Mendelian randomization studies do not support a role for raised circulating triglyceride levels influencing type 2 diabetes, glucose levels, or insulin resistance

De Silva, N. Maneka G. and Freathy, Rachel M. and Palmer, Tom M. and Donnelly, Louise A. and Luan, Jian'an and Gaunt, Tom and Langenberg, Claudia and Weedon, Michael N. and Shields, Beverley and Knight, Beatrice A. and Ward, Kirsten J. and Sandhu, Manjinder S. and Harbord, Roger M. and McCarthy, Mark I. and Smith, George Davey and Ebrahim, Shah and Hattersley, Andrew T. and Wareham, Nicholas and Lawlor, Debbie A. and Morris, Andrew D. and Palmer, Colin N. A. and Frayling, Timothy M. (2011) Mendelian randomization studies do not support a role for raised circulating triglyceride levels influencing type 2 diabetes, glucose levels, or insulin resistance. Diabetes Care, 60 (3). pp. 1008-1018. ISSN 0149-5992

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Abstract

OBJECTIVE: The causal nature of associations between circulating triglycerides, insulin resistance, and type 2 diabetes is unclear. We aimed to use Mendelian randomization to test the hypothesis that raised circulating triglyceride levels causally influence the risk of type 2 diabetes and raise normal fasting glucose levels and hepatic insulin resistance. RESEARCH DESIGN AND METHODS: We tested 10 common genetic variants robustly associated with circulating triglyceride levels against the type 2 diabetes status in 5,637 case and 6,860 control subjects and four continuous outcomes (reflecting glycemia and hepatic insulin resistance) in 8,271 nondiabetic individuals from four studies. RESULTS: Individuals carrying greater numbers of triglyceride-raising alleles had increased circulating triglyceride levels (SD 0.59 [95% CI 0.52-0.65] difference between the 20% of individuals with the most alleles and the 20% with the fewest alleles). There was no evidence that the carriers of greater numbers of triglyceride-raising alleles were at increased risk of type 2 diabetes (per weighted allele odds ratio [OR] 0.99 [95% CI 0.97-1.01]; P = 0.26). In nondiabetic individuals, there was no evidence that carriers of greater numbers of triglyceride-raising alleles had increased fasting insulin levels (SD 0.00 per weighted allele [95% CI -0.01 to 0.02]; P = 0.72) or increased fasting glucose levels (0.00 [-0.01 to 0.01]; P = 0.88). Instrumental variable analyses confirmed that genetically raised circulating triglyceride levels were not associated with increased diabetes risk, fasting glucose, or fasting insulin and, for diabetes, showed a trend toward a protective association (OR per 1-SD increase in log(10) triglycerides: 0.61 [95% CI 0.45-0.83]; P = 0.002). CONCLUSIONS: Genetically raised circulating triglyceride levels do not increase the risk of type 2 diabetes or raise fasting glucose or fasting insulin levels in nondiabetic individuals. One explanation for our results is that raised circulating triglycerides are predominantly secondary to the diabetes disease process rather than causal.

Item Type:
Journal Article
Journal or Publication Title:
Diabetes Care
Uncontrolled Keywords:
/dk/atira/pure/subjectarea/asjc/2900/2902
Subjects:
?? AGEDALLELESBLOOD GLUCOSECASE-CONTROL STUDIESDIABETES MELLITUS, TYPE 2FEMALEGENETIC VARIATIONGENOTYPEHUMANSINSULININSULIN RESISTANCEMALEMENDELIAN RANDOMIZATION ANALYSISMIDDLE AGEDPOLYMORPHISM, SINGLE NUCLEOTIDETRIGLYCERIDESINTERNAL MEDICINEENDOCRINOLOGY, D ??
ID Code:
73925
Deposited By:
Deposited On:
18 Jun 2015 05:56
Refereed?:
Yes
Published?:
Published
Last Modified:
15 Sep 2023 00:18