Non-alcoholic fatty liver disease (NAFLD)/non-alcoholic steatohepatitis (NASH)-related liver fibrosis: mechanisms, treatment and prevention

Abstract

Liver fibrosis is the excessive expression and accumulation of extracellular matrix proteins in the liver. Fibrotic scarring occurs as the consequence of chronic injury and inflammation. While the successful treatment of hepatitis B and C reduced the burden of liver disease related to viral hepatitis, non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steatohepatitis (NASH) are nowadays the leading causes of hepatic fibrosis worldwide. Although basic research activities have significantly advanced our understanding of the molecular disease pathogenesis, the present therapeutic options for fibrosis are still limited. In advanced disease stages, liver transplantation often remains the only curative treatment. This highlights the necessity of preventive strategies to avoid complications of fibrosis, particularly cirrhosis, portal hypertension and liver cancer. Lifestyle modifications (weight loss, exercise, healthy diet) are the basis for prevention and treatment of NAFLD-associated fibrosis. In the present review, we discuss recent advances in antifibrotic prevention and therapy. In particular, we review the current concepts for antifibrotic drug candidates in the treatment of NAFLD and NASH. While some compounds aim at reverting pathogenic liver metabolism, an alternative approach is to disconnect the injury (e.g., NAFLD) from inflammation and/or fibrosis. Investigational drugs typically target metabolic pathways, insulin resistance, hepatocyte death, inflammatory cell recruitment or activation, the gut-liver axis, matrix expression or matrix turnover. While several promising drug candidates failed in phase 2 or 3 clinical trials (including elafibranor, emricasan and selonsertib), promising results with the farnesoid X receptor agonist obeticholic acid, the pan-PPAR agonist lanifibranor and the chemokine receptor CCR2/CCR5 inhibitor cenicriviroc support the expectation of an effective pharmacological therapy for liver fibrosis in the near future. Tackling NAFLD-associated fibrosis from different directions by combinatorial drug treatment and effective lifestyle changes hold the greatest prospects.

Introduction

Persistent liver damage occurring in the context of metabolic (non-alcoholic fatty liver), viral hepatitis B or C, cholestatic, toxic (alcohol) or genetic (hemochromatosis, Wilson disease, etc.) diseases, usually causes a chronic inflammatory reaction. Similar to a misdirected wound healing reaction, chronic inflammation can cause scarring of the liver (1). Noteworthy, liver fibrosis is, in principle, independent of the noxious agent that causes hepatic insult, although the pattern of initial fibrosis (e.g., periportal vs. perisinusoidal) may vary. Untreated (and progressive) fibrosis can lead to cirrhosis, which is the complete architectural reconstruction with deposition of large quantities of connective tissue resulting in consecutive loss of hepatic function (2). Cirrhosis, in turn, can lead to portal hypertension, progressive liver failure and/or hepatocellular carcinoma (HCC). In recent years, it has become evident that this process is not irreversible. This offers a window of opportunity for preventive or therapeutic antifibrotic interventions.

During the past decade, the landscape of hepatology has substantially changed (3). While the effective antiviral treatment of hepatitis B and C significantly reduced the disease burden, alcohol-related liver disease remains a leading cause of liver-related mortality (4). The successful antiviral treatment against hepatitis B (viral suppression) and hepatitis C (viral eradication) provided clinical evidence that fibrosis regression can be achieved and is associated with a remarkable reduction in liver-related morbidity and mortality (5). For instance, hospital admissions related to hepatitis C-associated liver cirrhosis have tremendously decreased, signifying the enormous clinical benefit of direct-acting antivirals (DAA) in the treatment of hepatitis C (6).

