Effect of biventricular pacing on metabolism and perfusion in patients affected by dilated cardiomyopathy and left bundle branch block: evaluation by positron emission tomography

Europace. 2003 Jan;5(1):111-5. doi: 10.1053/eupc.2002.0272.

Abstract

Aims: Evaluate the possible changes in myocardial metabolism and perfusion induced by biventricular pacing (BIVP) in patients affected by dilated cardiomyopathy (DC) and left bundle branch block (LBBB).

Methods and results: Eight male patients (aged 60-79 years, mean 69) affected by DC (NYHA functional class III and ejection fraction <40%) were submitted to cardiac PET in basal condition and 3 weeks after the implantation of a biventricular device. Metabolism was evaluated using F18-fluorodeoxyglucose (FDG), by the glucose load-insulin technique, and perfusion by N13-ammonia (NH3), injected at rest. Visual and a semi quantitative analyses were performed, calculating by ROIs the septum to lateral uptake ratio (SLR). The myocardial blood flow (MBF) was also calculated in ml/min/g using a dynamic acquisition and a modified Patlak method. In all 8 patients a selective defect in FDG uptake in the septum was present in basal condition (mean SLR 0.59+/-0.17) with a 'reverse mismatch' effect with respect to NH3 (mean SLR 1.07+/-0.18). During BIVP the distribution of FDG in the septal area significatively improved (mean SLR 0.86+/-0.15 P=0.011 with respect to basal); on the contrary, no significant changes were found in NH3 uptake (mean SLR 1.02+/-0.23, P=ns). On quantitative analysis the mean MBF in the septum was 1.05+/-0.37 in basal condition and did not significantly change during BIVP (0.95+/-0.34, P=0.06).

Conclusions: Our results suggest that, in patients affected by DC and LBBB, BIVP improves the septal glucose metabolism without significant changes in myocardial perfusion.

MeSH terms

  • Aged
  • Ammonia
  • Bundle-Branch Block / diagnostic imaging*
  • Bundle-Branch Block / metabolism
  • Bundle-Branch Block / therapy*
  • Cardiac Pacing, Artificial*
  • Cardiomyopathy, Dilated / diagnostic imaging*
  • Cardiomyopathy, Dilated / metabolism
  • Cardiomyopathy, Dilated / therapy*
  • Fluorodeoxyglucose F18
  • Heart / diagnostic imaging*
  • Humans
  • Male
  • Myocardium / metabolism
  • Nitrogen Radioisotopes
  • Perfusion
  • Radiopharmaceuticals
  • Tomography, Emission-Computed*

Substances

  • Nitrogen Radioisotopes
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18
  • Ammonia