Background-We aimed to determine the prevalence of silent myocardial infarction (SMI) in people with newly diagnosed type 2 diabetes mellitus and its relationships to future myocardial infarction (MI) and all-cause mortality. Methods and Results-We examined data from the 5102 patients in the 30-year UK Prospective Diabetes Study (UKPDS) and used Cox proportional hazards regression to examine outcomes by SMI status. Of 1967 patients with complete baseline data, 326 (16.6%) had ECG evidence of SMI (Minnesota codes 1.1 or 1.2) at enrollment. Those with SMI were more likely to be older, female, sedentary, and nonsmokers compared with those without SMI. Their mean blood pressure was greater despite more intensive antihypertensive treatment; they were more likely to be taking aspirin and lipid-lowering therapy; and they had a greater prevalence of microangiopathy. Fully adjusted hazard ratios for those with versus those without SMI in multivariate models that included UKPDS Risk Engine variables were 1.58 (95% confidence interval, 1.22-2.05) for fatal MI and 1.31 (95% confidence interval,1.10-1.56) for all-cause mortality. Hazard ratios for first fatal or nonfatal MI and for first nonfatal MI were nonsignificant. The net reclassification index showed no improvement when SMI was added to these models, and the integrated discrimination index showed that SMI marginally improved the prediction of fatal MI and all-cause mortality. Conclusions-About 1 in 6 UKPDS patients with newly diagnosed type 2 diabetes mellitus had evidence of SMI, which was independently associated with an increased risk of fatal MI and all-cause mortality.
Davis et al Silent Myocardial Infarction in Type 2 Diabetes Mellitus 981The UK Prospective Diabetes Study (UKPDS) 9 affords the opportunity to assess the prognostic importance of SMI in newly diagnosed T2DM patients without significant comorbidities who were followed up over a longer period than in other studies. We have examined the prevalence of SMI in UKPDS participants at enrollment, its correlates, and its relationship with subsequent clinically evident MI and death.
Methods PatientsFull details of UKPDS participants have been published. 10 Briefly, 5102 of 7616 people referred by their general practitioners with newly diagnosed T2DM were enrolled. Exclusion criteria included severe vascular disease, MI or stroke within the previous year, and major systemic illness. The study received ethical committee approval in each of the 23 UK clinical centers and conformed to the Declaration of Helsinki guidelines. All patients gave informed consent before participation.
Study DesignThe UKPDS protocol has been reported in detail.9,10 Briefly, enrolled patients underwent baseline assessment and then after a 3-to 4-month dietary run-in period before allocation to diet (if fasting plasma glucose <15 mmol/L), sulfonylurea, insulin, or, if >120% ideal body weight, metformin therapy. All patients were seen quarterly in UKPDS clinics for a median within-trial follow-up to the end of September 1997 of 10 year...