- Open Access
Non-alcoholic fatty liver disease (NAFLD): a review of pathophysiology, clinical management and effects of weight loss
BMC Endocrine Disorders volume 22, Article number: 63 (2022)
Given the increasing prevalence of diabetes and obesity worldwide, the deleterious effects of non-alcoholic fatty liver disease (NAFLD) are becoming a growing challenge for public health. NAFLD is the most common chronic liver disease in the Western world. NAFLD is closely associated with metabolic disorders, including central obesity, dyslipidaemia, hypertension, hyperglycaemia and persistent abnormalities of liver function tests.
In general NAFLD is a common denominer for a broad spectrum of damage to the liver, which can be due to hepatocyte injury, inflammatory processes and fibrosis. This is normally seen on liver biopsy and can range from milder forms (steatosis) to the more severe forms (non-alcoholic steatohepatitis (NASH), advanced fibrosis, cirrhosis and liver failure). In these patients, advanced fibrosis is the major predictor of morbidity and liver-related mortality, and an accurate diagnosis of NASH and NAFLD is mandatory. Histologic evaluation with liver biopsy remains the gold standard to diagnose NAFLD. Diagnosis of NAFLD is defined as presence of hepatic steatosis, ballooning and lobular inflammation with or without fibrosis. Weight loss, dietary modification, and the treatment of underlying metabolic syndrome remain the mainstays of therapy once the diagnosis is established. Dietary recommendations and lifestyle interventions, weight loss, and the treatment of underlying metabolic syndrome remain the mainstays of therapy once the diagnosis is established with promising results but are difficult to maintain. Pioglitazone and vitamin E are recommended by guidelines in selected patients. This review gives an overview of NAFLD and its treatment options.
Non-alcoholic fatty liver disease (NAFLD) is a common cause of chronic liver disease worldwide. NAFLD is a spectrum of the disease characterized by hepatic steatosis when no other causes for secondary hepatic fat accumulation (e.g., excessive alcohol consumption) can be identified. NAFLD ranges from the more benign condition of non-alcoholic fatty liver (NAFL) to non-alcoholic steatohepatitis (NASH), which is at the more severe end of the spectrum. NAFLD may progress to fibrosis and cirrhosis [1, 2]. In NAFLD, hepatic steatosis is present without evidence of inflammation, whereas in NASH, hepatic steatosis is associated with lobular inflammation and apoptosis that can lead to fibrosis and cirrhosis [1,2,3,4].
Before the middle of the last decade, NASH was widely considered a serious condition, occurring almost exclusively in females with obesity, often associated with Type 2 Diabetes Mellitus (T2DM), and relatively benign prognosis, that are predictive risk factors of cardiovascular disease, stroke, and diabetes [1,2,3,4]. The prevalence of liver disease (NAFLD) has risen rapidly in Western countries, with a worldwide prevalence of 25%. NAFLD is becoming more common chronic liver disease in Western industrialized countries, particularly in patients with central obesity, T2DM, dyslipidaemia, and metabolic syndrome .
In terms of diagnostic tests, the gold standard to investigate any form of liver inflammation e.g. damage is a liver biopsy. In the diagnosis of NAFLD and related disorders, liver biopsies can be extremely helpful and its findings can range from triglyceride deposition as droplets in the hepatocyte to more extensive forms of non-alcoholic steatohepatitis (NASH). NASH is normally characterised by the earlier mentioned lipid droplets in hepatocytes, with concomitant inflammation and a variable degree of hepatic fibrosis. In the majority of the liver steatosis patients, the disease is ‘non-progressive’, however a small portion of these patients develop the earlier mentioned NASH, which can lead to liver failure and even hepatocellular carcinoma [5, 6].
NAFLD management’s US guidelines define NAFLD as steatosis with ≥5% fat infiltration in imaging or histology and b) no alcohol, drug, or viral-induced steatosis. NAFLD patients may present with elevated liver enzymes .
Patients with NAFLD often have one or more components of the metabolic syndrome (MS) like systemic hypertension, dyslipidaemia, Insulin resistance, or overt diabetes . There is increasing evidence that visceral obesity is a risk factor for NAFLD and it also has to be taken into account that MS is a known risk factor in cardiovascular disease development [5, 7]. Based on current literature cardiac and vascular diseases seem to be the most important cause of death in these patients, however the pathophysiological mechanisms connecting cardiovascular disease and NAFLD are not fully understood [5, 7]. It is thought that insulin resistance is a common factor in the pathogenesis linking both entities [5, 7].
Evaluation of abnormal liver enzyme levels in an otherwise healthy patient can pose a challenge to even an experienced clinician. NAFLD is a common explanation for abnormal liver test results in blood donors. It determines asymptomatic elevation of alanine aminotransferase (ALT) and asparate aminotransverase (AST) levels in up to 90% of cases, once other liver disease causes are excluded [8, 9]. The World Health Organization Global Health Observatory data in 2014 indicates that globally obesity occurs in 15% of women and 11% of men aged 18 and over [8, 9]. A study evaluating the prevalence of NASH estimated that 5.7–17% of the US population is affected [8, 9].
The spectrum of NAFLD and related disease, including its complex relationship with MS poses challenges for clinicians. This review aims to summarise the pathophysiology of NAFLD, risk factors, diagnostic measures and conservative and surgical treatment options.