During the last years, non-alcoholic steatohepatitis (NASH) has emerged as a major etiology of liver fibrosis in Western populations, and it is expected to become the leading indication for liver transplantation and liver-related mortality within a few years worldwide (7). Obesity, type 2 diabetes, insulin resistance, dyslipidemia, metabolic syndrome and several predisposing genetic factors (Figure 1) fuel non-alcoholic fatty liver disease (NAFLD). Alcohol-related liver disease and NAFLD are prime examples that liver fibrosis can be improved by changing life style, that means avoiding the uptake of compounds leading to the disease (i.e., alcohol) or by modifying disease drivers (overweight/obesity, insulin resistance, sedentary lifestyle). Importantly, such lifestyle-related risk factors for fatty liver disease remain relevant in patients with viral hepatitis as well, even if hepatitis C has been successfully cured (8).

Figure 1.

Clinical conditions from normal liver to NAFLD, NASH, cirrhosis, and HCC. About 25% of the general population have NAFLD, of which a substantial fraction (10–30%) is at risk for progressing towards relevant fibrosis. Between 0.3–3% of patients with fibrosis progress to cirrhosis and/or HCC per year. The pathogenesis is influenced by many factors including genetic factors, age, diabetes, obesity, alcohol, and lifestyle. Weight loss, physical exercise, consumption of coffee, Mediterranean diet, and a vegetable-rich diet have positive effects on disease outcome and are recommended to prevent NAFLD progression. NAFLD, non-alcoholic fatty liver disease; NASH, non-alcoholic steatohepatitis; HCC, hepatocellular carcinoma.

However, alcohol-related liver disease and NAFLD are also prime examples that liver fibrosis is the hepatic manifestation of a systemic disease. In case of alcohol and NAFLD, a large number of comorbidities exist in most patients (e.g., cardiovascular diseases, diabetes, psychiatric disorders), emphasizing that prevention and treatment of liver fibrosis is only one aspect of the patient management (9,10).

The substantial global burden of hepatic fibrosis to the public health systems demands the active search for effective therapies. However, despite the urgent need, approved drugs are still not available for this specific indication (11). This is majorly due to the complex molecular disturbances and the multifactorial symptoms associated with respective disease. Although lifestyle changes (particularly weight loss) are highly effective in blocking or even reversing fibrosis (12), only few patients successfully achieve a durable lifestyle change in clinical practice. Bariatric surgery is also beneficial in NASH (13), but is only available to a small fraction of morbidly obese patients. Several novel medications targeting different stages and molecular events in the disease process are currently in the pipeline, while other previously known drug candidates are used off-label or tested in clinical trials. These compounds offer new hope to patients and it is most likely that highly desirable future anti-fibrotic therapies will be established which will allow to attenuate or even reverse fibrosis and improve the quality of care in patients with liver fibrosis and cirrhosis. The histological regression of fibrosis has been accepted as a surrogate for clinically relevant endpoints in clinical trials investigating anti-NASH agents (11). This is based on the close association between fibrosis stage and “hard outcomes” including liver-related complications and mortality (14).

From a clinical perspective, it is well understood that histology is suboptimal to assess “antifibrotic” effects of an intervention (15). In cases of advanced fibrosis and cirrhosis, improving the hepatic venous pressure gradient (HVPG) might better indicate beneficial effects on portal hypertension and cirrhosis prognosis (16). Serum-based and imaging-based biomarkers may also provide information on treatment responses, but this require further prospective evaluation (17).

This review intends to summarize current concepts on strategies for the therapy and prevention of NAFLD-associated liver fibrosis.

