Key result
Simultaneous low-dose dual-isotope CZT-SPECT imaging in heart failure patients demonstrated that myocardial innervation defect sizes were significantly larger than perfusion defect sizes (29% vs 17%, p<0.001).
Why the study?
Sequential imaging shows a relationship between myocardial perfusion and adrenergic innervation in HF, but the feasibility of a simultaneous low-dose dual-isotope protocol using CZT-SPECT had not been evaluated.
Is simultaneous low-dose dual-isotope CZT SPECT imaging feasible for assessing myocardial perfusion and adrenergic innervation in patients with heart failure?
Cross-Sectional (n=55)
No
Is simultaneous low-dose dual-isotope CZT SPECT imaging feasible for assessing myocardial perfusion and adrenergic innervation in patients with heart failure?
Absolute Event Rate: 29% vs 17%
p-value: p=<0.001
A simultaneous low-dose dual-isotope CZT-SPECT protocol is feasible for assessing myocardial perfusion and adrenergic innervation in heart failure patients, showing significant correlations with LVEF.
Supports dual-isotope CZT-SPECT feasibility in HF; leaves open whether innervation-perfusion mismatch improves risk stratification.
In patients with heart failure (HF) sequential imaging studies have demonstrated a relationship between myocardial perfusion and adrenergic innervation. We evaluated the feasibility of a simultaneous low-dose dual-isotope 123 I/ 99m Tc-acquisition protocol using a cadmium-zinc-telluride (CZT) single-photon emission computed tomography (SPECT) camera. Thirty-six patients with HF underwent simultaneous low-dose 123 I-metaiodobenzylguanidine (MIBG)/ 99m Tc-sestamibi gated CZT-SPECT cardiac imaging. Perfusion and innervation total defect sizes and perfusion/innervation mismatch size (defined by 123 I-MIBG defect size minus 99m Tc-sestamibi defect size) were expressed as percentages of the total left ventricular (LV) surface area. LV ejection fraction (EF) significantly correlated with perfusion defect size ( P < .005), innervation defect size ( P < .005), and early ( P < .05) and late ( P < .01) 123 I-MIBG heart-to-mediastinum (H/M) ratio. In addition, late H/M ratio was independently associated with reduced LVEF ( P < .05). Although there was a significant relationship ( P < .001) between perfusion and innervation defect size, innervation defect size was larger than perfusion defect size ( P < .001). At multivariable linear regression analysis, 123 I-MIBG washout rate (WR) correlated with perfusion/innervation mismatch ( P < .05). In patients with HF, a simultaneous low-dose dual-isotope 123 I/ 99m Tc-acquisition protocol is feasible and could have important clinical implications.
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Assante et al. (2022) conducted a cross-sectional in Heart failure (n=55). Simultaneous low-dose dual-isotope 123I-MIBG/99mTc-sestamibi CZT-SPECT was evaluated on Innervation defect size vs perfusion defect size (% of total left ventricular surface area) (p=<0.001). Simultaneous low-dose dual-isotope CZT-SPECT imaging in heart failure patients demonstrated that myocardial innervation defect sizes were significantly larger than perfusion defect sizes (29% vs 17%, p<0.001).
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