Evidence-based clinical practice guidelines for nonalcoholic fatty liver disease/nonalcoholic steatohepatitis 2020

1Nonalcoholic fatty liver disease (NAFLD) has become the most prevalent cause of chronic liver disease worldwide and is now the fastest-growing indication for liver transplantation among waitlist registrants. There are more than 20 million NAFLD patients in Japan, and it is feared that this number will increase in the future. In recent years, hepatocellular carcinoma (HCC) based on non-viral liver disease has increased, and the need for a screening method has become urgent.

2The Japanese NAFLD/NASH guidelines were established in 2014. These clinical guidelines have received considerable attention and been widely used. However, new knowledge has since been reported relating to their concepts, diagnostic imaging methods, and treatment methods. Therefore, a joint committee of the Japanese Society of Gastroenterology and the Japanese Society of Hepatology has reviewed and revised these guidelines.

3The current guidelines summarize reports from 1983 to the end of October 2018, focusing on the following: (1) concept and clinical significance of liver fibrosis, (2) screening and follow-up systems for liver fibrosis, (3) surveillance of HCC, (4) a system for consultation with specialists regarding cardiovascular risk in NAFLD, and (5) new therapeutics. We hope that these guidelines will be used widely in clinical practice, and also hope to discuss and improve any problems that may arise in the clinical field so that further revisions may be made as necessary.

4In the 2014 guidelines, NAFLD was characterized by evidence of hepatic steatosis by either imaging or histology and the appropriate exclusion of other liver diseases. NAFLD is histologically characterized by macrovesicular steatosis and further categorized into nonalcoholic fatty liver (NAFL) and nonalcoholic steatohepatitis (NASH). In the revised guidelines, the concept and diagnosis of NAFLD are essentially the same (Table 1).

5NAFLD is characterized by evidence of hepatic steatosis as determined by either imaging or histology, associated with any metabolic factor. Other liver diseases, such as alcoholic liver disease, viral liver disease, and drug-induced liver disorder, are excluded.

6The European Association for the Study of the Liver (EASL) defines NAFLD as being characterized by “excessive hepatic fat accumulation associated with insulin resistance (IR)”. In Japan, 60–70% of NAFLD cases are complicated with diabetes mellitus or IR, while others may be complicated with obesity, hypertension, or dyslipidemia without IR. Therefore, we defined NAFLD as “hepatic steatosis associated with any metabolic factor.” Another issue is NAFL progression. McPherson et al. report that of 27 NAFL patients, 12 (44%) had progressed to NASH at the second biopsy. NAFL and NASH are not completely different diseases; there is a certain amount of overlap. Therefore, we specifically state in the guidelines that “NAFL and NASH are not completely different diseases. Some NAFL patients show slow progression of hepatic fibrosis.” In addition, the American Association for the Study of Liver Diseases (AASLD) and EASL management guidelines state that hepatic steatosis induced by drugs should be excluded from NAFLD. We, therefore, specify that “hepatic steatosis induced by drugs is treated as a drug-induced liver disorder, not as NAFLD.”

7After the publication of the 2014 guidelines, many cohort studies demonstrated that hepatic fibrosis, but no other histological features of NAFLD, was associated independently with long-term overall mortality, liver transplantation, and liver-related events in NAFLD patients. Therefore, we added the following statement to the revised guidelines: “the most important factor in the prognosis is hepatic fibrosis, and follow-up and treatment methods should be selected depending on the degree of hepatic fibrosis.”

8We also added new clinical questions (CQs).

9The stage of hepatic fibrosis is strongly associated with both total and liver-related mortalities. It is important to evaluate the grade of hepatic fibrosis in NAFLD patients. (Evidence Level A, Strength 1).

10The stage of hepatic fibrosis is strongly associated with both total and liver-related mortalities. It is important to evaluate the grade of hepatic fibrosis in NAFLD patients. (Evidence Level A, Strength 1).

11There is currently no overall flowchart for the screening and follow-up of hepatic fibrosis, HCC, or cardiovascular disease (CVD). As noted, the most important factor in the prognosis is hepatic fibrosis. We, therefore, propose that the first step on the flowchart be a screening system for NAFLD by a general physician (Fig. 1). Castera et al. report that simple inexpensive and widely available serum biomarkers, such as the FIB-4 index or the NAFLD fibrosis score (NFS), which have a high negative predictive value for ruling out advanced fibrosis, should be used as the first line. Patients with low risk of advanced fibrosis (FIB-4 < 1.3 or NFS < − 1.455) do not need further assessment, while liver stiffness should be measured by vibration-controlled transient elastography (VCTE) in those with intermediate risk (FIB-4 = 1.3–3.25 or NFS = − 1.455–0.672) or high risk (FIB-4 > 3.25 or NFS > 0.672).

