Nonalcoholic fatty liver disease: Evolving paradigms.

In the last years new evidence has accumulated on nonalcoholic fatty liver disease (NAFLD) challenging the paradigms that had been holding the scene over the previous 30 years. NAFLD has such an epidemic prevalence as to make it impossible to screen general population looking for NAFLD cases. Conversely, focusing on those cohorts of individuals exposed to the highest risk of NAFLD could be a more rational approach. NAFLD, which can be diagnosed with either non-invasive strategies or through liver biopsy, is a pathogenically complex and clinically heterogeneous disease. The existence of metabolic as opposed to genetic-associated disease, notably including "lean NAFLD" has recently been recognized. Moreover, NAFLD is a systemic condition, featuring metabolic, cardiovascular and (hepatic/extra-hepatic) cancer risk. Among the clinico-laboratory features of NAFLD we discuss hyperuricemia, insulin resistance, atherosclerosis, gallstones, psoriasis and selected endocrine derangements. NAFLD is a precursor of type 2 diabetes (T2D) and metabolic syndrome and progressive liver disease develops in T2D patients in whom the course of disease is worsened by NAFLD. Finally, lifestyle changes and drug treatment options to be implemented in the individual patient are also critically discussed. In conclusion, this review emphasizes the new concepts on clinical and pathogenic heterogeneity of NAFLD, a systemic disorder with a multifactorial pathogenesis and protean clinical manifestations. It is highly prevalent in certain cohorts of individuals who are thus potentially amenable to selective screening strategies, intensive follow-up schedules for early identification of liver-related and extrahepatic complications and in whom earlier and more aggressive treatment schedules should be carried out whenever possible.

Core tip: Nonalcoholic fatty liver disease (NAFLD) is a pandemic disease. Recent evidence highlights new concepts in clinical and pathogenic heterogeneity of NAFLD, a systemic disorder with a multifactorial pathogenesis and protean clinical manifestations. Other than the classical obese phenotype of NAFLD, a lean though metabolically abnormal variant has been recognized. Simple steatosis is no more considered a benign condition; insulin resistance is necessary but not sufficient for the disease progression, and NAFLD is not only a mere hepatic manifestation of metabolic syndrome, but may forerun the development of metabolic syndrome and cardio-renal complications. Several non-invasive diagnostic tests are now available and new drug treatment options are coming.

INTRODUCTION

Nonalcoholic fatty liver disease (NAFLD) features excess intrahepatic ectopic triglyceride deposition[1] in patients who are free of competing etiologies of liver disease[2]. It is the most frequent liver disease and is associated with a wide spectrum of hepatic disorders ranging from simple steatosis to nonalcoholic steatohepatitis (NASH), cirrhosis and hepatocellular carcinoma (HCC)[3]. Moreover, frequent co-morbidities of NAFLD include specific cardio-renal-metabolic conditions and increased hepatic/extrahepatic cancer risk[4].

NAFLD is a pandemic disease worldwide, which has been paralleling the ongoing epidemics of obesity, type 2 diabetes (T2D), and metabolic syndrome (MetS)[4]. The prevalence of NAFLD approaches 25%-30% in the Europe and United States general populations; but this figure surges to 80%-90% in selected cohorts of dysmetabolic individuals[5-7]. Patients with NAFLD have an increased risk of premature cardiovascular as well as of liver-related mortality[8]. Of concern, up to 50% of cases NAFLD-HCC may occur in the absence of cirrhosis, a circumstance which will often worsen the outcome[9,10].

Knowledge accumulated since 1980, when Ludwig named and described NASH[11], has challenged most of the paradigms that had been holding the scene over the previous 30 years. For example, NAFLD is now considered a multifaceted complex systemic condition[12,13] which exhibits a sexual dimorphisms[14] and follows a variable hepatic and extra-hepatic course[15,16]. In addition, recent evidence suggests that simple steatosis may progress to NASH and advanced liver fibrosis[17] challenging the previous dogma that “steatosis is a benign condition”.

Insulin resistance (IR) is often associated with NAFLD but it is “necessary but not sufficient” for the disease to progress[18]. Moreover, NAFLD may occur in lean individuals[19,20] and it is not only a mere “hepatic manifestation of MetS”, but may forerun the development of MetS[21,22]. NAFLD is associated with secretion of diabetogenic hepatokines and inflammatory biomarkers that increase the risk of incident T2D by adversely affecting glucose homeostasis[23]. Of concern, NAFLD and T2D are linked by a “vicious circle” which carries to accelerated worsening of liver disease[24], more difficult metabolic control and earlier appearance of T2D complications[25,26].

The historical “two-hit” pathogenic theory[27] has been replaced by a multi-factorial model, which more incisively recapitulates the complexity of the pathogenesis of the disease[28] by emphasizing the myriads of pathways leading to the same hepatic phenotype[29]. A better definition of the role played by genetics in the development of NAFLD[30] has led to the notion that, probably, two different NAFLD types exist: NAFLD associated with and NAFLD dissociated from MetS, and that each may differentially affect cardio-metabolic risk[31,32]. In addition, the declining gradient of risk of NAFLD in Hispanic patient populations compared to non-Hispanic whites and African Americans may potentially be accounted for by polymorphisms in genes that control metabolism[33]. The impressive amount of data implicating gut microbiota in the development of NAFLD may well illustrate the role of diet in increasing NAFLD risk[34-36] and significantly impact our understanding of NAFLD pathogenesis and treatment[4].

Over time, the diagnostic approach has also undergone substantial changes. Non-invasive physical and chemical biomarkers are now available[37]. Liver biopsy is reserved to selected NAFLD cases in clinical practice and is more extensively performed and repeated to evaluate novel drug agents[3,4,38,39]. Finally, new histological classifications have recently been proposed[40] and the pros and cons of each system must be carefully evaluated[41].

Within the complex frame of pathogenic and clinical heterogeneity of different NAFLD populations synthesized in Figure 1, this review aims at disseminating the most updated paradigms on NAFLD and the possible implications for both clinical practice and research purposes.

