Prevalence of NAFLD in adult population by region.
Nonalcoholic fatty liver disease (NAFLD) is a leading liver disease worldwide with a prevalence of approximately 25% among adult population. The highest prevalence is observed in Middle East and the lowest prevalence in Africa. NAFLD is a spectrum of liver disorders ranging from simple steatosis to nonalcoholic steatohepatitis (NASH). Pro-inflammatory diet, overweight/obesity, inflammation, insulin resistance, prediabetes, type 2 diabetes, dyslipidemia, disrupted gut microbiome, and impaired intestinal barrier function are important risk factors associated with and/or contributing to NAFLD. Gut microbiome is a complex and diverse microbial ecosystem essential for the maintenance of human health. It is influenced by several factors including diet and medications. Gut microbiome can be disrupted in NAFLD. Intestinal epithelial barrier is the largest and most important barrier against the external environment and plays an important role in health and disease. Several factors including diet and gut microbiome impact intestinal barrier function. NAFLD can be associated with impaired intestinal barrier function (increased intestinal permeability). There are no specific drugs that directly treat NAFLD. The first-line therapy of NAFLD is currently lifestyle intervention. Weight loss is an important component in the treatment of NAFLD subjects who have excess body weight. Gut microbiome and intestinal epithelial barrier are becoming promising targets for the treatment of several diseases including NAFLD. In the absence of approved pharmacotherapy for the treatment of NAFLD/NASH, in addition to lifestyle intervention and weight loss (in case of excess body weight), focus should also be on correcting gut microbiome and intestinal permeability (directly and/or through gut microbiome modulation) using diet (e.g., low-fat diet, high-fiber diet, and Mediterranean diet), prebiotics (nondigestible food ingredients), probiotics (nonpathogenic living microorganisms), synbiotics (combination of prebiotics and probiotics), and fecal microbiota transplantation (transfer of healthy stool).
- nonalcoholic fatty liver disease
- gut microbiome
- intestinal epithelial barrier
- targeted treatment
NAFLD is a leading liver disease worldwide with a prevalence of approximately 25% among adult population. It is the most common cause of chronic liver disease in Western countries. NAFLD is a spectrum of liver disorders ranging from simple steatosis to NASH [1, 2, 3, 4, 5, 6, 7, 8, 9].
Pro-inflammatory diet, overweight/obesity, inflammation, insulin resistance, prediabetes, type 2 diabetes, dyslipidemia, disrupted gut microbiome, and impaired intestinal barrier function are important risk factors associated with and/or contributing to NAFLD [2, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27].
Gut microbiome and intestinal epithelial barrier are becoming promising targets for the treatment of several diseases including NAFLD [4, 17, 18, 20, 21, 22, 24, 25, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43].
The liver is the largest visceral organ. It weighs approximately 1.5 kg. Macroscopically, the liver is divided into four lobes. The basic functional unit of the liver is the liver lobule which includes the hepatocytes. Approximately 30% of the liver volume is made up by blood (Figure 1) .
The liver is a vital organ. It has numerous important roles including secretion of bile (700–1,200 mL/day), metabolism of bilirubin, metabolism of nutrients (e.g., glucose homeostasis, fat synthesis, and albumin synthesis), endocrine function (e.g., production of angiotensinogen and activation of vitamin D), storage of minerals and vitamins (e.g., iron, copper, vitamin A, vitamin B12, and vitamin D), hematologic and vascular functions (e.g., hemostatic function and capacity to store/release large volume of blood), immunologic and protective functions, and metabolic inactivation and detoxification (e.g., catabolism or alteration of hormones, toxins, and drugs) .
2.2 Gut microbiome
Gut microbiome is a complex and diverse microbial ecosystem living in the digestive tract, mainly in the colon. It is established within the few first years of life and contains up to 100 trillion microbes, mainly bacteria (more than 1,000 species) but also fungi, protozoa, archaea, and viruses (Figure 2) [45, 46, 47, 48, 49, 50, 51].
Gut microbiome is involved in multiple physiological functions and is essential for the maintenance of human health [50, 51, 52, 53, 54, 55, 56, 57]. It is influenced by several factors including diet and medications [31, 32, 50, 53, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69].
2.3 Intestinal epithelial barrier
The intestine is lined by layer of epithelial cells that are connected by cell–cell junctions (tight junction, adherens junction, desmosome). These junctions are responsible for maintenance of tissue integrity, creation of a barrier, and signaling. The barrier, which is important for tissue homeostasis, controls the passage of water, ions, molecules, cells, and pathogens across the epithelial layer. Intestinal epithelial barrier is the largest and most important barrier against the external environment (barrier between luminal contents and the underlying immune system). It covers a surface of approximately 400 m2 and requires approximately 40% of the body energy expenditure (Figure 3) [23, 41, 42, 43, 70, 71].
Intestinal epithelial barrier is constantly challenged by gut microbiome. It plays an important role in health and disease [23, 41, 42, 43, 70, 71]. Several factors including diet and gut microbiome impact intestinal barrier function [20, 41, 42, 43]. A high-fiber diet has a beneficial effect while a high-fructose diet and a high-fat diet have a deleterious effect on intestinal barrier function.
NAFLD is a liver disease characterized by hepatic steatosis (≥ 5% fat deposit) on either imaging or histology, with no excessive alcohol consumption (< 30 g/day for men and < 20 g/day for women), in the absence of other causes of steatosis (e.g., viral hepatitis and medications). It is a spectrum of liver disorders ranging from simple steatosis to NASH. Up to 30% of NAFLD subjects develop NASH. NASH is the aggressive form of NAFLD that can progress to fibrosis, cirrhosis, and hepatocellular cancer. The presence of fibrosis is the strongest predictor of mortality (Figure 4) [1, 2, 3, 4, 5, 6, 7, 8, 9].
Recently, a consensus of international experts proposed to change the acronym NAFLD to MAFLD (metabolic dysfunction-associated fatty liver disease) .