12Following Castera et al., we propose a screening method for NAFLD with hepatic fibrosis by a general physician (Fig. 1). At the first screening for NAFLD, physicians are recommended to measure serum hepatic fibrosis markers, such as hyaluronic acid, Type IV collagen 7S, Mac-binding protein glycosylation isomer, and to use a fibrosis scoring system such as the FIB-4 index, NFS, or platelet count. If any data indicate liver fibrosis, consultation with a gastroenterology specialist should be considered.

13Figure 2 is a flowchart of the next screening, to be conducted by a gastroenterology specialist. First, the FIB-4 index or NFS is calculated. If the FIB-4 index is under 1.3 or the NFS is under − 1.455, the patient is at low risk of having fibrosis and should repeat the evaluation every 1 year. If moderate hepatic fibrosis (FIB-4 index of 1.3–2.66 or NFS of − 1.455–0.674) is suspected, liver biopsy or VCTE or magnetic resonance elastography (MRE) should be considered. If severe hepatic fibrosis (FIB-4 index: ≥ 2.67 or NFS: ≥ 0.675) is suspected, liver biopsy or elastography is recommended and, depending on fibrosis stage or liver stiffness, surveillance and therapy may be considered. The most important point is to evaluate hepatic fibrosis stage by liver biopsy, elastography, or some other method.

14Regarding HCC surveillance, we recommend that in NAFLD with F0-1, the evaluation for fibrosis stage should be performed after 1 year without HCC screening. In male NAFLD with F2 or F3 and female NAFLD with F3, patients have a mild risk of HCC and abdominal ultrasound (US) should be considered every 6–12 months.

15HCC screening should be performed by US and tumor markers every 6 months in NAFLD with liver cirrhosis (LC; F4). However, the best screening method in terms of cost and manpower remains to be determined. Loomba et al. recently reported on the American Gastroenterological Association (AGA) Clinical Practice Update on screening and surveillance for HCC in patients with NAFLD. Screening for HCC should be considered in patients with LC or advanced fibrosis. In the revised guidelines, we have added new CQs regarding HCC follow-up and screening in NAFLD/NASH patients.

16Depending on the grade of hepatic fibrosis, it is important to follow-up not only liver-related events, but also CVD and extrahepatic malignancies. (Evidence Level A, Strength 1).

17Depending on the grade of hepatic fibrosis, it is important to follow-up not only liver-related events, but also CVD and extrahepatic malignancies. (Evidence Level A, Strength 1).

18HCC screening should be performed depending on the stage of hepatic fibrosis and risk factors for HCC. However, the best screening method in terms of cost and manpower remains to be determined. (Evidence Level C, Strength 2).

19HCC screening should be performed depending on the stage of hepatic fibrosis and risk factors for HCC. However, the best screening method in terms of cost and manpower remains to be determined. (Evidence Level C, Strength 2).

20In terms of HCC risk factors, old age, male, advanced fibrosis, diabetes, and moderate alcohol intake have been reported to be risk factors for NAFLD-HCC.

21CVD, the most common death etiology in NAFLD patients, is another issue. Francque et al. reported the screening method for CVD in NAFLD patients. It is important to note that NASH and NAFLD with hepatic fibrosis increase the risk of cardiovascular event. In cases with hepatic fibrosis, CVD screening is recommended.

22Therefore, we propose the flowchart for cardiovascular event screening in NAFLD patients shown in Fig. 3. We first check for CVD complications and/or a past history of CVD, and perform an electrocardiogram (ECG). If any abnormality is found, we then consult a specialist in cardiology or neurology. In NAFLD with a reduced platelet count or increased FIB-4 index, we should evaluate risk based on cardiovascular examination, such as loaded ECG and/or US of the carotid artery. CQ5-3 concerns cardiovascular events in NAFLD patients.

23In NAFLD/NASH, cardiovascular events are increased, especially in the advanced hepatic fibrosis group. Examination for and evaluation of CVD should be considered in NAFLD patients with advanced fibrosis. (Evidence Level A, Strength 1).

24In NAFLD/NASH, cardiovascular events are increased, especially in the advanced hepatic fibrosis group. Examination for and evaluation of CVD should be considered in NAFLD patients with advanced fibrosis. (Evidence Level A, Strength 1).