Figure 1

Nonalcoholic fatty liver disease as a pathogenically and clinically heterogeneous condition. Schematic representation of the pathogenic and clinical heterogeneity of different NAFLD populations. Left: “Metabolic” NAFLD is associated with adipose tissue dysfunction and IR and may progress towards hepatic and extrahepatic complications. Right: “Genetic” NAFLD seems to be disconnected from adipose tissue dysfunction and IR, is associated with an increased risk of liver disease progression but is probably spared from extrahepatic complications. NAFLD: Nonalcoholic fatty liver disease; NASH: Nonalcoholic steatohepatitis; HCC: Hepatocellular carcinoma.

NAFLD: TO SCREEN OR NOT TO SCREEN. PRINCIPLES OF EPIDEMIOLOGY

An ongoing debate regards whether any screening campaigns should be ever conducted to identify NAFLD individuals[38,42]. Those supporting screening would argue that NAFLD patients are prone to excess liver-related morbidity/mortality and cardiovascular risk and thus in need of intensive follow-up schedules; those against would reply that there is no point in identifying NAFLD, a condition for which no licensed drug treatment schedule is available. At any rate, given the overwhelming prevalence of NAFLD in the general population worldwide, any sensitive approach should best be conducted based on our understanding of which specific cohorts of individuals are exposed to the highest risk of disease.

In the general population, the prevalence of NAFLD has been reported to widely range from 6.3% to 51% related to the different population/ethnicity evaluated as well as to the diagnostic methods utilized to assess the amount of intrahepatic fat content[43]. In particular, the diagnostic technique used to capture cases of NAFLD has undoubtedly affected the results. For example, liver enzymes are far less sensitive than ultrasonographic scanning; in its turn, MR spectroscopy is the most sensitive although this technique is expensive and not universally available[3]. Based on meta-analytic data, Younossi et al[6] have reported that, in Europe and in United States, the overall prevalence of NAFLD in the general population approximates 25%. However, there are areas of the world, such as south America and middle East, wherein the average prevalence peaks > 30%; conversely, Africa has the minimum prevalence of NAFLD worldwide[6]. These impressive data clearly imply that no society worldwide can invest so many resources as to screen the general population for NAFLD. It is of interest, therefore, that modifiers of risk might assist health authorities as well as practicing physician in identifying individuals who are particularly prone to developing NAFLD. For example: male gender, middle age and Hispanic ethnicity, all reinforce the risk of NAFLD and, conversely, young women of Afro-American descent have the lowest risk of this disease[7]. Further to the above physiological modifiers, a set of metabolic modifiers have also been identified. They include arterial hypertension and the MetS (whose presence doubles the prevalence of NAFLD up to 50% of individuals); obesity, dyslipidemia and T2D[7]. In the general population, women are protected from developing NAFLD owing to their hormonal profile and/or set of chromosomes. Conversely, women with T2D are exposed to the same risk of NAFLD as men, indicating that T2D abrogates such a gender-related protection[7,14].

PATHOGENESIS OF NAFLD: FROM TWO TO MULTIPLE HITS

In recent years, it has increasingly become evident that what had initially been called the NAFLD “two hit hypothesis”, in which IR acted as the “first hit” by inducing lipid accumulation in the hepatocytes and increasing the vulnerability of the liver to further insults, referred to as the “second hit”, that, in their turn, promoted hepatic injury, inflammation and fibrosis, is probably over-simplistic[27,44]. Human NAFLD is rather a multi-factorial, non-communicable disease resulting from a complex interaction between multiple environmental and metabolic “hits” and a predisposing genetic background[45] (Figure 2). A “multiple parallel hits hypothesis” seems more appropriate to recapitulate the complexity of NAFLD pathogenesis[28], which results from numerous events originating within liver, adipose tissue, gastrointestinal tract and the muscle[45].

Figure 2

Nonalcoholic fatty liver disease pathogenesis: from two to multiple parallel hits. Schematic representation of the increasing grade of complexity gained in moving from earlier theories[27] to more updated pathogenic paradigms[28]. Top: Former “two hits” hypothesis: steatosis, the first ‘hit’, sensitizes the liver to the second “hits”: oxidative stress, endotoxin, ATP depletion and adduct formation[44]. Bottom: The "multiple hits" hypothesis considers multiple insults acting together on genetically predisposed subjects to induce NAFLD and provides a more accurate explanation of NAFLD pathogenesis. Such hits include IR, hormones secreted from the adipose tissue, nutritional factors, gut microbiota and genetic and epigenetic factors[28]. NAFLD: Nonalcoholic fatty liver disease; TLRs: Toll-like receptors.

An unhealthy lifestyle, characterized by sedentariness and high-calorie diet, is crucial for NAFLD development and progression. The unbalance between caloric intake and expenditure determines the expansion of fat depots, which become inflamed and insulin resistant, and release increased amounts of free fatty acids into the bloodstream, leading to ectopic fat accumulation in the liver, skeletal muscles and pancreas[46]. The hepatic lipid content mainly derives from the increased lipolysis of triglycerides in the adipose tissue and, to a lesser extent, from dietary fats and sugars, and from de novo lipogenesis[47]. Moreover, the dysfunctional adipose tissue overproduces pro-inflammatory cytokines, such as leptin and resistin, whereas the release of anti-inflammatory adipokines, such as adiponectin, is reduced, so further enhancing NAFLD progression[48]. The role of intra-hepatocytic accumulation of specific toxic lipids, via lipotoxicity and inflammation, has emerged as a key player in the pathogenesis of NASH and its systemic complications[49]. Saturated fatty acids have been found elevated in NASH patients and induce inflammation and hepatocyte apoptosis through activation of JNK/endoplasmic reticulum stress and oxidative stress/mitochondrial dysfunction[50]. The accumulation of diacylglycerol and ceramide in the liver impairs hepatic insulin signaling, fuels gluconeogenesis and promotes the development of persisting hyperglycemia and, eventually, T2D[51].

Unhealthy lifestyle also results in dysbiosis, i.e. quantitative and qualitative changes of gut microbiota composition[52]. In NAFLD an increased Firmicutes/Bacteroidetes ratio and changes in metagenomic-based functional aspects of gut microbiota have all been described[53]. Gut microbiota may contribute to the development and progression of NAFLD by triggering (both directly or via end-products of bacterial metabolism) different signaling pathways, by increasing the efficiency of caloric extraction from the food, and by inducing translocation of bacterial products via increased gut permeability[54-57]. Circulating pathogen-associated molecular pattern (PAMPs) and damage-associated molecular patterns (DAMPs) interact with the family of pattern recognition receptors (toll-like receptors, TLRs) within the liver and induce several pro-inflammatory pathways, including over-expression of cytokines/chemokines, production of reactive oxygen species and activation of the inflammasome[58,59]. Of note, activation of Nod-like receptor protein 3 inflammasome, upregulated by TLRs in response to the presence of PAMPs and DAMPs, has been associated with a novel cell death mechanism, referred to as hepatocyte pyroptosis[60].