NAFLD is a pandemic with a prevalence of approximately 25% among adult population worldwide. The highest prevalence is observed in Middle East and the lowest prevalence in Africa. More than 1 billion people are affected by NAFLD worldwide (Table 1) [3, 8]. The differences in prevalence can be explained, at least partially, by genetic background and lifestyle. NAFLD prevalence continues to rise in all age groups, including in the adolescent population, especially in the setting of the obesity pandemic.
The pathophysiology underlying NAFLD is complex with both non-genetic and genetic components [2, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 75, 76, 77, 78, 79].
Pro-inflammatory diet, overweight/obesity, inflammation, insulin resistance, prediabetes, type 2 diabetes, dyslipidemia, disrupted gut microbiome, and impaired intestinal barrier function are important risk factors associated with and/or contributing to NAFLD [2, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27]. In addition, some miscellaneous endocrine disorders including growth hormone (GH) deficiency, hypothyroidism, polycystic ovary syndrome, and hypogonadism and deficiency in epigenetic regulators such as sirtuin 1 have been reported as possible contributing factors to NAFLD [75, 76, 77, 78, 79].
There are several genetic forms of NAFLD including variations in patatin-like phospholipase domain-containing protein 3 (
Excessive fat deposition in the liver (hepatocytes) leading to NAFLD can result from one or several combined mechanisms including increased delivery of lipids to the liver from diet or adipose tissue, increased
3.3.1 Pro-inflammatory diet
Various common food components have pro-inflammatory potential and by contributing to chronic inflammation, can promote the development of NAFLD . They can either directly alter liver metabolism or act through disruption of gut microbiome. The Western diet which is a diet rich in saturated fat, red meat, fructose, alcohol, and salt is associated with an increased risk of NAFLD.
3.3.2 Overweight/obesity, inflammation
Excess body weight (overweight and obesity) is considered as the main cause of several abnormalities that are contributing to the pathogenesis of NAFLD (e.g., inflammation and insulin resistance). NAFLD is commonly associated with overweight/obesity . It is independently associated with both subcutaneous and visceral obesity. The adipose tissue inflammation observed in overweight/obesity and characterized by increased cytokine production leads to systemic inflammation which is responsible for insulin resistance [10, 11, 80]. Clinical studies have shown that cellular and molecular adipose tissue inflammation correlate with the degree of liver inflammation and the importance of liver disease.
|< 18.5 (n = 445)||0.4%|
|18.5 to < 24.0 (n = 4,899)||12.7%|
|24.0 to < 28.0 (n = 2,801)||49.2%|
|≥ 28.0 (672)||82.4%|
3.3.3 Insulin resistance, prediabetes, type 2 diabetes
Insulin resistance plays an important role in the in the development of NAFLD. Overweight/obesity and systemic inflammation are responsible for insulin resistance which in its turn is an important contributing factor to the pathogenesis of prediabetes, type 2 diabetes, and NAFLD [2, 10, 80]. NAFLD is highly correlated with prediabetes and type 2 diabetes. There is a reciprocal association between prediabetes/type 2 diabetes and NAFLD . The global prevalence of NAFLD in subjects with prediabetes and type 2 diabetes is around 48% and more than 55%, respectively (Figure 5) [5, 10, 12, 15].
Dyslipidemia is a significant risk factor for NAFLD and associated cardiovascular disease. The mechanism by which dyslipidemia increases the risk of NAFLD may be related to an increased accumulation of lipids in the hepatocytes .
3.3.5 Disrupted gut microbiome
Profound changes affecting the diversity and the abundance of gut microbiome (dysbiosis) are associated with several metabolic disorders including NAFLD [4, 10, 17, 18, 19, 20, 21, 22, 23, 24, 25, 83]. Gut microbiome plays a major role in the pathogenesis of NAFLD. Disrupted gut microbiome (e.g., increase in pro-inflammatory bacteria and decrease in protective bacteria) can promote or aggravate NAFLD through several mechanisms including change in intestinal permeability and change in the amount of absorbed energy (this can cause overweight/obesity, an important risk factor for NAFLD). Microbial metabolites and cell components contribute to the development of inflammation and hepatic steatosis.
Several clinical studies have shown the association of qualitative and quantitative changes in gut microbiome (e.g., increased
3.3.6 Impaired intestinal barrier function
Increased intestinal permeability is most likely caused by the disruption of intercellular tight junctions of the intestinal epithelium [26, 71]. It promotes translocation of bacteria-derived products (e.g., SCFAs, alcohol, and LPS) into the portal circulation, exposing the liver to substances capable of inducing hepatic steatosis and fibrosis [17, 20, 21, 22, 23]. Several studies have reported that serum zonulin, a marker of intestinal permeability, correlates significantly with the severity of hepatic steatosis in subjects with NAFLD .
3.3.7 Miscellaneous endocrine disorders
Several miscellaneous endocrine disorders may contribute to the development of secondary NAFLD . GH deficiency through different mechanisms including inflammation and insulin resistance may promote NAFLD. Hypothyroidism by causing impaired glucose and lipid metabolism and altered energy homeostasis can be linked to NAFLD. Polycystic ovary syndrome through multiple factors (e.g., obesity, inflammation, insulin resistance, and hyperandrogenism) may promote NAFLD. Hypogonadism can be associated with NAFLD through several mechanisms including obesity, insulin resistance, dyslipidemia, estrogen deficiency, and dehydroepiandrosterone deficiency.
3.3.8 Sirtuin 1 deficiency
Sirtuins are a group of proteins belonging to the family of silent information regulator 2. Humans have seven sirtuins. Sirtuin 1 is widely recognized as an important epigenetic regulator involved in multiple biological processes and its deficiency contributes to the pathogenesis of several diseases including NAFLD [76, 77, 78, 79]. Exposure to sirtuin 1 inhibitors (e.g., fructose, alcohol, and LPS) leads to defective sirtuin 1 function and can promote NAFLD.
