Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: descriptive characteristics of the epidemiological studies within the IMI DIRECT Consortium.
T2 - Diabetologia
UR - http://dx.doi.org/10.1007/s00125-019-4906-1
UR - https://www.ncbi.nlm.nih.gov/pubmed/31203377
UR - https://link.springer.com/article/10.1007%2Fs00125-019-4906-1
UR - http://hdl.handle.net/10044/1/71790
VL - 62
ER -