PURPOSE OF REVIEW: The purpose of this review is to discuss the influence of obesity, insulin resistance, type 2 diabetes (T2D), and nonalcoholic fatty liver disease (NAFLD) on bile acid metabolism and to analyze whether these findings reinforce current beliefs about the role of bile acids in the pathophysiology of these diseases. RECENT FINDINGS: Discordant results on plasma bile acid alterations in NAFLD patients have been reported. Obesity, insulin resistance, and T2D, common comorbidities of NAFLD, have been associated with bile acid changes, but the individual bile acid species variations differ between studies (summarized in this review), perhaps because of clinicobiological differences between the studied patient populations and the heterogeneity of statistical analyses applied. SUMMARY: The regulatory role of bile acids in metabolic and cellular homeostasis renders bile acids attractive candidates as players in the pathophysiology of NAFLD. However, considering the complex relationship between NAFLD, obesity, insulin resistance and T2D, it is difficult to establish clear and independent associations between bile acid alterations and these individual diseases. Though bile acid alterations may not drive NAFLD progression, signaling pathways activated by bile acids remain potent therapeutic targets for its treatment. Further studies with appropriate matching or adjustment for potential confounding factors are necessary to determine which pathophysiological conditions drive the alterations in bile acid metabolism.
PURPOSE OF REVIEW: The purpose of this review is to discuss the influence of obesity, insulin resistance, type 2 diabetes (T2D), and nonalcoholic fatty liver disease (NAFLD) on bile acid metabolism and to analyze whether these findings reinforce current beliefs about the role of bile acids in the pathophysiology of these diseases. RECENT FINDINGS: Discordant results on plasma bile acid alterations in NAFLD patients have been reported. Obesity, insulin resistance, and T2D, common comorbidities of NAFLD, have been associated with bile acid changes, but the individual bile acid species variations differ between studies (summarized in this review), perhaps because of clinicobiological differences between the studied patient populations and the heterogeneity of statistical analyses applied. SUMMARY: The regulatory role of bile acids in metabolic and cellular homeostasis renders bile acids attractive candidates as players in the pathophysiology of NAFLD. However, considering the complex relationship between NAFLD, obesity, insulin resistance and T2D, it is difficult to establish clear and independent associations between bile acid alterations and these individual diseases. Though bile acid alterations may not drive NAFLD progression, signaling pathways activated by bile acids remain potent therapeutic targets for its treatment. Further studies with appropriate matching or adjustment for potential confounding factors are necessary to determine which pathophysiological conditions drive the alterations in bile acid metabolism.
Authors: Merel van den Broek; Loek J M de Heide; Fianne L P Sips; Martijn Koehorst; Tim van Zutphen; Marloes Emous; Martijn van Faassen; Albert K Groen; Natal A W van Riel; Jan F de Boer; André P van Beek; Folkert Kuipers Journal: Int J Obes (Lond) Date: 2021-01-15 Impact factor: 5.551
Authors: Guillaume Grzych; Oscar Chávez-Talavera; Amandine Descat; Dorothée Thuillier; An Verrijken; Mostafa Kouach; Vanessa Legry; Hélène Verkindt; Violeta Raverdy; Benjamin Legendre; Robert Caiazzo; Luc Van Gaal; Jean-Francois Goossens; Réjane Paumelle; Sven Francque; François Pattou; Joel T Haas; Anne Tailleux; Bart Staels Journal: JHEP Rep Date: 2020-12-16