3.3.9 Genetic predisposition
Common genetic forms of NAFLD include variations in
3.3.10 Combination of several factors
Several of the above-mentioned factors can be present in subjects with NAFLD, especially when they are interrelated. For example, a subject with obesity may have inflammation, insulin resistance (with prediabetes or type 2 diabetes), gut microbiome dysbiosis, and leaky gut.
NAFLD is a liver disease characterized by hepatic steatosis (≥ 5% fat deposit) on either imaging or histology. Several tests (non-invasive and invasive) can be performed to support and/or confirm the diagnosis of NAFLD and the presence of fibrosis, and optimize the intervention [1, 5, 6, 9, 84, 85, 86, 87, 88]. There are several national and international guidelines related to the diagnosis and the management of NAFLD (e.g., American Association for the Study of Liver Diseases “AASLD”, National Institute for Health and Care Excellence “NICE”, European Association for the Study of the Liver “EASL”, Italian Association for the Study of the Liver “AISF”, and Asia-Pacific guidelines) [1, 89].
3.4.1 Non-invasive tests
To establish the diagnosis of NAFLD, conventional liver biochemistry is used first. It may show an increase in liver enzymes including aspartate aminotransferase (AST), alanine aminotransferase (ALT), and gamma-glutamyl transpeptidase (GGT). However, up to approximately 75% of subjects with NAFLD may have normal liver enzymes. Additional biomarkers and scores have been proposed (e.g., cytokeratin-18 fragment, fatty liver index, Zhejiang University index, and NAFLD liver fat score) (non-exhaustive list).
Imaging of the liver can be obtained with several tools including ultrasound, computed tomography (CT), and magnetic resonance imaging (MRI) (Figure 7). Based on most guidelines, abdominal ultrasound should be the first-line examination for the identification of hepatic steatosis. Although ultrasound has some limitations in morbidly obese subjects and in subjects with liver fat content below 20%, it has the advantage of being widely available with low cost. MRI remains the gold standard for assessing and quantifying hepatic steatosis since it can detect a liver fat content as low as 5%. However, its use is limited due to high cost and a long time of execution. Another promising imaging technique is the ultrasonography-based transient elastography using continuous attenuation parameter.
For the assessment of liver fibrosis, several biomarkers, scores, and imaging techniques have been proposed (e.g., AST/ALT ratio, AST to platelet ratio index, enhanced liver fibrosis score, NAFLD fibrosis score, and magnetic resonance elastography) (non-exhaustive list) [6, 84, 88].
All the non-imaging assessments of NAFLD have limitations and alone cannot replace liver biopsy.
3.4.2 Invasive tests
Liver biopsy is the gold standard test in the assessment of NAFLD to diagnose NASH and stage liver fibrosis. It is potentially harmful and carries a low risk of morbidity and extremely low risk of mortality. Therefore, it should be reserved to selected subjects (Figure 8) [1, 90]. One important limitation of liver biopsy is that it explores only a small portion of the liver (approximately 1/50,000), not representative of the entire organ.
Because NAFLD/NASH is associated with increased morbidity and higher risk of death mainly related to cardiovascular and liver diseases, it is essential to initiate a treatment as soon as the diagnosis is made. In the absence of approved pharmacotherapy for the treatment of NAFLD/NASH, the first-line therapy of NAFLD remains lifestyle intervention with weight loss (in case of excess body weight) [1, 2, 8, 28, 29, 30]. Gut microbiome and intestinal epithelial barrier are becoming promising targets for the treatment of several diseases including NAFLD [4, 17, 18, 20, 21, 22, 24, 25, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43]. When treating NAFLD/NASH, in addition to lifestyle changes and weight loss (in case of excess body weight), focus should also be on correcting gut microbiome and intestinal permeability directly and/or through gut microbiome modulation [4, 17, 18, 20, 21, 22, 24, 25, 35, 36, 37, 38, 39, 40, 43]. Several drugs for the treatment of NAFLD/NASH are currently under investigation [6, 8, 91]. It is also important to treat the associated morbidities other than overweight/obesity (e.g., type 2 diabetes and dyslipidemia).
3.5.1 Lifestyle intervention
Lifestyle intervention which includes diet and exercise is the first-line therapy in NAFLD but is difficult to maintain (Table 3) [1, 2, 8, 28, 29, 30]. Diet is a powerful tool in the management of NAFLD. Diet relates to the amount and the composition of food that is consumed on a daily basis. There are several types of diets with different caloric content and different composition of macronutrients, fiber, minerals, and vitamins. They include hypocaloric diet, low-carbohydrate diet, low-fat, high-protein diet, high-fiber diet, and Mediterranean diet (non-exhaustive list) [8, 29, 30, 92]. In NAFLD subjects, hypocaloric diet is usually a deficit of 500–1,000 kcal/day. For macronutrient composition and according to most recommendations, carbohydrate intake should be between 40 and 50% (with exclusion of fructose from foods and beverages), fat intake no more than 30% (with saturated fat below 10%), and protein intake between 15 and 20% . Even without significant weight loss, anti-inflammatory diets like Mediterranean diet (a mainly plant-based low-carbohydrate and high-unsaturated fat diet) have beneficial properties both in the prevention and treatment of NAFLD [8, 10, 25, 27, 28, 29, 93]. The omega-3 polyunsaturated fatty acids present in the Mediterranean diet may reduce hepatic steatosis. A diet containing sirtuin 1 activators (e.g., magnesium and zinc) can be beneficial in NAFLD subjects .
|Healthy diet||Low-carbohydrate diet, Low-fat diet, High-fiber diet, Mediterranean diet, etc.|
|Diet for weight loss (in case of excess body weight)||Hypocaloric diet|
|Exercise||Aerobic activities, Resistance training|
The objective in NAFLD subjects with excess body weight is a weight loss of 7–10%. To achieve weight loss, in addition to lifestyle intervention, other tools including drugs, medical devices, and bariatric surgery can also be used when needed and indicated [2, 28, 94, 95, 96, 97]. Rapid sudden weight loss should be avoided (risk of aggravation of liver failure).
Lean NAFLD subjects may have visceral obesity that is not detected by BMI. These subjects may also benefit from diet and weight loss.
