4.4 Article

Prognostic Value of Admission Fasting Glucose Levels in Patients With Acute Coronary Syndrome

Journal

AMERICAN JOURNAL OF CARDIOLOGY
Volume 104, Issue 4, Pages 470-474

Publisher

EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC
DOI: 10.1016/j.amjcard.2009.04.006

Keywords

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Funding

  1. National Heart, Lung, and Blood Institute, Bethesda, Maryland [K23 HL0733 10-01]
  2. Mardigan Fund, Detroit, Michigan, Sanofi-Aventis, Bridgewater, New Jersey
  3. Hewlett Foundation, Menlo Park, California

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Data are limited regarding the best prognostic glucose measure for patients admitted for an acute coronary event. We examined the admission fasting glucose levels among patients with acute coronary syndrome (ACS) from the University of Michigan ACS registry. The glucose levels were grouped into 3 categories (>= 70 to < 100, 100 to < 126, and >= 126 mg/dl). The primary outcome measures included mortality and a composite end point (stroke, recurrent infarction, and death) in hospital and at 6 months after the ACS event. Of the 1,525 patients (29% with diabetes) for whom glucose levels were available, a fasting glucose level of >= 100 mg/dl was associated with increased in-hospital mortality, after adjusting for the Global Registry of Acute Coronary Events risk score and gender. A fasting glucose level of >= 126 mg/dl in patients with no known history of diabetes was associated with in-hospital adverse events (odds ratio 3.37, 95% confidence interval 1.51 to 7.51). The fasting glucose level was associated with an increased risk of 6-month mortality among nondiabetics (odds ratio 3.03, 95% confidence interval 1.35 to 6.81 for patients with a glucose level of 100 to 125 mg/dl; and odds ratio 2.81, 95% confidence interval 1.07 to 7.36 for patients with a glucose level of >= 126 mg/dl) but not for diabetic patients. In conclusion, we observed a strong association between the admission fasting glucose level and mortality, particularly among nondiabetic patients. Whether improving the diagnosis and treatment of hyperglycemia would result in reductions in adverse events after ACS remains unclear. (C) 2009 Elsevier Inc. All rights reserved. (Am J Cardiol 2009;104:470-474)

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