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J Am Coll Cardiol Img, 2009; 2:1159-1166, doi:10.1016/j.jcmg.2009.06.012
© 2009 by the American College of Cardiology Foundation
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Influence of Abnormal Glucose Metabolism on Coronary Microvascular Function After a Recent Myocardial Infarction

Brian B. Løgstrup, MD*,*, Dan E. Høfsten, MD, PhD*, Thomas B. Christophersen, MD*, Jacob E. Møller, MD, DMsc{dagger}, Hans E. Bøtker, MD, DMsc{ddagger}, Patricia A. Pellikka, MD§, Kenneth Egstrup, MD, DMsc*

* Department of Medical Research, Funen Hospital, Svendborg, Denmark
{dagger} Department of Cardiology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark
{ddagger} Department of Cardiology, Aarhus University Hospital Skejby, Aarhus, Denmark
§ Division of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota

* Reprint requests and correspondence: Dr. Brian B. Løgstrup, Department of Medical Research, Funen Hospital Svendborg, 5700 Svendborg, Denmark (Email: bbl{at}dadlnet.dk).

Objectives: This study sought to assess the association between abnormal glucose metabolism and abnormal coronary flow reserve (CFR) in patients with a recent acute myocardial infarction (AMI).

Background: Mortality and morbidity after AMI is high among patients with abnormal glucose metabolism, which may be related to abnormal microcirculation.

Methods: We studied 183 patients with a first AMI. In 161 patients with no history of diabetes mellitus (DM), an oral glucose tolerance test was performed, and patients were categorized according to World Health Organization criteria for whole blood glucose into 3 groups. After coronary angiography and revascularization, a comprehensive transthoracic echocardiogram and noninvasive assessment of CFR was performed in the distal part of left descending artery, as an indicator of microvascular function. Adenosine was administered by intravenous infusion (140 µg/kg/min) to obtain the hyperemic flow profiles. The CFR was defined as the ratio of hyperemic to baseline peak diastolic coronary flow velocities.

Results: Median CFR was 1.9 (interquartile range [IQR] 1.4 to 2.4], and 109 (60%) patients had a CFR ≤2. The lowest CFR was seen in patients with a history of DM (1.4 [IQR 1.4 to 1.7], n = 22) and in patients with newly diagnosed DM (1.6 [IQR 1.3 to 2], n = 39), whereas CFR did not differ in patients with abnormal glucose tolerance (2.1 [IQR 1.4 to 2.6], n = 58) and in patients with normal glucose tolerance (2.2 [IQR 1.7 to 2.6], n = 62). In a stepwise logistic regression model adjusting for age, sex, site and size of AMI, heart rate, risk factors of the metabolic syndrome, degree of angiographic evidence of coronary artery disease, and medical therapy, newly diagnosed DM (odds ratio: 3.0) and a history of DM (odds ratio: 9.9) remained significant predictors of CFR <2, whereas impaired glucose tolerance was not.

Conclusions: CFR is decreased in patients with known or newly diagnosed DM even after adjustment of possible confounders, whereas CFR in patients with impaired glucose tolerance seems less affected. (Coronary Flow Reserve and Glucometabolic State [CFRGS]; NCT00845468 [ClinicalTrials.gov] )

Key Words: coronary flow reserve • transthoracic echocardiography • acute myocardial infarction • dysglycemia • impaired glucose tolerance • oral glucose tolerance test

Abbreviations and Acronyms
  AMI = acute myocardial infarction
  CFR = coronary flow reserve
  DM = diabetes mellitus
  IGT = impaired glucose tolerance
  LAD = left anterior descending artery
  NSTEMI = non–ST-segment elevation myocardial infarction
  OGTT = oral glucose tolerance test
  OR = odds ratio
  PCI = percutaneous coronary intervention
  STEMI = ST-segment elevation myocardial infarction






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