Several nuclear receptors with their molecular cascades are promising pharmacological targets for the treatment of NAFLD, given their pivotal role in the regulation of energy homeostasis and metabolic pathways. Owing to the development of specific targeted drugs, peroxisome proliferator-activated receptors (PPARs), farnesoid X receptor (FXR) and liver X receptors (LXRs), now deserve full attention. The PPARs superfamily includes PPAR-α, PPAR-β/δ and PPAR-γ. PPAR-α, mainly expressed in liver and muscle, modulates the rates of fatty acids catabolism, lipogenesis and ketone body synthesis by acting as a nutrient sensor. PPAR-γ, abundantly expressed in the adipose tissue, promotes adipocyte differentiation and storage of triglycerides, and regulates glucose homeostasis. PPAR-β/δ, universally expressed in all organ tissues, regulates glucose and lipoprotein metabolism and exerts an anti-inflammatory role. FXR, mainly expressed in the liver and gut, acts as a sensor of bile acids and mediates the signaling effects exerted by bile acid on glucose and lipid metabolism. LXRs serve as lipid sensors in the liver and participate in regulating the metabolism of cholesterol and fatty acids. The role of nuclear receptors in NAFLD pathophysiology has been comprehensively reviewed elsewhere[15].

The role of skeletal muscle in the pathogenesis of NAFLD is a matter of increasing research[23]. Intra-myocellular lipid storage is an early step of ectopic fat accumulation and systemic IR, leads to increased delivery of glucose to the liver, where it becomes substrate for hepatic de novo lipogenesis, and has been associated with NAFLD[61,62]. Accordingly, sarcopenia, a pathological condition featured by generalized loss of skeletal mass and strength, has recently been proposed as an additional key factor in the pathogenesis of NAFLD[63-65]. The myokines, such as irisin, which is produced in response to physical activity and exerts several beneficial metabolic effects, may partly account for these associations[66,67].

NAFLD AS A HETEROGENEOUS DISEASE ENTITY: THE ROLE OF GENETICS

NAFLD is a complex disorder with a variable natural history. Subtle inter-patient genetic variation and environmental factors combine to determine variation in disease progression[68]. Several clinical features are clues to genetics playing a major role in NAFLD. First, up to a quarter of the general population are at risk of progressive disease; however only a minority will experience associated liver-related morbidity[69]. Second, both the development and the progression of disease tend to cluster as distinct traits among “NAFLD families”[7,70]. Third, among non-diabetics, NAFLD will typically affect men more often than women[7] which, further to hormonal variations, may mirror genetic factors. Fourth, although NAFLD is strictly linked with obesity[7] not all obese subjects will develop NAFLD and, more importantly, NAFLD can also be found in non-obese individuals[20]. On these grounds, in the last few years scientific attention has focused on NAFLD genetic features.

Role of PNPLA3, TM6SF2 and MBOAT7

Among all analyzed genes patatin-like phospholipase domain-containing protein 3 (PNPLA3, also called adiponutrin) and trans-membrane 6 super family 2 (TM6SF2) are deemed to play the most significant role. More recently, membrane bound O-acyltransferase domain-containing 7 gene (MBOAT7) has also gained attention. They are all involved in the process of intrahepatic accumulation of triglycerides.

PNPLA3 gene encodes for a 481-aminoacid protein expressed in the liver and adipose tissues, with function of triglyceride hydrolase and acetytil-CoA-indipendent transacylase, suggesting a double role of catabolic lipase activity and anabolic lipogenic activity[71-73]. The nonsynonymous variant rs738409 of PNPLA3 is a genetic polymorphism characterized by the substitution of isoleucine to methionine at position 148 (I148M). Studies consistently show a strong association between I148M variant and hepatocellular triglycerides accumulation[74-76]. I148M variant is a loss of function allele that determines an altered hepatic lipid metabolism, eventually leading to hepatic droplet lipid accumulation, lower hepatic VLDL secretion and lower adiponectin production[77]. Adiponectin is a protein with anti-inflammatory activity and onco-suppressive properties; lower circulating levels of adiponectin can account for the propensity of I148M variant to the progression from NAFLD to NASH and the increased risk of HCC[77,78].

TM6SF2, also known as KIAA 1926, is a gene at the 19p13.11 locus, with unknown biological function that encodes a protein high expressed in the small intestine, kidney and liver. It is involved in the pathophysiology of NAFLD by modifying hepatic lipid secretion; a decreased hepatic expression of this protein is associated with an increased size and number of hepatocytic lipid droplets[79]. In particular, studies have shown that a variant of TM6SF2, rs58542926 c.449 C>T (E167K), is associated with NAFLD evolution, also with dyslipidemia and cardiovascular risk. The minor variant allele (T) is linked with a reduction of the excretion of hepatic VLDL and a lower level of circulating triglyceride and LDL-cholesterol. Conversely, C-allele is associated with a higher hepatic excretion of VLDL, serum triglyceride and cholesterol. Thus, the minor allele exhibits a higher risk of advanced hepatic disease, though protecting from metabolic and cardiovascular disease[80]. Conversely, increased metabolic risk is associated with C-allele[81]. Morris et al[82]. based on their large meta-analysis have hypothesized a correlation with T-allele variant and risk developing T2D, but this theory remains to be confirmed[82]. Recently, it has been shown that TM6SF2 (E167K) gene variant is associated with an altered lipidomic profile featuring deficiency of polyunsaturated phosphatidylcholine and excess of polyunsaturated free fatty acids in the liver. This lipidomic profile leads to decreased concentrations of circulating VLDL and increased liver fat content[83]. Moreover, the same polymorphism has been found to modulate postprandial lipidmetabolism, nutrient oxidation and glucose homeostasis in response to dietary fat[84]. These findings are compatible with the above reported notion that carriers of TM6SF2 polymorphisms may be specifically exposed to liver-related as opposed to vascular manifestations of NAFLD.

