熊去氧胆酸
医学
原发性硬化性胆管炎
药品
疾病
内科学
胃肠病学
免疫系统
肝损伤
肝病
药理学
免疫学
作者
Martin Wagner,Peter Fickert
出处
期刊:Annual Review of Pharmacology and Toxicology
[Annual Reviews]
日期:2020-01-06
卷期号:60 (1): 503-527
被引量:39
标识
DOI:10.1146/annurev-pharmtox-010818-021059
摘要
Though ursodeoxycholic acid (UDCA) remains the baseline treatment for most cholestatic liver diseases, UDCA treatment leaves approximately one-third of patients with primary biliary cholangitis (PBC) and all patients with primary sclerosing cholangitis (PSC) at risk for disease progression. New anticholestatic agents, including nuclear receptor agonists, choleretics, and bile acid synthesis suppressors, will likely increase response rates to therapy in PBC and PSC. Strategies that target early immune-mediated injury have so far been disappointing, hampered by the lack of biomarkers to detect early disease states, which then could profit from immunomodulatory therapy. Future concepts need to personalize treatments according to disease stage, progression, and phase, and to combine multiple drugs to target different pathogenic pathways.
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