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PMID: 12106931 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Altered myocardial fatty acid and glucose metabolism in idiopathic dilated cardiomyopathy.

Journal of the American College of Cardiology ·Vol. 40 ·No. 2 ·2002-07-17 ·Pages 271-7

Dávila-Román VG, Vedala G, Herrero P, de las Fuentes L, Rogers JG, Kelly DP, Gropler RJ

Abstract

The purpose of this study was to determine whether patients with idiopathic dilated cardiomyopathy (IDCM) exhibit alterations in myocardial fatty acid and glucose metabolism. Alterations in myocardial metabolism have been implicated in the pathogenesis of heart failure (HF); however, studies of myocardial metabolic function in human HF have yielded conflicting results. Animal models of HF have shown a downregulation of the expression of enzymes of fatty acid beta-oxidation that recapitulates the fetal energy metabolic program, in which fatty acid metabolism is decreased and glucose metabolism is increased. Seven patients with IDCM (mean left ventricular ejection fraction 27 +/- 8%) and 12 normal controls underwent positron emission tomography for measurements of myocardial blood flow (MBF), myocardial oxygen consumption (MVO(2)), myocardial glucose utilization (MGU), myocardial fatty acid utilization (MFAU) and myocardial fatty acid oxidation (MFAO). The systolic and diastolic blood pressures, plasma substrates and insulin levels, MBF and MVO(2), were similar between groups. The rates of MFAU and MFAO were significantly lower in IDCM than in the normal control group (MFAU: 134 +/- 44 vs. 213 +/- 49 nmol/g/min, p = 0.003; and MFAO: 113 +/- 50 vs. 205 +/- 49 nmol/g/min, p = 0.001) and the rates of MGU were significantly higher in IDCM than the normal control group (MGU: 247 +/- 63 vs. 125 +/- 64 nmol/g/min, p < 0.001). Patients with IDCM exhibit alterations in myocardial metabolism characterized by decreased fatty acid metabolism and increased myocardial glucose metabolism, a pattern similar to that shown in animal models of HF. Whether alterations in myocardial metabolism constitute an adaptive response or mediate the development of HF remains to be determined.

MeSH Terms
Adult Carbon Radioisotopes Cardiomyopathy, Dilated/diagnostic imaging,metabolism Case-Control Studies Fatty Acids/metabolism Female Glucose/metabolism Humans Male Middle Aged Myocardium/metabolism Oxygen Consumption Radionuclide Imaging
Chemicals
Carbon Radioisotopes Fatty Acids Glucose
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Dávila-Román Víctor G
Cardiovascular Imaging and Clinical Research Core Laboratory, Cardiovascular Division, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA. [email protected]
Vedala Giridhar
Herrero Pilar
de las Fuentes Lisa
Rogers Joseph G
Kelly Daniel P
Gropler Robert J
Article Info
Journal
Journal of the American College of Cardiology
Abbr.
J Am Coll Cardiol
ISSN
0735-1097
Published
2002-07-17
Pages
271-7
Language
English
Region
United States
NLM ID
8301365
Subset
IM
Grants
NCRR NIH HHS · M01 RR 00036 · United States
NHLBI NIH HHS · P01 HL 13851 · United States
NIA NIH HHS · R01 AG 15466 · United States
NHLBI NIH HHS · R01 HL 58878 · United States
NCRR NIH HHS · S10 RR 14778 · United States
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