Pathophysiology of NAFLD/NASH
The development of NASH is a complex process and is not completely understood. In the recent years a lot of animal research has been conducted investigating the pathophysiology of NAFLD and NASH, mainly difference in dietary models (high fructose, high fat or methionine/choline deficient diet (MCD) [10, 11]. Based on this body of evidence, it has been suggested that the development of NASH is a two-step process. The first step of this process is fat deposition in the liver that will increase insulin resistance. The second part of this process is cellular and molecular changes involving oxidative stress, and oxidation of fatty acids in the liver due to a variety of factors (cytokine injury, hyperinsulinemia, hepatic iron and/or lipid peroxidation, variation of the extracelular matrix, energy homeostasis, and change in the immune system function) [9, 12]. The development of insulin resistance is an intricate process. In the setting of the MS, as is the case for many patients with NASH, the increase in fat mass and adipocyte differentiation plays a key role in developing insulin resistance.
NAFLD can be divided into two distinct types. The first type of NAFLD has a narrow relationship with metabolic syndrome and the current beliefs are that insulin resistance is the primary pathophysiological mechanism. The second type of NAFLD has a relationship with infectious pathologies that can lead to the occurrence of liver steatosis. In this case infections like hepatitis C and HIV can be a cause, but it is also associated with medication (total parenteral nutrition, glucocorticoids, tamoxifen, tetracycline, amiodaron, methotrexate, valproic acid, vinyl chloride) and specific toxins or inherited/acquired metabolic diseases (e.g. lipodystrophy or cachexia or intestinal bypass surgery) [13, 14].
People with NAFLD generally have characteristics of MS, with the associated cardiovascular disease risk factors [15, 16]. As stated earlier NAFLD is closely related to metabolic syndrome and obesity, type 2 diabetes mellitus (T2DM), and dyslipidaemia are considered to be important risk factors for NAFLD . Studies have shown the increased prevalence of cardiovascular disease (CVD) in patients with NAFLD, without and without diabetes [18, 19]. Thus, NAFLD is generally associated with an unhealthy lifestyle, with evidence, to suggest that changes in unhealthy lifestyles can reduce the transaminase levels and improve NAFLD . A study of patients with T2DM found a higher prevalence of peripheral vascular, coronary and cerebrovascular diseases in subjects with NAFLD than without, with coronary, cerebrovascular and peripheral vascular disease was greater among those with NAFLD than among those without this disease, aside from normal CVD risk factors, medication use and diabetes-related variables . Byrne et al. stated there are over 20 published studies, both prospective and retrospective, that have studied the relationship between NAFLD and cardiovascular disease and concluded that CVD is a clear and present threat , which continues to be confirmed in on-going studies .
The relationship between NAFLD and smoking is controversial [23, 24]. Overall, smoking is a major risk factor for the development of chronic, non-communicable diseases (NCD) such as cancer, T2DM, respiratory and cardiovascular conditions globally . A study of obese rats found that cigarette smoke increased the histological severity of NAFLD . A cross-sectional study of NAFLD patients (smokers and non-smokers) found the proportions of patients with liver significant fibrosis and advanced liver fibrosis among the smokers were significantly higher than those among the non-smokers . A systematic review and meta-analysis of 20 published studies found smoking is greatly associated with NAFLD, and recommended further studies to understand the underlying mechanisms of the association . Smoking was considered an independent risk factor for the development of NAFLD , however, a cross-sectional study of 933 patients (368 smokers and 565 non-smokers as controls) found no difference in the prevalence of NAFLD in the two groups (22.2% versus 29%), nor with heavy smokers (> 20 packs of cigarettes per year) .
Symptoms and signs
The majority of the patients with NAFLD do not experience any symptoms, however some of them may complain of fatigue, right upper quadrant discomfort, hepatomegaly, acanthosis nigricans, and lipomatosis . A significant amount of patients with cirrhosis can be present themselves with end-stage liver disease. In approximately 48-100% NASH can be asymptomatic and very often it is discovered during medical evaluations for other reasons. Although clinical stigmata of chronic liver failure are rarely seen in this population, one study showed that at the time of diagnosis splenomegaly was present in 25% of the patients .
Very often a diagnosis like NASH or NAFLD is discovered due to abnormal liver function tests such as aminotransferases (ALT and AST) or incidental finding of hepatic steatosis on radiologic abdominal finding. Hepatomegaly can present during physical examination and this is caused by the liver’s fatty infiltration .
When performing laboratory tests, serum markers like aminotransferases (AST, ALT), are mild to moderately elevated . However, the AST and ALT levels can be aspecific in patients with NAFLD or related conditions. In other words, AST and ALT levels can either be elevated or normal, but both do exclude the presence of NAFLD [30,31,32]. In patients with NAFLD, ALT elevations are more common than elevations of AST. The ALT levels tend to be higher in NASH than in simple steatosis. Elevated serum ferritin levels are commonly elevated in patients with NAFLD, and increased transferrin saturation is found in 6–11% of patients [30,31,32].
Other markers of interest are alkaline phosphatase (ALP) and clotting factors. In patients with NAFLD ALP can be abnormal and even be elevated 2-3 times the upper limit of its normal value.
In addition, other laboratory values can be helpful in diagnosing NAFLD. Both albumin and bilirubin levels may be high in patients who have developed chronic progressive disease. In cirrhotic patients laboratory measurements of clotting times can be abnormal. Most of the time patients who have developed cirrhosis have a prolonged prothrombin time, thrombocytopenia, and a concomitant neutropenia [30,31,32].