25The reported prevalence of NAFLD varies widely depending on the population studied and the definition or method used. Age, gender, and ethnic differences have an effect on both the prevalence and severity of NAFLD/NASH. These differences are also seen in the prevalence of obesity and metabolic syndrome. The prevalence of NAFLD is reported to be 20–40% in Western countries and 12–30% in Asian countries. Annual health checkup data show that 9–30% of Japanese adults have US-diagnosed NAFLD, and NASH is diagnosed in 10–20% or more of NAFLD cases. The estimated prevalence of NASH is approximately 3–5% worldwide. NAFLD/NASH is predominantly diagnosed in middle-aged men and postmenopausal women. A Markov model has estimated there to be approximately 22,600,000 NAFLD patients in Japan and 3,700,000 NASH patients, and by 2030, the prevalence of NASH and advanced fibrosis will have increased.

26Regarding the rate of HCC development from NAFLD, Younossi et al. report global data showing that the incidence of HCC among NAFLD and NASH patients is 0.44 per 1000 person-years (range 0.29–0.66) and 5.29 per 1000 person-years (range 0.75–37.56), respectively. It is higher in LC due to NAFLD, at 2–3% per year.

27Given the important role of insulin resistance and oxidative stress in the pathophysiology of NAFLD/NASH, several studies have attempted to investigate their effects.

28The I148M variant of patatin-like phospholipase domain-containing 3 (PNPLA3) is widely known to be associated with the occurrence and progression of NAFLD/NASH worldwide. The mechanism remains unknown, however, it has been suggested that the 148M variant disrupts ubiquitylation and proteasomal degradation of PNPLA3, resulting in an accumulation of PNPLA3-148M and impaired mobilization of triglycerides (TGs) from lipid droplets (LDs). There is known to be a significant association between HCC and the 148M variant. TM6SF2, GCKR, GATAD2A and DYSF have been reported as genomic background candidates. In addition, there has been a recent focus on the relationship between NAFLD and gut dysbiosis. Henao-Mejia et al. found that inflammasome-mediated dysbiosis regulates the progression of NAFLD and obesity, however, a more detailed analysis using human samples is needed. Sarcopenia has also been examined.

29The diagnosis of NAFLD is described as part of the concept and definition of NAFLD (Table 1). ‘‘Nonalcoholic’’ is defined as an upper limit of alcohol drinking of 30 g/day in males and 20 g/day in females. NASH is diagnosed from liver biopsy on the basis of the presence of steatohepatitis, however, liver biopsy has several drawbacks. It is an expensive and invasive procedure and there is potential for sampling error and variability in interpretation by pathologists. However, liver biopsies remain the gold standard for the diagnosis of NASH and are, therefore, often recommended, particularly in NAFLD with suspected advanced fibrosis and in suspected coexisting chronic liver disease, where there is a need to distinguish NASH from other chronic liver diseases.

30Regarding the noninvasive assessment of NASH and advanced fibrosis, there are no practically useful surrogate markers for diagnosing NASH. Platelet count and scoring systems such as the NFS and the FIB-4 index have proven to be useful for predicting fibrosis in the Japanese population and worldwide. However, care must be taken, because age is one of the factors in the FIB-4 index, and higher FIB-4 index titers in older patients do not necessarily reflect actual liver stiffness or fibrosis grade.

31A number of imaging modalities can detect liver fat and liver stiffness, including VCTE, which measures liver stiffness noninvasively, has shown promising results for assessing the severity of liver fibrosis. Recently, MRE was found to have statistically significantly higher diagnostic accuracy than VCTE in the detection of each stage of fibrosis. MRE and VCTE each have a role to play in the detection of fibrosis in patients with NAFLD, depending on the level of accuracy desired.

32Figure 4 is a flowchart of therapy for NAFLD patients. It is similar to that in the previous guidelines. NAFLD is usually associated with metabolic disturbance such as visceral obesity, insulin resistance, type 2 diabetes mellitus, or dyslipidemia, and these underlying conditions play a crucial role in its pathogenesis. Therefore, it makes sense to treat not only the liver disease itself but also these associated metabolic morbidities, and it is likewise essential to prevent stimulation or pathogenesis of these diseases, so-called “2nd hits,” in the management of NAFLD/NASH. Treatments for these associated conditions include lifestyle modification, weight loss, and increased physical activity, all of which have been shown to be effective and represent the cornerstone of treatment.

