Bile Acids as Emerging Players at the Intersection of Steatotic Liver Disease and Cardiovascular Diseases.
Josh BilsonEleonora ScorlettiJonathan R SwannChristopher D ByrnePublished in: Biomolecules (2024)
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.
Keyphrases
- cardiovascular disease
- insulin resistance
- type diabetes
- high fat diet induced
- metabolic syndrome
- adipose tissue
- high fat diet
- skeletal muscle
- public health
- healthcare
- polycystic ovary syndrome
- cardiovascular events
- fatty acid
- risk factors
- cardiovascular risk factors
- left ventricular
- low density lipoprotein
- early onset
- mouse model
- liver fibrosis
- heart failure
- health information
- coronary artery disease
- atrial fibrillation