Effects of Genetic Susceptibility for Type 2 Diabetes on the Evolution of Glucose Homeostasis Traits Before and After Diabetes Diagnosis Data From the DESIR Study

被引:9
作者
Gautier, Alain [1 ]
Roussel, Ronan [2 ]
Lange, Celine [3 ,4 ]
Piguel, Xavier [1 ]
Cauchi, Stephane [5 ]
Vol, Sylviane [6 ]
Froguel, Philippe [7 ]
Balkau, Beverley [3 ,4 ]
Bonnet, Fabrice [1 ]
机构
[1] Univ Rennes 1, INSERM, U991, Serv Endocrinol,Ctr Hosp Univ Rennes,Hop Sud, Rennes, France
[2] Univ Paris 07, Hop Bichat, AP HP, INSERM,U695, Paris, France
[3] INSERM, Ctr Rech Epidennol & Sante Populat, U1018, Villejuif, France
[4] Univ Paris 11, UMRS 1018, Villejuif, France
[5] Univ Lille 2, Inst Pasteur, Ctr Natl Rech Sci, Inst Biol,UMR 8090, Lille, France
[6] Inst Inter Reg Sante La Riche, La Riche, France
[7] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, London, England
关键词
BETA-CELL FUNCTION; INSULIN-SECRETION; TCF7L2; GENE; RISK-FACTORS; SENSITIVITY; PROGRESSION; VARIANTS; ONSET; POLYMORPHISMS; DYSFUNCTION;
D O I
10.2337/db10-1442
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-To assess the impact of genetic susceptibility on evolution toward type 2 diabetes (T2D) by analyzing time trajectories of fasting glucose, glycated hemoglobin (HbA(1c)), insulin sensitivity (homeostasis model assessment [HOMA2%S]), and beta-cell secretion (HOMA2%B) in a large nondiabetic cohort. We also examined whether baseline HbA(1c) modified the effect of genetic predisposition on the time trajectories. RESEARCH DESIGN ANT METHODS-Time trajectories were drawn in 4,744 participants from the French Data from an Epidemiological Study on the Insulin Resistance Syndrome (D.E.S.I.R.) cohort based on samples collected every 3 years over a 9-year follow-up. Trajectories were analyzed according to the TCF7L2 common variant, a family history of T2D, and a combination of at-risk alleles from nine T2D-associated genes. RESULTS-There was a marked decrease in HOMA2%B in parallel to a steep increase in HbA(1c), over the 3 years before incident diabetes, which was not influenced by genetic predisposition when considered alone. However, after the onset of T2D, the TCF7L2 at-risk variant was associated with a greater decrease in HOMA2%B. There was a joint effect of a family history of T2D with the presence of the TCF7L2 risk allele with a greater rise in HbA(1c) conferred by the coexistence of a family history and the T risk allele. An HbA(1c) >= 5.7% at baseline was associated with a greater increase in both glycemia and HbA(1c) levels in the presence of a combination of diabetes at-risk alleles. CONCLUSIONS-After incident T2D, TCF7L2 at-risk variants were associated with a faster decrease in beta-cell function compared with those with the CC genotype. There was a joint effect of family history of T2D and TCF7L2 risk variant on the rise in glycemia and the decrease in insulin secretion at the end of follow-up, suggesting the joint influence of the combination of diabetes genetic predisposition with familial factors on the evolution of glycemia over time. Diabetes 60:2654-2663, 2011
引用
收藏
页码:2654 / 2663
页数:10
相关论文
共 29 条
[2]   Anti-proliferative effect of pro-inflammatory cytokines in cultured β cells is associated with extracellular signal-regulated kinase 1/2 pathway inhibition:: protective role of glucagon-like peptide-1 [J].
Blandino-Rosano, M. ;
Perez-Arana, G. ;
Mellado-Gil, J. M. ;
Segundo, C. ;
Aguilar-Diosdado, M. .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2008, 41 (1-2) :35-44
[3]   TCF7L2 variation predicts hyperglycentia incidence in a French general population -: The Data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) study [J].
Cauchi, Stephane ;
Meyre, David ;
Choquet, Helene ;
Dina, Christian ;
Born, Catherine ;
Marre, Michel ;
Balkau, Beverley ;
Froguel, Philippe .
DIABETES, 2006, 55 (11) :3189-3192
[4]   Mode of onset of type 2 diabetes from normal or impaired glucose tolerance [J].
Ferrannini, E ;
Nannipieri, M ;
Williams, K ;
Gonzales, C ;
Haffner, SM ;
Stern, MP .
DIABETES, 2004, 53 (01) :160-165
[5]   The natural course of β-cell function in nondiabetic and diabetic individuals -: The insulin resistance atherosclerosis study [J].
Festa, A ;
Williams, K ;
D'Agostino, R ;
Wagenknecht, LE ;
Haffner, SM .
DIABETES, 2006, 55 (04) :1114-1120
[6]   β-Cell dysfunction in subjects with impaired glucose tolerance and early type 2 diabetes -: Comparison of surrogate markers with first-phase insulin secretion from an intravenous glucose tolerance test [J].
Festa, Andreas ;
Williams, Ken ;
Hanley, Anthony J. G. ;
Haffner, Steven M. .
DIABETES, 2008, 57 (06) :1638-1644
[7]   TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program [J].
Florez, Jose C. ;
Jablonski, Kathleen A. ;
Bayley, Nick ;
Pollin, Toni I. ;
de Bakker, Paul I. W. ;
Shuldiner, Alan R. ;
Knowler, William C. ;
Nathan, David M. ;
Altshuler, David .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (03) :241-250
[8]   Type 2 Diabetes Susceptibility Gene TCF7L2 and Its Role in β-Cell Function [J].
Gloyn, Anna L. ;
Braun, Matthias ;
Rorsman, Patrik .
DIABETES, 2009, 58 (04) :800-802
[9]   Assessing progression to impaired glucose tolerance and type 2 diabetes mellitus [J].
Guerrero-Romero, F. ;
Rodriguez-Moran, M. .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2006, 36 (11) :796-802
[10]   Exendin-4 modulates diabetes onset in nonobese diabetic mice [J].
Hadjiyanni, Irene ;
Baggio, Laurie L. ;
Poussier, Philippe ;
Drucker, Daniel J. .
ENDOCRINOLOGY, 2008, 149 (03) :1338-1349