Finally, it has been recently shown that the rs641738 C>T variant in MBOAT7 gene, which is involved in phosphatidylinositol acyl-chain remodeling, increases the risk of developing NAFLD; inflammation and fibrosis[85,86].

Lean NAFLD

As previously reported in this review, genetic factors play a major role in development and progression of NAFLD. Such a role of genetics is further reinforced when lean NAFLD patients are taken into consideration. It is well-known that NAFLD is often found in obese and dysmetabolic patients. Accordingly, the “Lean NAFLD” phenotype has attracted interest among researchers in as much as it features selectively expanded visceral adiposity though preserving a normal body mass index and, sometimes, even a normal waist circumference. Worryingly, these individuals develop IR and atherogenic dyslipidemia similarly to obese patients and have, therefore, in the past been alluded to as “metabolically obese, normal weight”[87]. Lean NAFLD cases have been described among different ethnic population, mainly among Asians, who tend to develop the metabolic complications of obesity for BMI values inferior to those of Caucasians[88,89]. The mechanism(s) through which lean NAFLD develop(s) is/are poorly characterized and the disease goes often under-recognized. Though the role of genetic factors is likely to be more substantial in “lean NAFLD” than that found in “obese NAFLD”[90], a recent statistically sophisticated study has suggested that both lean and obese NAFLD patients share cardio-metabolic risk commonalities and that the former, despite normal body weight, nonetheless have excess of abdominal adiposity and other MetS features[19]. Accordingly, also lean NAFLD patients may benefit from increased physical activity which is effective in reducing visceral fat[91]. Of note, the findings of a very recent study confirm that NAFLD development and progression derive from a complex interplay between genetic and environmental factor, by clearly demonstrating the presence of a synergy between adiposity and the genetic risk of NAFLD conferred by multiple loci[92].

DIAGNOSTIC STRATEGIES

Diagnosis and staging of NAFLD fully rely on liver biopsy. Histological examination of liver tissue specimens is the gold-standard for quantitating steatosis, diagnosing NASH and staging fibrosis. The last of these three tasks bears major prognostic significance given that fibrosis is associated with long-term liver-related and, probably, cardiovascular outcomes[93-95]. Over the past two decades, different criteria have been suggested for scoring and staging histological lesions, and different definitions of NASH have been used[40,96-99]. Besides discrepancies and subjectivity in interpretation, liver biopsy has additional limitations such as cost, invasiveness and sampling variability which limit the feasibility of this procedure in all the patients with suspected NAFLD and have called for the development of alternative non-invasive diagnostic and staging procedures. Despite some intrinsic and specific drawbacks[100,101], these non-invasive tools, especially if used in combination or sequentially, may help in restricting the number of and assist in a better selection of potential candidates to liver biopsy[102].

Histological classification: what’s new?

Steatosis, namely a minimal threshold of 5% of hepatocytes containing fat droplets in biopsy specimen, is a prerequisite for the diagnosis of NAFLD. The histological definition of adult NASH is based on a combination of three elementary lesions, i.e., steatosis, hepatocellular ballooning and lobular inflammation[41,97].

Four main pathologic classifications of NAFLD have been proposed: Matteoni’s, Brunt’s, Kleiner’s classification with the NAFLD Activity Score (NAS) and the recent Fatty Liver Inhibition of Progression (FLIP) algorithm with the Steatosis, Activity, and Fibrosis (SAF) score[40,96-99].

In 2005 the NASH Clinical Research Network designed and validated a histological feature scoring system that addressed the full spectrum of lesions of NAFLD. Currently, NAS is the most widely used histological classification for NAFLD/NASH and its use is recommended for defining and quantifying disease activity in clinical trials[98]. NAS, ranging from 0 to 8, is derived from the sum of steatosis (0-3), ballooning (0-2) and lobular inflammation (0-3). However, at least two out of its three components show a high variability among pathologists; and data increasingly suggest that NAS is poorly correlated with metabolic risk factors[103], is unable to predict fibrosis progression[104] and to prognosticate liver-related and overall mortality in NAFLD patients[93,94,105].

More recently, Bedossa and the FLIP Consortium created a simple histological algorithm (FLIP algorithm) based on a scoring system, the SAF score (Steatosis, Activity, Fibrosis) intended for pathologists to reliably diagnose NASH, assess disease severity and limit interobservervariation[40,99]. The SAF score separately assesses steatosis, activity and fibrosis. Activity, which ranges from 0 to 4, is derived from the combination of the semi-quantitative values of hepatocellular ballooning (0-2) and lobular inflammation (0-2). NASH according to the FLIP algorithm is diagnosed when steatosis, ballooning and lobular inflammation are all scored ≥ 1. The main discrepancy between NAS and SAF scores is that SAF does not include steatosis in the activity score, owing to the questionable role of steatosis per se as a marker of disease progression and prognosis. Moreover, fibrosis stage, the strongest predictor of outcomes in chronic liver disease, was not included in the NAS. This novel histological classification has shown excellent applicability and reproducibility among pathologists for the assessment of liver lesions in morbidly obese patients and in NAFLD patients with MetS[40,99]. However, it will have to undergo further validation in clinical practice. Table 1 shows the main features of NAS and SAF scores and highlights the main differences between these scoring systems.

Table 1

Main features and differences between Nonalcoholic Steatohepatitis Activity score and Steatosis, Activity, and Fibrosis score

	NAS	SAF
Scoring system	Steatosis + Lobular Inflammation + Ballooning: 0-8	Steatosis, Activity (Lobular Inflammation + Ballooning), Fibrosis: S0-3, A0-4, F0-4
Details of scoring	Steatosis	Steatosis
	0: < 5%	0: < 5%
	1: 5%-33%	1: 5%-33%
	2: 34%-66%	2: 34%-66%
	3: > 67%	3: > 67%
	Lobular inflammation	Lobular inflammation
	0:00	0:00
	1: < 2/20X	1: < 2/20X
	2: 2-4/20X	2: ≥ 2/20X
	3: > 4/20X
	Ballooning (number of ballooned hepatocytes)	Ballooning (size and shape of hepatocytes)
	0: None	0: normal hepatocytes
	1: Few	1: clusters, reticulated cytoplasm
	2: Many	2: enlarged hepatocytes
	Fibrosis stage	Fibrosis stage
	F0: None	F0: 0
	F1a: zone 3 perisinusoidal, delicate	F1: zone 3 perisinusoidal (all), or portal only
	F1b: perisinusoidal, dense	F2: zone 3 + portal
	F1c: portal only	F3: bridging
	F2: 1a or 1b + portal	F4: cirrhosis
	F3: bridging
	F4: cirrhosis

NAS: NASH activity score; SAF: Steatosis, Activity, and Fibrosis score; NASH: Nonalcoholic steatohepatitis.