Imaging in NAFLD
In liver diseases such as NAFLD and NASH, various imaging modalities can be used to substantiate the diagnosis, however none of them are routinely used for differentiating between (histological) subtypes of NAFLD or NASH . Computed tomography (CT) scans, abdominal ultrasound (US), or Magnetic Resonance Imaging (MRI) can detect these liver diseases. Imaging findings in patients with NAFLD include increased echogenicity on ultrasound, decreased hepatic attenuation on CT, and an increased fat signal on MRI .
US often reveals a hyperechoic texture or a bright liver because of diffuse fatty infiltration . The sensitivity and the specificity of US are respectively 89 and 93% in detecting increased fibrosis and steatosis . However, the US is the cheapest method and has been the most common modality used in clinical practice. The sensitivity of US is decreased in patients with obesity [36, 37]. The US showing hyperechogenic liver tissue in contrast to the spleen or kidney echogenicity is suggestive of steatosis. However, the sensitivity of the US is only 60–94% in these instances .
Vibration-controlled transient Elastography (VCTE)
VCTE is a non-invasive method for excluding advanced fibrosis in measuring liver stiffness with VCTE [39,40,41]. A meta-analysis of 19 biopsy-controlled studies including over 2700 patients, the optimal cut-off value for steatosis grade > S0 was 248 dB/m (95% Confidence Interval (CI) 237-261) and for steatosis grade > S1 was 268 dB/m (95% CI 257-284) .
CT, MRI, and magnetic resonance spectroscopy (MRS)
Both imaging modalities are able to detect steatosis, but lack sensitivity to detect inflammatory or fibrotic process of the liver .
Unfortunately MRS has a higher sensitivity to detect the earlier mentioned pathological processes it is (not yet) widely available . In general the sensitivity of CT, MRI and MRS to detect steatosis of the liver was 33, 50, and 88%, respectively. Specificity of all three for detection of hepatic steatosis was 100, 83, and 63%, respectively .
Histological findings in NAFLD
The liver biopsy is the Gold standard for diagnosis of NASH or NAFLD. Performing a liver biopsy on every patient with suspected NAFLD remains controversial. The general indications for performing a liver biopsy in patients with NAFLD confirm or exclude the diagnosis. To many, the liver biopsy is considered to be the golden standard in diagnosing NAFLD, but a pre-emptive diagnosis is mostly made up using the medical history, laboratory work and imaging of the patient. A liver biopsy can be very helpful in assessing the amount of hepatic damage in general, but also in patients that remain to have an unclear diagnosis after non-invasive assessments [45,46,47].
Limitations of liver biopsy are sampling error variability, inter and intra-observer variability, and risk and complications—problems with a pathological diagnosis that may lead to misdiagnosis and staging inaccuracies. Many studies have shown sampling variability and uneven distribution of NASH histologic lesions during the evaluation of paired biopsies [45,46,47].
The NAFLD Activity Score (NAS) is a validated score that is used to grade disease activity in patients with NAFLD . The NAS has several components and each of them has a minimum and maximum score; steatosis (0 to 3), lobular inflammation (0 to 3), hepatocellular ballooning (0 to 2) . Fibrosis is not included in the NAS. In the original study that derived the NAS, scores of 0 to 2 occurred in cases mainly considered not diagnostic of NASH; scores of 3 to 4 were evenly divided among those considered not diagnostic, borderline, or positive for NASH; and scores of 5 to 8 occurred in cases that were considered mainly diagnostic of NASH .
The treatment of NAFLD and related diseases (including but not limited to components of MS) consists of several tiers of which conservative and surgical therapies are known treatments. Very often the treatment of patients with NAFLD consists of a multimodal intervention targeting multiple aspects like weight loss, lifestyle modifications and possible medication optimisation.
Conservative treatment - lifestyle modifications and weight loss
To date, there is no specific drug treatment for NAFLD, however it is believed that a combination of treatment goals (lifestyle adjustments, increasing physical activity and smoking/ alcohol cessation) can be beneficial [49, 50].
NAFLD patients, whether living with obesity are not, should be encouraged and educated to partake in a healthy lifestyle approach, which exists irrespective of weight-loss . A healthy diet i.e. reduction of caloric intake and high-glycaemic index (GI) foods, increased consumption of monounsaturated fatty acids, omega-3 fatty acids, fibers, and specific protein sources such as fish and poultry are suggested to have beneficial effects . Studies suggest that a Mediterranean diet, defined as reduced carbohydrate intake (especially sugars and refined carbohydrates) and increased monosaturated and omega-3 fatty acid intake, can reduce liver fat and thus positively contribute to the management of NAFLD [50, 52]. Research into the effect of diet on risk and management of NAFLD found that prolonged consumption of sugary drinks had a positive correlation to NAFLD  and many people with NAFLD tended to consume high levels of sugary drinks and red meat compared to others . Whilst the reduction of and type of carbohydrates on prevention and management of NAFLD has been widely studied, the effects of protein consumption are not as widely known [55, 56]. A high protein diet is suggested to be beneficial for NAFLD management, but the source of protein needs to be considered given the evidence on consumption of red meat on cardiovascular disease, and consideration of proteins in a vegetarian diet .
Other dietary components can also be beneficial in the treatment of NAFLD, like changes in Vitamin E, caffeine and polyphenol intake. Vitamin E is a fat-soluble vitamin that works as an antioxidant . Current data support the use of Vitamin E in non-diabetic patients with nonalcoholic fatty liver disease. However, it should not be considered as the first option for treatment . Vitamin E therapy should be considered as treatment if lifestyle modifications do not produce the expected results due to non-compliance or ineffectiveness .
