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Volume 17, Issue 1, Pages 94-99 (1 February 2010)


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Diabetes as a coronary artery disease risk equivalent: before a change of paradigm?

Christoph H. Saelyab, Stefan Aczelab, Lorena Kocha, Fabian Schmida, Thomas Marteab, Kurt Huberc, Heinz DrexelabdeCorresponding Author Informationemail address

Received 20 March 2009; accepted 16 July 2009.

Background

Current guidelines consider diabetes per se as a coronary artery disease (CAD) risk equivalent. We aimed at investigating the contribution of baseline coronary atherosclerosis to the risk of diabetic patients for future vascular events.

Design

Prospective cohort study.

Methods

Vascular events were recorded over 4 years in 750 consecutive patients undergoing coronary angiography for the evaluation of stable CAD.

Results

From our patients, 244 had neither type 2 diabetes (T2DM) nor significant CAD (i.e. coronary stenoses ≥50%) at the baseline angiography, 50 had T2DM but not significant CAD, 342 did not have T2DM but had significant CAD, and 114 had both T2DM and significant CAD. Nondiabetic patients without significant CAD had an event rate of 9.0%. The event rate was similar in T2DM patients without significant CAD (8.0%, P=0.951), but higher in nondiabetic patients with significant CAD (24.9%, P<0.001). Patients with T2DM and significant CAD had the highest event rate (43.0%). Importantly, T2DM patients without significant CAD had a significantly lower event rate than nondiabetic patients with significant CAD (P=0.008).

Conclusion

T2DM per se is not a CAD risk equivalent. Moderate-risk diabetic patients without significant CAD and very high-risk diabetic patients with significant CAD add up to a grand total of high-risk diabetic patients, this is why diabetes seems to be a CAD risk equivalent in many epidemiological studies.

a Vorarlberg Institute for Vascular Investigation and Treatment (VIVIT)

b Department of Medicine, Academic Teaching Hospital Feldkirch, Feldkirch

c 3rd Department of Medicine, Cardiology and Emergency Medicine, Wilhelminenhospital, Vienna, Austria

d Private University in the Principality of Liechtenstein, Triesen, Liechtenstein

e Drexel University College of Medicine, Philadelphia, Pennsylvania, USA

Corresponding Author InformationCorrespondence to Heinz Drexel, MD, FESC, Chairman of the Department of Medicine and Cardiology and of the VIVIT Institute, Academic Teaching Hospital Feldkirch, Carinagasse 47, Feldkirch A-6807, Austria and Full Professor of Medicine, Private University of the Principality of Liechtenstein, Triesen, Liechtenstein Tel: +43 5522 303 2670; fax: +43 5522 303 7533;

PII: S1741-8267(10)17113-8

doi:10.1097/01.hjr.0b013e32833100f0


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