Role of imaging techniques

Imaging methods are the most commonly used non-invasive tools for the diagnosis of steatosis. The main advantages of ultrasonography are its safety, low cost, wide availability and the overall scanning of abdominal organs. Traditionally, ultrasonography has been considered a technique with a low sensitivity in identifying fatty liver infiltration when less than 30% of hepatocytes are steatotic. Of note, a recent study has demonstrated that ultrasonography, especially when implemented with standardized measurements and semi-quantitative scores, is sensitive for an amount of steatosis as low as 10%[106] and may predict metabolic derangements and liver histology changes[106-108]. Further studies are necessary to confirm these novel findings. The main limitations of ultrasonography are its inability in differentiating steatosis from fibrosis, the issues with morbid obese individuals, and its operator and machinery dependency.

The controlled attenuation parameter (CAP) is a new promising screening method that measures ultrasound attenuation in the liver using signals obtained by the Vibration Controlled Transient Elastometry (TE) (Fibroscan®). Interestingly, CAP appears to be more sensitive in detecting lesser degrees of steatosis compared to other widely available imaging methods. Moreover, being coupled with liver stiffness measurements, it has the advantage of simultaneously estimating liver fibrosis[108-110]. However, the underlying disease, BMI and T2D may affect the findings and thus must be taken into consideration in the interpretation of CAP results[111].

Over the last 10 years, several ultrasound elastographic techniques have been implemented, including TE, acoustic radiation force impulse (ARFI) elastography, 2D shear-wave elastography and real-time strain elastography. TE, is the most studied elastographic method for the estimation of liver fibrosis in chronic liver disease; in NAFLD, TE can be used to confidently rule out severe fibrosis and cirrhosis (with a nearly 90% negative predictive value) and for monitoring disease progression[11,112]. Of note, the amount of steatosis has emerged as a significant factor affecting the performance of liver stiffness measurements with TE[112,113]. For this reason, it has been suggested that taking into account CAP values may improve the prediction of liver fibrosis by TE[113].

Magnetic resonance imaging techniques, and particularly magnetic resonance spectroscopy, are able to accurately quantify liver fat content; the advantages include high sensitivity for assessing small amounts of intrahepatic triglycerides and sampling a large liver volume[114]. More recently, magnetic resonance elastography and multiparametric magnetic resonance offer the possibility of performing a thorough characterization of liver tissue by assessing steatosis, fibrosis and haemosiderosis at the same time[115,116], and have been shown to be able to predict clinical outcomes in patients with various chronic liver disease, notably including NAFLD[117]. Cost and limited availability, however, restrict their use to research purposes.

Performance and limitations of biomarkers

Several serum biomarker panels have been developed for predicting steatosis, diagnosing NASH and estimating fibrosis[118] which are, in theory, the preferred diagnostic tool for large-scale screening and epidemiological studies on NAFLD[4,38]. For example, Bedogni’s Fatty Liver Index (FLI) has been largely used to capture steatosis in epidemiological studies[119]. The strength of FLI as a surrogate marker comes from the demonstration that it can predict clinical outcomes related to the MetS, such as risk of T2D, accelerated atherosclerosis and cardiovascular risk, as well as hepatic, cardiovascular and cancer-related mortality[120,121]. While clinically relevant, these associations might be conveyed independently of steatosis per se since FLI incorporatesvariables that are part of the MetS phenotype[101]. In fact, recent studies have found only a limited correlation between FLI and the amount of liver fat per se, as defined by liver biopsy or magnetic resonance spectroscopy[101,122,123]. As for the FLI, other steatosis biomarkers, such as the NAFLD liver fat score, the Hepatic Steatosis Index and the Lipid Accumulation Product, generally show good performance in identifying steatosis, though they are unable to predict liver fat content and are confounded by hepatic histological changes other than steatosis, mainly necro-inflammation and fibrosis[101,123].

With regard to the possibility of non-invasively differentiating NASH from simple steatosis, several biomarkers (acute-phase proteins, cytokines, markers of oxidative stress and apoptosis, as is the case of cytokeratin-18 fragments) and multiple complex models have been investigated, but the majority of them lack external validation, have only been tested among selected populations and have been inconsistent in their performance of detecting NASH[102,118].

Several simple non-invasive fibrosis scoring systems, notably including NAFLD Fibrosis Score and Fib-4 can, however, reliably exclude advanced fibrosis in a high proportion of NAFLD patients, allowing a more targeted use of liver biopsy[124]. Their use in clinical practice is recommended by updated hepatological guidelines[4,38], and they reliably predict liver-related and cardiovascular complications and death in NAFLD patients[125-127]. However, they were principally developed and validated in patients aged < 65 years of age, hence their cut-offs need to be adapted in the elderly[128]. It has been shown that the combination or the sequential use of different scoring systems or different non-invasive techniques (TE plus biomarker) improve the diagnostic accuracy in detecting severe liver fibrosis, thus further reducing the need for liver biopsy[129,130].

Recently, several miRNAs[131], epigenetic biomarkers[132], lipidomic[133,134], metabolomics[135] and proteomic[136] profiles have been found differently expressed in NAFLD patients and could be used as surrogate markers of progressive liver injury. Probably, a multi-domain, multi-component approach which integrates variables from a diverse set of data sources deriving from phenotypic, genomic, lipidomic, metabolomic and proteomic domains will be the avenue for future investigations in the noninvasive assessment of NAFLD[136,137].

NAFLD: CLINICO-LABORATORY FEATURES

Usually asymptomatic, NAFLD is a phenotypically polymorphic disease which, owing to its systemic nature, has a variable clinical presentation, a multitude of potentially associated disease and a rich spectrum of laboratory features[4,12,138]. Understanding this remarkable phenotypic polymorphism is key in guiding the diagnostic process in the individual patient.