Mechanisms of liver fibrogenesis

Fibrogenesis is initiated as a consequence of parenchymal cell damage that can be induced by different hepatotoxic agents and mechanisms. In general, an inflammatory response is initiated after tissue injury, which involves the local vascular system, the immune system, and an orchestrated local as well as systemic mobilization of soluble mediators. This response is orchestrated by non-parenchymal cells (endothelium, stellate and Kupffer cells) and resident immune cells (macrophages, dendritic cells, and mast cells) that are equipped with specialized surface receptors that recognize specific pathogen-associated molecular patterns (PAMPs) such as bacterial toxins and damage-associated molecular patterns (DAMPs). After binding, they trigger the synthesis and/or release of a large variety of different inflammatory and pro-fibrogenic mediators within the injured liver tissue. Subsequently, these soluble mediators lead to the recruitment of inflammatory immune cells into the liver tissue (18) as well as to the activation of matrix-producing cell populations driving scar tissue synthesis (1). There is an intimate crosstalk between (stressed/injured) hepatocytes, (activated) macrophages and stellate cells in the liver, which ultimately drives matrix protein deposition (19). Understanding the fibrogenic signals may offer new targets for therapeutic interventions. For instance, the recognition of liver injury by Kupffer cells, the resident phagocytes of the liver, promotes the release of chemokines including CCL2, which then promotes the recruitment of inflammatory, fibrogenic monocytes into the injured liver (20,21).

The main matrix-producing cell types in liver fibrosis are hepatic stellate cells (HSCs) that transition into myofibroblasts (MFBs). Fibrogenic mediators or cell-cell contacts promote HSC activation by triggering distinct signaling cascades (22). New technologies such as single-cell RNA sequencing (scRNAseq) have helped to elucidate such activation profiles of HSC/MFB, but revealed also a striking heterogeneity among MFBs (23). For instance, HSCs partition into topographic regions, with specific differences between portal vein-associated and central vein-associated HSCs (24). Moreover, different functional aspects of HSC—e.g., chemokine/cytokine release vs. matrix production—can be assigned to different HSC/MFB subpopulations by scRNAseq (25). This ambiguity offers potential therapeutic options, as innovative drugs might specifically target defined myofibroblast populations (26). While targeting HSC activation and drug delivery to MFBs works already quite well in preclinical models, translation into human diseases has remained challenging (27).

Liver fibrogenesis is closely linked to pathological angiogenesis. Inflammatory signals, particularly from infiltrating macrophages, promote the expansion of hepatic blood vessels (28). These newly formed vessels have a different, dysfunctional, dedifferentiated phenotype compared to healthy sinusoidal endothelial cells (29). The crosstalk between pro-angiogenic endothelial cells and activated stellate cells is not only relevant during progression, but also during regression of fibrosis (30). Very likely, the fibrosis-induced angiogenesis favors the development of HCC in fibrotic livers (31). Intriguingly, changes in sinusoidal endothelial cells including loss of fenestrae (“capillarization”) or the reduced ability to generate vasodilator agents occur quite early in NAFLD and can precede fibrosis, making these cells an interesting target for therapeutic interventions (32).

Antifibrotic therapeutic targets

Based on the high complexity of mediators and signaling pathways as well as the different cellular players involved in hepatic fibrogenesis, there are several new treatment options currently under evaluation. Due to the high burden of NAFLD, most antifibrotic drugs are being evaluated in patients with NASH-associated fibrosis. Liver disease in NASH is oftentimes viewed as the hepatic manifestation of the metabolic syndrome, due to the similar pathomechanisms driving obesity-associated metabolic alterations and NAFLD progression, such as oxidative stress, free fatty acids, hyperinsulinemia or systemic inflammation (33). Figure 2 provides an overview of selected therapeutic targets in NASH-related fibrosis. The different strategies can be summarized into two goals: (I) reverting pathogenic liver metabolism (in order to stop the underlying fibrosis-promoting mechanism) or (II) disconnecting NAFLD from inflammation and/or fibrosis (i.e., target “downstream” pathways so that the metabolic stress does not translate into inflammation or fibrosis).

Figure 2.

