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UK Prospective Diabetes Study (UKPDS) 14: association of angiotensin-converting enzyme insertion/deletion polymorphism with myocardial infarction in NIDDM

UK Prospective Diabetes Study (UKPDS) 14: association of angiotensin-converting enzyme insertion/deletion polymorphism with myocardial infarction in NIDDM
UK Prospective Diabetes Study (UKPDS) 14: association of angiotensin-converting enzyme insertion/deletion polymorphism with myocardial infarction in NIDDM

The deletion allele of the insertion/deletion polymorphism of the angiotensin-converting enzyme gene has been suggested to be an independent risk factor for myocardial infarction, particularly in subjects judged to be "low-risk" by the criteria of lipid status and body mass index. In a prospective, matched case-control study, we have investigated the role of this polymorphism as a risk factor for myocardial infarction in 173 newly-diagnosed British Caucasian non-insulin-dependent diabetic subjects taken from the United Kingdom Prospective Diabetes Study who subsequently developed myocardial infarction and 297 control subjects from the same study population matched for known cardiovascular risk factors including age at diagnosis of diabetes, gender, blood pressure, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglyceride and smoking habit. A trend towards increased risk conferred by homozygosity for the deletion allele was observed in cases (odds ratio 1.63, p=0.09). When the population was stratified according to the matched risk factors, the deletion allele was associated with myocardial infarction in those with low plasma low-density lipoprotein cholesterol (odds ratio 3.67, p=0.002), or low triglyceride (odds ratio 3.14, p=0.005). The strongest association of the deletion allele with myocardial infarction was observed in subjects with both low low-density lipoprotein cholesterol and low triglyceride levels (odds ratio 9.0, p<0.001). These results show that the deletion allele is a risk factor for myocardial infarction in non-insulin-dependent diabetic patients who have a favourable lipid profile.

angiotensin-converting enzyme, genetics, myocardial infarction, Non-insulin-dependent diabetes mellitus, risk factors
0012-186X
948-952
Keavney, B. D.
92fd4f0e-2f41-475c-b168-e9d80055905d
Dudley, C. R.K.
760db4cf-0b3a-4e49-9d75-ff69ce2071ab
Stratton, I. M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Holman, R. R.
336fb2f7-edb5-4d65-a7b0-465111cbd047
Matthews, D. R.
ba1a878d-6510-45c5-896c-d4ade423caca
Ratcliffe, P. J.
5873e945-bfe9-432a-b24c-311104fd345e
Turner, R. C.
9c4a3b92-5186-43ae-b750-08990e742e4e
Keavney, B. D.
92fd4f0e-2f41-475c-b168-e9d80055905d
Dudley, C. R.K.
760db4cf-0b3a-4e49-9d75-ff69ce2071ab
Stratton, I. M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Holman, R. R.
336fb2f7-edb5-4d65-a7b0-465111cbd047
Matthews, D. R.
ba1a878d-6510-45c5-896c-d4ade423caca
Ratcliffe, P. J.
5873e945-bfe9-432a-b24c-311104fd345e
Turner, R. C.
9c4a3b92-5186-43ae-b750-08990e742e4e

Keavney, B. D., Dudley, C. R.K., Stratton, I. M., Holman, R. R., Matthews, D. R., Ratcliffe, P. J. and Turner, R. C. (1995) UK Prospective Diabetes Study (UKPDS) 14: association of angiotensin-converting enzyme insertion/deletion polymorphism with myocardial infarction in NIDDM. Diabetologia, 38 (8), 948-952. (doi:10.1007/BF00400584).

Record type: Article

Abstract

The deletion allele of the insertion/deletion polymorphism of the angiotensin-converting enzyme gene has been suggested to be an independent risk factor for myocardial infarction, particularly in subjects judged to be "low-risk" by the criteria of lipid status and body mass index. In a prospective, matched case-control study, we have investigated the role of this polymorphism as a risk factor for myocardial infarction in 173 newly-diagnosed British Caucasian non-insulin-dependent diabetic subjects taken from the United Kingdom Prospective Diabetes Study who subsequently developed myocardial infarction and 297 control subjects from the same study population matched for known cardiovascular risk factors including age at diagnosis of diabetes, gender, blood pressure, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglyceride and smoking habit. A trend towards increased risk conferred by homozygosity for the deletion allele was observed in cases (odds ratio 1.63, p=0.09). When the population was stratified according to the matched risk factors, the deletion allele was associated with myocardial infarction in those with low plasma low-density lipoprotein cholesterol (odds ratio 3.67, p=0.002), or low triglyceride (odds ratio 3.14, p=0.005). The strongest association of the deletion allele with myocardial infarction was observed in subjects with both low low-density lipoprotein cholesterol and low triglyceride levels (odds ratio 9.0, p<0.001). These results show that the deletion allele is a risk factor for myocardial infarction in non-insulin-dependent diabetic patients who have a favourable lipid profile.

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Published date: August 1995
Keywords: angiotensin-converting enzyme, genetics, myocardial infarction, Non-insulin-dependent diabetes mellitus, risk factors

Identifiers

Local EPrints ID: 486947
URI: http://eprints.soton.ac.uk/id/eprint/486947
ISSN: 0012-186X
PURE UUID: e7291eed-b10c-4716-b9a7-fe29564f8fb3
ORCID for I. M. Stratton: ORCID iD orcid.org/0000-0003-1172-7865

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Date deposited: 08 Feb 2024 17:45
Last modified: 18 Mar 2024 04:01

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Contributors

Author: B. D. Keavney
Author: C. R.K. Dudley
Author: I. M. Stratton ORCID iD
Author: R. R. Holman
Author: D. R. Matthews
Author: P. J. Ratcliffe
Author: R. C. Turner

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