The PIVENS study showed that a 2-year period of treatment with Vitamin E at 800 IU / day in adult patients significantly reverses steatohepatitis and significantly reduced hepatic steatosis and alanine aminotransferase (ALT), but did not had significant changes in fibrosis compared to placebo [58, 60]. Long-term safety is of concern, several meta-analyses suggest increased mortality in patients taking Vitamin E supplements. Some of them showed a 20% increased risk of haemorrhagic stroke; and another test suggested an increased risk of prostate cancer in men over the age of 50 .
Caffeine is a strong antioxidant that could help reduce the burden of oxidative stress and inflammation in the liver and may provide hepatoprotective effect . Many studies have linked coffee consumption to improvement in liver enzymes in a dose-dependent manner in individuals who are at risk of liver diseases . There is an evident protective role of more than 3 cups of coffee consumption per day but not less than 2 cups according a meta-analysis study .
Finally, polyphenols are a heterogeneous class of plant-derived compounds that include several hydro soluble antioxidants reported as health promoting agents and proposed in the treatment of different metabolic disorders . Natural polyphenols are present in nature and particularly have been found in high quantities in many foods and plants, such as vegetables, fruits, cereals, spices, mushrooms, tea, microalgae, medical plants, wild fruits, and flowers .
There exists a considerable amount of evidence indicating the hepatoprotective effects of these biomolecules, unless they are in cultured cells and animal models. Their optimal dose and the concomitant length of the treatment period are not known .
Weight loss – conservative and surgical
Weight loss is the primary therapy for most patients with NAFLD. Weight loss can improve liver biochemical tests, liver histology, serum insulin levels, and quality of life in patients with NAFLD [65,66,67,68,69].
A significant body of literature has shown that weight loss induces a clinical improvement in patients with NAFLD or NASH. Several studies showed improvement of liver biochemistry after significant weight loss [65,66,67,68,69,70]. In a study of 25 Japanese individuals aminotransferases, cholesterol and fasting glucose improved significantly after a 3-months of combined exercise and dieting . In a study done by Knobler et al. in 48 patients these results were substantiated by the fact that the majority of the patients had improved liver biochemistry and half of them had a complete normalisation of their transaminase profiles .
In the last few years there have been promising outcomes using pioglitazone (and related medication) [71, 72], but also the use of Glucagon-like peptide-1 (GLP-1) receptor agonists has shown significant improvement in hepatic outcomes in patients with NAFLD [73, 74].
In the last years, bariatric and metabolic surgery has made enormous developments. Its benefits regarding weight loss and improvement of several metabolic diseases, like T2DM has been well established [75, 76]. It even has lead to a significantly better long-term overall survival compared to patients treated conservatively [75,76,77].
Specifically looking at NAFLD related outcomes, bariatric and metabolic surgery has not been taken into account as treatment option in many meta-analyses to date, despite the increasing body of evidence and properly designed studies on this subject. Lassailly et al.  found that bariatric and metabolic surgery results in resolution of NAFLD/NASH in the majority of the patients (64.2% in patients that underwent Roux-Y Gastric Bypass (RYGB) and 5.5% in Sleeve Gastrectomy (SG)). Secondly they found regression of the present liver fibrosis .
A meta-analysis on 48 studies showed that the combination of pioglitazone and Roux-en Y Gastric Bypass surgery had the best effects on the NAFLD Activity Score. This suggests a possible causal connection between glucose metabolism and NAFLD development . It needs to be said that bariatric and metabolic surgery solely can impact the amelioration of NAFLD and related disorders, but also its impact on postoperative outcomes after surgery needs to be taken into account .
It has to be said that a small proportion of the patients undergoing bariatric and metabolic surgery develop NASH or suffer from aggravation of the disease (NAFLD/NASH/ live fibrosis) after bariatric surgery . Also the patients on the ‘end of the spectrum’, with liver cirrhosis are in need of special preparation before and after bariatric and metabolic surgery, as highlighted in the systematic reviews done by Jan et al.  and Ahmed et al.  We need to consider that different surgical procedures have different effects on postoperative physiological remodelling and also can lead to (liver-related) complications. (See Fig. 1).
With the growing obesity pandemic and the rising prevalence of comorbid conditions like T2DM and NAFLD, the management of these patients has become even more complex. There are some treatment methods, however there is lack of high-quality studies that compared different treatment methods with each other. Considering that bariatric surgery is increasingly utilized, prospective studies answering the remaining questions on the connection of insulin resistance, fatty liver, and fibrosis progression should become available in the near future.
Availability of data and materials
Ahmed A, Wong RJ, Harrison SA. Nonalcoholic fatty liver disease review: diagnosis, treatment, and outcomes. Clin Gastroenterol Hepatol. 2015;13(12):2062–70.
Machado MV, Diehl AM. Pathogenesis of nonalcoholic Steatohepatitis. Gastroenterology. 2016;150(8):1769–77.
Nasr P, Ignatova S, Kechagias S, Ekstedt M. Natural history of nonalcoholic fatty liver disease: a prospective follow-up study with serial biopsies. Hepatol Commun. 2018;2(2):199–210.
Younossi Z, Anstee QM, Marietti M, Hardy T, Henry L, Eslam M, et al. Global burden of NAFLD and NASH: trends, predictions, risk factors and prevention. Nat Rev Gastroenterol Hepatol. 2018;15(1):11–20.
