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Scar imaging in the dyssynchronous left ventricle: Accuracy of myocardial metabolism by positron emission tomography and function by echocardiographic strain.
Int J Cardiol. 2023 02 01; 372:122-129.IJ

Abstract

PURPOSE

Response to cardiac resynchronization therapy (CRT) is reduced in patients with high left ventricular (LV) scar burden, in particular when scar is located in the LV lateral wall or septum. Late gadolinium enhancement (LGE) cardiac magnetic resonance (CMR) can identity scar, but is not feasible in all patients. This study investigates if myocardial metabolism by 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) and contractile function by echocardiographic strain are alternatives to LGE-CMR.

METHODS

In a prospective multicenter study, 132 CRT candidates (91% with left bundle branch block) were studied by speckle tracking strain echocardiography, and 53 of these by FDG-PET. Regional myocardial FDG metabolism and peak systolic strain were compared to LGE-CMR as reference method.

RESULTS

Reduced FDG metabolism (<70% relative) precisely identified transmural scars (≥50% of myocardial volume) in the LV lateral wall, with area under the curve (AUC) 0.96 (95% confidence interval (CI) 0.90-1.00). Reduced contractile function by strain identified transmural scars in the LV lateral wall with only moderate accuracy (AUC = 0.77, CI 0.71-0.84). However, absolute peak systolic strain >10% could rule out transmural scar with high sensitivity (80%) and high negative predictive value (96%). Neither FDG-PET nor strain identified septal scars (for both, AUC < 0.80).

CONCLUSIONS

In CRT candidates, FDG-PET is an excellent alternative to LGE-CMR to identify scar in the LV lateral wall. Furthermore, preserved strain in the LV lateral wall has good accuracy to rule out transmural scar. None of the modalities can identify septal scar.

CLINICAL TRIAL REGISTRATION

The present study is part of the clinical study "Contractile Reserve in Dyssynchrony: A Novel Principle to Identify Candidates for Cardiac Resynchronization Therapy (CRID-CRT)", which was registered at clinicaltrials.gov (identifier NCT02525185).

Authors+Show Affiliations

Institute for Surgical Research, Oslo University Hospital and University of Oslo, Oslo, Norway; Department of Cardiology, Oslo University Hospital, Oslo, Norway.Department of Cardiology, University Hospital of Rennes and University of Rennes, Rennes, France.Department of Cardiovascular Diseases, University Hospitals Leuven and Department of Cardiovascular Sciences, KU Leuven - University of Leuven, Leuven, Belgium.Institute for Surgical Research, Oslo University Hospital and University of Oslo, Oslo, Norway; Department of Cardiology, Oslo University Hospital, Oslo, Norway.Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway; Department of Physics, University of Oslo, Oslo, Norway.Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway; Oslo Metropolitan University, Oslo, Norway.Department of Nuclear Medicine, University Hospitals Leuven and Department of Imaging and Pathology, KU Leuven - University of Leuven, Leuven, Belgium.Department of Nuclear Medicine, University Hospitals Leuven and Department of Imaging and Pathology, KU Leuven - University of Leuven, Leuven, Belgium.Department of Nuclear Medicine, Cliniques Universitaires Saint-Luc and Institute of Clinical and Experimental Research (IREC), Université Catholique de Louvain, Brussels, Belgium.Department of Cardiology, Akershus University Hospital, Lorenskog, Norway.Ostlandske Hjertesenter, Moss, Norway.Department of Cardiology, Oslo University Hospital, Oslo, Norway.Department of Radiology, University Hospitals Leuven, Leuven, Belgium.Department of Cardiology, Oslo University Hospital, Oslo, Norway.Cardiovascular Center, OLV Clinic, Aalst, Belgium.Department of Cardiovascular Diseases, University Hospitals Leuven and Department of Cardiovascular Sciences, KU Leuven - University of Leuven, Leuven, Belgium.Department of Cardiology, University Hospital of Rennes and University of Rennes, Rennes, France.Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.Institute for Surgical Research, Oslo University Hospital and University of Oslo, Oslo, Norway; Department of Cardiology, Oslo University Hospital, Oslo, Norway. Electronic address: otto.smiseth@gmail.com.

