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
[11]   Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution [J].
Helgason, Agnar ;
Palsson, Snaebjorn ;
Thorleifsson, Gudmar ;
Grant, Struan F. A. ;
Emilsson, Valur ;
Gunnarsdottir, Steinunn ;
Adeyemo, Adebowale ;
Chen, Yuanxiu ;
Chen, Guanjie ;
Reynisdottir, Inga ;
Benediktsson, Rafn ;
Hinney, Anke ;
Hansen, Torben ;
Andersen, Gitte ;
Borch-Johnsen, Knut ;
Jorgensen, Torben ;
Schaefer, Helmut ;
Faruque, Mezbah ;
Doumatey, Ayo ;
Zhou, Jie ;
Wilensky, Robert L. ;
Reilly, Muredach P. ;
Rader, Daniel J. ;
Bagger, Yu ;
Christiansen, Claus ;
Sigurdsson, Gunnar ;
Hebebrand, Johannes ;
Pedersen, Oluf ;
Thorsteinsdottir, Unnur ;
Gulcher, Jeffrey R. ;
Kong, Augustine ;
Rotimi, Charles ;
Stefansson, Kari .
NATURE GENETICS, 2007, 39 (02) :218-225
[12]   Glycemia Determines the Effect of Type 2 Diabetes Risk Genes on Insulin Secretion [J].
Heni, Martin ;
Ketterer, Caroline ;
Thamer, Claus ;
Herzberg-Schaefer, Silke A. ;
Guthoff, Martina ;
Stefan, Norbert ;
Machicao, Fausto ;
Staiger, Harald ;
Fritsche, Andreas ;
Haering, Hans-Ulrich .
DIABETES, 2010, 59 (12) :3247-3252
[13]   Updated Genetic Score Based on 34 Confirmed Type 2 Diabetes Loci Is Associated With Diabetes Incidence and Regression to Normoglycemia in the Diabetes Prevention Program [J].
Hivert, Marie-France ;
Jablonski, Kathleen A. ;
Perreault, Leigh ;
Saxena, Richa ;
McAteer, Jarred B. ;
Franks, Paul W. ;
Hamman, Richard F. ;
Kahn, Steven E. ;
Haffner, Steven ;
Meigs, James B. ;
Altshuler, David ;
Knowler, William C. ;
Florez, Jose C. .
DIABETES, 2011, 60 (04) :1340-1348
[14]   Dipeptidyl Peptidase IV Inhibition With MK0431 Improves Islet Graft Survival in Diabetic NOD Mice Partially via T-Cell Modulation [J].
Kim, Su-Jin ;
Nian, Cuilan ;
Doudet, Doris J. ;
McIntosh, Christopher H. S. .
DIABETES, 2009, 58 (03) :641-651
[15]   Long-term changes and variability in diabetes risk factors prior to the development of impaired glucose homeostasis [J].
Laspa, E. ;
Christen, A. ;
Efstathiadou, Z. ;
Johnston, D. G. ;
Godsland, I. F. .
DIABETIC MEDICINE, 2007, 24 (11) :1269-1278
[16]   TCF7L2 polymorphisms modulate proinsulin levels and β-cell function in a British europid population [J].
Loos, Ruth J. F. ;
Franks, Paul W. ;
Francis, Richard W. ;
Barroso, Ines ;
Gribble, Fiona M. ;
Savage, David B. ;
Ong, Ken K. ;
O'Rahilly, Stephen ;
Wareham, Nicholas J. .
DIABETES, 2007, 56 (07) :1943-1947
[17]   Insulin Resistance, β-Cell Dysfunction, and Conversion to Type 2 Diabetes in a Multiethnic Population The Insulin Resistance Atherosclerosis Study [J].
Lorenzo, Carlos ;
Wagenknecht, Lynne E. ;
D'Agostino, Ralph B., Jr. ;
Rewers, Marian J. ;
Karter, Andrew J. ;
Haffner, Steven M. .
DIABETES CARE, 2010, 33 (01) :67-72
[18]   Predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes [J].
Lyssenko, V ;
Almgren, P ;
Anevski, D ;
Perfekt, R ;
Lahti, K ;
Nissén, M ;
Isomaa, B ;
Forsen, B ;
Homström, N ;
Saloranta, C ;
Taskinen, MR ;
Groop, L ;
Tuomi, T .
DIABETES, 2005, 54 (01) :166-174
[19]   Clinical Risk Factors, DNA Variants, and the Development of Type 2 Diabetes. [J].
Lyssenko, Valeriya ;
Jonsson, Anna ;
Almgren, Peter ;
Pulizzi, Nicolo ;
Isomaa, Bo ;
Tuomi, Tiinamaija ;
Berglund, Goran ;
Altshuler, David ;
Nilsson, Peter ;
Groop, Leif .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (21) :2220-2232
[20]   Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes [J].
Lyssenko, Valeriya ;
Lupi, Roberto ;
Marchetti, Piero ;
Del Guerra, Silvia ;
Orho-Melander, Marju ;
Almgren, Peter ;
Sjogren, Marketa ;
Ling, Charlotte ;
Eriksson, Karl-Fredrik ;
Lethagen, Asa-Linda ;
Mancarella, Rita ;
Berglund, Goran ;
Tuomi, Tiinamaija ;
Nilsson, Peter ;
Del Prato, Stefano ;
Groop, Leif .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (08) :2155-2163