Browning JD, Szczepaniak LS, Dobbins R, Nuremberg P, Horton JD, Cohen JC, et al. Prevalence of hepatic steatosis in an urban population in the United States: impact of ethnicity. Hepatology (Baltimore, Md). 2004;40(6):1387–95.
Chalasani N, Younossi Z, Lavine JE, Diehl AM, Brunt EM, Cusi K, et al. The diagnosis and management of non-alcoholic fatty liver disease: practice guideline by the American Gastroenterological Association, American Association for the Study of Liver Diseases, and American College of Gastroenterology. Gastroenterology. 2012;142(7):1592–609.
Dixon JB, Bhathal PS, O'Brien PE. Nonalcoholic fatty liver disease: predictors of nonalcoholic steatohepatitis and liver fibrosis in the severely obese. Gastroenterology. 2001;121(1):91–100.
Clark JM, Brancati FL, Diehl AM. The prevalence and etiology of elevated aminotransferase levels in the United States. Am J Gastroenterol. 2003;98(5):960–7.
Edmison J, McCullough AJ. Pathogenesis of non-alcoholic steatohepatitis: human data. Clin Liver Dis. 2007;11(1):75–104, ix.
Erbas O, Erdogan MA, Khalilnezhad A, Gürkan FT, Yiğittürk G, Meral A, et al. Neurobehavioral effects of long-term maternal fructose intake in rat offspring. Int J Dev Neurosci. 2018;69:68–79.
Lau JK, Zhang X, Yu J. Animal models of non-alcoholic fatty liver disease: current perspectives and recent advances. J Pathol. 2017;241(1):36–44.
Day CP, Saksena S. Non-alcoholic steatohepatitis: definitions and pathogenesis. J Gastroenterol Hepatol. 2002;17(Suppl 3):S377–84.
Chitturi S, Farrell GC. Etiopathogenesis of nonalcoholic steatohepatitis. Semin Liver Dis. 2001;21(1):27–41.
Fromenty B, Pessayre D. Impaired mitochondrial function in microvesicular steatosis. Effects of drugs, ethanol, hormones and cytokines. J Hepatol. 1997;26(Suppl 2):43–53.
Byrne CD, Targher G. NAFLD: a multisystem disease. J Hepatol. 2015;62(1):S47–64.
Anstee QM, Targher G, Day CP. Progression of NAFLD to diabetes mellitus, cardiovascular disease or cirrhosis. Nat Rev Gastroenterol Hepatol. 2013;10(6):330–44.
EASL. EASD&EASO clinical practice guidelines for the management of non-alcoholic fatty liver disease. J Hepatol. 2016;64(6):1388–402.
Bhatia LS, Curzen NP, Calder PC, Byrne CD. Non-alcoholic fatty liver disease: a new and important cardiovascular risk factor? Eur Heart J. 2012;33(10):1190–200.
Targher G, Day CP, Bonora E. Risk of cardiovascular disease in patients with nonalcoholic fatty liver disease. N Engl J Med. 2010;363(14):1341–50.
Ou H, Fu Y, Liao W, Zheng C, Wu X. Association between smoking and liver fibrosis among patients with nonalcoholic fatty liver disease. Can J Gastroenterol Hepatol. 2019;2019:6028952.
Targher G, Bertolini L, Padovani R, Rodella S, Tessari R, Zenari L, et al. Prevalence of nonalcoholic fatty liver disease and its association with cardiovascular disease among type 2 diabetic patients. Diabetes Care. 2007;30(5):1212–8.
Lonardo A, Sookoian S, Pirola CJ, Targher G. Non-alcoholic fatty liver disease and risk of cardiovascular disease. Metabolism. 2016;65(8):1136–50.
Hamabe A, Uto H, Imamura Y, Kusano K, Mawatari S, Kumagai K, et al. Impact of cigarette smoking on onset of nonalcoholic fatty liver disease over a 10-year period. J Gastroenterol. 2011;46(6):769–78.
Akhavan Rezayat A, Dadgar Moghadam M, Ghasemi Nour M, Shirazinia M, Ghodsi H, Rouhbakhsh Zahmatkesh MR, et al. Association between smoking and non-alcoholic fatty liver disease: a systematic review and meta-analysis. SAGE Open Med. 2018;6:2050312117745223.
Control CfD. Current cigarette smoking among adults - United States, 2011. MMWR Morb Mortal Wkly Rep. 2012;61(44):889–94.
Azzalini L, Ferrer E, Ramalho LN, Moreno M, Domínguez M, Colmenero J, et al. Cigarette smoking exacerbates nonalcoholic fatty liver disease in obese rats. Hepatology. 2010;51(5):1567–76.
Al-Dayyat HM, Rayyan YM, Tayyem RF. Non-alcoholic fatty liver disease and associated dietary and lifestyle risk factors. Diabetes Metab Syndr. 2018;12(4):569–75.
Chavez-Tapia NC, Lizardi-Cervera J, Perez-Bautista O, Ramos-Ostos MH, Uribe M. Smoking is not associated with nonalcoholic fatty liver disease. World J Gastroenterol. 2006;12(32):5196–200.
Bacon BR, Farahvash MJ, Janney CG, Neuschwander-Tetri BA. Nonalcoholic steatohepatitis: an expanded clinical entity. Gastroenterology. 1994;107(4):1103–9.
Mofrad P, Contos MJ, Haque M, Sargeant C, Fisher RA, Luketic VA, et al. Clinical and histologic spectrum of nonalcoholic fatty liver disease associated with normal ALT values. Hepatology (Baltimore, Md). 2003;37(6):1286–92.
