- Posted Friday June 22, 2018
Findings could eventually lead to new treatments for patients with NASH, the nation’s leading cause of chronic liver disease
PHOENIX, Ariz. — June 22, 2018 — A fatty liver disease known as NASH — non-alcoholic steatohepatitis — is the nation’s major cause of chronic liver disease, and is projected to become the most common indicator for liver transplants.
The number of Americans with NASH has soared in recent decades to more than 6 million. NASH is strongly associated with patients who are obese and those with type 2 diabetes. Yet, despite the growing number of patients, there are no effective treatments for this disease, which most often progresses to liver inflammation, fibrosis, cirrhosis and death.
In an effort towards discovering a drug target, scientists at the Translational Genomics Research Institute (TGen), an affiliate of City of Hope, for the first time have identified significant gene expression patterns associated with obesity-related NASH inflammation and fibrosis.
The study, which was done in collaboration with the Geisinger Obesity Institute and Temple University, was published June 5 in the Journal of the Endocrine Society.
“These patients are in desperate need of effective new treatments,” said Dr. Johanna DiStefano, Professor and Head of TGen’s Diabetes and Fibrotic Disease Unit, and the study’s senior author. “Our study results suggest that there may be a genomic framework around which new treatments might be based.”
The researchers sequenced mRNA to profile the liver samples of obese patients from 24 healthy individuals, 53 with inflammation, and 65 with some degree of fibrosis or cirrhosis. They discovered 176 genes specific to fibrosis, revealing three associated cellular pathways, and 16 genes previously associated with liver fibrosis and cirrhosis.
“The results obtained in this study demonstrate that advanced NASH fibrosis is characterized by a distinct set of molecular changes that are shared with other causes of cirrhosis,” said Dr. DiStefano. “Future investigations, including validation in independent cohorts and functional characterization of dysregulated genes and pathways, will be important to extend these findings.”
Funding for this study — Transcriptomic profiling of obesity-related nonalcoholic steatohepatitis reveals a core set of fibrosis-specific genes — was provided by the National Institute of Diabetes and Digestive and Kidney Diseases, part of the National Institutes of Health, the nation’s medical research agency.
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Translational Genomics Research Institute (TGen) is a Phoenix, Arizona-based non-profit organization dedicated to conducting groundbreaking research with life changing results. TGen is focused on helping patients with neurological disorders, cancer, diabetes, and infectious diseases, through cutting edge translational research (the process of rapidly moving research towards patient benefit). TGen physicians and scientists work to unravel the genetic components of both common and rare complex diseases in adults and children. Working with collaborators in the scientific and medical communities literally worldwide, TGen makes a substantial contribution to help our patients through efficiency and effectiveness of the translational process. TGen is affiliated with City of Hope, a world-renowned independent research and cancer and diabetes treatment center: www.cityofhope.org. This precision medicine affiliation enables both institutes to complement each other in research and patient care, with City of Hope providing a significant clinical setting to advance scientific discoveries made by TGen. For more information, visit: www.tgen.org. Follow TGen on Facebook, LinkedIn and Twitter @TGen.
TGen Senior Science Writer