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Effect of ET‐A blockade on portal pressure and hepatic arterial perfusion in patients with cirrhosis: A proof of concept study
Author(s) -
Zipprich Alexander,
Gittinger Fleur,
Winkler Matthias,
Dollinger Matthias M.,
Ripoll Cristina
Publication year - 2021
Publication title -
liver international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.873
H-Index - 110
eISSN - 1478-3231
pISSN - 1478-3223
DOI - 10.1111/liv.14757
Subject(s) - portal venous pressure , medicine , portal hypertension , cirrhosis , antagonist , hemodynamics , endothelin receptor antagonist , cardiology , vasoconstriction , receptor
Background/aim Endothelin causes vasoconstriction via the endothelin‐A receptor (ET‐A) in the intrahepatic circulation in cirrhosis and its increase leads to portal hypertension. The aim of the study was to investigate the acute effect of a selective ET‐A antagonist in patients with portal hypertension and cirrhosis. Methods Proof‐of‐concept study with two different substudies: (a) local intrahepatic administration of the ET‐A antagonist BQ 123 and (b) systemic oral administration of the ET‐A antagonist Ambrisentan. Portal pressure was determined by hepatic venous pressure gradient (HVPG, both substudies) and hepatic arterial blood flow (HABF) by intra‐arterial Doppler measurements (substudy 1) before and under the ET‐A antagonist. Systemic haemodynamic parameters were measured in substudy 2. Results Twelve patients (Child‐Pugh [CP] B/C n = 7/5) were included in substudy 1 and 14 patients (CP A/B/C n = 4/6/4) in substudy 2. The relative decrease in HVPG was −12.5% (IQR: −40% to 0%; P = .05) in substudy 1 and −5.0% (IQR: −11.5% to 0%; P = .01) in substudy 2. Substudy 1 revealed higher decrease in HVPG in CP B patients. HABF increased significantly and patients without portal pressure decrease showed a higher increase of HABF. Substudy 2 showed a slight decrease in the mean arterial pressure without changes of other systemic haemodynamic parameters. Conclusion Administration of a selective ET‐A antagonist decreases the portal pressure in cirrhotic patients. This decrease was higher in CP B patients and the non‐responders showed a higher increase in hepatic arterial flow. Selective ET‐A antagonists might be a future treatment option in patients with portal hypertension.