Noguchi H, Tazawa Y, Nishinomiya F, Takada G. The relationship between serum transaminase activities and fatty liver in children with simple obesity. Acta Paediatr Jpn Overseas Edition. 1995;37(5):621–5.
Charatcharoenwitthaya P, Lindor KD, Angulo P. The spontaneous course of liver enzymes and its correlation in nonalcoholic fatty liver disease. Dig Dis Sci. 2012;57(7):1925–31.
Schwenzer NF, Springer F, Schraml C, Stefan N, Machann J, Schick F. Non-invasive assessment and quantification of liver steatosis by ultrasound, computed tomography and magnetic resonance. J Hepatol. 2009;51(3):433–45.
Lonardo A, Bellini M, Tondelli E, Frazzoni M, Grisendi A, Pulvirenti M, et al. Nonalcoholic steatohepatitis and the "bright liver syndrome": should a recently expanded clinical entity be further expanded? Am J Gastroenterol. 1995;90(11):2072–4.
Hernaez R, Lazo M, Bonekamp S, Kamel I, Brancati FL, Guallar E, et al. Diagnostic accuracy and reliability of ultrasonography for the detection of fatty liver: a meta-analysis. Hepatology (Baltimore, Md). 2011;54(3):1082–90.
Mottin CC, Moretto M, Padoin AV, Swarowsky AM, Toneto MG, Glock L, et al. The role of ultrasound in the diagnosis of hepatic steatosis in morbidly obese patients. Obes Surg. 2004;14(5):635–7.
de Moura AA, Cotrim HP, Barbosa DB, de Athayde LG, Santos AS, Bitencourt AG, et al. Fatty liver disease in severe obese patients: diagnostic value of abdominal ultrasound. World J Gastroenterol. 2008;14(9):1415–8.
Adams LA, Talwalkar JA. Diagnostic evaluation of nonalcoholic fatty liver disease. J Clin Gastroenterol. 2006;40(Suppl 1):S34–8.
Wong GL, Wong VW. Fat and fiber: how the controlled attenuation parameter complements noninvasive assessment of liver fibrosis. Dig Dis Sci. 2015;60(1):9–12.
Karlas T, Petroff D, Sasso M, Fan JG, Mi YQ, de Lédinghen V, et al. Individual patient data meta-analysis of controlled attenuation parameter (CAP) technology for assessing steatosis. J Hepatol. 2017;66(5):1022–30.
Shi KQ, Tang JZ, Zhu XL, Ying L, Li DW, Gao J, et al. Controlled attenuation parameter for the detection of steatosis severity in chronic liver disease: a meta-analysis of diagnostic accuracy. J Gastroenterol Hepatol. 2014;29(6):1149–58.
Rofsky NM, Fleishaker H. CT and MRI of diffuse liver disease. Semin Ultrasound CT MR. 1995;16(1):16–33.
Szczepaniak LS, Nurenberg P, Leonard D, Browning JD, Reingold JS, Grundy S, et al. Magnetic resonance spectroscopy to measure hepatic triglyceride content: prevalence of hepatic steatosis in the general population. Am J Physiol Endocrinol Metab. 2005;288(2):E462–8.
Borra RJ, Salo S, Dean K, Lautamäki R, Nuutila P, Komu M, et al. Nonalcoholic fatty liver disease: rapid evaluation of liver fat content with in-phase and out-of-phase MR imaging. Radiology. 2009;250(1):130–6.
Merriman RB, Ferrell LD, Patti MG, Weston SR, Pabst MS, Aouizerat BE, et al. Correlation of paired liver biopsies in morbidly obese patients with suspected nonalcoholic fatty liver disease. Hepatology (Baltimore, Md). 2006;44(4):874–80.
Arun J, Jhala N, Lazenby AJ, Clements R, Abrams GA. Influence of liver biopsy heterogeneity and diagnosis of nonalcoholic steatohepatitis in subjects undergoing gastric bypass. Obes Surg. 2007;17(2):155–61.
Ratziu V, Charlotte F, Heurtier A, Gombert S, Giral P, Bruckert E, et al. Sampling variability of liver biopsy in nonalcoholic fatty liver disease. Gastroenterology. 2005;128(7):1898–906.
Kleiner DE, Brunt EM, Van Natta M, Behling C, Contos MJ, Cummings OW, et al. Design and validation of a histological scoring system for nonalcoholic fatty liver disease. Hepatology (Baltimore, Md). 2005;41(6):1313–21.
Nseir W, Hellou E, Assy N. Role of diet and lifestyle changes in nonalcoholic fatty liver disease. World J Gastroenterol. 2014;20(28):9338–44.
Romero-Gómez M, Zelber-Sagi S, Trenell M. Treatment of NAFLD with diet, physical activity and exercise. J Hepatol. 2017;67(4):829–46.
Freidoony L, Kong ID. Practical approaches to the nutritional management of nonalcoholic fatty liver disease. Integr Med Res. 2014;3(4):192–7.
Pintó X, Fanlo-Maresma M, Corbella E, Corbella X, Mitjavila MT, Moreno JJ, et al. A Mediterranean diet rich in extra-virgin olive oil is associated with a reduced prevalence of nonalcoholic fatty liver disease in older individuals at high cardiovascular risk. J Nutr. 2019;149(11):1920–9.
Siddiqi Z, Karoli R, Fatima J, Khanduri S, Varshneya S, Ahmad SS. Soft drinks consumption and the risk of nonalcoholic fatty liver disease. J Assoc Physicians India. 2017;65(5):28–32.
