» Articles » PMID: 8142201

Insulin in Ischaemic Heart Disease: Are Associations Explained by Triglyceride Concentrations? The Caerphilly Prospective Study

Overview
Journal Br Heart J
Date 1994 Mar 1
PMID 8142201
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: To investigate the predictive value of fasting insulin concentrations for subsequent fatal or non-fatal ischaemic heart disease at five year follow up and to examine the associations between insulin and other indicators of risk.

Design: A prospective population study among 2512 men aged 45 to 59 at recruitment.

Setting: A whole population sample of men resident in Caerphilly, South Wales.

Measurements: At recruitment fasting blood samples were taken for measurement of plasma lipids and serum insulin. Men were re-examined at a five year follow up and ischaemic heart disease events during this period were assessed from hospital notes, death certificates, and electrocardiograms.

Main Results: Diabetic men and those men with a fasting blood glucose of > or = 8 mmol/l were excluded from all analyses. In a univariate analysis the incidence of ischaemic heart disease increased with increasing concentration of fasting insulin, such that for men in the top 20% of the insulin distribution the odds of developing ischaemic heart disease were 1.87 relative to men in the bottom 20%. On multivariate analysis this relation disappeared on adjusting for plasma triglycerides, body mass index, and evidence of ischaemic heart disease at recruitment.

Conclusion: In this population in South Wales there was no evidence that the fasting insulin concentration is an independent risk factor for ischaemic heart disease. The univariate association between insulin and incident disease was almost entirely explained by the association of both with triglycerides and body mass index.

Citing Articles

The effect of insulin resistance on prognosis of non-diabetic patients who underwent percutaneous coronary intervention.

Yun K, Jeong M, Kim K, Hong Y, Park H, Kim J J Korean Med Sci. 2006; 21(2):212-6.

PMID: 16614503 PMC: 2733993. DOI: 10.3346/jkms.2006.21.2.212.


Plasma insulin and cardiovascular mortality in non-diabetic European men and women: a meta-analysis of data from eleven prospective studies.

Diabetologia. 2004; 47(7):1245-1256.

PMID: 15241592 DOI: 10.1007/s00125-004-1433-4.


Leg length, insulin resistance, and coronary heart disease risk: the Caerphilly Study.

Smith G, Greenwood R, Gunnell D, Sweetnam P, Yarnell J, Elwood P J Epidemiol Community Health. 2001; 55(12):867-72.

PMID: 11707479 PMC: 1731819. DOI: 10.1136/jech.55.12.867.


Beneficial and detrimental effects of intensive glycaemic control, with emphasis on type 2 diabetes mellitus.

Camacho P, Pitale S, Abraira C Drugs Aging. 2001; 17(6):463-76.

PMID: 11200307 DOI: 10.2165/00002512-200017060-00004.


Is metabolic syndrome a discrete entity in the general population? Evidence from the Caerphilly and Speedwell population studies.

Yarnell J, Patterson C, Bainton D, Sweetnam P Heart. 1998; 79(3):248-52.

PMID: 9602657 PMC: 1728632. DOI: 10.1136/hrt.79.3.248.


References
1.
BUCOLO G, David H . Quantitative determination of serum triglycerides by the use of enzymes. Clin Chem. 1973; 19(5):476-82. View

2.
. PLASMA insulin in man. Am J Med. 1960; 29:1-8. DOI: 10.1016/0002-9343(60)90002-4. View

3.
Tobey T, Greenfield M, Kraemer F, Reaven G . Relationship between insulin resistance, insulin secretion, very low density lipoprotein kinetics, and plasma triglyceride levels in normotriglyceridemic man. Metabolism. 1981; 30(2):165-71. DOI: 10.1016/0026-0495(81)90167-0. View

4.
Cullen K, STENHOUSE N, Wearne K, Welborn T . Multiple regression analysis of risk factors for cardiovascular disease and cancer mortality in Busselton, Western Australia--13-year study. J Chronic Dis. 1983; 36(5):371-7. DOI: 10.1016/0021-9681(83)90169-8. View

5.
Orchard T, Becker D, Bates M, Kuller L, Drash A . Plasma insulin and lipoprotein concentrations: an atherogenic association?. Am J Epidemiol. 1983; 118(3):326-37. DOI: 10.1093/oxfordjournals.aje.a113639. View