Objective We investigated the impact of cardiac presynaptic norepinephrine recycling in patients with long-QT syndrome (LQTS) using positron emission tomography (PET) with 11C-meta-hydroxyephedrine ([11C]mHED-PET).
Methods [11C]mHED-PET was performed in 25 patients with LQTS (LQT1: n=14; LQT2: n=11) and 20 healthy controls and correlated with clinical parameters. [11C]mHED-PET images were analysed for global and regional retention indices (RI) and washout rates (WO) reflecting dynamic parameters of the tracer activity.
Results Global and regional RI values were similar between patients with LQTS and controls. Although the global WO rates were similar between these groups, regional WO rates were on average higher in the lateral left ventricle (LV) wall in patients with LQTS (dose, mean ±SD; 0.08±0.14 vs 0.00%±0.09% min–1; p=0.033). In addition, patients with LQTS with a longer QTc interval showed a higher global WO rate. Clinical symptoms correlated with higher global WO rates. In the presence of normal global WO rates, asymptomatic LQTS patients showed higher global RI values.
Conclusion The increased regional WO rate of [11C]mHED in the lateral LV suggests an imbalance of presynaptic catecholamine reuptake and release, resulting in a higher synaptic catecholamine concentration, in particular in LQT1 patients. This might enhance β-adrenoceptor signalling and thereby aggravate inherited ion channel dysfunction and may facilitate occurrence of ventricular tachyarrhythmias. Detection of regional differences in LV sympathetic nervous function may modify disease expression and potentially serve as a non-invasive risk marker in congenital LQTS.
Trial registration number 2006-002767-41;Results.
- long-QT syndrome
- 11C hydroxyephedrine PET
- cardiac sympathetic innervation
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Contributors Substantial contributions to the conception and design of the work: SZ, AV, LS, MS, ES-B. Acquisition, analysis and interpretation of data: SZ, AV, LS, PK, CW, ME, JM, GS, MP, KS, BS, MS, ES-B. Drafting the work or revising it critically for important intellectual content: SZ, AV, LS, PK, CW, ME, JM, GS, MP, KS, BS, MS, ES-B. Final approval of the version published: SZ, AV, LS, PK, CW, ME, JM, GS, MP, KS, BS, MS, ES-B.
Funding This work was supported by grants of the Fondation Leducq, Paris, France (to ES-B), the German Research Foundation, Bonn, Germany (DFG SFB 6565C1), and the Interdisciplinary Center for Clinical Research, Münster, Germany.
Competing interests None declared.
Patient consent Obtained.
Ethics approval Federal Institute for Drugs and Medical Devices (BfArM), the Federal Office for Radiation Protection (BfS) and the local ethics committee.
Provenance and peer review Not commissioned; externally peer reviewed.
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