Zelber-Sagi S, Nitzan-Kaluski D, Goldsmith R, Webb M, Blendis L, Halpern Z, et al. Long term nutritional intake and the risk for non-alcoholic fatty liver disease (NAFLD): a population based study. J Hepatol. 2007;47(5):711–7.
Hallsworth K, Adams LA. Lifestyle modification in NAFLD/NASH: facts and figures. JHEP Rep. 2019;1(6):468–79.
Ampong I, Watkins A, Gutierrez-Merino J, Ikwuobe J, Griffiths HR. Dietary protein insufficiency: an important consideration in fatty liver disease? Br J Nutr. 2020;123(6):601–9.
De Chiara F, Ureta Checcllo C, Ramón AJ. High protein diet and metabolic plasticity in non-alcoholic fatty liver disease: myths and truths. Nutrients. 2019;11(12):2985. https://doi.org/10.3390/nu11122985.
Miller EF. Nutrition management strategies for nonalcoholic fatty liver disease: treatment and prevention. Clin Liver Dis. 2020;15(4):144–8.
Perumpail BJ, Li AA, John N, Sallam S, Shah ND, Kwong W, et al. The role of vitamin E in the treatment of NAFLD. Diseases (Basel, Switzerland). 2018;6(4):86. https://doi.org/10.3390/diseases6040086.
Bugianesi E. Non-alcoholic fatty liver disease: a 360-degree overview. Switzerland: Springer Nature; 2020. https://doi.org/10.1007/978-3-319-95828-6.
Wijarnpreecha K, Thongprayoon C, Ungprasert P. Coffee consumption and risk of nonalcoholic fatty liver disease: a systematic review and meta-analysis. Eur J Gastroenterol Hepatol. 2017;29(2):e8–e12.
Chen YP, Lu FB, Hu YB, Xu LM, Zheng MH, Hu ED. A systematic review and a dose-response meta-analysis of coffee dose and nonalcoholic fatty liver disease. Clin Nutr (Edinburgh, Scotland). 2019;38(6):2552–7.
Abenavoli L, Milic N, Luzza F, Boccuto L, De Lorenzo A. Polyphenols treatment in patients with nonalcoholic fatty liver disease. J Transl Intern Med. 2017;5(3):144–7.
Li S, Tan HY, Wang N, Cheung F, Hong M, Feng Y. The potential and action mechanism of polyphenols in the treatment of liver diseases. Oxidative Med Cell Longev. 2018;2018:8394818.
Petersen KF, Dufour S, Befroy D, Lehrke M, Hendler RE, Shulman GI. Reversal of nonalcoholic hepatic steatosis, hepatic insulin resistance, and hyperglycemia by moderate weight reduction in patients with type 2 diabetes. Diabetes. 2005;54(3):603–8.
Promrat K, Kleiner DE, Niemeier HM, Jackvony E, Kearns M, Wands JR, et al. Randomized controlled trial testing the effects of weight loss on nonalcoholic steatohepatitis. Hepatology (Baltimore, Md). 2010;51(1):121–9.
Keating SE, Hackett DA, George J, Johnson NA. Exercise and non-alcoholic fatty liver disease: a systematic review and meta-analysis. J Hepatol. 2012;57(1):157–66.
Knobler H, Schattner A, Zhornicki T, Malnick SD, Keter D, Sokolovskaya N, et al. Fatty liver--an additional and treatable feature of the insulin resistance syndrome. QJM. 1999;92(2):73–9.
Ueno T, Sugawara H, Sujaku K, Hashimoto O, Tsuji R, Tamaki S, et al. Therapeutic effects of restricted diet and exercise in obese patients with fatty liver. J Hepatol. 1997;27(1):103–7.
Vilar-Gomez E, Martinez-Perez Y, Calzadilla-Bertot L, Torres-Gonzalez A, Gra-Oramas B, Gonzalez-Fabian L, et al. Weight Loss Through Lifestyle Modification Significantly Reduces Features of Nonalcoholic Steatohepatitis. Gastroenterology. 2015;149(2):367–78 e5 quiz e14-5.
Colca JR, Scherer PE. The metabolic syndrome, Thiazolidinediones, and implications for intersection of chronic and inflammatory disease. Mol Metab. 2021;101409. https://doi.org/10.1016/j.molmet.2021.101409.
Takahashi H, Kessoku T, Kawanaka M, Nonaka M, Hyogo H, Fujii H, et al. Ipragliflozin improves the hepatic outcomes of patients with diabetes with NAFLD. Hepatol Commun. 2022;6(1):120–32. https://doi.org/10.1002/hep4.1696.
Ghosal S, Datta D, Sinha B. A meta-analysis of the effects of glucagon-like-peptide 1 receptor agonist (GLP1-RA) in nonalcoholic fatty liver disease (NAFLD) with type 2 diabetes (T2D). Sci Rep. 2021;11(1):22063.
Rezaei S, Tabrizi R, Nowrouzi-Sohrabi P, Jalali M, Atkin SL, Al-Rasadi K, et al. GLP-1 receptor agonist effects on lipid and liver profiles in patients with nonalcoholic fatty liver disease: systematic review and Meta-analysis. Can J Gastroenterol Hepatol. 2021;2021:8936865.
Sjöström L, Narbro K, Sjöström CD, Karason K, Larsson B, Wedel H, et al. Effects of bariatric surgery on mortality in Swedish obese subjects. N Engl J Med. 2007;357(8):741–52.
