EM2605G"Genetics of Steatotic Liver Disease: Pathogenesis, Prognosis and Implications for Treatment" (IM GR-051526)
Purpose and Overview
Steatotic liver disease (SLD) is a leading cause of liver-related morbidity and mortality worldwide. Obesity, insulin resistance, and chronic alcohol intake are its major risk factors, but genetic differences strongly influence disease susceptibility. Human genetic studies have identified key genetic modifiers of SLD risk, both those that confer susceptibility and resistance, thereby deepening our understanding of disease pathogenesis.
Target Audience
UT Southwestern faculty, fellows, residents and medical students, community physicians, nurse clinicians, physician assistants and nurses.
Learning Objectives
At the conclusion of this activity, the participant should be able to:
- Describe the physiologic basis of hepatic steatosis.
- Explain why PNPLA3(148M) is the genetic risk factor with the greatest clinical impact on steatotic liver disease (SLD).
- Summarize the current and emerging therapeutic strategies for the prevention and treatment of SLD.

Helen H. Hobbs, M.D., M.Sc.
Professor & Chief of Clinical Genetics
Dallas Heart Ball Chair in Cardiology Research
Department of Internal Medicine
UT Southwestern Medical Center
Available Credit
- 1.00 AMA
Price
Required Hardware/software
Activities should be run with recent versions of common browsers, including Internet Explorer, Firefox and Google Chrome

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