TY - JOUR
T1 - Profiles of glucose metabolism in different prediabetes phenotypes, classified by fasting glycemia, 2-hour OGTT, glycated hemoglobin, and 1-hour OGTT
T2 - An IMI DIRECT study
AU - IMI DIRECT Consortium
AU - Tura, Andrea
AU - Grespan, Eleonora
AU - Göbl, Christian S.
AU - Koivula, Robert W.
AU - Franks, Paul W.
AU - Pearson, Ewan R.
AU - Walker, Mark
AU - Forgie, Ian M.
AU - Giordano, Giuseppe N.
AU - Pavo, Imre
AU - Ruetten, Hartmut
AU - Dermitzakis, Emmanouil T.
AU - McCarthy, Mark I.
AU - Pedersen, Oluf
AU - Schwenk, Jochen M.
AU - Adamski, Jerzy
AU - De Masi, Federico
AU - Tsirigos, Konstantinos D.
AU - Brunak, Søren
AU - Viñuela, Ana
AU - Mahajan, Anubha
AU - McDonald, Timothy J.
AU - Kokkola, Tarja
AU - Vangipurapu, Jagadish
AU - Cederberg, Henna
AU - Laakso, Markku
AU - Rutters, Femke
AU - Elders, Petra J. M.
AU - Koopman, Anitra D. M.
AU - Beulens, Joline W.
AU - Ridderstråle, Martin
AU - Hansen, Tue H.
AU - Allin, Kristine H.
AU - Hansen, Torben
AU - Vestergaard, Henrik
AU - Mari, Andrea
N1 - © 2021 by the American Diabetes Association.
PY - 2021/9/1
Y1 - 2021/9/1
N2 - Differences in glucose metabolism among categories of prediabetes have not been systematically investigated. In this longitudinal study, participants (N = 2,111) underwent a 2-h 75-g oral glucose tolerance test (OGTT) at baseline and 48 months. HbA1c was also measured. We classified participants as having isolated prediabetes defect (impaired fasting glucose [IFG], impaired glucose tolerance [IGT], or HbA1c indicative of prediabetes [IA1c]), two defects (IFG+IGT, IFG+IA1c, or IGT+IA1c), or all defects (IFG+IGT+IA1c). β-Cell function (BCF) and insulin sensitivity were assessed from OGTT. At baseline, in pooling of participants with isolated defects, they showed impairment in both BCF and insulin sensitivity compared with healthy control subjects. Pooled groups with two or three defects showed progressive further deterioration. Among groups with isolated defect, those with IGT showed lower insulin sensitivity, insulin secretion at reference glucose (ISRr), and insulin secretion potentiation (P < 0.002). Conversely, those with IA1c showed higher insulin sensitivity and ISRr (P < 0.0001). Among groups with two defects, we similarly found differences in both BCF and insulin sensitivity. At 48 months, we found higher type 2 diabetes incidence for progressively increasing number of prediabetes defects (odds ratio >2, P < 0.008). In conclusion, the prediabetes groups showed differences in type/degree of glucometabolic impairment. Compared with the pooled group with isolated defects, those with double or triple defect showed progressive differences in diabetes incidence.
AB - Differences in glucose metabolism among categories of prediabetes have not been systematically investigated. In this longitudinal study, participants (N = 2,111) underwent a 2-h 75-g oral glucose tolerance test (OGTT) at baseline and 48 months. HbA1c was also measured. We classified participants as having isolated prediabetes defect (impaired fasting glucose [IFG], impaired glucose tolerance [IGT], or HbA1c indicative of prediabetes [IA1c]), two defects (IFG+IGT, IFG+IA1c, or IGT+IA1c), or all defects (IFG+IGT+IA1c). β-Cell function (BCF) and insulin sensitivity were assessed from OGTT. At baseline, in pooling of participants with isolated defects, they showed impairment in both BCF and insulin sensitivity compared with healthy control subjects. Pooled groups with two or three defects showed progressive further deterioration. Among groups with isolated defect, those with IGT showed lower insulin sensitivity, insulin secretion at reference glucose (ISRr), and insulin secretion potentiation (P < 0.002). Conversely, those with IA1c showed higher insulin sensitivity and ISRr (P < 0.0001). Among groups with two defects, we similarly found differences in both BCF and insulin sensitivity. At 48 months, we found higher type 2 diabetes incidence for progressively increasing number of prediabetes defects (odds ratio >2, P < 0.008). In conclusion, the prediabetes groups showed differences in type/degree of glucometabolic impairment. Compared with the pooled group with isolated defects, those with double or triple defect showed progressive differences in diabetes incidence.
UR - http://www.scopus.com/inward/record.url?scp=85115388774&partnerID=8YFLogxK
U2 - 10.2337/db21-0227
DO - 10.2337/db21-0227
M3 - Article
C2 - 34233929
SN - 0012-1797
VL - 70
SP - 2092
EP - 2106
JO - Diabetes
JF - Diabetes
IS - 9
ER -