4.7 Review

Modulation of Bile Acid Metabolism to Improve Plasma Lipid and Lipoprotein Profiles

期刊

JOURNAL OF CLINICAL MEDICINE
卷 11, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/jcm11010004

关键词

bile acids; cholesterol; triglycerides; lipoproteins; bile acid sequestrants; ABST inhibitors; FXR agonists

资金

  1. China Scholarship Council
  2. University Medical Center Groningen [CSC202006170047]
  3. Nutrition and Health initiative of the University of Groningen
  4. Netherlands Heart Foundation (IN CONTROL) [CVON2018-27]
  5. Noaber Foundation, Lunteren
  6. Netherlands CardioVascular Research Initiative: 'the Dutch Heart Foundation
  7. Dutch Federation of University Medical Centers
  8. Netherlands Organization for Health Research and Development
  9. Royal Netherlands Academy of Sciences [CVON2017-2020]
  10. Netherlands Heart Foundation [2015T068]

向作者/读者索取更多资源

This review evaluates the potential of new drugs targeting bile acid metabolism in the treatment of cholestatic liver diseases, NAFLD, and NASH. The review also explores the impact of changes in bile acid metabolism on plasma cholesterol, triglycerides, and cardiovascular outcomes. The findings highlight the need for further research on the interactions between bile acid and lipid and lipoprotein metabolism.
New drugs targeting bile acid metabolism are currently being evaluated in clinical studies for their potential to treat cholestatic liver diseases, non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH). Changes in bile acid metabolism, however, translate into an alteration of plasma cholesterol and triglyceride concentrations, which may also affect cardiovascular outcomes in such patients. This review attempts to gain insight into this matter and improve our understanding of the interactions between bile acid and lipid metabolism. Bile acid sequestrants (BAS), which bind bile acids in the intestine and promote their faecal excretion, have long been used in the clinic to reduce LDL cholesterol and, thereby, atherosclerotic cardiovascular disease (ASCVD) risk. However, BAS modestly but consistently increase plasma triglycerides, which is considered a causal risk factor for ASCVD. Like BAS, inhibitors of the apical sodium-dependent bile acid transporter (ASBTi's) reduce intestinal bile acid absorption. ASBTi's show effects that are quite similar to those obtained with BAS, which is anticipated when considering that accelerated faecal loss of bile acids is compensated by an increased hepatic synthesis of bile acids from cholesterol. Oppositely, treatment with farnesoid X receptor agonists, resulting in inhibition of bile acid synthesis, appears to be associated with increased LDL cholesterol. In conclusion, the increasing efforts to employ drugs that intervene in bile acid metabolism and signalling pathways for the treatment of metabolic diseases such as NAFLD warrants reinforcing interactions between the bile acid and lipid and lipoprotein research fields. This review may be considered as the first step in this process.

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