Therapeutic targets in liver fibrosis. The understanding of molecular processes leading to hepatic fibrosis offers emerging therapeutic targets for preventing fibrosis and enhancing therapy. Effective drugs are beneficial to prevent cell death, inflammation, and reactive oxygen species formation. Other drugs target hepatic fat metabolism, the gut-liver axis, and matrix expression or turnover. The figure is based on (34). ACC, acetyl-CoA carboxylase; DNL, de novo lipogenesis; ER, endoplasmic reticulum; FGF, fibroblast growth factor; FFA, free fatty acids; FXR, farnesoid X receptor; PPAR, peroxisome proliferator- activated receptor; ROS, reactive oxygen species; SHP, small heterodimer partner; SREBP1, Sterol regulatory element binding protein-1; TGR5, G protein-coupled bile acid receptor 1 (GPBAR1); THRβ, thyroid hormone receptor-β; TNF, tumor necrosis factor.

Reverting pathogenic liver metabolism

Many metabolic risk factors contribute to the pathogenesis of NAFLD and NASH. In particular, low high-density lipoprotein (HDL), high triglycerides, hypercholesterolemia, and type 2 diabetes mellitus have been discussed as independent predictors of poor outcome in NAFLD. A recent meta-analysis of 22 population-based cohort studies suggested that type 2 diabetes and obesity as measured by body mass index (BMI) are the most important factors that are associated with more severe liver disease (35). Therefore, strategies targeting insulin resistance and diabetes are promising for ameliorating metabolic disturbances in NASH. Modern antidiabetic drugs that have a beneficial impact on weight loss may therefore also alleviate NASH. Such drug candidates are agonists of the glucagon-like peptide-1 (GLP-1), which promotes insulin secretion in a glucose-dependent manner, or inhibitors of the sodium-glucose transport protein 2 (SGLT2), also called gliflozins, which inhibit glucose reabsorption in the kidney. GLP-1 receptor agonists (liraglutide, semaglutide) are currently being tested in NASH, also in non-diabetic patients. An initial pilot study demonstrated improvement of histological features of NASH by using liraglutide (36).

Besides “repurposing” anti-diabetes drugs, several strategies for targeting aspects of aberrant (liver) metabolism are in focus. Potential targets include correction of insulin resistance, interference with free fatty acid generation, triglyceride uptake, lipolysis and prevention of autophagy, endoplasmic reticulum stress, and mitochondrial functions (Figure 2, Table 1).

Table 1. Selected examples for pharmacotherapies under evaluation for the treatment of NASH and/or NASH fibrosis.

Mechanism	Selected compounds	Effects on fibrosis	Stage of development
FXR agonism	Obeticholic acid (OCA); tropifexor; cilofexor	Fibrosis regression (OCA)	Phase 3 (OCA); phase 2 (others)
PPAR agonism	Elafibranor (α/δ); saroglitazar (α/γ); lanifibranor (α/γ/δ)	No effect on fibrosis (α/δ) vs. fibrosis regression (α/γ/δ)	Phase 2–3
ACC inhibition	Firsocostat; PF-05221304	Possible de-activation of stellate cells	Phase 2
THRβ agonism	Resmetirom	Indirect antifibrotic effects	Phase 3
FGF19/FGF21 mimetics	Aldafermin (FGF19); pegbelfermin (FGF21)	Indirect antifibrotic effects	Phase 2
SCD1 inhibition	Aramchol	Indirect antifibrotic effects	Phase 2–3
CCR2/CCR5 inhibition	Cenicriviroc	Fibrosis regression	Phase 3

NASH, non-alcoholic steatohepatitis

One key factor contributing to metabolic stress pathways are bile acid receptors such as the farnesoid X-activated receptor (FXR) that is involved in energy expenditure and metabolism. It is involved in pathways that control lipogenesis-inducing enzymes such as the sterol regulatory element-binding transcription factor 1 (SREBP-1) and reducing endogenous bile acid production, thereby having a critical role in glucose and lipid metabolism. Drugs with agonistic FXR activity such as obeticholic acid are currently approved for the treatment of patients with primary biliary cholangitis, and was shown to be particular useful to improve insulin sensitivity in NAFLD patients suffering from type 2 diabetes (37,38). These positive attributes of obeticholic acid were also confirmed in the multicenter, randomized, placebo-controlled “FXR ligand obeticholic acid in NASH treatment” (FLINT) phase 2 trial, in which NASH patients showed significant improvements in inflammation and fibrosis (39). Based on this positive finding, obeticholic acid is currently tested in a large phase 3 long-term trial in over 2,400 patients with NASH, including ~2,100 patients with stage 2 or 3 liver fibrosis (40). The interim analyses from this trial are very promising, as obeticholic acid at a dose of 25 mg daily significantly improved fibrosis and key histological components of NASH disease activity after 72 weeks of therapy (41). Based on these data, it is expected that the FDA and EMEA will conditionally approve this drug for the treatment of NASH patients with advanced fibrosis.

