Research across Cirrhosis
Related studies from across the Cirrhosis family.
Questions about Liver Fibrosis
Are there new immunomodulation strategies to treat liver fibrosis?
Yes, new immunomodulation strategies for liver fibrosis focus on reprogramming macrophages, targeting specific immune subsets, and using metabolic therapies like GLP-1 analogues and THRβ activators.
Full answer →Can nanotechnology be used to treat liver fibrosis?
Nanotechnology shows promise for treating liver fibrosis by delivering drugs directly to liver cells, improving how treatments work, and reducing side effects compared to traditional methods.
Full answer →What are the new antifibrotic therapies for liver fibrosis?
New antifibrotic therapies focus on reprogramming immune cells like macrophages and using metabolic drugs that reduce liver fat, rather than just targeting scar tissue directly.
Full answer →Do PON1 genetic variants affect my risk for liver fibrosis?
Specific genetic variants in the PON1 gene can change how well the enzyme works, which directly influences a person's risk for developing liver fibrosis and related metabolic issues.
Full answer →How do machine learning models help diagnose liver fibrosis?
Machine learning models analyze patient data to predict liver fibrosis with moderate accuracy, often outperforming traditional tests like FIB-4, but they are not yet standard in clinical practice.
Full answer →Can gene modulation help treat liver fibrosis and MASH?
Yes, gene modulation is a promising experimental approach for liver fibrosis and MASH, with several strategies showing preclinical success, though human treatments are not yet available.
Full answer →All Liver Fibrosis Articles
- Salvia miltiorrhiza components show potential for hepatocyte protection and hepatic stellate cell control
- cGAS-STING pathway serves as a central axis for innate immune activation in MASLD and HCC
- Hepatic macrophage metabolic reprogramming and bidirectional signaling dictate the balance between liver injury and regeneration
- Lactylation Targeting Shows Preclinical Anti-Fibrotic Potential in Liver Fibrosis
- Transcriptomic analysis identifies 846 genes and key pathways associated with MASLD fibrosis progression
- Dioscin shows therapeutic potential for various liver disorders including MASLD and hepatocellular carcinoma
- Phase 2 Trial Evaluating Zalfermin and Semaglutide Combinations for Metabolic Dysfunction Associated Steatohepatitis
- Narrative review explores macrophage reprogramming for liver fibrosis and MASH
- Systematic review and meta-analysis evaluates ML and DL models for diagnosing MASH and fibrosis
- Review of liver disease immunomodulation strategies notes precision over broad suppression
- PON1 genetic variants rs2057681 and rs854572 modulate PONase activity and dysmetabolic risk in MASLD
- Review of bile acid homeostasis regulation in liver disease and cancer
- Hospitalized malignant neoplasm patients show high comorbidity burden and distinct disease patterns across 163 Chinese hospitals
- Perspective reviews emerging antifibrotic therapies for metabolic dysfunction-associated steatohepatitis