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U.K. Prospective Diabetes Study XV: Relationship of renin-angiotensin system gene polymorphisms with microalbuminuria in NIDDM

U.K. Prospective Diabetes Study XV: Relationship of renin-angiotensin system gene polymorphisms with microalbuminuria in NIDDM
U.K. Prospective Diabetes Study XV: Relationship of renin-angiotensin system gene polymorphisms with microalbuminuria in NIDDM

We performed a case-control study to determine whether molecular variants of genes of the renin-angiotensin system were associated with the presence of albuminuria in non-insulin dependent diabetes mellitus (NIDDM). A total of 180 diabetic patients with persistent microalbuminuria [median urinary albumin (interquartile range) of 74 (54 to 126 mg/liter)] were matched with two control groups of diabetic patients without microalbuminuria [median urinary albumin 7 (5 to 10) mg/liter] for variables known to be associated with raised urinary albumin concentration including hemoglobin Alc and triglyceride. One control group was also matched for blood pressure and the other group was not, to allow assessment of interactions with hypertension. Association with the I/D polymorphism of the ACE gene and M235T variant of the angiotensinogen gene (AGT) with microalbuminuria and retinopathy was examined. There were no significant differences in genotype frequency between cases and controls for ACE or AGT irrespective of blood pressure matching. However, among subjects with microalbuminuria, those with the ACE DD genotype had a significantly greater urinary albumin excretion than individuals with a non-DD genotype [median 88 (68 to 170) mg/liter vs. 67 (53 to 113) mg/liter, P < 0.001]. More subjects with the DD than non-DD genotype had persistent albuminuria > 100 mg/liter, twice the upper normal range (60% vs. 38%, P = 0.006). When increased albumin excretion occurs, the presence of the ACE DD genotype appears to be associated with higher urinary albumin levels. No association with retinopathy was observed.

0085-2538
1907-1911
Dudley, C. R.K.
760db4cf-0b3a-4e49-9d75-ff69ce2071ab
Keavney, B.
d7f31a20-b9aa-4cd2-a1e3-87175cad3c62
Stratton, I. M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Turner, R. C.
9c4a3b92-5186-43ae-b750-08990e742e4e
Ratcliffe, P. J.
5873e945-bfe9-432a-b24c-311104fd345e
Dudley, C. R.K.
760db4cf-0b3a-4e49-9d75-ff69ce2071ab
Keavney, B.
d7f31a20-b9aa-4cd2-a1e3-87175cad3c62
Stratton, I. M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Turner, R. C.
9c4a3b92-5186-43ae-b750-08990e742e4e
Ratcliffe, P. J.
5873e945-bfe9-432a-b24c-311104fd345e

Dudley, C. R.K., Keavney, B., Stratton, I. M., Turner, R. C. and Ratcliffe, P. J. (1995) U.K. Prospective Diabetes Study XV: Relationship of renin-angiotensin system gene polymorphisms with microalbuminuria in NIDDM. Kidney International, 48 (6), 1907-1911. (doi:10.1038/ki.1995.490).

Record type: Article

Abstract

We performed a case-control study to determine whether molecular variants of genes of the renin-angiotensin system were associated with the presence of albuminuria in non-insulin dependent diabetes mellitus (NIDDM). A total of 180 diabetic patients with persistent microalbuminuria [median urinary albumin (interquartile range) of 74 (54 to 126 mg/liter)] were matched with two control groups of diabetic patients without microalbuminuria [median urinary albumin 7 (5 to 10) mg/liter] for variables known to be associated with raised urinary albumin concentration including hemoglobin Alc and triglyceride. One control group was also matched for blood pressure and the other group was not, to allow assessment of interactions with hypertension. Association with the I/D polymorphism of the ACE gene and M235T variant of the angiotensinogen gene (AGT) with microalbuminuria and retinopathy was examined. There were no significant differences in genotype frequency between cases and controls for ACE or AGT irrespective of blood pressure matching. However, among subjects with microalbuminuria, those with the ACE DD genotype had a significantly greater urinary albumin excretion than individuals with a non-DD genotype [median 88 (68 to 170) mg/liter vs. 67 (53 to 113) mg/liter, P < 0.001]. More subjects with the DD than non-DD genotype had persistent albuminuria > 100 mg/liter, twice the upper normal range (60% vs. 38%, P = 0.006). When increased albumin excretion occurs, the presence of the ACE DD genotype appears to be associated with higher urinary albumin levels. No association with retinopathy was observed.

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Published date: December 1995

Identifiers

Local EPrints ID: 486924
URI: http://eprints.soton.ac.uk/id/eprint/486924
ISSN: 0085-2538
PURE UUID: 26be1ae4-f481-493c-91b8-b5b06d9dcd44
ORCID for I. M. Stratton: ORCID iD orcid.org/0000-0003-1172-7865

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Date deposited: 08 Feb 2024 17:42
Last modified: 18 Mar 2024 04:01

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Contributors

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

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