Genetic Risk Score of 46 Type 2 Diabetes Risk Variants Associates With Changes in Plasma Glucose and Estimates of Pancreatic β-Cell Function Over 5 Years of Follow-Up

被引:37
作者
Andersson, Ehm A. [1 ]
Allin, Kristine H. [1 ]
Sandholt, Camilla H. [1 ]
Borglykke, Anders [2 ]
Lau, Cathrine J. [2 ]
Ribel-Madsen, Rasmus [1 ]
Sparso, Thomas [1 ]
Justesen, Johanne M. [1 ]
Harder, Marie N. [1 ]
Jorgensen, Marit E. [3 ]
Jorgensen, Torben [2 ,4 ,5 ]
Hansen, Torben [1 ,6 ]
Pedersen, Oluf [1 ,3 ,7 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Sect Metab Genet, Novo Nordisk Fdn,Ctr Basic Metab Res, Copenhagen, Denmark
[2] Glostrup Univ Hosp, Res Ctr Prevent & Hlth, Glostrup, Denmark
[3] Steno Diabet Ctr AS, Gentofte, Denmark
[4] Univ Copenhagen, Fac Hlth & Med Sci, Copenhagen, Denmark
[5] Aalborg Univ, Fac Med, Aalborg, Denmark
[6] Univ Southern Denmark, Fac Hlth Sci, Odense, Denmark
[7] Univ Aarhus, Fac Hlth Sci, Aarhus, Denmark
关键词
POLYMORPHISMS; POPULATION; PREVENTION; PREDICTION; AGE;
D O I
10.2337/db13-0362
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
More than 40 genetic risk variants for type 2 diabetes have been validated. We aimed to test whether a genetic risk score associates with the incidence of type 2 diabetes and with 5-year changes in glycemic traits and whether the effects were modulated by changes in BMI and lifestyle. The Inter99 study population was genotyped for 46 variants, and a genetic risk score was constructed. During a median follow-up of 11 years, 327 of 5,850 individuals developed diabetes. Physical examinations and oral glucose tolerance tests were performed at baseline and after 5 years (n = 3,727). The risk of incident type 2 diabetes was increased with a hazard ratio of 1.06 (95% CI 1.03-1.08) per risk allele. While the population in general had improved glucose regulation during the 5-year follow-up period, each additional allele in the genetic risk score was associated with a relative increase in fasting, 30-min, and 120-min plasma glucose values and a relative decrease in measures of -cell function over the 5-year period, whereas indices of insulin sensitivity were unaffected. The effect of the genetic risk score on 5-year changes in fasting plasma glucose was stronger in individuals who increased their BMI. In conclusion, a genetic risk score based on 46 variants associated strongly with incident type 2 diabetes and 5-year changes in plasma glucose and -cell function. Individuals who gain weight may be more susceptible to the cumulative impact of type 2 diabetes risk variants on fasting plasma glucose.
引用
收藏
页码:3610 / 3617
页数:8
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