Background: Biventricular pacing induces well-known effects on myocardial wall function, apparently providing better results in comparison with conventional right pacing in patients presenting with dilated cardiomyopathy (DCM). However, at the moment the secondary changes in myocardial metabolism induced by pacing devices are unclear. The aim of our study was to evaluate the possible changes in myocardial metabolism and perfusion induced by cardiac pacing in these patients.
Methods: Twenty-eight patients presenting with DCM were submitted to positron emission tomography. Eighteen patients were examined during cardiac pacing, 6 had dual chamber pacemakers implanted for conventional reasons (group A), 12 biventricular pacemakers (group B) for resynchronization purposes; the other 10 patients were considered as controls. Myocardial metabolism was evaluated using 18F-fluorodeoxyglucose (FDG), by the glucose load-insulin technique and perfusion using 13N-ammonia (NH3), injected at rest. A visual and a semiquantitative analysis were performed, calculating on the basis of the regions of interest the septum to lateral uptake (S/L) ratio.
Results: In all the 6 patients of group A, a selective defect in FDG uptake was observed in the septum (mean S/L ratio 0.67 +/- 0.15, p < 0.01 with respect to controls), while both the patients in group B and the controls presented a homogeneous distribution of FDG uptake in the myocardial wall (mean S/L ratio 1.01 +/- 0.10 and 0.95 +/- 0.13 respectively, p = NS). On the contrary, at the NH3 positron emission tomography studies no significant difference in myocardial perfusion was found in the three groups of patients, both at the visual and at the semiquantitative analysis (mean S/L ratio group A 1.01 +/- 0.21, group B 0.99 +/- 0.17, controls 0.94 +/- 0.11, p = NS).
Conclusions: Our experience could suggest that, in patients with DCM, conventional right pacing could induce interference in the metabolism of the septum not correlated with perfusion changes. On the other hand, biventricular pacing improves myocardial wall function without interfering with myocardial metabolism and perfusion.
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BMC Nutr
January 2025
Department of Community Nutrition, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Razi Blvd, Shiraz, 7153675541, Iran.
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J Transl Med
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Department of Cardiovascular Ultrasound, The First Hospital of China Medical University, Shenyang, China.
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Instituto do Coração (InCor), Faculdade de Medicina, Hospital das Clínicas HCFMUSP, Universidade de São Paulo, São Paulo, Brazil.
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Key Laboratory of Bioactive Materials for the Ministry of Education, College of Life Sciences, State Key Laboratory of Medicinal Chemical Biology, and Frontier of Science Center for Cell Response, Nankai University, Tianjin, 300071, China.
Nanozymes play a pivotal role in mitigating excessive oxidative stress, however, determining their specific enzyme-mimicking activities for intracellular free radical scavenging is challenging due to endo-lysosomal entrapment. In this study, we employ a genetic engineering strategy to generate ionizable ferritin nanocages (iFTn), enabling their escape from endo-lysosomes and entry into the cytoplasm. Specifically, ionizable repeated Histidine-Histidine-Glutamic acid (9HE) sequences are genetically incorporated into the outer surface of human heavy chain FTn, followed by the assembly of various chain-like nanostructures via a two-armed polyethylene glycol (PEG).
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