القائمة الرئيسية

الصفحات

Follow-up glucose control in patients with type 2 diabetes for 10 years

 Follow-up glucose control in patients with type 2 diabetes for 10 years


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.



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