An Imaging Biomarker for Assessing Hepatic Function in Patients With Primary Sclerosing Cholangitis

• Published in: Clinical gastroenterology and hepatology Vol. 17; no. 1; pp. 192 - 199.e3
• Main Authors: Schulze, Jennifer, Lenzen, Henrike, Hinrichs, Jan B., Ringe, Burckhardt, Manns, Michael P., Wacker, Frank, Ringe, Kristina I.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2019
• Subjects: Adolescent; Adult; Aged; Aged, 80 and over; Biomarkers - analysis; Cholangitis, Sclerosing - complications; Contrast Media - administration & dosage; Contrast Media - analysis; Female; Gadolinium DTPA - administration & dosage; Gadolinium DTPA - analysis; Humans; Liver Diseases - diagnostic imaging; Liver Diseases - etiology; Liver Diseases - pathology; Magnetic Resonance Imaging - methods; Male; Middle Aged; Predicted Outcome; Prognosis; Prognostic Factor; Prospective Studies; Risk Factor; Sensitivity and Specificity; Young Adult; CHE; PSC; AST; Prognosis; Predicted Outcome; MRI; ROC; ALT; IQR; INR; AP; RE; MELD; MRCP; SI; HBP; ERCP; LFT; Risk Factor; Prognostic Factor
• ISSN: 1542-3565; 1542-7714
• DOI: 10.1016/j.cgh.2018.05.011

We aimed to evaluate the potential of hepatobiliary phase magnetic resonance imaging (MRI) as parameter for assessment of hepatocellular function in patients with primary sclerosing cholangitis (PSC). We collected data from 111 patients (83 male, 28 female; median, 44 years old), from March 2012 through March 2016, with a confirmed diagnosis of PSC who underwent MRI evaluation before and after injection (hepatobiliary phase) of a hepatocyte-specific contrast agent (gadoxetate disodium). Signal intensities were measured in each liver segment. Mean relative enhancement values were calculated and correlated with findings from liver functions tests, prognostic scoring systems (model for end-stage liver disease [MELD] score; Mayo risk score; Amsterdam-Oxford-PSC score), abnormalities detected by endoscopic retrograde cholangiopancreatography (using the Amsterdam cholangiographic classification system), and clinical endpoints (liver transplantation, cholangiocarcinoma, liver-related death). Our primary aim was to associate relative enhancement values with liver function and patient outcomes. Most patients had moderate-stage disease and had intermediate levels of risk (median MELD score, 8 and median Mayo score, 0.27). Clinical endpoints were reached by 21 patients (6 developed cholangiocarcinoma, 8 underwent liver transplantation, and 7 patients died). The highest levels of correlations were observed for relative enhancement 20 min after contrast injection and level of alkaline phosphatase (r = –0.636), bilirubin (r = –0.646), albumin (r = 0.538); as well as international normalized ratio (r = 0.456); MELD score (r = –0.587); Mayo risk score (r = –0.535), and Amsterdam-Oxford model score (r = –0.595) (P < .0001). Relative enhancement correlated with all clinical endpoints (all P < .05). A cutoff relative enhancement value of 0.65 identified patients with a clinical endpoint with 73.9% sensitivity 92.9% specificity (area under the receiver operating characteristic curve, 0.901; likelihood ratio, 10.34; P < .0001). In an analysis of 111 patients with PSC, we found MRI-measured relative enhancement, using a hepatocyte-specific contrast agent, to identify patients with clinical outcomes with 73.9% sensitivity 92.9% specificity. Long-term, multicenter studies are needed to further evaluate this marker of PSC progression.