Bile Acids as Emerging Players at the Intersection of Steatotic Liver Disease and Cardiovascular Diseases

被引:6
作者
Bilson, Josh [1 ,2 ]
Scorletti, Eleonora [1 ,2 ,3 ]
Swann, Jonathan R. [1 ,2 ]
Byrne, Christopher D. [1 ,2 ]
机构
[1] Univ Southampton, Fac Med, Sch Human Dev & Hlth, Southampton SO16 6YD, England
[2] Univ Southampton, Univ Hosp Southampton Natl Hlth Serv Fdn Trust, Natl Inst Hlth Res Southampton Biomed Res Ctr, Southampton SO16 6YD, England
[3] Univ Penn, Perelman Sch Med, Div Genet, Philadelphia, PA 19104 USA
关键词
metabolic dysfunction-associated steatotic liver disease; cardiovascular disease; cardiac disease; obeticholic acid; farnesoid X receptor; resmetirom; bile acids; bile acid receptors; NONALCOHOLIC STEATOHEPATITIS; ACTIVATION; SEVERITY; INJURY; LEVEL; NAFLD;
D O I
10.3390/biom14070841
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Affecting approximately 25% of the global population, steatotic liver disease (SLD) poses a significant health concern. SLD ranges from simple steatosis to metabolic dysfunction-associated steatohepatitis and fibrosis with a risk of severe liver complications such as cirrhosis and hepatocellular carcinoma. SLD is associated with obesity, atherogenic dyslipidaemia, and insulin resistance, increasing cardiovascular risks. As such, identifying SLD is vital for cardiovascular disease (CVD) prevention and treatment. Bile acids (BAs) have critical roles in lipid digestion and are signalling molecules regulating glucose and lipid metabolism and influencing gut microbiota balance. BAs have been identified as critical mediators in cardiovascular health, influencing vascular tone, cholesterol homeostasis, and inflammatory responses. The cardio-protective or harmful effects of BAs depend on their concentration and composition in circulation. The effects of certain BAs occur through the activation of a group of receptors, which reduce atherosclerosis and modulate cardiac functions. Thus, manipulating BA receptors could offer new avenues for treating not only liver diseases but also CVDs linked to metabolic dysfunctions. In conclusion, this review discusses the intricate interplay between BAs, metabolic pathways, and hepatic and extrahepatic diseases. We also highlight the necessity for further research to improve our understanding of how modifying BA characteristics affects or ameliorates disease.
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页数:16
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