The Role of Red Cell Distribution Width as a Prognostic Marker in Chronic Liver Disease: A Literature Review.

Hunain Aslam, Fouzia Oza, Khalid Ahmed, Jonathan Kopel, Mark M Aloysius, Aman Ali, Dushyant Singh Dahiya, Muhammad Aziz, Abhilash Perisetti, Hemant Goyal

Journal: International journal of molecular sciences 2023;24(4):3487

PMID: 36834895

Abstract

Liver disease is one of the leading public health problems faced by healthcare practitioners regularly. As such, there has been a search for an inexpensive, readily available, non-invasive marker to aid in monitoring and prognosticating hepatic disorders. Recently, red blood cell distribution width (RDW) has been found to be associated with various inflammatory conditions with implications for its use as a potential marker for assessing disease progression and prognosis in multiple conditions. Multiple factors effect red blood cell production whereby a dysfunction in any process can lead to anisocytosis. Furthermore, a chronic inflammatory state leads to increased oxidative stress and produces inflammatory cytokines causing dysregulation and increased intracellular uptake and use of both iron and vitamin B12, which leads to a reduction in erythropoiesis causing an increase in RDW. This literature review reviews in-depth pathophysiology that may lead to an increase in RDW and its potential correlation with chronic liver diseases, including hepatitis B, hepatitis C, hepatitis E, non-alcoholic fatty liver disease, autoimmune hepatitis, primary biliary cirrhosis, and hepatocellular carcinoma. In our review, we examine the use of RDW as a prognostic and predictive marker for hepatic injury and chronic liver disease.

Address: The Wright Center for Graduate Medical Education, 501 S. Washington Ave, Scranton, PA 18505, USA.; Department of Medicine, The Wright Center for Graduate Medical Education, 501 S. Washington Ave, Scranton, PA 18505, USA.; Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.; Department of Internal Medicine, Central Michigan University College of Medicine, Saginaw, MI 48603, USA.; Department of Gastroenterology and Hepatology, University of Toledo Medical Center, Toledo, OH 43614, USA.; Department of Gastroenterology and Hepatology, Kansas City VA Medical Center, Kansas City, KS 64128, USA.; Center for Interventional Gastroenterology at UT (iGUT), Division of Gastroenterology, Hepatology, and Nutrition, The University of Texas Health Science Center, 6431 Fannin, MSB 4.234, Houston, TX 77030, USA.
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.