In addition to the type of diet, the timing and the frequency of the meals may also influence NAFLD. It is recommended to consume more daily calories in the morning versus the evening and avoid skipping meals .
Regular exercise including moderate intensity aerobic activities (3–5 weekly sessions with approximately 40 minutes per session) and resistance training can reduce hepatic steatosis even without significant weight loss [1, 8, 28, 29]. Combination of exercise and diet has greater benefit than exercise or diet alone.
3.5.2 Gut microbiome modulation
The prevention and management of NAFLD may benefit from modulation and correction of gut microbiome [4, 17, 18, 20, 21, 22, 24, 25, 35, 36, 37, 38, 39, 40]. Gut microbiome can be modulated through diet, antibiotics, prebiotics, probiotics, synbiotics, and fecal microbiota transplantation [4, 17, 18, 20, 21, 22, 24, 25, 33, 34, 35, 36, 37, 38, 39, 40, 58, 59, 60, 61, 62, 63, 64, 65]. To optimize the efficacy of these therapies, focus should be on the altered gut microbiome (e.g., taxa responsible for high alcohol and LPS production) .
Diet is an important tool for the modulation of gut microbiome. The amount of daily caloric intake and the content of food significantly affect gut microbiome. A diet that is low in calories (when weight loss is needed), low in fat, and high in fiber has a favorable effect on weight control and gut microbiome (increase in richness, decrease in Firmicutes-to-Bacteroidetes phyla ratio) [58, 59, 60, 61, 62, 63, 64].
Antibiotics are medications used to fight local or systemic infection .
Antibiotics affect gut microbiome [4, 24, 59, 65]. They can deplete or alter gut microbiome (e.g., increase in Firmicutes phylum) and reduce liver disease development. However, their clinical use is limited since they may eliminate important beneficial bacterial species and cause antibiotic resistance.
Prebiotics are chemicals (nondigestible food ingredients) inducing growth and/or activity of intestinal bacteria (e.g., inulin, lactulose, and resistant starch) [31, 69]. Some dietary fibers are prebiotics . Prebiotics can be found in many foods (e.g., leek, asparagus, onion, soybean, apple, and banana) (Figure 9).
Prebiotics can positively modulate gut microbiome and improve NAFLD [4, 21, 24, 25, 35]. They lower the production of LPS. Treatment with oligofructose (16 g/day for 8 weeks) in subjects with NASH showed a significant decrease of AST .
Probiotics are nonpathogenic living microorganisms with direct or indirect effect on gut microbiome [31, 32, 68]. Probiotics can be found in several foods (e.g., yogurt, cheese, and milk) (Figure 10).
Probiotics can positively impact gut microbiome and improve NAFLD [4, 21, 24, 36, 37, 38, 39]. They reduce the production of LPS. Administration of
Synbiotics are combination of prebiotics and probiotics. They have the potential to induce more effects than prebiotics or probiotics used alone.
There are few studies assessing the effects of synbiotics on NAFLD subjects. They showed several beneficial effects including reduction of inflammation and hepatic steatosis [4, 24, 40]. Administration of
126.96.36.199 Fecal microbiota transplantation
Fecal microbiota transplantation consists of transfer of feces from a healthy donor to a recipient. The addition of healthy stool can be done through colonoscopy, orogastric tube, esophagogastroduodenoscopy, or oral capsule (Figure 11) .
Fecal microbiota transplantation is an exciting therapy with important potential indications. It was first approved by the United States Food and Drug Administration for the treatment of
3.5.3 Intestinal permeability correction
Restoring the intestinal epithelial barrier is an attractive therapeutic approach in NAFLD subjects. Currently, there is no approved drug for this indication. Intestinal permeability can be targeted and corrected directly (with diet) and/or through gut microbiome modulation [17, 18, 43].
A study using high-fiber diet for 6 months in subjects with NAFLD showed a decrease in intestinal permeability as demonstrated by a reduction of approximately 90% of serum zonulin, and a significant reduction of liver enzymes (e.g., AST, ALT, and GGT) and hepatic steatosis .
There are no approved drugs for the treatment of NAFLD/NASH. Several investigational drugs are currently in various stages of clinical trials. They can impact at least four pathways related to NAFLD development and progression (hepatic fat accumulation, oxidative stress, gut microbiome, and hepatic fibrosis) [7, 8, 91]. Some of these investigational drugs have shown promising preliminary results (e.g., lanifibranor, cenicriviroc, and resmetirom) (non-exhaustive list) [6, 8, 91].
Any drug that is currently used in the treatment of NAFLD/NASH (e.g., antidiabetic drugs, lipid-lowering drugs, and vitamin E) should be considered as an off-label treatment [1, 2, 6, 7, 8, 9, 14, 15, 16, 28, 91, 100]. Among the antidiabetic drugs, pioglitazone has shown a strong efficacy and became the first-line therapy in subjects who have type 2 diabetes and NAFLD [1, 2, 6, 14, 15, 28, 100].
The summary of different tools available in the United States of America (USA) or under investigation for the treatment of NAFLD/NASH is reported in Table 4.
|Lifestyle intervention||Diet, Exercise|
|Anti-obesity drug||Xenical®, Qsymia®, Contrave®, Saxenda®|
|Anti-obesity medical device||Lap-Band®, AspireAssist®, Orbera® Intragastric Balloon System, TransPyloric Shuttle®, Obalon® Balloon System, Plenity®|
|Bariatric surgery||Sleeve gastrectomy, Roux-en-Y gastric bypass|
|Gut microbiome modulation||Diet, Antibiotics, Prebiotics, Probiotics, Synbiotics, Fecal microbiota transplantation|
|Intestinal permeability correction||High-fiber diet, Gut microbiome modulation|
|Off-label drug||Antidiabetic drugs, Vitamin E, etc.|
|Investigational drug||Lanifibranor, Cenicriviroc, Resmetirom, etc.|
3.5.5 Liver transplantation
NASH is becoming one of the leading causes of liver transplantation. Currently, in the USA, NASH ranks as the second most common reason for liver transplantation after hepatitis C .