Many companies now developed FXR agonists without chemical similarities to bile acids. Such “non-steroidal” FXR agonist may potentially show a more favorable safety profile, as obeticholic acid has relevant side effects such as itching and elevated LDL cholesterol serum levels. Representative non-steroidal FXR agonists are tropifexor (Novartis), GS-9674 (Gilead), AKN-083 (Allergan) and LBM763 (Novartis).

Another pathway involving bile acid biology in NASH is the chemical inhibition of the apical sodium-dependent bile acid transporter (ASBT), which blocks bile acid reuptake and stimulates hepatic bile acid production. The ASBT inhibitor volixibat increased bile acid synthesis and decreased cholesterol in NASH patients, but did not show clear signals of histological benefits in a phase 2 clinical trial (42).

Other therapeutic targets are offered by the family of fibroblast growth factors (FGF) and their receptors. This growth factor family comprises 22 members that bind to five distinct receptors (FGFR1-4, FGFRL1) and signal through several downstream pathways relevant in the initiation of fibrosis (43). They have not only a substantial influence of fibrogenesis, but also impact development, regeneration, hepatocyte proliferation and recruitment of progenitor cells during acute and chronic liver injury (44). In particular, the hepatoprotective properties and beneficial effects on inflammation and fibrosis have brought FGF19 and FGF21 into the focus as novel targets for drug development. Mice lacking FGF21 showed increased hepatic fatty acid activation and β-oxidation and subcutaneous infusions of FGF21 reduced steatosis and peroxidative damage in a mouse NASH model (45). The PEGylated FGF21 analogue pegbelfermin (BMS-986036) demonstrated beneficial metabolic effects and reduced hepatic fat content in a 16-week application in NASH patients (46). The engineered FGF19 analogue NGM282 seems to be very effective in reducing hepatic steatosis as well (47,48). Its concomitant changes in circulating lipids, including increases of LDL cholesterol, can be effectively managed by coadministering rosuvastatin, as demonstrated in clinical trials (49).

An interesting group of drugs are agonists for proliferator-activated receptors (PPARs). PPARs represent a family of transcription factors that act as lipid sensors in various tissues (50). They are responsive to specific ligands, especially fatty acids, phospholipids, and prostaglandins. The family consists of three different receptors (PPARα, PPARβ/δ, and PPARγ) that are expressed at different levels in various tissues and are targeted by different ligands. PPARs play critical roles in the regulation of liver homeostasis, fatty acid oxidation, triglyceride metabolism, and adipogenesis. They prevent fibrogenesis by keeping HSC in the quiescent phase and regulating the inflammatory response, increase insulin sensitivity and regulate triglyceride storage in adipose tissue (51). PPAR stimulation may provide therapeutic benefit against steatohepatitis and insulin resistance. Several medical compounds acting on one, two or even three PPARs already exist. Pioglitazone or rosiglitazone targeting PPARγ improved histological features in NAFLD (52) and may even ameliorate fibrosis (53). However, the use of these drugs in clinical routine is limited by their propensity to induce weight gain (34). In a phase 2 trial, the dual PPARα/δ agonist elafibranor improved histological features and showed beneficial effects on lipid profiles, glucose, liver enzymes and inflammatory marker expression in NASH but failed to improve hepatic fibrosis (54). However, interim analyses from a phase 3 clinical trial reported that elafibranor failed to reach its primary endpoint, as elafibranor did not significantly improve the rate of patients achieving histological resolution of NASH compared to placebo.

