JACC
HOME SUBSCRIPTIONS CURRENT ISSUE PAST ISSUES CARDIOSOURCE SEARCH HELP FEEDBACK
 QUICK SEARCH:   [advanced]


     


J Am Coll Cardiol, 2007; 50:2051-2058, doi:10.1016/j.jacc.2007.07.070 (Published online 5 November 2007).
© 2007 by the American College of Cardiology Foundation
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
j.jacc.2007.07.070v1
50/21/2051    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Naoumova, R. P.
Right arrow Articles by Camici, P. G.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Naoumova, R. P.
Right arrow Articles by Camici, P. G.
Related Collections
Right arrowRelated Article

CLINICAL RESEARCH

Pioglitazone Improves Myocardial Blood Flow and Glucose Utilization in Nondiabetic Patients With Combined Hyperlipidemia

A Randomized, Double-Blind, Placebo-Controlled Study

Rossi P. Naoumova, MD, PhD, FAHA, MRCP*, Heiko Kindler, MD, MRCP*, Lucia Leccisotti, MD*,{dagger}, Marco Mongillo, MD, PhD*, Muhammad T. Khan, MD, FRCS*, Clare Neuwirth, RN*, Mary Seed, MA, DM, FRCPath, FREP{ddagger}, Paul Holvoet, PhD, FAHA§, John Betteridge, PhD, MD, FAHA, FRCP|| and Paolo G. Camici, MD, FESC, FACC, FAHA, FRCP*,#,*

* Medical Research Council Clinical Sciences Centre, Imperial College, Hammersmith Hospital, London, United Kingdom
# National Heart and Lung Institute, Imperial College, Hammersmith Hospital, London, United Kingdom
{dagger} Institute of Nuclear Medicine, Catholic University of the Sacred Heart, Rome, Italy
{ddagger} Lipid Clinic, Charing Cross Hospital, London, United Kingdom
§ Department of Cardiovascular Diseases, Faculty of Medicine, Katholieke Universiteit Leuven, Leuven, Belgium
|| Department of Medicine, University College London, University College Hospitals, London, United Kingdom. Supported in part by an unrestricted grant from Takeda Europe.

Manuscript received October 31, 2006; revised manuscript received July 6, 2007, accepted July 18, 2007.

* Reprint requests and correspondence: Prof. Paolo G. Camici, MRC Clinical Sciences Centre, Hammersmith Hospital, Du Cane Road, London W12 0NN, United Kingdom. (Email: paolo.camici{at}csc.mrc.ac.uk).

Objectives: This study's aim was to examine whether treatment with pioglitazone, added to conventional lipid-lowering therapy, would improve myocardial glucose utilization (MGU) and blood flow (MBF) in nondiabetic patients with familial combined hyperlipidemia (FCHL).

Background: Thiazolidinediones were found to improve insulin sensitivity and MGU in type 2 diabetes and MBF in Mexican Americans with insulin resistance. Familial combined hyperlipidemia is a complex genetic disorder conferring a high risk of premature coronary artery disease, characterized by high serum cholesterol and/or triglyceride, low high-density lipoprotein (HDL) cholesterol, and insulin resistance.

Methods: We undertook a randomized, double-blind, placebo-controlled study in 26 patients with FCHL, treated with pioglitazone or matching placebo 30 mg daily for 4 weeks, followed by 45 mg daily for 12 weeks. Positron emission tomography was used to measure MBF at rest and during adenosine-induced hyperemia and MGU during euglycemic hyperinsulinemic clamp at baseline and after treatment.

Results: Whereas no change was observed in the placebo group after treatment, patients receiving pioglitazone showed a significant increase in whole body glucose disposal (3.93 ± 1.59 mg/kg/min to 5.24 ± 1.65 mg/kg/min; p = 0.004) and MGU (0.62 ± 0.26 µmol/g/min to 0.81 ± 0.14 µmol/g/min; p = 0.0007), accompanied by a significant improvement in resting MBF (1.11 ± 0.20 ml/min/g to 1.25 ± 0.21 ml/min/g; p = 0.008). Furthermore, in the pioglitazone group HDL cholesterol (+28%; p = 0.003) and adiponectin (+156.2%; p = 0.0001) were increased and plasma insulin (–35%; p = 0.017) was reduced.

Conclusions: In patients with FCHL treated with conventional lipid-lowering therapy, the addition of pioglitazone led to significant improvements in MGU and MBF, with a favorable effect on blood lipid and metabolic parameters. (A study to investigate the effect of pioglitazone on whole body and myocardial glucose uptake and myocardial blood flow/coronary vasodilator reserve in patients with familial combined hyperlipidaemia; http://www.controlled-trials.com/mrct/trial/230761/ISRCTN78563659; ISRCTN78563659 [controlled-trials.com] )

Abbreviations and Acronyms
  BMI = body mass index
  CAD = coronary artery disease
  CFR = coronary flow reserve
  FCHL = familial combined hyperlipidemia
  FDG = 2-[18F]fluoro-2-deoxy-D-glucose
  H2 15O = oxygen-15–labeled water
  HDL = high-density lipoprotein cholesterol
  LDL = low-density lipoprotein cholesterol
  M = whole body glucose disposal
  MBF = myocardial blood flow
  MGU = myocardial glucose utilization
  PAI = plasminogen activator inhibitor
  PET = positron emission tomography


Related Article

Physiologic Straws in the Wind: In Which Direction Do They Bend?
Richard Lewanczuk and Paul W. Armstrong
J. Am. Coll. Cardiol. 2007 50: 2059-2060. [Full Text] [PDF]



This article has been cited by other articles:


Home page
J Am Coll CardiolHome page
R. Lewanczuk and P. W. Armstrong
Physiologic Straws in the Wind: In Which Direction Do They Bend?
J. Am. Coll. Cardiol., November 20, 2007; 50(21): 2059 - 2060.
[Full Text] [PDF]




HOME SUBSCRIPTIONS CURRENT ISSUE PAST ISSUES CARDIOSOURCE SEARCH HELP FEEDBACK
Copyright © 2007 by the American College of Cardiology Foundation.