Most patients will seek medical advice on the grounds of otherwise inexplicably deranged liver tests/ultrasonographic findings compatible with fatty changes. Collectively, these laboratory/ultrasonographic abnormalities tend to be often discovered either during routine medical check-up performed by asymptomatic individuals or by patients who have nonspecific and causally unrelated complaints[139,140].

Insulin resistance, hyperuricemia and atherogenic dyslipidemia

The association of NAFLD with IR and its close connection with the MetS was independently reported by three unrelated groups of investigators as early as 1999[141-143]. In particular, Marchesini et al[141] by comparing 46 patients with NAFLD to 92 age and sex-matched healthy controls with the homeostasis model assessment method found that NAFLD was associated with IR and hyperinsulinemia even in lean subjects with normal glucose tolerance. Consistently, Cortez-Cortez-Pinto et al[142] in 30 patients with NAFLD found that 80% were either obese or dyslipidemic; 50% had arterial hypertension and 33% T2D; moreover, glucose metabolism was altered in 69% and hyperinsulinemia and hyperleptinemia were common. Along the same line, Lonardo, based on his systematic search of the available literature, concluded that fatty liver most commonly affected middle-aged men with obesity, altered glucose metabolism, hyperlipidemia, and hypertension[143].

Over time, these pioneer studies suggesting an intimate connection of NAFLD with IR and the MetS have extensively been confirmed and carried further. For example Ballestri et al[144] have recently shown that HOMA-IR, a widely used index of IR, along with serum uric acid concentrations, is an independent predictor of both steatosis and ballooning; waist circumference predicts both ballooning and hepatic fibrosis[144]. Moreover, the same group of investigators, also found that baseline NAFLD predicts the development of incident T2D and MetS over a median 5-year follow-up[22]. Taken collectively, these findings strongly support the notion that NAFLD should no longer be considered a mere “hepatic manifestation of the MetS” but rather, and more appropriately, both a precursor and a consequence of the MetS[21,31,145-147].

Lonardo et al[139] were first in reporting that both fasting insulin (a sensitive marker of IR) and uric acid were independent predictors of NAFLD. These findings have been independently confirmed by several studies[148-152], including two meta-analytic reviews[153,154]. Of interest, although serum uric acid concentrations are associated with indices of IR, both parameters are independently associated with NASH, at least in children and adolescents[155], suggesting that each probably carries an independent contribution to the development of progressive liver disease.

NAFLD is typically characterized by atherogenic dyslipidemia featuring larger and triglyceride over-enriched circulating very-low-density lipoproteins (VLDLs), small dense low-density lipoproteins (LDLs) and low and dysfunctional high-density lipoproteins (HDLs). Of note, when NAFLD progresses to severe fibrosis and cirrhosis, dyslipidemia will apparently improve, probably owing to failing hepatic synthetic capacity[144,156-159].

Liver tests, parameters of iron metabolism and non-organ specific autoantibodies

Liver tests are typically normal or mildly elevated in NAFLD. Gamma-glutamyltransferase (GGT) may be slightly elevated and is increasingly recognized as a marker of metabolic disturbances and cardiovascular risk[160]. Aminotransferases do not identify progressive disease, given that patients with normal liver enzymes are spared neither from NASH nor significant fibrosis[161].

The diagnostic process followed to investigate a suspect liver disease may include the determination of parameters of iron metabolism and non-organ specific autoantibodies (NOSA). Elevated serum ferritin, closely associated with hepatic iron deposition, is common in NAFLD and is strongly correlated with IR, more advanced disease and increased mortality[162-164]. Whether therapeutic strategies aimed at correcting iron metabolism may be beneficial in NAFLD remains controversial.

It is important to highlight that the positivity of NOSA, in the appropriate clinical and epidemiological context, is compatible with NAFLD. Loria et al[165], in their pilot study, were first in reporting that NOSA positivity in NAFLD was more prevalent than in the general population and that high-titer ANA was associated with IR. Bringing this line of research further, the clinical research network, in a multicenter study including a total of 864 NAFLD patients found that NOSA are frequently positive in NAFLD in the absence of autoimmune hepatitis and their occurrence is not associated with more advanced histological features[166].

NAFLD AS A MULTISYSTEM DISEASE: CARDIO-METABOLIC AND CANCER RISK

As early as 1995, was it first suggested that NAFLD was a systemic condition with a specific cardio-metabolic involvement[167], a notion which is now universally accepted[12,168].

In particular, our understanding of the close and mutual relationship of NAFLD with the MetS has evolved and the bidirectional relationship among the two conditions is now largely acknowledged (Figure 3)[4,31,146,147]. IR, in its turn, will drive the course of liver disease to progressively fibrosing liver disease culminating with cirrhosis, but also promote the development of T2D[169]. NAFLD almost doubles the risk of incident T2D[22]. However, NAFLD patients usually die of extra-hepatic causes, frequently for cardiovascular diseases, which underpins the importance to early diagnose and aggressively treat CVD risk factors, as extensively discussed elsewhere[170]. A meta-analysis of 27 cross-sectional studies has shown a robust association between NAFLD and several markers of subclinical atherosclerosis burden, such as an increased risk, independent of classical CVD risk factors, of coronary artery calcification, carotid intima-media thickness, impaired flow-mediated vasodilatation and arterial stiffness[171]. Moreover, studies have shown that NAFLD is also associated with increased risk of atrial fibrillation and aortic valve sclerosis[172-175].

Figure 3

The closed loop nonalcoholic fatty liver disease-metabolic syndrome circuit. Schematic representation illustrating the mutual cause-and-effect relationship of NAFLD with the Metabolic syndrome[4,31,146,147]. NAFLD: Nonalcoholic fatty liver disease; NASH: Nonalcoholic steatohepatitis.

While cardiovascular mortality is the leading cause of death in NAFLD patients, malignancies, mainly affecting the gastrointestinal tract (liver, colon, esophagus, stomach, and pancreas) and extra-intestinal sites (kidney in men, and breast in women) rank second[176,177]. The association between NAFLD and colorectal cancer (CRC) has been investigated: some studies have shown a higher prevalence of CRC in NAFLD population than patients without, and this association is increased in presence of NASH[178].

NAFLD AND T2D: A DANGEROUS COMBINATION

T2D accounts for more than 90% of those 415 million people worldwide who live with diabetes; T2D may lead to micro-macrovascular complications that cause profound sufferings and put a heavy burden on health-care systems worldwide[179].