Sjöström L, Lindroos AK, Peltonen M, Torgerson J, Bouchard C, Carlsson B, et al. Lifestyle, diabetes, and cardiovascular risk factors 10 years after bariatric surgery. N Engl J Med. 2004;351(26):2683–93.
Carlsson LMS, Sjöholm K, Jacobson P, Andersson-Assarsson JC, Svensson PA, Taube M, et al. Life expectancy after bariatric surgery in the Swedish obese subjects study. N Engl J Med. 2020;383(16):1535–43.
Lassailly G, Caiazzo R, Buob D, Pigeyre M, Verkindt H, Labreuche J, et al. Bariatric surgery reduces features of nonalcoholic Steatohepatitis in morbidly obese patients. Gastroenterology. 2015;149(2):379–88 quiz e15-6.
Panunzi S, Maltese S, Verrastro O, Labbate L, De Gaetano A, Pompili M, et al. Pioglitazone and bariatric surgery are the most effective treatments for non-alcoholic steatohepatitis: a hierarchical network meta-analysis. Diabetes Obes Metab. 2021;23(4):980–90.
Goossens N, Hoshida Y, Song WM, Jung M, Morel P, Nakagawa S, et al. Nonalcoholic Steatohepatitis is associated with increased mortality in obese patients undergoing bariatric surgery. Clin Gastroenterol Hepatol. 2016;14(11):1619–28.
Eilenberg M, Langer FB, Beer A, Trauner M, Prager G, Staufer K. Significant liver-related morbidity after bariatric surgery and its reversal-a case series. Obes Surg. 2018;28(3):812–9.
Jan A, Narwaria M, Mahawar KK. A systematic review of bariatric surgery in patients with liver cirrhosis. Obes Surg. 2015;25(8):1518–26.
Ahmed S, Pouwels S, Parmar C, Kassir R, de Luca M, Graham Y, et al. Outcomes of bariatric surgery in patients with liver cirrhosis: a systematic review. Obes Surg. 2021;31(5):2255–67.
Brolin RE, Bradley LJ, Taliwal RV. Unsuspected cirrhosis discovered during elective obesity operations. Arch Surg (Chicago, Ill : 1960). 1998;133(1):84–8.
Dallal RM, Mattar SG, Lord JL, Watson AR, Cottam DR, Eid GM, et al. Results of laparoscopic gastric bypass in patients with cirrhosis. Obes Surg. 2004;14(1):47–53.
Kral JG, Thung SN, Biron S, Hould FS, Lebel S, Marceau S, et al. Effects of surgical treatment of the metabolic syndrome on liver fibrosis and cirrhosis. Surgery. 2004;135(1):48–58.
Sarr MG. Is a bariatric procedure appropriate in patients with portal hypertension secondary to cirrhosis? Surgery for obesity and related diseases : official journal of the American Society for Bariatric. Surgery. 2006;2(3):405–6 discussion 6-7.
Takata MC, Campos GM, Ciovica R, Rabl C, Rogers SJ, Cello JP, et al. Laparoscopic bariatric surgery improves candidacy in morbidly obese patients awaiting transplantation. Surg Obes Relat Dis. 2008;4(2):159–64 discussion 64-5.
Shimizu H, Phuong V, Maia M, Kroh M, Chand B, Schauer PR, et al. Bariatric surgery in patients with liver cirrhosis. Surg Obes Relat Dis. 2013;9(1):1–6.
Rebibo L, Gerin O, Verhaeghe P, Dhahri A, Cosse C, Regimbeau JM. Laparoscopic sleeve gastrectomy in patients with NASH-related cirrhosis: a case-matched study. Surg Obes Relat Dis. 2014;10(3):405–10 quiz 565.
Woodford RM, Burton PR, O'Brien PE, Laurie C, Brown WA. Laparoscopic adjustable gastric banding in patients with unexpected cirrhosis: safety and outcomes. Obes Surg. 2015;25(10):1858–62.
Lin MY, Tavakol MM, Sarin A, Amirkiai SM, Rogers SJ, Carter JT, et al. Safety and feasibility of sleeve gastrectomy in morbidly obese patients following liver transplantation. Surg Endosc. 2013;27(1):81–5.
Pestana L, Swain J, Dierkhising R, Kendrick ML, Kamath PS, Watt KD. Bariatric surgery in patients with cirrhosis with and without portal hypertension: a single-center experience. Mayo Clin Proc. 2015;90(2):209–15.
Wolter S, Duprée A, Coelius C, El Gammal A, Kluwe J, Sauer N, et al. Influence of liver disease on perioperative outcome after bariatric surgery in a northern German cohort. Obes Surg. 2017;27(1):90–5.
Hanipah ZN, Punchai S, McCullough A, Dasarathy S, Brethauer SA, Aminian A, et al. Bariatric surgery in patients with cirrhosis and portal hypertension. Obes Surg. 2018;28(11):3431–8.
García-Sesma A, Calvo J, Manrique A, Cambra F, Justo I, Caso O, et al. Morbidly obese patients awaiting liver transplantation-sleeve Gastrectomy: safety and efficacy from a liver transplant unit experience. Transplant Proc. 2019;51(1):33–7.
Moulla Y, Lyros O, Blüher M, Simon P, Dietrich A. Feasibility and safety of bariatric surgery in high-risk patients: a single-center experience. J Obes. 2018;2018:7498258.
Miñambres I, Rubio MA, de Hollanda A, Breton I, Vilarrasa N, Pellitero S, et al. