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Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study

Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study
Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study

Objective. To determine the relation between exposure to glycaemia over time and the risk of macrovascular or microvascular complications in patients with type 2 diabetes. Design. Prospective observational study Setting. 23 hospital based clinics in England, Scotland, and Northern Ireland. Participants. 4585 white, Asian Indian, and Afro-Caribbean UKPDS patients, whether randomised or not to treatment, were included in analyses of incidence; of these, 3642 were included in analyses of relative risk. Outcome measures. Primary predefined aggregate clinical outcomes: any end point or deaths related to diabetes and all cause mortality. Secondary aggregate outcomes: myocardial infarction, stroke, amputation (including death from peripheral vascular disease), and microvascular disease (predominantly retinal photo-coagulation). Since end points: non-fatal heart failure and cataract extraction. Risk reduction associated with a 1% reduction in updated mean HbA(1c) adjusted for possible confounders at diagnosis of diabetes. Results. The incidence of clinical complications was significantly associated with glycaemia. Each 1% reduction in updated mean HbA(1c) was associated with reductions in risk of 21% for any end point related to diabetes (95% confidence interval 17% to 24%, P < 0.0001), 21%, for deaths related to diabetes (15% to 27%, P < 0.0001), 14% for myocardial infarction (8%, to 21%, P < 0.0001), and 37% for microvascular complications (33% to 41%, P < 0.0001). No threshold of risk was observed for any end point. Conclusions. In patients with type 2 diabetes the risk of diabetic complications was strongly associated with previous hyperglycaemia. Any reduction in HbA(1c) is likely to reduce the risk of complications, with the lowest risk being in those with HbA(1c) values in the normal range (< 6.0%).

0959-8146
405-412
Stratton, Irene M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Adler, Amanda I.
d02dfdd6-ca6f-4cdc-91ab-8eb79ff94d7f
Neil, H. Andrew W.
ded0352b-edc2-499f-a8b9-51f82489f985
Matthews, David R.
ba1a878d-6510-45c5-896c-d4ade423caca
Manley, Susan E.
46bacfff-cf40-4894-86d8-4aa07e302e70
Cull, Carole A.
ae95233f-ce25-4c32-a5b9-368419e07826
Hadden, David
4285fe4d-6716-4cef-ae5f-0c6b2aa838ef
Turner, Robert C.
f974acc5-a17a-49c4-8bb7-84fa4d449863
Holman, Rury R.
336fb2f7-edb5-4d65-a7b0-465111cbd047
on behalf of the UK Prospective Diabetes Study Group
Stratton, Irene M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Adler, Amanda I.
d02dfdd6-ca6f-4cdc-91ab-8eb79ff94d7f
Neil, H. Andrew W.
ded0352b-edc2-499f-a8b9-51f82489f985
Matthews, David R.
ba1a878d-6510-45c5-896c-d4ade423caca
Manley, Susan E.
46bacfff-cf40-4894-86d8-4aa07e302e70
Cull, Carole A.
ae95233f-ce25-4c32-a5b9-368419e07826
Hadden, David
4285fe4d-6716-4cef-ae5f-0c6b2aa838ef
Turner, Robert C.
f974acc5-a17a-49c4-8bb7-84fa4d449863
Holman, Rury R.
336fb2f7-edb5-4d65-a7b0-465111cbd047

Stratton, Irene M., Adler, Amanda I., Neil, H. Andrew W., Matthews, David R., Manley, Susan E., Cull, Carole A., Hadden, David, Turner, Robert C. and Holman, Rury R. , on behalf of the UK Prospective Diabetes Study Group (2000) Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study. British medical journal, 321 (7258), 405-412. (doi:10.1136/bmj.321.7258.405).

Record type: Article

Abstract

Objective. To determine the relation between exposure to glycaemia over time and the risk of macrovascular or microvascular complications in patients with type 2 diabetes. Design. Prospective observational study Setting. 23 hospital based clinics in England, Scotland, and Northern Ireland. Participants. 4585 white, Asian Indian, and Afro-Caribbean UKPDS patients, whether randomised or not to treatment, were included in analyses of incidence; of these, 3642 were included in analyses of relative risk. Outcome measures. Primary predefined aggregate clinical outcomes: any end point or deaths related to diabetes and all cause mortality. Secondary aggregate outcomes: myocardial infarction, stroke, amputation (including death from peripheral vascular disease), and microvascular disease (predominantly retinal photo-coagulation). Since end points: non-fatal heart failure and cataract extraction. Risk reduction associated with a 1% reduction in updated mean HbA(1c) adjusted for possible confounders at diagnosis of diabetes. Results. The incidence of clinical complications was significantly associated with glycaemia. Each 1% reduction in updated mean HbA(1c) was associated with reductions in risk of 21% for any end point related to diabetes (95% confidence interval 17% to 24%, P < 0.0001), 21%, for deaths related to diabetes (15% to 27%, P < 0.0001), 14% for myocardial infarction (8%, to 21%, P < 0.0001), and 37% for microvascular complications (33% to 41%, P < 0.0001). No threshold of risk was observed for any end point. Conclusions. In patients with type 2 diabetes the risk of diabetic complications was strongly associated with previous hyperglycaemia. Any reduction in HbA(1c) is likely to reduce the risk of complications, with the lowest risk being in those with HbA(1c) values in the normal range (< 6.0%).

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Published date: 12 August 2000

Identifiers

Local EPrints ID: 486999
URI: http://eprints.soton.ac.uk/id/eprint/486999
ISSN: 0959-8146
PURE UUID: d70e9885-2488-4057-baf0-f48921e96f53
ORCID for Irene M. Stratton: ORCID iD orcid.org/0000-0003-1172-7865

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Date deposited: 09 Feb 2024 17:37
Last modified: 06 Jun 2024 02:10

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Contributors

Author: Irene M. Stratton ORCID iD
Author: Amanda I. Adler
Author: H. Andrew W. Neil
Author: David R. Matthews
Author: Susan E. Manley
Author: Carole A. Cull
Author: David Hadden
Author: Robert C. Turner
Author: Rury R. Holman
Corporate Author: on behalf of the UK Prospective Diabetes Study Group

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