Emerging role of obeticholic acid in the management of nonalcoholic fatty liver disease

Abstract

Nonalcoholic fatty liver disease (NAFLD) is the commonest chronic liver disease and its prevalence is increasing driven by the pandemic of obesity and type 2 diabetes mellitus. NAFLD can progress to cirrhosis and is associated with increased risk for cardiovascular disease and hepatocellular cancer. Diet and exercise are limited by suboptimal long-term adherence in patients with NAFLD. On the other hand, current pharmacological treatment of NAFLD has limited efficacy and unfavorable safety profile. In this context, obeticholic acid (OCA), a selective agonist of the farnesoid X receptors, might represent a useful option in these patients. Preclinical studies suggest that OCA improves hepatic steatosis, inflammation and fibrosis. A proof-of-concept study and the randomized, placebo-controlled Farnesoid X Receptor Ligand Obeticholic Acid in non-alcoholic steatohepatitis Treatment (FLINT) trial also showed improvements in liver histology in patients with NAFLD who received OCA. Weight loss and reduction in blood pressure were also observed. However, the effects of OCA on insulin resistance are conflicting and the lipid profile is adversely affected by this agent. In addition, pruritus is frequently observed during treatment with OCA and might lead to treatment discontinuation. However, given the limitations of existing treatments for NAFLD, OCA might represent a useful therapeutic option in selected patients with NAFLD.

Key Words: Nonalcoholic fatty liver disease; Obeticholic acid; Farnesoid X receptors; Insulin resistance; Fibrosis; Dyslipidemia; Steatosis; Hepatocellular cancer

Core tip: Nonalcoholic fatty liver disease (NAFLD) is the commonest chronic liver disease in Western countries, can progress to cirrhosis and is associated with increased all-cause and cardiovascular disease mortality risk. Current pharmacological treatment of NAFLD has limited efficacy and therefore, there is a pressing need to develop more effective and safe agents for this common and life-threatening disease. Obeticholic acid (OCA), a selective agonist of the farnesoid X receptors, might be a useful agent in the management of NAFLD. In the Farnesoid X Receptor Ligand Obeticholic Acid in non-alcoholic steatohepatitis (NASH) Treatment (FLINT) trial in patients with NASH, OCA administration was associated with improvements in liver histology, while weight loss and reduction in blood pressure were also observed. Although its adverse effects on the lipid profile and insulin sensitivity are worrisome, given the increased cardiovascular risk of this population, OCA might be considered in selected patients with NAFLD/NASH, particularly in those with adequately controlled glucose and lipid levels.

INTRODUCTION

Nonalcoholic fatty liver disease (NAFLD) is defined as hepatic steatosis in the absence of secondary hepatic fat accumulation such as significant alcohol consumption, use of steatogenic medication or hereditary disorders. NAFLD is asymptomatic in most patients but can progress to cirrhosis and hepatocellular carcinoma. The prevalence of NAFLD is steadily increasing and is currently 20%-30% in Western countries and 5%-18% in Asia[1-3]. NAFLD is the commonest cause of elevated liver enzymes and is even more prevalent in patients with metabolic diseases such as obesity and type 2 diabetes mellitus (T2DM)[4]. Consequently, its prevalence is expected to increase in the near future as an aftermath of the increasing adoption of a sedentary lifestyle and an unhealthy diet[3,4].

Patients with NAFLD have higher all-cause mortality risk than general population[5]. Moreover, cardiovascular disease represents the leading cause of death in these patients, whereas liver-related mortality is less frequent[5,6]. Lifestyle modifications, including diet and exercise, are imperative for achieving weight loss and reducing insulin resistance and hepatic steatosis /inflammation in patients with NAFLD[7,8]. Despite the short-term effectiveness of such measures, adherence to lifestyle changes wanes with time underlining the need for pharmacological therapy[7,9]. The therapeutic interventions that are used for the treatment of NAFLD aim at the underpinning pathophysiologic mechanisms of the disease but are hampered by suboptimal efficacy and safety[1,10]. Therefore, there is a pressing need to develop more effective and safe agents for this common and life-threatening disease.

