10-year follow-up of intensive glucose control in type 2 diabetes

被引:5532
作者
Holman, Rury R. [1 ,4 ]
Paul, Sanjoy K. [1 ]
Bethel, M. Angelyn [1 ]
Matthews, David R. [1 ,4 ]
Neil, H. Andrew W. [1 ,2 ,3 ,4 ]
机构
[1] Churchill Hosp, Diabet Trials Unit, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LJ, England
[2] Div Publ Hlth & Primary Hlth Care, Oxford, England
[3] NIHR, Sch Primary Care Res, Oxford, England
[4] NIHR, Oxford Biomed Res Ctr, Oxford, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1056/NEJMoa0806470
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: During the United Kingdom Prospective Diabetes Study (UKPDS), patients with type 2 diabetes mellitus who received intensive glucose therapy had a lower risk of microvascular complications than did those receiving conventional dietary therapy. We conducted post-trial monitoring to determine whether this improved glucose control persisted and whether such therapy had a long-term effect on macrovascular outcomes. Methods: Of 5102 patients with newly diagnosed type 2 diabetes, 4209 were randomly assigned to receive either conventional therapy (dietary restriction) or intensive therapy (either sulfonylurea or insulin or, in overweight patients, metformin) for glucose control. In post-trial monitoring, 3277 patients were asked to attend annual UKPDS clinics for 5 years, but no attempts were made to maintain their previously assigned therapies. Annual questionnaires were used to follow patients who were unable to attend the clinics, and all patients in years 6 to 10 were assessed through questionnaires. We examined seven prespecified aggregate clinical outcomes from the UKPDS on an intention-to-treat basis, according to previous randomization categories. Results: Between-group differences in glycated hemoglobin levels were lost after the first year. In the sulfonylurea-insulin group, relative reductions in risk persisted at 10 years for any diabetes-related end point (9%, P=0.04) and microvascular disease (24%, P=0.001), and risk reductions for myocardial infarction (15%, P=0.01) and death from any cause (13%, P=0.007) emerged over time, as more events occurred. In the metformin group, significant risk reductions persisted for any diabetes-related end point (21%, P=0.01), myocardial infarction (33%, P=0.005), and death from any cause (27%, P=0.002). Conclusions: Despite an early loss of glycemic differences, a continued reduction in microvascular risk and emergent risk reductions for myocardial infarction and death from any cause were observed during 10 years of post-trial follow-up. A continued benefit after metformin therapy was evident among overweight patients. (UKPDS 80; Current Controlled Trials number, ISRCTN75451837.).
引用
收藏
页码:1577 / 1589
页数:13
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