In experimental mouse models, also the PPARα/γ agonist saroglitazar and the triple PPARα/γ/δ agonist lanifibranor (IVA337) were highly effective in protecting the liver from metabolic disorders and fibrosis (55,56). In mice subjected to choline-deficient high-fat diet-induced NASH, saroglitazar reduced hepatic steatosis, inflammation, ballooning and prevented fibrogenesis (55). Similar preventive and curative effects were shown for lanifibranor in preclinical mouse models of NASH (56). Most importantly, lanifibranor synergistically combined beneficial effects of agonism on PPARα (on hepatocytes), PPARγ (on stellate cells) and PPARδ (on macrophages) in mouse models of NASH (57). A clinical trial using lanifibranor in NASH patients is ongoing.

Improvement of NASH by increasing hepatic fat metabolism and reducing lipotoxicity was also found by usage of the liver-directed, orally active, selective thyroid hormone receptor-β (THRβ) agonist resmetirom (MGL-3196) (58). THRβ is a nuclear hormone receptor for triiodothyronine and are associated with the control of a wide variety of effects related to development, differentiation, growth, and metabolism (59). Binding to THRβ affects metabolic processes by lowering serum lipids, cholesterol, serum triglycerides, and other metabolic factors. Several thyroid hormone analogues are currently under development that vary regarding selectivity (60).

Inhibition of acetyl-coenzyme carboxylase (ACC) catalyzing the rate-limiting step in de novo lipogenesis by drugs such as firsocostat (GS-0976) or PF-05221304 showed also beneficial effects on hepatic steatosis, fibrogenic marker expression and liver histology in a phase 2 randomized placebo-controlled trials of patients with NASH (61). More recent evidence suggests direct anti-fibrotic activities in addition to the beneficial metabolic effects of inhibiting ACC (62).

Disconnecting NAFLD from inflammation and/or fibrosis

It is well known that inflammation and fibrosis are key characteristics of disease progression in NAFLD. This observation fuels the concept that blocking inflammation and/or activation of MFBs or matrix deposition would provide clinically meaningful benefit to patients. Cell death and activation of inflammatory signaling pathways (in hepatocytes and non-parenchymal cells) would represent logical targets for “anti-inflammatory” interventions (63). In this direction, selonsertib, an apoptosis signal-regulating kinase 1 (ASK1) inhibitor, was proposed. In fact, selonsertib demonstrated potent antifibrotic activity in rodent models (64,65). However, two large phase 3 trials in NASH patients with either advanced fibrosis or cirrhosis failed, as selonsertib did not improve liver fibrosis after 48 weeks of therapy compared to placebo (66).

One of the key findings of NASH progression towards fibrosis is the accumulation of macrophages in the liver (67). These disease-promoting fibrogenic macrophages originate from monocytes that are recruited to the liver (68) and display a unique, metabolically activated and inflammatory phenotype (69). Monocyte recruitment to NASH livers can be effectively inhibited by the chemokine receptor CCR2/CCR5 inhibitor cenicriviroc (70). In patients with NASH and fibrosis, cenicriviroc treatment was associated with a higher rate of fibrosis improvement after 1 year of therapy (71). The antifibrotic efficacy was less clear after 2 years of cenicriviroc therapy, but this drug was exceptionally safe and well tolerated (72). A phase 3 trial evaluating cenicriviroc in NASH patients with fibrosis is currently ongoing (73).