The common soil and the mutual relationship

The prevalence of NAFLD is increased among those with T2D and T2D rescinds the typical gender dimorphism of NAFLD[7,180,181]. Conversely, NAFLD is associated with a 2-to-5-fold risk of developing T2D after adjustment for several metabolic confounders[22,169,182].

Common features in the epidemiology, risk factors and natural history of NAFLD and T2D can be identified: overweight and obesity[183-185]; a hypercaloric diet coupled with a sedentary behavior leading to weight gain[186,187]; IR and MetS components, including combined dyslipidemia[147,188].

As previously highlighted, NAFLD is not only a consequence, but also a cause of T2D and MetS generating a “vicious circle” and worsens the course of T2D[21,24,31,189]. It is mandatory to interrupt this circle and in this regard, it is encouraging that even transient remission/improvement of NAFLD is independently associated with reduced incidence of T2D[190,191].

The consequences of the association

T2D and NAFLD interact in enhancing the risk of promoting endothelial dysfunction, atherosclerosis, cardiovascular diseases, chronic kidney disease and advanced retinopathy[21,168,192,193]. The coexistence of T2D and NAFLD predicts the development of hepatic fibrosis[194-198]. Treatment of NAFLD, by affecting those pathogenic factors linking fatty liver with atherosclerosis (hence the so called “atherogenic liver”) was predicted to be able to reduce cardiovascular risk a few years ago[199]. Consistent with such a prediction, a recent study reported that reduced CIMT progression in the entire cohort of 92 patients was independently associated with decreased liver fat content assessed with magnetic resonance spectroscopy[200].

T2D and NAFLD are also associated with an increased incidence and mortality from several cancer types and, similarly, mortality for malignancies is the second cause of mortality in patients with NAFL[178,201-203]. Similar to NAFLD, T2D enhances the risk of developing HCC and may aggravates HCC outcomes[204-206].

NAFLD in those with T2D will follow a worse prognosis via hastened progression to NASH, liver cirrhosis and its complications and increased risk of developing NAFLD-HCC[43,207-210]. Specularly, concurrent NAFLD will often worsen the course of T2D[211].

Diagnostic issues

An early diagnosis and treatment of NAFLD may potentially increase life expectancy of T2D patients[209]. Conversely, in subjects with NAFLD, periodical screening for T2D is encouraged, given that poor metabolic control will lead to progressive liver disease which,in its turn, is associated with enhanced cardiometabolic risk[38,193,212].

NAFLD: A LARGE SPECTRUM OF CLINICAL ASSOCIATIONS

An impressively heterogeneous spectrum of clinical conditions have been associated with NAFLD spanning from carotid atherosclerosis through polycystic ovarian syndrome[23]. Some will be shortly reviewed here; others have recently been covered in detail elsewhere[4,213,214].

Atherosclerosis and gallstones

A pioneer study by Lonardo et al[215] evaluated the triangular association of NAFLD, gallstones and atherosclerosis. A decade later, we now know that the most severe NAFLD forms are strongly associated with excess cardiovascular mortality, probably as a direct/indirect result of hepatic fibrosis[193,212]. Concerning the NAFLD-gallstone duo, a systematic review and meta-analysis conducted in 12 observational studies (9 cross-sectional studies, 2 cohort studies and 1 case-control study) found that gallstones are significantly associated with NAFLD[216]. Further studies should be conducted regarding the underlying mechanism of this association. However, it is now clear that bile acids are no longer “a detergent which facilitates the absorption of fatty foodstuffs” such as it was deemed in the past; but rather, they must be regarded as signaling molecules, which coordinately regulate metabolism and inflammation acting not only in entero-hepatic tissues, but in peripheral organs as well[217].

Psoriasis

This line of research was almost anecdotally inaugurated by a report of three cases from the POLI.ST.E.N.A study[218]. Several systematic studies have subsequently confirmed this novel association and a recent systematic review and meta-analysis supports an association between psoriasis and NAFLD suggesting that screening for NAFLD may be warranted among those with psoriasis[219].

Endocrine derangements

Again, this topic was originally initiated by pioneer clinical observations. First, it was reported that endocrine derangements may eventually be conducive to NAFLD as a result of hormones being master regulators of body fat distribution and cell metabolism[220]. Next, endocrine pathways specifically leading to NASH were identified[221]. Among these, hypothyroidism has been associated to the whole NAFLD spectrum, steatosis to NASH-HCC[156,221-224].

A large Rotterdam population-based survey, aimed at investigating the association between variations in thyroid function and NAFLD, prospectively, in 9419 adults with a median follow-up time of 10 years; the presence of fibrosis in those with NAFLD was assessed with TE[225]. Data have shown that, compared to euthyroid individuals, hypothyroid ones were exposed to a higher risk of NAFLD and of clinically relevant fibrosis; consistently, on the opposite side of the spectrum, hyperthyroidism was associated with a protection from developing NAFLD[225]. These findings may potentially disclose novel treatment strategies.

NAFLD: PRINCIPLES OF TREATMENT

It is widely accepted that lifestyle changes, namely diet and physical exercise are the mainstay of treatment of NAFLD, a condition no drugs are specifically licensed for[4,38].

Diet

A 3%-5% weight loss will improve steatosis; however, 5%-7% reductions are necessary to decrease hepatic inflammatory changes and 7%-10% to obtain remission of NAFLD/NASH and regression of fibrosis. Calorie restriction per se rather than specific diets are deemed to be beneficial[226]. In particular, despite emphasis is usually put in restricting dietary carbohydrates, moderate-carbohydrate diets do not induce a more profound reduction in liver enzymes (a non-validated surrogate index of NAFLD severity) than low/moderate-fat diets[227].

Physical exercise

Exercise effectively reduces visceral and perhaps liver fat. A recent meta-analysis found that aerobic exercise but not resistance training exercise was effective in reducing visceral fat in overweight/obese adults with T2D[228]. The benefits of exercise in reducing intrahepatic triglyceride content will typically occur with minimal or no body weight loss[227,229], suggesting that diet and physical exercise will improve NAFLD and should be associated whenever possible given that they act via different pathways. Indeed, diet combined with exercise is associated with improvement in NAFLD activity score[227].

