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18 F-FAPI PET/CT in chronic liver disease: myocardial fibroblast activation and its correlates
Yangyang Wang1,2, Guangjie Yang2, Wenlong Yan3
1Department of Nuclear Medicine, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu Province.
Insights
Fibroblast activation in the heart, detected by fluorine-18 (18F)-labeled fibroblast activation protein inhibitor (FAPI) PET/CT, is linked to clinical factors in chronic liver disease patients. This imaging may help identify early cardiac changes noninvasively.
Area of Science:
- Cardiology
- Hepatology
- Nuclear Medicine
Background:
- Chronic liver disease (CLD) is associated with cardiovascular complications.
- Cardiac fibroblast activation is implicated in heart disease pathogenesis.
- Noninvasive markers for cardiac fibroblast activation in CLD are needed.
Purpose of the Study:
- To investigate the relationship between cardiac fibroblast activation and clinical parameters, electrophysiological findings, serum fibrosis markers, and hepatic fibroblast activation in patients with CLD.
- To assess the utility of fluorine-18 (18F)-labeled fibroblast activation protein inhibitor (FAPI) PET/CT for detecting cardiac fibroblast activation in CLD.
Main Methods:
- Prospective study of 46 CLD patients (December 2021-April 2022).
- 18F-FAPI PET/CT imaging and 12-lead electrocardiogram (ECG) were performed.
- Abnormal cardiac 18F-FAPI uptake defined as uptake greater than blood pool.
Main Results:
- 14 out of 46 patients showed positive myocardial 18F-FAPI uptake.
- Positive uptake was significantly associated with older age and greater epicardial fat volume (EFV).
- Myocardial FAPI uptake correlated with hepatic FAPI uptake and serum laminin levels.
Conclusions:
- Cardiac fibroblast activation is detectable using 18F-FAPI PET/CT in CLD patients.
- This activation is associated with electrophysiological parameters, hepatic FAPI uptake, and serum fibrosis markers.
- 18F-FAPI PET/CT may serve as a noninvasive tool for identifying early myocardial changes in CLD.
Objectives:
This study investigated the relationship between cardiac fibroblast activation and clinical parameters, electrophysiological findings, serum fibrosis markers, and hepatic fibroblast activation in patients with chronic liver disease.
Methods:
In this prospective study conducted from December 2021 to April 2022, 46 patients with chronic liver disease underwent fluorine-18 ( 18 F)-labeled fibroblast activation protein inhibitor (FAPI) PET/computed tomography (CT) imaging and 12-lead electrocardiogram (ECG). Abnormal cardiac 18 F-FAPI uptake was defined as uptake greater than that of the blood pool.
Results:
Among 46 patients with chronic liver disease analyzed, 14 showed positive myocardial FAPI uptake and 32 were negative. Significant differences were observed between positive and negative myocardial 18 F-FAPI PET/CT imaging groups in terms of age ( P = 0.006), epicardial fat volume (EFV) ( P = 0.004), Cornell voltage QRS amplitude ( P = 0.022), and QRS duration ( P = 0.032). The multivariable logistic regression analysis demonstrated a significant association between EFV [odds ratio (OR) = 1.019; P = 0.024] and age (OR = 1.162; P = 0.019) and positive myocardial FAPI uptake. Myocardial maximum target-to-background ratio (TBR max ) was positively correlated with hepatic TBR max ( r = 0.405; P = 0.005) and hepatic TBR mean ( r = 0.412, P = 0.004). Moreover, myocardial maximum standardized uptake value was positively correlated with serum laminin levels ( r = 0.367; P = 0.042).
Conclusions:
In patients with chronic liver disease, FAPI PET/CT imaging observed cardiac fibroblast activation, which was associated with electrophysiological parameters, hepatic FAPI uptake, and serum liver fibrosis markers. These findings suggest that 18 F-FAPI PET/CT imaging may offer a noninvasive approach for identifying early myocardial changes in chronic liver disease.
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