Document Detail


Impact of type 2 diabetes on myocardial insulin sensitivity to glucose uptake and perfusion in patients with coronary artery disease.
MedLine Citation:
PMID:  16984986     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND AND HYPOTHESIS: Myocardial insulin resistance (IR) is a feature of coronary artery disease (CAD) with reduced left ventricular ejection fraction (LVEF). Whether type 2 diabetes mellitus (T2DM) with CAD and preserved LVEF induces myocardial IR and whether insulin in these patients acts as a myocardial vasodilator is debated. METHODS: We studied 27 CAD patients (LVEF > 50%): 12 with T2DM (CAD+DM), 15 without T2DM (CAD-NoDM). Regional myocardial and skeletal glucose uptake, myocardial and skeletal muscle perfusion were measured with positron emission tomography. Myocardial muscle perfusion was measured at rest and during hyperemia in nonstenotic and stenotic regions with and without acute hyperinsulinemia. RESULTS: Myocardial glucose uptake was similar in CAD+DM and CAD-NoDM in both nonstenotic and stenotic regions [0.38 +/- 0.08 and 0.36 +/- 0.11 micromol/g.min; P value nonsignificant (NS)] and (0.35 +/- 0.09 and 0.37 +/- 0.13 micromol/g.min; P = NS). Skeletal glucose uptake was reduced in CAD+DM (0.05 +/- 0.04 vs. 0.10 +/- 0.05 micromol/g.min; P = 0.02), and likewise, whole-body glucose uptake was reduced in CAD+DM (4.0 +/- 2.8 vs. 7.0 +/- 2.4 mg/kg.min; P = 0.01). Insulin did not alter myocardial muscle perfusion at rest or during hyperemia. Insulin increased skeletal muscle perfusion in CAD-NoDM (0.11 +/- 0.03 vs. 0.06 +/- 0.03 ml/g.min; P = 0.02), but not in CAD+DM (0.08 +/- 0.04 and 0.09 +/- 0.05 ml/g.min; P = NS). CONCLUSION: Myocardial IR to glucose uptake is not an inherent feature in T2DM patients with preserved LVEF. Acute physiological insulin exposure exerts no coronary vasodilation in CAD patients irrespective of T2DM.
Authors:
Hanne M Søndergaard; Morten Bøttcher; Mette Marie Madsen; Ole Schmitz; Søren B Hansen; Torsten T Nielsen; Hans Erik Bøtker
Related Documents :
18485566 - Real-time myocardial contrast stress echocardiography using bolus application.
8557276 - Angiographic severity and morphological spectrum of coronary artery disease in non insu...
21254206 - Three-directional acceleration phase mapping of myocardial function.
12382156 - Hyperhomocysteinemia: a potential risk factor for cervical artery dissection following ...
23074446 - Functional cardiac magnetic resonance imaging (mri) in the assessment of myocardial via...
16890486 - Left bundle branch block as a risk factor for progression to heart failure.
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't     Date:  2006-09-19
Journal Detail:
Title:  The Journal of clinical endocrinology and metabolism     Volume:  91     ISSN:  0021-972X     ISO Abbreviation:  J. Clin. Endocrinol. Metab.     Publication Date:  2006 Dec 
Date Detail:
Created Date:  2006-12-06     Completed Date:  2007-01-25     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  0375362     Medline TA:  J Clin Endocrinol Metab     Country:  United States    
Other Details:
Languages:  eng     Pagination:  4854-61     Citation Subset:  AIM; IM    
Affiliation:
Department of Cardiology B, Aarhus University Hospital (SKS), Brendstrupgaardsvej 100, DK-8200 Aarhus N, Denmark.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Aged
Blood Glucose / analysis
Blood Pressure
Coronary Artery Disease / complications*,  metabolism*
Diabetes Mellitus, Type 2 / complications*,  metabolism*
Female
Fluorodeoxyglucose F18 / pharmacokinetics
Glucose / metabolism*
Heart Rate
Humans
Insulin Resistance*
Male
Middle Aged
Muscle, Skeletal / metabolism
Myocardium / metabolism*
Perfusion / methods
Positron-Emission Tomography
Chemical
Reg. No./Substance:
0/Blood Glucose; 50-99-7/Glucose; 63503-12-8/Fluorodeoxyglucose F18

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Association between neuromedin U gene variants and overweight and obesity.
Next Document:  Progesterone regulation of human granulosa/luteal cell viability by an RU486-independent mechanism.