OBETICHOLIC ACID IN NAFLD

Farnesoid X receptors (FXRs) represent an attractive target for the management of NAFLD. FXRs are nuclear receptors that are abundantly expressed and play several roles including regulation of bilirubin, carbohydrate and lipid metabolism and modulation of liver growth[11-14]. Activation of FXRs ameliorates hyperlipidemia, glucose intolerance and insulin resistance, protects against cholestasis-induced liver injury and induces hepatocyte regeneration[11-14]. Bile acids are the natural ligands of the FXRs. Obeticholic acid (OCA, 6α-ethyl-chenodeoxycholic acid) is a semi-synthetic bile acid analogue of chenodeoxycholic acid (CDCA) with a 100-fold higher affinity for FXR, compared to CDCA, and represents the first selective FXR agonist to be used in human studies[15-17]. Similarly to ursodeoxycholic acid (UDCA), OCA has anti-apoptotic action and increases bile flow and the concentrations of bile acid transport proteins, such as multidrug resistance-associated protein 2. However, UDCA is a very weak FXR agonist[13,15-17] (Figure 1).

Figure 1 Molecular structures of obeticholic acid and ursodeoxycholic acid.

Accumulating data suggest that OCA might be a useful agent in the management of NAFLD[18,19]. In a rabbit model of NAFLD, OCA induced weight loss and improved glucose tolerance[20]. In a rat model of NAFLD [Zucker (fa/fa) rats], in which a loss of function mutation leads to T2DM, visceral adiposity and hepatic steatosis[21,22], OCA ameliorated these consequences by reducing hepatic expression of genes involved in fatty acid synthesis, lipogenesis and gluconeogenesis[21]. In other animal models of NAFLD, OCA exerted anti-inflammatory and antifibrotic effects[23-26]. However, opposite effects have also been reported; indeed, OCA induced hepatic steatosis, ballooning and inflammation in an animal study[27]. The effects of OCA on liver carcinogenesis are also controversial. In animal study, activation of FXR inhibited hepatocarcinogenesis by regulating nuclear factor κB-mediated hepatic inflammatory reactions[28]. In contrast, in another recent report using 3 mouse models, loss of FXR was associated with liver carcinogenesis in diabetic animals[29].

Regarding human studies, OCA in patients with NAFLD was first evaluated in a double-blind, placebo-controlled, proof-of-concept study[19]: patients with NAFLD and T2DM were randomly assigned to receive 25 mg OCA (n = 20), 50 mg OCA (n = 21) or placebo (n = 23) for 6 weeks[19]. Insulin resistance was evaluated using hyperinsulinemic-euglycemic clamp[19]. Insulin sensitivity improved by 28.0% and 20.1% in patients treated with 25 and 50 mg OCA, respectively, whereas it worsened in the placebo group (a 5.5% reduction)[19]. A dose-dependent weight loss was observed in patients treated with OCA[19]. Moreover, alanine transaminase (ALT) and γ-glutamyltransferase (γGT) levels declined in both OCA groups[19]. The Enhanced Liver Fibrosis test, a non-invasive marker of hepatic fibrosis, improved in patients treated with 25 mg OCA and remained stable in patients treated with 50 mg OCA[19]. On the other hand, aspartate transaminase (AST) levels remained stable and alkaline phosphatase (ALP) levels increased in both OCA groups[19]. In addition, serum low-density lipoprotein cholesterol (LDL-C) levels increased with both OCA doses and serum high-density lipoprotein cholesterol (HDL-C) decreased in patients under 50 mg OCA[19]. Serum triglyceride levels also decreased in the 50 mg OCA group[19]. These lipid effects have also been reported in animal studies and were attributed to inhibition of conversion of cholesterol to bile acids and to reduction of intestinal cholesterol absorption[30]. Regarding OCA safety, adverse reactions were comparable in all groups[19].