NAFLD is the most common chronic liver disease worldwide. It is a spectrum of liver disorders ranging from simple steatosis to NASH. NAFLD subjects have overweight/obesity in the majority of cases and the disease can be associated with disrupted gut microbiome and impaired intestinal barrier function.
In the absence of approved pharmacotherapy for the treatment of NAFLD/NASH, in addition to lifestyle intervention with weight loss (in case of excess body weight), targeting gut microbiome and intestinal epithelial barrier with diet, prebiotics, probiotics, synbiotics, and fecal microbiota transplantation represents a promising novel therapeutic approach.
Conflict of interest
The author declares no conflict of interest.
Leoni S, Tovoli F, Napoli L, Serio I, Ferri S, Bolondi L. Current guidelines for the management of non-alcoholic fatty liver disease: A systematic review with comparative analysis. World Journal of Gastroenterology. 2018; 24:3361-3373. DOI: 10.3748/wjg.v24.i30.3361
Mundi MS, Velapati S, Patel J, Kellogg TA, Abu Dayyeh BK, Hurt RT. Evolution of NAFLD and its management. Nutrition in Clinical Practice. 2020; 35:72-84. DOI: 10.1002/ncp.10449
Younossi ZB, Koenig AB, Abdelatif D, Fazel Y, Henry L, Wymer M. Global epidemiology of nonalcoholic fatty liver disease – Meta-analytic assessment of prevalence, incidence, and outcomes. Hepatology. 2016; 64:73-84. DOI: 10.1002/hep.28431
Safari Z, Gérard P. The links between the gut microbiome and non-alcoholic fatty liver disease (NAFLD). Cellular and Molecular Life Sciences. 2019; 76:1541-1558. DOI: 10.1007/s00018-019-03011-w
Yki-Järvinen. Diagnosis of non-alcoholic fatty liver disease (NAFLD). Diabetologia. 2016; 59:1104-1111. DOI: 10.1007/s00125-016-3944-1
Drescher HK, Weiskirchen S, Weiskirchen R. Current status in testing for nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH). Cells. 2019; 8:845. DOI: 10.3390/cells8080845
Oseini AM, Sanyal AJ. Therapies in non-alcoholic steatohepatitis (NASH). Liver International. 2017; 37(Suppl 1):97-103. DOI: 10.1111/liv.13302
Pydyn N, Miękus K, Jura J, Kotlinowski J. New therapeutic strategies in nonalcoholic fatty liver disease: A focus on promising drugs for nonalcoholic steatohepatitis. Pharmacological Reports. 2020; 72:1-12. DOI: 10.1007/s43440-019-00020-1
Gharaibeh NE, Rahhal MN, Rahimi L, Ismail-Beigi F. SGLT-2 inhibitors as promising therapeutics for non-alcoholic fatty liver disease: Pathophysiology, clinical outcomes, and future directions. Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 2019; 12:1001-1012. DOI: 10.2147/DMSO.S212715
Tilg H, Adolph TE, Moschen AR. Multiple parallel hits hypothesis in nonalcoholic fatty liver disease: Revisited after a decade. Hepatology. DOI: 10.1002/hep.31518
Alisi A, Carpino G, Oliveira FL, Panera N, Nobili V, Gaudio E. The role of tissue macrophage-mediated inflammation on NAFLD pathogenesis and its clinical implications. Mediators of Inflammation. DOI: 10.1155/2017/8162421
Vesa CM, Behl T, Nemeth S, et al. Prediction of NAFLD occurrence in prediabetes patients. Experimental and Therapeutic Medicine. 2020; 20:190. DOI: 10.3892/etm.2020.9320
Radaelli MG, Martucci F, Perra S, et al. NAFLD/NASH in patients with type 2 diabetes and related treatment options. Journal of Endocrinological Investigation. 2018; 41:509-521. DOI: 10.1007/s40618-017-0799-3
Tacelli M, Celsa C, Magro B, et al. Antidiabetic drugs in NAFLD: The accomplishment of two goals at once. Pharmaceuticals. 2018; 11:121. DOI: 10.3390/ph11040121
Kim KS, Lee BW. Beneficial effect of anti-diabetic drugs for nonalcoholic fatty liver disease. Clinical and Molecular Hepatology. 2020; 26:430-443. DOI: 10.3350/cmh.2020.0137
Iqbal U, Perumpail BJ, John N, et al. Judicious use of lipid lowering agents in the management of NAFLD. Diseases. 2018; 6:87. DOI: 10.3390/diseases6040087
Zhu L, Baker RD, Baker SS. Gut microbiome and nonalcoholic fatty liver diseases. Pediatric Research. 2015; 77:245-251. DOI: 10.1038/pr.2014.157
Vespasiani-Gentilucci U, Gallo P, Picardi A. The role of intestinal microbiota in the pathogenesis of NAFLD: Starting points for intervention. Archives of Medical Science. 2018; 14:701-706. DOI: 10.5114/aoms.2016.58831
Grabherr F, Grander C, Effenberger M, Adolph TE, Tilg H. Gut dysfunction and non-alcoholic fatty liver disease. Frontiers in Endocrinology. 2019; 10:611. DOI: 10.3389/fendo.2019.00611
Kolodziejczyk AA, Zheng D, Shibolet O, Elinav E. The role of the microbiome in NAFLD and NASH. EMBO Molecular Medicine. 2019; 11:e9302. DOI: 10.15252/emmm.201809302
Durate SMB, Stefano JT, Oliveira CP. Microbiota and nonalcoholic fatty liver disease/nonalcoholic steatohepatitis (NAFLD/NASH). Annals of Hepatology. 2019; 18:416-421. DOI: 10.1016/j.aohep.2019.04006
Liu Q, Liu S, Chen L, et al. Role and effective therapeutic target of gut microbiota in NAFLD/NASH (review). Experimental and Therapeutic Medicine. 2019; 18:1935-1944. DOI: 10.3892/etm.2019.7781
