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Eur J Cardiothorac Surg 2004;26:736-741
© 2004 Elsevier Science NL

Sympathetic reinnervation after heart transplantation, assessed by iodine-123 metaiodobenzylguanidine imaging, and heart rate variability

^a Department of Cardiology, University Medical Centre, Zaloska 7, Ljubljana, SI 1000, Slovenia
^b Department of Nuclear Medicine, University Medical Centre, Ljubljana, Slovenia
^c Department for Communication and Computer Networks, Jozef Stefan Institute, Ljubljana, Slovenia
^d Department of Cardiovascular Surgery, University Medical Centre, Ljubljana, Slovenia

Received 13 April 2004; received in revised form 24 June 2004; accepted 7 July 2004.

^* Corresponding author. Tel.: +386-1-5222844; fax: +386-1-5222828. (E-mail: silvia.samarin{at}kclj.si).

Objective: Complete allograft denervation occurs during heart transplantation. Partial ventricular sympathetic reinnervation may develop one year or later after transplantation and can be measured with iodine-123-meta-iodobenziylguanidine (MIBG) uptake. Aim of this study was to assess sinus node sympathetic reinnervation measured with heart rate variability and ventricular sympathetic reinnervation evaluated with MIBG. Methods: Twelve patients and 14 healthy controls were included. In patients, MIBG scintigraphy with early and late imaging was performed. Heart to mediastinum ratio (HMR) was calculated and patients were divided in groups with (HMR>1.3) and without left ventricular reinnervation (HMR<1.3). Bipolar ECG with high sampling rate and resolution was recorded over 8.5min in supine position and in upright position after 10min interval. R–R intervals in time domain and heart rate variability in frequency domain through spectral power analysis of R–R intervals were analysed to evaluate sinus node reinnervation. Spectral power in low frequency range (0.04–0.15Hz) above 4.5ms² was considered as sinus node sympathetic reinnervation. Results: Six (50%) patients had evidence of left ventricular sympathetic reinnervation on scintigraphy. Sinus node sympathetic reinnervation based on heart rate variability was detected in 6 (50%) patients in supine, and in 4 (33%) patients in upright body position. Four patients groups were discerned: (1) with ventricular and sinus node sympathetic reinnervation, (2) with sinus node sympathetic reinnervation, (3) with ventricular sympathetic reinnervation and (4) without atrial or ventricular sympathetic reinnervation. Ventricular reinnervation process was time dependent and sinus node reinnervation was not. Conclusions: Simultaneous ventricular sympathetic reinnervation assessed by MIBG and sinus node sympathetic reinnervation assessed by heart rate variability in supine as in upright position were detected only in two patients (17%). The results of our study show that eventual sinus node sympathetic reinnervation and left ventricular sympathetic reinnervation do not occur simultaneously.