33Lifestyle-related interventions such as diet and exercise therapies have been reported to improve serum transaminase levels as well as liver fat as measured by US and magnetic resonance imaging (MRI) in NAFLD patients. Musso et al. evaluated the effects of weight loss in NAFLD in eight randomized controlled trials, four of which included posttreatment histology. Their meta-analysis showed that a 5% or greater weight loss improved hepatic steatosis, and a 7% or greater weight loss correlated with improvement in the NAFLD Activity Score (NAS). Unfortunately, only 50% of subjects were able to attain a weight loss of 7% or greater even with significant intervention. Vilar-Gomez et al. evaluated the effects of weight loss through lifestyle modifications in 261 patients with paired liver biopsies, finding that the degree of weight loss was associated independently with improvements in all NASH-related histology. Furthermore, for those individuals who lost 10% or more of their body weight, 45% experienced regression of fibrosis, 90% had resolution of steatohepatitis, and 100% demonstrated improvements in NAS. These findings indicate the effectiveness of body weight reduction for patients with obesity-related NAFLD/NASH. In almost all reports of dietary interventions for patients with obesity-related NAFLD, a low-calorie diet is prescribed and, in terms of dietary contents, the proportions of energy intake from carbohydrates and lipids are often restricted to 50–60% and 20–25%, respectively. Recent attention has focused on low-carbohydrate and Mediterranean diets, and coffee intake has been reported to inhibit hepatic fibrosis and hepatocarcinogenesis.

34Exercise therapy is another useful lifestyle-related intervention for NAFLD/NASH. Consistent aerobic exercise in 30- to 60-min sessions held 3–4 times weekly for 4–12 weeks in patients with NAFLD complicated by obesity has been shown to improve liver fat content, even without accompanying body weight reduction. Oh et al. report that physical activity of moderate to vigorous intensity for ≥ 250 min/week as part of lifestyle management improves NAFLD pathophysiology in obese men in Japan. The benefits seem to be acquired through reducing inflammation and oxidative stress levels and altering the fatty acid metabolism. While these reports do not examine histological changes, liver fat are thought to improve even with exercise therapy alone.

35Body weight reduction through a low-calorie diet improves liver function and fatty changes in the liver in patients with NAFLD. To improve NAFLD/NASH, we recommend prioritizing the optimization of energy intake and restricting lipids or carbohydrates in terms of the proportions of nutrient intake. (Evidence Level C, Strength 2).

36Body weight reduction through a low-calorie diet improves liver function and fatty changes in the liver in patients with NAFLD. To improve NAFLD/NASH, we recommend prioritizing the optimization of energy intake and restricting lipids or carbohydrates in terms of the proportions of nutrient intake. (Evidence Level C, Strength 2).

37Although the effects of exercise on liver histology have not been fully clarified, we recommend implementing exercise therapy because, even alone, it improves liver function and liver fat in the liver in patients with NAFLD. (Evidence Level B, Strength 2).

38Although the effects of exercise on liver histology have not been fully clarified, we recommend implementing exercise therapy because, even alone, it improves liver function and liver fat in the liver in patients with NAFLD. (Evidence Level B, Strength 2).

39Vitamin E and pioglitazone have been shown to improve liver function and liver histological findings. However, their safety over the long term remains to be evaluated.

40Vitamin E improves hepatic biological and histological parameters in patients with NASH, and is recommended. However, its safety over the long term in patients with CVD, congestive heart failure, or bladder cancer has not yet been fully assessed.

41Vitamin E improves hepatic biological and histological parameters in patients with NASH, and is recommended. However, its safety over the long term in patients with CVD, congestive heart failure, or bladder cancer has not yet been fully assessed.

42Pioglitazone is recommended for NASH patients with insulin resistance. (Evidence Level A, Strength 2).

43Pioglitazone is recommended for NASH patients with insulin resistance. (Evidence Level A, Strength 2).

44Other studies have focused on other diabetic drugs such as incretin-related drugs like glucagon-like peptide-1 (GLP-1) receptor analogue dipeptidyl peptidase 4 (DPP-4) inhibitor, and sodium glucose co-transporter 2 (SGLT2) inhibitor. Both GLP-1 analogue and SGLT2 inhibitor not only decrease body weight but also improve the glucose metabolism. As SGLT2 inhibitor is known to be effective to heart failure, additional effects can reasonably be expected in NASH patients. Some reports have demonstrated that GLP-1 analogue and SGLT2 improve liver function and liver histological findings. In the revised guidelines, two drugs have been added.

45In NAFLD/NASH patients with type 2 diabetes, SGLT2 inhibitor improves liver enzymes and histological findings, and its administration is, therefore, suggested. SGLT2 inhibitor is not adaptive for insurance of NAFLD/NASH. (Evidence Level C, Strength 2).

