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.
Abstract