Drugs

Drug treatment (better if within the frame of a clinical trial) should be reserved to those NASH individuals who do not respond to lifestyle changes. Drugs used to treat concurrent metabolic disorders (e.g., statins and antidiabetics) should be differentiated from drugs aimed at treating NASH per se.

Statins, glitazones and liraglutide belong to the first group. Our appreciation of the role of statins in hepatology has undergone a dramatic evolution from under-prescription based on fears of hepatotoxicity[230] to their identification as potentially protectors from the full spectrum of liver damage in NASH, notably including liver fibrosis and HCC[231-238].

As regards the oral antidiabetic agents glitazones, a meta-analysis of five eligible randomized controlled trials showed that these drugs improved neither fibrosis nor IR; however, lobular inflammation decreased in NASH patients who received TZD treatment[239]. However, a more recent meta-analytic review was specifically aimed at investigating the role of thiazolidinediones in advanced hepatic fibrosis in those with NASH analyzed 8 RCTs (5 evaluating pioglitazone and 3 evaluating rosiglitazone) enrolling 516 patients with biopsy-proven NASH for a duration of 6 to 24 mo. Among all studies combined, thiazolidinedione therapy was associated with improved advanced fibrosis, fibrosis of any stage and NASH resolution. Analyses restricted to RCTs enrolling patients without diabetes yielded similar results. All effects were accounted for by pioglitazone use[240]. Weight gain and lower limb edema occurred more frequently with thiazolidinedione therapy[240]. These novel data indicate that pioglitazone improves advanced fibrosis in NASH, even in patients without diabetes.

A phase 2 randomized study conducted on 52 patients (26 per arm) tested the efficacy of liraglutide (1.8 mg/daily via subcutaneous route) vs placebo. The use of liraglutide was associated with a 39% NASH resolution rate vs 9% in the placebo arm (RR = 4.3, 95%CI: 1.0-17.7, P = 0.019). This study was funded by the manufacturers of liraglutide[241].

A few drugs, such as vitamin E and obeticholic acid (OCA) have specifically been tested against NASH. Based on a meta-analysis of five RCTs vitamin E significantly reduced liver enzymes (AST, ALT, ALP); steatosis, inflammation and hepatocellular ballooning compared to the control group. Vitamin E treatment in adult NASH was also associated with reduction of fibrosis[242]. Concerns have been raised, however, on the long-term safety of Vitamin E and the lack of data in patients with T2D and cirrhosis. A network meta-analysis found that pentoxyphylline and OCA improve fibrosis, and vitamin E, TZDs, and OCA improve ballooning degeneration in patients with NASH[243]. A subsequent network meta-analysis substantially confirmed these findings by showing that OCA significantly improves fibrosis, while vitamin E and TZDs result in a significant increase in NASH resolution[244]. Table 2 compares the findings from the above two meta-analytic studies[243,244].

Table 2

Drugs useful in treating nonalcoholic steatohepatitis - A neck-to-neck comparison of findings from two different meta-analytic studies

	Sawangjit et al[244]	Singh et al[243]
Fibrosis	OCA1 improves fibrosis.PTX2, TZDs plus Metformin2, TZDs plus Losartan2 might potentially be effective.	PTX1 and OCA1 improve fibrosis
Resolution of NASH	TZDs1 and Vitamin E1 use is associated with resolution of NASH	Vitamin E1, TZDs1, and OCA1 improve ballooning degeneration
NAS	PTX1, OCA1, vitamin E1, and TZDs1 improve NAS
Steatosis		PTX1, Vitamin E2, TZD1 and OCA2 significantly improve steatosis
Lobular inflammation		PTX1, TZDs1 and OCA2 significantly improve lobular Inflammation

High quality of evidence;

Moderate quality of evidence. NASH: Nonalcoholic steatohepatitis; NAS: NASH activity score; OCA: Obeticholic acid; PTX: Pentoxyphylline; TZDs: Thiazolidinediones.

Thinking out of the box. Innovative treatment strategies

Further to the above discussed notions on the relationship of the entire NAFLD spectrum with endocrine and metabolic derangements, a line of innovative treatment options can be envisaged. For example, administration of thyroid receptor agonists (GC-1 and KB2115) improves NAFLD in a ob/ob mouse model and a xantine oxidase inhibitor (febuxostat) antagonizes the development of disease in a rodent NASH model[245,246].

Also our understanding of the role of nuclear receptors in the pathogenesis and natural course of NAFLD may lead to novel treatments[15]. The above-mentioned OCA exerts its effects by agonizing FXR. Elafibranor, a dual PPAR-α/δ agonist, has been shown to resolve NASH without fibrosis worsening and to improve the cardiometabolic profile in a recent phase 2 randomized trial of patients with NASH[247]. Oltipraz is a synthetic inhibitor of LXR-α whose antisteatosic properties have previously been shown in a mouse model. A recent phase 2 randomized controlled trial found that, in patients with NAFLD, a 24-wk course of oltipraz significantly reduced intrahepatic fat content assessed with magnetic resonance spectroscopy in a dose-dependent manner; however IR, liver enzymes, lipids and cytokines were unaltered[248].

CONCLUSION

NAFLD is an emerging multifaceted systemic disease with a heavy epidemiological burden. Further to hepatic risks, NAFLD also affects cardiovascular, metabolic, renal and endocrine systems as well as cancer development with a significant hepatic and extra-hepatic impact on morbidity and mortality[4]. The bi-directional relationship between NAFLD and MetS-T2D is an important emerging topic underpinning the mutual influence and the need to interrupt the vicious circle associating liver and dysmetabolism. However, we now know that IR is a necessary though not sufficient requisite of the development of NAFLD and that gender, genetic background and microbiota also play a major role[4,14]. It is anticipated that pathogenic complexity and multi-factoriality will have to be translated into more finely tailored diagnostic and treatment strategies. This implies that “ad hoc” studies are necessary to more precisely identify the individual target populations to be addressed. Presently, lifestyle changes effected via dietary restrictions and physical exercising remain the only recommended treatment of NAFLD; in all overweight/obese patients, weight loss is mandatory[4]. However, given that only a small minority of such individuals will succeed in maintaining their ideal body weight, and that no currently marketed drugs are specifically licensed for NASH, data of ongoing studies are eagerly awaited to offer these numerous and heterogeneous patients effective and safe tailored drug treatment options.