TY - JOUR
T1 - Reappearance of cardiac presynaptic sympathetic nerve terminals in the transplanted heart
T2 - Correlation between PET using 11C-hydroxyephedrine and invasively measured norepinephrine release
AU - Odaka, K.
AU - Von Scheidt, W.
AU - Ziegler, S. I.
AU - Ueberfuhr, P.
AU - Nekolla, S. G.
AU - Reichart, B.
AU - Bengel, Frank Michael
AU - Schwaiger, M.
PY - 2001
Y1 - 2001
N2 - Previously, sympathetic reinnervation of the transplanted heart has been described using invasive catheterization techniques and noninvasive radionuclide imaging techniques. However, little is known about the agreement between these 2 methods. Thus, correlation between 11C-hydroxyephedrine (HED) PET and invasively measured norepinephrine (NE) release was investigated in transplant recipients in this study, Methods: Using PET and the catecholamine analog HED, 17 patients were studied between 2 mo and 13.6 y after transplantation. Based on results in completely denervated hearts, areas with HED retention >7%/min were defined as reinnervated. Additionally, transcardiac NE release induced by intravenous tyramine (55 uμg/kg) was measured by coronary sinus and aortic catheterization within 1 wk of the PET study. NE levels between coronary sinus and aortic root, ΔNECS-Ao, were calculated at baseline and after tyramine administration. Differences of more than 3 SD of baseline (>163 pg/mL) were interpreted as reinnervation. Results: HED retention indicated reinnervation in 10 patients. Maximal HED retention ranged from 4.3%/min to 16.4%/min./-ΔNECS-Ao 1 min after tyramine administration ranged between -10 pg/mL and 1157 pg/mL, and 8 patients were above the reinnervation threshold. Fisher's exact test demonstrated good agreement between results of PET and ANECS-Ao measurements (P = 0.002). Maximal HED retention was also significantly correlated with NE release (r = 0.69; P = 0.001). Conclusion: Results of invasively measured NE release and noninvasive 11C-HED PET are well correlated. This study further supports the usefulness of PET as a noninvasive approach for detection of reappearance of catecholamine uptake sites after heart transplantation.
AB - Previously, sympathetic reinnervation of the transplanted heart has been described using invasive catheterization techniques and noninvasive radionuclide imaging techniques. However, little is known about the agreement between these 2 methods. Thus, correlation between 11C-hydroxyephedrine (HED) PET and invasively measured norepinephrine (NE) release was investigated in transplant recipients in this study, Methods: Using PET and the catecholamine analog HED, 17 patients were studied between 2 mo and 13.6 y after transplantation. Based on results in completely denervated hearts, areas with HED retention >7%/min were defined as reinnervated. Additionally, transcardiac NE release induced by intravenous tyramine (55 uμg/kg) was measured by coronary sinus and aortic catheterization within 1 wk of the PET study. NE levels between coronary sinus and aortic root, ΔNECS-Ao, were calculated at baseline and after tyramine administration. Differences of more than 3 SD of baseline (>163 pg/mL) were interpreted as reinnervation. Results: HED retention indicated reinnervation in 10 patients. Maximal HED retention ranged from 4.3%/min to 16.4%/min./-ΔNECS-Ao 1 min after tyramine administration ranged between -10 pg/mL and 1157 pg/mL, and 8 patients were above the reinnervation threshold. Fisher's exact test demonstrated good agreement between results of PET and ANECS-Ao measurements (P = 0.002). Maximal HED retention was also significantly correlated with NE release (r = 0.69; P = 0.001). Conclusion: Results of invasively measured NE release and noninvasive 11C-HED PET are well correlated. This study further supports the usefulness of PET as a noninvasive approach for detection of reappearance of catecholamine uptake sites after heart transplantation.
KW - C-hydroxy-ephedrine
KW - Heart transplantation
KW - Norepinephrine
KW - PET
KW - Sympathetic reinnervation
UR - http://www.scopus.com/inward/record.url?scp=0034955643&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034955643&partnerID=8YFLogxK
M3 - Article
C2 - 11438620
AN - SCOPUS:0034955643
SN - 0161-5505
VL - 42
SP - 1011
EP - 1016
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 7
ER -