Imaging of cardiac fibroblast activation in patients with chronic thromboembolic pulmonary hypertension

Purpose The aim of this study was to explore the association of cardiac fibroblast activation with clinical parameters and cardiovascular magnetic resonance (CMR) imaging parameters in patients with chronic thromboembolic pulmonary hypertension (CTEPH). Methods Thirteen CTEPH patients were prospecti...

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Veröffentlicht in:European journal of nuclear medicine and molecular imaging 2022-03, Vol.49 (4), p.1211-1222
Hauptverfasser: Chen, Bi-Xi, Xing, Hai-Qun, Gong, Juan-Ni, Guo, Xiao-Juan, Xi, Xiao-Ying, Yang, Yuan-Hua, Huo, Li, Yang, Min-Fu
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Sprache:eng
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Zusammenfassung:Purpose The aim of this study was to explore the association of cardiac fibroblast activation with clinical parameters and cardiovascular magnetic resonance (CMR) imaging parameters in patients with chronic thromboembolic pulmonary hypertension (CTEPH). Methods Thirteen CTEPH patients were prospectively enrolled. All of the patients underwent cardiac 68 Gallium-labelled fibroblast activation protein inhibitor ( 68  Ga-FAPI-04)-positron emission tomography/computed tomography (PET/CT), right heart catheterisation, and echocardiography, and 11 of them additionally underwent CMR. Thirteen control subjects were selected to establish the normal range of cardiac 68  Ga-FAPI-04 uptake. Cardiac 68  Ga-FAPI-04 uptake higher than that in the blood pool was defined as abnormal. The global and segmental maximum standardised uptake values (SUV max ) of the right ventricle (RV) were measured and further expressed as target-to-background ratio (TBR RV ) with left ventricular lateral wall activity as background. Late gadolinium enhancement (LGE) was visually evaluated, and native-T1 times, enhanced-T1 times, and extracellular volume (ECV) were quantitatively measured. Results Ten CTEPH patients (77%) had abnormal 68  Ga-FAPI-04 uptake in RV, mainly located in the free wall, which was significantly higher than that in controls (TBR RV : 2.4 ± 0.9 vs 1.0 ± 0.1, P  
ISSN:1619-7070
1619-7089
DOI:10.1007/s00259-021-05577-9