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Potential pharmacotherapy pathways in metabolic dysfunction-associated steatotic liver disease
Paweł Rajewski1,2, Jakub Cieściński3, Piotr Rajewski4
1Department of Internal and Infectious Diseases, Provincial Infectious Disease Hospital, Bydgoszcz, Poland.
Metabolic dysfunction-associated steatotic liver disease (MASLD) affects 30% of adults globally and is rising due to obesity. Current treatments focus on lifestyle and managing related conditions, with limited direct liver therapies available.
Area of Science:
- Hepatology
- Metabolic Disorders
- Pharmacology
Background:
- Metabolic dysfunction-associated steatotic liver disease (MASLD) is a prevalent global liver condition.
- It is a significant risk factor for cirrhosis, liver cancer, and cardiovascular disease.
- MASLD prevalence is increasing, projected to double by 2030 due to the obesity epidemic.
Purpose of the Study:
- To review current pharmacological treatments for MASLD.
- To explore potential future pharmacotherapy for MASLD's hepatic complications.
- To highlight the limited efficacy of current treatments targeting steatosis, steatohepatitis, or fibrosis alone.
Main Methods:
- Literature review of current pharmacological options for MASLD.
- Analysis of ongoing clinical trials for novel MASLD pharmacotherapies.
- Discussion of treatment strategies for MASLD-related hepatic complications.
Main Results:
- Current treatment primarily relies on weight reduction, diet, physical activity, and managing associated metabolic conditions like diabetes and hypertension.
- Pharmacological treatment specifically for hepatic steatosis, steatohepatitis, or fibrosis in MASLD is limited.
- Numerous drugs targeting MASLD's hepatic manifestations are under investigation in clinical trials.
Conclusions:
- Effective MASLD management requires a multi-faceted approach including lifestyle changes and addressing cardiometabolic risk factors.
- The development of targeted pharmacotherapies for MASLD's liver manifestations is an active area of research.
- Future treatments may offer more direct options for hepatic steatosis, steatohepatitis, and fibrosis.
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