Jadhav K, Cohen TS. Can you trust your gut? Implicating a disrupted intestinal microbiome in the progression of NAFLD/NASH. Frontiers in Endocrinology. 2020; 11:592157. DOI: 10.3389/fendo.2020.592157
Hu H, Lin A, Kong M, et al. Intestinal microbiome and NAFLD: Molecular insights and therapeutic perspectives. Journal of Gastroenterology. 2020; 55:142-158. DOI: 10.1007/s00535-019-01649-8
Pérez-Montes de Oca A, Julián MT, Ramos A, Puig-Domingo M, Alonso N. Microbiota, fiber, and NAFLD: Is there any connection? Nutrients. 2020; 12:3100. DOI: 10.3390/nu12103100
Luther J, Garber JJ, Khalili H, et al. Hepatic injury in nonalcoholic steatohepatitis contributes to altered intestinal permeability. Cellular and Molecular Gastroenterology and Hepatology. 2015; 1:222-232. DOI: 10.1016/j.jcmgh.2015.01.001
Biolato M, Manca F, Marrone G, et al. Intestinal permeability after Mediterranean diet and low-fat diet in non-alcoholic fatty liver disease. World Journal of Gastroenterology. 2019; 25:509-520. DOI: 10.3748/wjg.v25.i4.509
Hossain N, Kanwar P, Mohanty SR. A comprehensive updated review of pharmaceutical and nonpharmaceutical treatment for NAFLD. Gastroenterology Research and Practice. DOI: 10.1155/2016/7109270
El-Agroudy NN, Kurzbach A, Rodionov RN, et al. Are lifestyle therapies effective for NAFLD treatment? Trends in Endocrinology & Metabolism. 2019; 30:701-709. DOI: 10.1016/j.tem.2019.07.013
Plaz Torres MC, Aghemo A, Lleo A, et al. Mediterranean diet and NAFLD: What we know and questions that still need to be answered. Nutrients. 2019; 11:2971. DOI: 10.3390/nu11122971
Dahiya DK, Renuka, Puniya M, et al. Gut microbiota modulation and its relationship with obesity using prebiotics fibers and probiotics: A review. Frontiers in Microbiology. 2017; 8:563. DOI: 10.3389/fmicb.2017.00563
Kobyliak N, Conte C, Cammarota G, et al. Probiotics in prevention and treatment of obesity: A critical view. Nutrition and Metabolism. 2016; 13:14. DOI: 10.1186/s12986-016-0067-0
Jayasinghe TN, Chiavaroli V, Holland DJ, Cutfield WS, O’Sullivan JM. The new era of treatment for obesity and metabolic disorders: Evidence and expectations for gut microbiome transplantation. Frontiers in Cellular and Infection Microbiology. 2016; 6:15. DOI: 10.3389/fcimb.2016.00015
Marotz CA, Zarrinpar A. Treating obesity and metabolic syndrome with fecal microbiota transplantation. Yale Journal of Biology and Medicine. 2016; 89:383-388
Daubioul CA, Horsmans Y, Lambert P, Danse E, Delzenne NM. Effects of oligofructose on glucose and lipid metabolism in patients with nonalcoholic steatohepatitis: Results of a pilot study. European Journal of Clinical Nutrition. 2005; 59:723-726. DOI: 10.1038/sj.ejcn.1602127
Vajro P, Mandato C, Licenziati MR, et al. Effects of Lactobacillus rhamnosusstrain GG in pediatric obesity-related liver disease. Journal of Pediatric Gastroenterology and Nutrition. 2011; 52:740-743. DOI: 10.1097/MPG.0b013e31821f9b85
Ma YY, Li L, Yu CH, Shen Z, Chen LH, Li YM. Effects of probiotics on nonalcoholic fatty liver disease: A meta-analysis. World Journal of Gastroenterology. 2013; 19:6911-6918. DOI: 10.3748/wjg.v19.i40.6911
Alisi A, Bedogni G, Baviera G, et al. Randomized clinical trial: The beneficial effects of VSL#3 in obese children with non-alcoholic steatohepatitis. Alimentary Pharmacology and Therapeutics. 2014; 39:1276-1285. DOI: 10.1111/apt.12758
Lavekar AS, Raje DV, Manohar T, Lavekar AA. Role of probiotics in the treatment of nonalcoholic fatty liver disease: A meta-analysis. Euroasian Journal of Hepato-Gastroenterology. 2017; 7:130-137
Malaguarnera M, Vacante M, Antic T, et al. Bifidobacterium longumwith fructo-oligosaccharides in patients with non alcoholic steatohepatitis. Digestive Diseases and Sciences. 2012; 57:545-553. DOI: 10.1007/s10620-011-1887-4
Bischoff SC, Barbara G, Buurman W, et al. Intestinal permeability – A new target for disease prevention and therapy. BMC Gastroenterology. 2014; 14:189. DOI: 10.1186/s12876-014-0189-7
Odenwald MA, Turner JR. The intestinal epithelial barrier: A therapeutic target? Nature Reviews. Gastroenterology & Hepatology. 2017; 14:9-21. DOI: 10.1038/nrgastro.2016.169
Krawczyk M, Maciejewska D, Ryterska K, et al. Gut permeability might be improved by dietary fiber in individuals with nonalcoholic fatty liver disease (NAFLD) undergoing weight reduction. Nutrients. 2018; 10:1793. DOI: 10.3390/nu10111793
Ozougwu JC. Physiology of the liver. International Journal of Research in Pharmacy and Biosciences. 2017; 4:13-24
The Human Microbiome Project Consortium. Structure, function and diversity of the healthy human microbiome. Nature. 2012; 486:207-214. DOI: 10.1038/nature11234
Lozupone CA, Stombaugh JI, Gordon JI, Jansson JK, Knight R. Diversity, stability and resilience of the human gut microbiota. Nature. 2012; 489:220-230. DOI: 10.1038/nature11550
Kundu P, Blacher E, Elinav E, Pettersson S. Our gut microbiome: The evolving inner self. Cell. 2017; 171:1481-1493. DOI: 10.1016/j.cell.2017.11.024