Pub Type(s)

Multicenter Study
Journal Article
Comment

Language

eng

PubMed ID

36460211

Citation

Larsen, Camilla Kjellstad, et al. "Scar Imaging in the Dyssynchronous Left Ventricle: Accuracy of Myocardial Metabolism By Positron Emission Tomography and Function By Echocardiographic Strain." International Journal of Cardiology, vol. 372, 2023, pp. 122-129.
Larsen CK, Galli E, Duchenne J, et al. Scar imaging in the dyssynchronous left ventricle: Accuracy of myocardial metabolism by positron emission tomography and function by echocardiographic strain. Int J Cardiol. 2023;372:122-129.
Larsen, C. K., Galli, E., Duchenne, J., Aalen, J. M., Stokke, C., Fjeld, J. G., Degtiarova, G., Claus, P., Gheysens, O., Saberniak, J., Sirnes, P. A., Lyseggen, E., Bogaert, J., Kongsgaard, E., Penicka, M., Voigt, J. U., Donal, E., Hopp, E., & Smiseth, O. A. (2023). Scar imaging in the dyssynchronous left ventricle: Accuracy of myocardial metabolism by positron emission tomography and function by echocardiographic strain. International Journal of Cardiology, 372, 122-129. https://doi.org/10.1016/j.ijcard.2022.11.042
Larsen CK, et al. Scar Imaging in the Dyssynchronous Left Ventricle: Accuracy of Myocardial Metabolism By Positron Emission Tomography and Function By Echocardiographic Strain. Int J Cardiol. 2023 02 1;372:122-129. PubMed PMID: 36460211.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Scar imaging in the dyssynchronous left ventricle: Accuracy of myocardial metabolism by positron emission tomography and function by echocardiographic strain. AU - Larsen,Camilla Kjellstad, AU - Galli,Elena, AU - Duchenne,Jürgen, AU - Aalen,John M, AU - Stokke,Caroline, AU - Fjeld,Jan Gunnar, AU - Degtiarova,Ganna, AU - Claus,Piet, AU - Gheysens,Olivier, AU - Saberniak,Jorg, AU - Sirnes,Per Anton, AU - Lyseggen,Erik, AU - Bogaert,Jan, AU - Kongsgaard,Erik, AU - Penicka,Martin, AU - Voigt,Jens-Uwe, AU - Donal,Erwan, AU - Hopp,Einar, AU - Smiseth,Otto A, Y1 - 2022/11/29/ PY - 2022/09/02/received PY - 2022/10/20/revised PY - 2022/11/22/accepted PY - 2022/12/3/pubmed PY - 2023/1/4/medline PY - 2022/12/2/entrez KW - Dyssynchrony KW - Glucose metabolism KW - Heart failure KW - Late gadolinium enhancement cardiac magnetic resonance KW - Myocardial scar KW - Positron emission tomography KW - Speckle tracking echocardiography KW - Strain SP - 122 EP - 129 JF - International journal of cardiology JO - Int J Cardiol VL - 372 N2 - PURPOSE: Response to cardiac resynchronization therapy (CRT) is reduced in patients with high left ventricular (LV) scar burden, in particular when scar is located in the LV lateral wall or septum. Late gadolinium enhancement (LGE) cardiac magnetic resonance (CMR) can identity scar, but is not feasible in all patients. This study investigates if myocardial metabolism by 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) and contractile function by echocardiographic strain are alternatives to LGE-CMR. METHODS: In a prospective multicenter study, 132 CRT candidates (91% with left bundle branch block) were studied by speckle tracking strain echocardiography, and 53 of these by FDG-PET. Regional myocardial FDG metabolism and peak systolic strain were compared to LGE-CMR as reference method. RESULTS: Reduced FDG metabolism (<70% relative) precisely identified transmural scars (≥50% of myocardial volume) in the LV lateral wall, with area under the curve (AUC) 0.96 (95% confidence interval (CI) 0.90-1.00). Reduced contractile function by strain identified transmural scars in the LV lateral wall with only moderate accuracy (AUC = 0.77, CI 0.71-0.84). However, absolute peak systolic strain >10% could rule out transmural scar with high sensitivity (80%) and high negative predictive value (96%). Neither FDG-PET nor strain identified septal scars (for both, AUC < 0.80). CONCLUSIONS: In CRT candidates, FDG-PET is an excellent alternative to LGE-CMR to identify scar in the LV lateral wall. Furthermore, preserved strain in the LV lateral wall has good accuracy to rule out transmural scar. None of the modalities can identify septal scar. CLINICAL TRIAL REGISTRATION: The present study is part of the clinical study "Contractile Reserve in Dyssynchrony: A Novel Principle to Identify Candidates for Cardiac Resynchronization Therapy (CRID-CRT)", which was registered at clinicaltrials.gov (identifier NCT02525185). SN - 1874-1754 UR - https://www.unboundmedicine.com/medline/citation/36460211/Scar_imaging_in_the_dyssynchronous_left_ventricle:_Accuracy_of_myocardial_metabolism_by_positron_emission_tomography_and_function_by_echocardiographic_strain_ DB - PRIME DP - Unbound Medicine ER -