More recently, the Farnesoid X Receptor Ligand Obeticholic Acid in NASH Treatment (FLINT) trial, a multicentre, double-blind, placebo-controlled clinical trial in patients with non-alcoholic steatohepatitis (NASH) but without cirrhosis, was published[31]. In this trial, 283 patients were randomized to receive OCA 25 mg daily or placebo for 72 wk[31]. The primary outcome was a decrease in NAFLD activity score by at least 2 points without deterioration of fibrosis. Fifty of 110 patients in the OCA group (45%) met the primary endpoint at 72 weeks compared with 23 of 109 patients in the placebo group (21%; P = 0.0002)[31]. These results did not change after pre-specified sensitivity analyses with adjustment for confounders, including weight loss[31]. Moreover, 35% of patients treated with OCA had reduction in fibrosis, compared with 19% of patients treated with placebo (P = 0.04)[31]. However, the rates of resolution of NASH did not differ between the two groups (22% vs 13%, respectively, P = 0.08)[31]. Treatment with OCA resulted in a reduction in AST, ALT and γGT levels but increased ALP levels[31]. OCA induced weight loss and lowered systolic blood pressure but increased glucose levels and insulin resistance[31]. Its contrasting effects on insulin resistance in the FLINT trial and in the earlier proof-of-concept study[19] might be due to differences in the study population (only patients with T2DM in the latter study[19], patients with and without T2DM in FLINT trial[31]). Notable, insulin resistance was evaluated using homeostasis model in the FLINT trial, which is less accurate than hyperinsulinemic-euglycemic clamp[31]. Regarding the effects on lipid profile, OCA increased serum LDL-C and reduced HDL-C levels whereas TG levels did not change at 72 wk[31]. A study in healthy subjects also reported that OCA treatment for 14-20 d increased LDL-C and decreased HDL-C levels regardless of dose (5, 10 or 25 mg daily)[32]. After treatment discontinuation, differences in liver function tests, lipid profile and insulin resistance between groups were no longer apparent[31]. Finally, side effects were non-severe and occurred at similar rates, but a higher frequency of pruritus was observed in OCA group, compared to placebo group (23% vs 6%)[31]. These high rates of pruritus have also been reported in patients using OCA for other liver diseases, including primary biliary cirrhosis[33].

In light of these findings, how does OCA fit into the management of NAFLD? According to current guidelines, pharmacological treatment is recommended only in non-diabetic patients with biopsy-proven NASH[8]. Vitamin E is recommended as first-line agent whereas pioglitazone could also be used[8]. These recommendations are primarily based on the results of Pioglitazone versus Vitamin E versus Placebo for the Treatment of Nondiabetic Patients with Nonalcoholic Steatohepatitis (PIVENS) trial[34], which randomized 247 non-diabetic patients with NASH to receive vitamin E, pioglitazone or placebo. Both vitamin E and pioglitazone reduced hepatic steatosis and inflammation but not fibrosis[34]. In contrast, OCA improved all histological features of NAFLD (steatosis, inflammation and fibrosis)[31]. Moreover, FLINT trial included patients with T2DM (52% of the study population, n = 149) and OCA was equally effective in both patients with and without T2DM[31]. On the other hand, vitamin E has no substantial metabolic effects whereas pioglitazone reduces insulin resistance and improves the lipid profile but induces weight gain[34]. OCA appears to reduce body weight but might aggravate insulin resistance and dyslipidemia[32]. However, adverse lipid effects of OCA can be mitigated using statins, which are frequently required for the management of dyslipidemia in patients with NAFLD and appear to be safe and to reduce cardiovascular morbidity in this population[8,35]. Finally, long-term studies in other populations suggest an increased risk for all-cause mortality in patients treated with vitamin E[36] and an increased risk for edema, heart failure and bone fractures in patients treated with pioglitazone[37,38]. On the other hand, the long-term safety of treatment with OCA is unknown.

CONCLUSION

OCA appears to represent a promising treatment for patients with NAFLD, since it improves fibrosis, induces weight loss and appears to be effective in patients with T2DM. On the other hand, the adverse effects on the lipid profile and insulin sensitivity are worrisome, given the increased cardiovascular risk of this population. Therefore, and given the suboptimal efficacy and safety of other pharmacotherapies in NAFLD, lifestyle changes should be recommended as first-line management in these patients whereas OCA might be considered in selected patients, particularly those with T2DM and adequately controlled glucose and lipid levels.