Barko PC, McMichael MA, Swanson KS, Williams DA. The gastrointestinal microbiome: A review. Journal of Veterinary Internal Medicine. 2018; 32:9-25. DOI: 10.1111/jvim.14875
Schmidt TSB, Raes J, Bork P. The human gut microbiome: From association to modulation. Cell. 2018; 172:1198-1215. DOI: 10.1016/j.cell.2018.02.044
Heshmati HM. Gut microbiome in obesity management. In: Himmerich H, editor. Weight Management. London: IntechOpen; 2020. p. 255-268. DOI: 10.5772/intechopen.91974
Conrad R, Vlassov AV. The human microbiota: Composition, functions, and therapeutic potential. Medical Science Review. 2015; 2:92-103. DOI: 10.12659/MSRev.895154
Ramakrishna BS. Role of the gut microbiota in human nutrition and metabolism. Journal of Gastroenterology and Hepatology. 2013; 28(Suppl 4):9-17. DOI: 10.1111/jgh.12294
Kovatcheva-Datchary P, Nilsson A, Akrami R, et al. Dietary fiber-induced improvement in glucose metabolism is associated with increased abundance of Prevotella. Cell Metabolism. 2015; 22:971-982. DOI: 10.1016/j.cmet.2015.10.001
Gerard C, Vidal H. Impact of gut microbiota on host glycemic control. Frontiers in Endocrinology. 2019; 10:29. DOI: 10.3389/fendo.2019.00029
Covasa M, Stephens RW, Toderean R, Cobuz C. Intestinal sensing by gut microbiota: Targeting gut peptides. Frontiers in Endocrinology. 2019; 10:82. DOI: 10.3389/fendo.2019.00082
Fu J, Bonder MJ, Cenit MC. The gut microbiome contributes to a substantial proportion of the variation in blood lipids. Circulation Research. 2015; 117:817-824. DOI: 10.1161/CIRCRESAHA.115.306807
Chen YC, Greenbaum J, Shen H, Deng HW. Association between gut microbiota and bone health: Potential mechanisms and prospective. The Journal of Clinical Endocrinology & Metabolism. 2017; 102:3635-3646. DOI: 10.1210/jc.2017-00513
Moschen AR, Wieser V, Tilg H. Dietary factors: Major regulators of the gut’s microbiota. Gut and Liver. 2012; 6:411-416. DOI: 10.5009/gnl.20126.4.411
Voreades N, Kozil A, Weir TL. Diet and the development of the human intestinal microbiome. Frontiers in Microbiology. 2014; 5:494. DOI: 10.3389/fmicb.2014.00494
Graf D, Di Cagno R, Fåk F, et al. Contribution of diet to the composition of the human gut microbiota. Microbial Ecology in Health and Disease. 2015; 26:26164. DOI: 10.3402/mehd.v26.26164
Bibbò S, Ianiro G, Giorgio V, et al. The role of diet on gut microbiota composition. European Review for Medical and Pharmacological Sciences. 2016; 20:4742-4749
Singh RK, Chang HW, Yan D, et al. Influence of diet on the gut microbiome and implications for human health. Journal of Translational Medicine. 2017; 15:73. DOI: 10.1186/s12967-017-1175-y
David LA, Maurice CF, Carmody RN, et al. Diet rapidly and reproducibly alters the human gut microbiome. Nature. 2014; 505:559-563. DOI: 10.1038/nature12820
Wu GD, Chen J, Hoffmann C, et al. Linking long-term dietary patterns with gut microbial enterotypes. Science. 2011; 334:105-108. DOI: 10.1126/science.1208344
Raymond F, Ouameur AA, Déraspe M, et al. The initial state of the human gut microbiome determines its reshaping by antibiotics. The ISME Journal. 2016; 10:707-720. DOI: 10.1038/ismej.2015.148
Le Bastard Q, Al-Ghalith GA, Grégoire M, et al. Systematic review: Human gut dysbiosis induced by non-antibiotic prescription medications. Alimentary Pharmacology & Therapeutics. 2018; 47:332-345. DOI: 10.1111/apt.14451
Maier L, Pruteanu M, Kuhn M, et al. Extensive impact of non-antibiotic drugs on human gut bacteria. Nature. 2018; 555:623-628. DOI: 10.1038/nature25979
Hill C, Guarner F, Reid G, et al. The International Scientific Association for Probiotics and Prebiotics consensus statement on the scope and appropriate use of the term probiotic. Nature Reviews. Gastroenterology & Hepatology. 2014; 11:506-514. DOI: 10.1038/nrgastro.2014.66
Carnahan S, Balzer A, Panchal SK, Brown L. Prebiotics in obesity. Panminerva Medica. 2014; 56:165-175
Citi S. Intestinal barriers protect against disease. Leaky cell-cell junctions contribute to inflammatory and autoimmune diseases. Science. 2018; 359:1097-1098. DOI: 10.1126/science.aat0835
Dai X, Wang B. Role of gut barrier function in the pathogenesis of nonalcoholic fatty liver disease. Gastroenterology Research and Practice. DOI: 10.1155/2015/287348
Bianco C, Romeo S, Petta S, Long MT, Valenti L. MAFLD vs NAFLD: Let the contest begin. Liver International. 2020; 40:2079-2081. DOI: 10.1111/liv.14620
Ballestri S, Nascimbeni F, Baldelli E, Marrazzo A, Romagnoli D, Lonardo A. NAFLD as a sexual dimorphic disease: Role of gender and reproductive status in the development and progression of nonalcoholic fatty liver disease and inherent cardiovascular risk. Advances in Therapy. 2017; 34:1291-1326. DOI: 10.1007/s12325-017-0556-1
Wang L, Guo J, Lu J. Risk factor compositions of nonalcoholic fatty liver disease change with body mass index in males and females. Oncotarget. 2016; 7:35632-35642