While the clinical development of cenicriviroc in liver fibrosis is quite advanced, many other anti-inflammatory approaches have been proposed as well. For instance, blocking inflammatory macrophage activation or polarization by interfering with toll-like receptor (TLR) signaling (e.g., with the TLR4 inhibitor serelaxin) or with galectin-3 (e.g., with the inhibitor belapectin) may hold antifibrotic potential (74). Similarly, monocytes upregulate the medium chain fatty acid receptor GPR84 upon inflammatory activation. Pharmacological inhibition of GPR84 reduces myeloid cell infiltration in NASH mouse models, which subsequently ameliorates steatohepatitis and fibrosis (64). Such data underline the potential of disconnecting NAFLD from inflammation and/or fibrosis as a valid therapeutic strategy.

Targeting the activation of stellate cells directly has remained challenging. While this can be achieved in preclinical models, e.g., by innovative nanotheranostic drug delivery approaches, the translation into clinical trials is currently pending (27).

The role of physical activity and lifestyle changes for treatment and prevention

Despite the promising results from research with new pharmacological strategies, drug treatment by itself is likely not sufficient, if the unhealthy lifestyle is not corrected. Lack of physical activity is one critical factor having impact of the outcome of hepatic diseases. Undoubtedly, exercise can be very beneficial, even in advanced stages of liver fibrosis or cirrhosis (75). It has been shown that in response to exercise a large number of endogenous active mediators are produced that endorse anti-inflammatory effects (76). Therefore, it is not surprising that physical activity and aerobic exercise of moderate intensity for at least 20 to 60 min on at least 5 days a week in combination with resistance training performed thrice weekly has entered into the practical recommendations for the prevention and treatment of NAFLD (77).

Similarly, interventions promoting weight loss, preventing overnutrition, and reducing hepatic fat have been shown to attenuate NASH-related inflammation and fibrosis (78). Weight loss of 1 kg/week is recommended for overweight and obese subjects suffering from NAFLD and NASH (79). The beneficial effects of weight loss on histological features of NAFLD/NASH are well documented, and strategies to overcome barriers in adopting dietary recommendations in the management of patients have been proposed and validated (80).

Several macronutrients and micronutrients are known to either support or prevent NAFLD pathogenesis. Prototypically, fructose is a key carbohydrate that is associated with insulin resistance and NAFLD development, while the consumption of soluble or insoluble fibers is beneficial for the outcome of hepatic disease because they promote satiety, restrict caloric intake, slow stomach emptying, and reduce glucose and cholesterol uptake (79). Saturated fatty acids are another factor contributing to the pathogenesis of NASH/NAFLD, while the uptake of monounsaturated or polyunsaturated fatty acids has been shown to be beneficial against NAFLD (79). Among micronutrients, vitamin E, vitamin C, vitamin D, and several polyphenols (e.g., resveratrol, curcumin, caffeine, quercetin) have been successfully tested in preclinical models and clinical studies (43,79). They counteract intracellular reactive oxygen species formation, prevent hepatic infiltration with circulating blood cells, or target pro-inflammatory and pro-fibrotic signaling pathways and mediators that critically contribute to generation of extracellular matrix compounds (43). Nevertheless, most of these beneficial attributes of these compounds have only been shown in experimental models and the translation to humans and the initiation of human trials is perennially hampered by many factors (43).

Conclusions

Liver fibrosis, i.e., scarring of the liver as the characteristic response to chronic injury, is the main determinant of long-term outcome in patients with liver diseases. The global epidemic of obesity and the metabolic syndrome made NAFLD the leading cause of liver fibrosis to date. Lifestyle modifications, particularly weight loss, healthy diet and physical activity, are key to preventing fibrosis progression. Extensive research over the past decade has unraveled cellular and molecular mechanisms of hepatic fibrogenesis. These findings have resulted in a large number of clinical investigations on antifibrotic drugs. While several promising drug candidates failed in phase 2 or 3 clinical trials (including elafibranor and selonsertib), promising results with obeticholic acid and cenicriviroc support the expectation of an effective pharmacological therapy for liver fibrosis in the near future. To the authors’ opinion, tackling NAFLD-associated fibrosis from different directions by combinatorial drug treatment and effective lifestyle changes hold the greatest prospects.

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