Published in the journal Hepatology. Here is a link to the article.
Regenstrief Institute authors: Wanzhu Tu, PhD.
In a clinical trial comparing treatments for severe alcohol-associated hepatitis, patients receiving anakinra plus zinc (A+Z) experienced higher rates and severity of acute kidney injury (AKI) than those treated with prednisone (PRED). AKI occurred in 45% of A+Z patients versus 22% of PRED patients. Biomarker analysis showed elevated urine neutrophil-gelatinase–associated lipocalin levels in A+Z-treated patients with AKI, indicating possible nephrotoxicity. Multivariable analysis confirmed A+Z treatment as an independent risk factor for AKI.
Authors:
Kavish R Patidar 1,2, Wanzhu Tu 3, Thomas G Cotter 4, Douglas A Simonetto 5, Amon Asgharpour 6, Muhammad Y Jan 7, Qing Tang 3, Yunpeng Yu 3, Yang Li 3, Moyinoluwa Taiwo 8, Prashanth Thevkar Nagesh 9, Srinivasan Dasarathy 8, Patrick S Kamath 5, Craig J McClain 10, Naga Chalasani 1, Gyongyi Szabo 9, Ramon Bataller 11,12, Mack Mitchell 4, Wajahat Z Mehal 13,14, Laura E Nagy 15, Vijay H Shah 5, Samer Gawrieh 1, Arun J Sanyal 6; AlcHepNet Investigators
Affiliations:
1Division of Gastroenterology and Hepatology, Department of Internal Medicine, Indiana University, Indianapolis, Indiana, USA
2Department of Internal Medicine, Section of Gastroenterology and Hepatology, Baylor College of Medicine and Michael E. DeBakey Veterans Affairs Medical Center, Houston, Texas, USA
3Department of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA
4Division of Digestive and Liver Diseases, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, Texas, USA
5Division of Gastroenterology and Hepatology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA
6Division of Gastroenterology, Department of Internal Medicine, Hepatology and Nutrition, Virginia Commonwealth University, Richmond, Virginia, USA
7Division of Nephrology, Department of Internal Medicine, Indiana University, Indianapolis, Indiana, USA
8Division of Gastroenterology and Hepatology, Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, Ohio, USA
9Division of Gastroenterology, Department of Internal Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA
10Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of Louisville, Louisville, Kentucky, USA
11Division of Gastroenterology and Hepatology and Nutrition, Department of Internal Medicine, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA
12School of Medicine and Health Sciences, Liver Unit, Hospital Clinic, Institut d’Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Barcelona, Spain
13Department of Internal Medicine, Section of Digestive Diseases, Yale University, New Haven, Connecticut, USA
14Department of Internal Medicine, Veterans Affairs Medical Center, West Haven, Connecticut, USA
15Department of Inflammation and Immunity, Cleveland Clinic Foundation, Cleveland, Ohio, USA