Lonardo A, Mantovani A, Lugari S, Targher G. NAFLD in some common endocrine diseases: Prevalence, pathophysiology, and principles of diagnosis and management. International Journal of Molecular Sciences. 2019; 20:2841. DOI: 10.3390/ijms20112841
Lee IH. Mechanisms and disease implications of sirtuin-mediated autophagic regulation. Experimental & Molecular Medicine. 2019; 51:102. DOI: 10.1038/s12276-019-0302-7
Nassir F, Ibdah JA. Sirtuins and nonalcoholic fatty liver disease. World Journal of Gastroenterology. 2016; 22:10084-10092. DOI: 10.3748/wjg.v22.i46.10084
Martins I. The future of genomic medicine involves the maintenance of sirtuin I in global populations. International Journal of Molecular Biology. 2017; 2:42-45. DOI: 10.15406/ijmboa.2017.02.00013
Martins IJ. Nutrition therapy regulates caffeine metabolism with relevance to NAFLD and induction of type 3 diabetes. Journal of Diabetes and Metabolic Disorders. 2017; 4:019. DOI: 10.24966/DMD-201X/100019
Ye J. Mechanisms of insulin resistance in obesity. Frontiers of Medicine. 2013; 7:14-24. DOI: 10.1007/s11684-013-0262-6
Niriella MA, Kasturiratne A, Pathmeswaran A, et al. Lean non-alcoholic fatty liver disease (lean NAFLD): Characteristics, metabolic outcomes and risk factors from a 7-year prospective, community cohort study from Sri Lanka. Hepatology International. 2019; 13:314-322. DOI: 10.1007/s12072-018-9916-4
Ye Q, Zou B, Yeo YH, et al. Global prevalence, incidence, and outcomes of non-obese or lean non-alcoholic fatty liver disease: A systematic review and meta-analysis. Lancet Gastroenterology & Hepatology. 2020; 5:739-752. DOI: 10.1016/S2468-1253(20)30077-7
Holmes E, Li JV, Athanasiou T, Ashrafian H, Nicholson JK. Understanding the role of gut microbiome-host metabolic signal disruption in health and disease. Trends in Microbiolgy. 2011; 19:349-359. DOI: 10.1016/j.tim.2011.05.006
Cleveland E, Bandy A, VanWagner LB. Diagnostic challenges of nonalcoholic fatty liver disease/nonalcoholic steatohepatitis. Clinical Liver Disease. 2018; 11:98-104
Zhou JH, Cai JJ, She ZG, Li HL. Noninvasive evaluation of nonalcoholic fatty liver disease: Current evidence and practice. World Journal of Gastroenterology. 2019; 25:1307-1326. DOI: 10.3748/wjg.v25.i11.1307
Lee DH. Noninvasive evaluation of nonalcoholic fatty liver disease. Endocrinology and Metabolism. 2020; 35:243-259. DOI: 10.3803/EnM.2020.35.2.243
Fu CP, Ali H, Rachakonda VP, Oczypok EA, DeLany JP, Kershaw EE. The ZJU index is a powerful surrogate marker for NAFLD in severely obese North American women. Plos One. 2019; 14:e0224942. DOI: 10.1371/journal.pone.0224942
Kaswala DH, Lai M, Afdhal NH. Fibrosis assessment in nonalcoholic fatty liver disease (NAFLD) in 2016. Digestive Diseases and Sciences. 2016; 61:1356-1364. DOI: 10.1007/s10620-016-4079-4
Paul S, Davis AM. Diagnosis and management of nonalcoholic fatty liver disease. Journal of the American Medical Association. 2018; 320:2474-2475
Bedossa P. Histological assessment of NAFLD. Digestive Diseases and Sciences. 2016; 61:1348-1355. DOI: 10.1007/s10620-016-4062-0
Sumida Y, Yoneda M. Current and future pharmacological therapies for NAFLD/NASH. Journal of Gastroenterology. 2018; 53:362-376. DOI: 10.1007/s00535-017-1415-1
Freedman MR, King J, Kennedy E. Popular diets: A scientific review. Obesity Research. 2001; 9(Suppl 1):1S–40S
Tyrovolas S, Panagiotakos DB, Georgousopoulou EN, et al. The anti-inflammatory potential of diet and nonalcoholic fatty liver disease: The ATTICA study. Therapeutic Advances in Gastroenterology. 2019; 12:1-11. DOI: 10.1177/1756284819858039
Gadde KM, Martin CK, Berthoud HR, Heymsfield SB. Obesity. Pathophysiology and management. Journal of the American College of Cardiology. 2018; 71:69-84. DOI: 10.1016/j.jacc.2017.11.011
Saxon DR, Iwamoto SJ, Mettenbrink CJ, et al. Antiobesity medication use in 2.2 million adults across eight large health care organizations: 2009-2015. Obesity. 2019; 27:1975-1981. DOI: 10.1002/oby.22581
Heshmati HM. Anti-obesity medical devices. In: Himmerich H, editor. Weight Management. London: IntechOpen; 2020. p. 239-253. DOI: 10.5772/intechopen.91697
Radvinsky D, Iskandar M, Ferzli G. Bariatric surgery today: The good, the bad, and the ugly. Annals of Laparoscopic and Endoscopic Surgery. 2017; 2:52. DOI: 10.21037/ales.2017.02.26
Coates ARM, Halls G, Hu Y. Novel classes of antibiotics or more of the same? British Journal of Pharmacology. 2011; 163:184-194. DOI: 10.1111/j.1476-5381.2011.01250.x
Wang JW, Kuo CH, Kuo FC, et al. Fecal microbiota transplantation: Review and update. Journal of the Formosan Medical Association. 2019; 118:S23-S31. DOI: 10.1016/j.jfma.2018.08.011
Sawangjit R, Chongmelaxme B, Phisalprapa P, et al. Comparative efficacy of interventions on nonalcoholic fatty liver disease (NAFLD). A PRISMA-compliant systematic review and network meta-analysis. Medicine. 2016; 95:32(e4529). DOI: 10.1097/MD.0000000000004529