Aims/hypothesis: Variation in fasting plasma glucose (FPG) within the normal range is a known risk factor for the development of type 2 diabetes. Several reports have shown that genetic variation in the genes for glucokinase (GCK), glucokinase regulatory protein (GCKR), islet-specific glucose 6 phosphatase catalytic subunit-related protein (G6PC2) and melatonin receptor type 1B (MTNR1B) is associated with FPG. In this study we examined whether these loci also contribute to type 2 diabetes susceptibility. Methods: A random selection from the Dutch New Hoorn Study was used for replication of the association with FGP (2,361 non-diabetic participants). For the genetic association study we extended the study sample with 2,628 participants with type 2 diabetes. Risk allele counting was used to calculate a four-gene risk allele score for each individual. Results: Variants of the GCK, G6PC2 and MTNR1B genes but not GCKR were associated with FPG (all, p∈ in;0.23). Combining these four genes in a risk allele score resulted in an increase of 0.05 mmol/l (0.04-0.07) per additional risk allele (p∈= ∈2∈×∈10-13). Furthermore, participants with less than three or more than five risk alleles showed significantly different type 2 diabetes susceptibility compared with the most common group with four risk alleles (OR 0.77 [0.65-0.93], p∈=∈0.005 and OR 2.05 [1.50-2.80], p∈=∈4∈×∈10-6 respectively). The age at diagnosis was also significantly associated with the number of risk alleles (p∈=∈0.009). Conclusions: A combined risk allele score for single-nucleotide polymorphisms in four known FPG loci is significantly associated with FPG and HbA1c in a Dutch population-based sample of non-diabetic participants. Carriers of low or high numbers of risk alleles show significantly different risks for type 2 diabetes compared with the reference group. © 2009 Springer-Verlag.
CITATION STYLE
Reiling, E., Van ’T Riet, E., Groenewoud, M. J., Welschen, L. M. C., Van Hove, E. C., Nijpels, G., … ’T Hart, L. M. (2009). Combined effects of single-nucleotide polymorphisms in GCK, GCKR, G6PC2 and MTNR1B on fasting plasma glucose and type 2 diabetes risk. Diabetologia, 52(9), 1866–1870. https://doi.org/10.1007/s00125-009-1413-9
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