46In NAFLD/NASH patients with type 2 diabetes, SGLT2 inhibitor improves liver enzymes and histological findings, and its administration is, therefore, suggested. SGLT2 inhibitor is not adaptive for insurance of NAFLD/NASH. (Evidence Level C, Strength 2).

47In NAFLD with type 2 diabetes, GLP-1 analogue has been found to improve liver function and liver histological findings. SGLT2 inhibitor is not adaptive for insurance of NAFLD/NASH. The effect of DPP-4 inhibitor is not constant. (Evidence Level C, Strength 2).

48In NAFLD with type 2 diabetes, GLP-1 analogue has been found to improve liver function and liver histological findings. SGLT2 inhibitor is not adaptive for insurance of NAFLD/NASH. The effect of DPP-4 inhibitor is not constant. (Evidence Level C, Strength 2).

49Regarding to both drugs, randomized trials with greater numbers of patients are needed.

50Drugs for dyslipidemia and hypertension are reported to improve liver enzymes, as described in previous guideline.

51HMG-CoA reductase inhibitors (statins) are recommended for NAFLD/NASH patients with hypercholesterolemia. However, the effect of ezetimibe is not constant. (Evidence Level C, Strength 2).

52HMG-CoA reductase inhibitors (statins) are recommended for NAFLD/NASH patients with hypercholesterolemia. However, the effect of ezetimibe is not constant. (Evidence Level C, Strength 2).

53We recommend an ARB or ACE for NASH patients with hypertension. (Evidence Level C, Strength 2).

54We recommend an ARB or ACE for NASH patients with hypertension. (Evidence Level C, Strength 2).

55Ursodeoxycholic acid (UDCA) and biguanides have no significant effect on liver histology and we do not recommend them as a specific treatment for liver disease in patients with NASH, as described in previous guideline.

56We do not recommend UDCA at conventional dose levels for the treatment of NAFLD/NASH.

57We do not recommend UDCA at conventional dose levels for the treatment of NAFLD/NASH.

58We do not recommend biguanides for the treatment of NAFLD/NASH, because there is no evidence, suggesting improvement of liver enzyme and liver histology in NAFLD/NASH patients. (Evidence Level B, Strength 2).

59We do not recommend biguanides for the treatment of NAFLD/NASH, because there is no evidence, suggesting improvement of liver enzyme and liver histology in NAFLD/NASH patients. (Evidence Level B, Strength 2).

60There are several ongoing drug trials for NAFLD/NASH therapy, including trials of obeticholic acid (OCA), elafibranor, selonsertib (SEL), apoptosis signal-regulating kinase 1 (ASK1), cenicriviroc (CVC), fibroblast growth factor (FGF)-21, Aramchol, acetyl-CoA carboxylase (ACC) inhibitor (GS-0976), FGF19 (NGM-282), pemafibrate, emricasan, toll-like receptor 4 (TLR4) inhibitor (JKB-21), solithromycin, SSAO/VAP-1 inhibitor (BI 1467335), IMM-124E, galectin-3 inhibitor (GR-MD-02), and heat shock protein (HSP) 47 to be addressed in future research questions.

61Nevertheless, the trials for NAFLD/NASH had several problems. First, even in placebo groups, about 20% of patients improved due to lifestyle improvements. Second, to confirm improvement of liver fibrosis, which associated with prognosis, an observation period of 5 years or more is necessary. In addition, histological evaluation differs among pathologists. It is also problematic that NAFLD is a syndrome, and therefore, includes many pathogeneses. The effects of drugs are, therefore, not always constant. Finally, the prevalence of the PNPLA3 variant, which is a risk factor of progression of NASH, is different among races. It is expected that these problems will be resolved, and that new drugs will be approved for NASH therapy.

62Elucidating the pathogenesis of NAFLD/NASH and developing therapies are now worldwide issues, and it is important that Japanese medical studies of NAFLD/NASH advance. For that purpose, these guidelines were prepared by searching for relevant evidence worldwide without regard to ethnic characteristics, and the obtained evidence was then summarized from a Japanese perspective. Of course, ethnic differences correlate with susceptibility to metabolic syndrome-related diseases including NAFLD/NASH, possibly as a result of genomic polymorphism. Therefore, it is also important to develop Japanese-based clinical research work and to interpret other countries’ evidence in light of ethnic considerations. The revised guidelines not only summarize the current clinical state of NAFLD/NASH but also point to future directions for study.