Associations between a polymorphism in the pleiotropic GCKR and Age-related phenotypes: the HALCyon programme
- PMID: 23894584
- PMCID: PMC3720952
- DOI: 10.1371/journal.pone.0070045
Associations between a polymorphism in the pleiotropic GCKR and Age-related phenotypes: the HALCyon programme
Abstract
Background: The glucokinase regulatory protein encoded by GCKR plays an important role in glucose metabolism and a single nucleotide polymorphism (SNP) rs1260326 (P446L) in the gene has been associated with several age-related biomarkers, including triglycerides, glucose, insulin and apolipoproteins. However, associations between SNPs in the gene and other ageing phenotypes such as cognitive and physical capability have not been reported.
Methods: As part of the Healthy Ageing across the Life Course (HALCyon) collaborative research programme, men and women from five UK cohorts aged between 44 and 90+ years were genotyped for rs1260326. Meta-analysis was used to pool within-study genotypic associations between the SNP and several age-related phenotypes, including body mass index (BMI), blood lipid levels, lung function, and cognitive and physical capability.
Results: We confirm the associations between the minor allele of the SNP and higher triglycerides and lower glucose levels. We also observed a triglyceride-independent association between the minor allele and lower BMI (pooled beta on z-score= -0.04, p-value=0.0001, n=16,251). Furthermore, there was some evidence for gene-environment interactions, including physical activity attenuating the effects on triglycerides. However, no associations were observed with measures of cognitive and physical capability.
Conclusion: Findings from middle-aged to older adults confirm associations between rs1260326 GCKR and triglycerides and glucose, suggest possible gene-environment interactions, but do not provide evidence that its relevance extends to cognitive and physical capability.
Conflict of interest statement
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References
-
- Kirkwood TBL (2008) A systematic look at an old problem. Nature 451: 644–647 doi:10.1038/451644a - DOI - PubMed
-
- Kuh D, Cooper R, Hardy R, Guralnik J, Richards M (2009) Lifetime cognitive performance is associated with midlife physical performance in a prospective national birth cohort study. Psychosom Med 71: 38–48 doi:10.1097/PSY.0b013e31818a1620 - DOI - PMC - PubMed
-
- Enright PL, McBurnie MA, Bittner V, Tracy RP, McNamara R, et al. (2003) The 6-min walk test: a quick measure of functional status in elderly adults. Chest 123: 387–398. - PubMed
-
- Deary IJ, Whalley LJ, Batty GD, Starr JM (2006) Physical fitness and lifetime cognitive change. Neurology 67: 1195–1200 doi:10.1212/01.wnl.0000238520.06958.6a - DOI - PubMed
-
- Sayer AA, Dennison EM, Syddall HE, Gilbody HJ, Phillips DIW, et al. (2005) Type 2 diabetes, muscle strength, and impaired physical function: the tip of the iceberg? Diabetes Care 28: 2541–2542. - PubMed
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