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

Ehm A Andersson, Kristine Højgaard Allin, Camilla H Sandholt, Anders Borglykke, Cathrine J Lau, Rasmus Ribel-Madsen, Thomas Sparsø, Johanne Marie Justesen, Marie Neergaard Harder, Marit Eika Jørgensen, Torben Jørgensen, Torben Hansen, Oluf Pedersen

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36 Citationer (Scopus)

Abstract

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 β-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 β-cell function. Individuals who gain weight may be more susceptible to the cumulative impact of type 2 diabetes risk variants on fasting plasma glucose.

OriginalsprogEngelsk
TidsskriftDiabetes
Vol/bind62
Udgave nummer10
Sider (fra-til)3610-3617
Antal sider8
ISSN0012-1797
DOI
StatusUdgivet - okt. 2013

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