Mendelian Randomization Studies Do Not Support a Role for Raised Circulating Triglyceride Levels Influencing Type 2 Diabetes, Glucose Levels, or Insulin Resistance

被引:69
作者
De Silva, N. Maneka G. [1 ]
Freathy, Rachel M. [1 ]
Palmer, Tom M. [2 ]
Donnelly, Louise A. [3 ]
Luan, Jian'an [4 ]
Gaunt, Tom [2 ]
Langenberg, Claudia [4 ]
Weedon, Michael N. [1 ]
Shields, Beverley [5 ]
Knight, Beatrice A. [5 ]
Ward, Kirsten J. [6 ]
Sandhu, Manjinder S. [4 ,7 ]
Harbord, Roger M. [2 ,8 ]
McCarthy, Mark I. [9 ,10 ,11 ]
Smith, George Davey [2 ]
Ebrahim, Shah [6 ]
Hattersley, Andrew T. [5 ]
Wareham, Nicholas [4 ]
Lawlor, Debbie A. [2 ]
Morris, Andrew D. [3 ]
Palmer, Colin N. A. [3 ]
Frayling, Timothy M. [1 ]
机构
[1] Univ Exeter, Inst Biomed & Clin Sci, Peninsula Coll Med & Dent, Exeter, Devon, England
[2] Univ Bristol, MRC, Ctr Causal Analyses Translat Epidemiol, Sch Social & Community Med, Bristol, Avon, England
[3] Univ Dundee, Ninewells Hosp & Med Sch, Biomed Res Inst, Dundee DD1 9SY, Scotland
[4] Addenbrookes Hosp, MRC, Inst Metab Sci, Cambridge, England
[5] Univ Exeter, Peninsula Natl Inst Hlth Res NIHR, Clin Res Facil, Peninsula Coll Med & Dent, Exeter, Devon, England
[6] Kings Coll London, Dept Twin Res & Genet Epidemiol, London WC2R 2LS, England
[7] Univ Cambridge, Dept Publ Hlth & Primary Care, Strangeways Res Lab, Cambridge, England
[8] Univ Bristol, Sch Social & Community Med, Bristol, Avon, England
[9] Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[10] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England
[11] Churchill Hosp, Oxford NIHR, Biomed Res Ctr, Oxford OX3 7LJ, England
基金
英国惠康基金; 美国国家卫生研究院; 英国医学研究理事会;
关键词
PANCREATIC BETA-CELL; CORONARY-ARTERY-DISEASE; LIPOPROTEIN-LIPASE; FASTING GLUCOSE; BLOOD-PRESSURE; PLASMA TRIGLYCERIDES; RISK-FACTORS; FATTY LIVER; MELLITUS; BEZAFIBRATE;
D O I
10.2337/db10-1317
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. Diabetes 60:1008-1018, 2011
引用
收藏
页码:1008 / 1018
页数:11
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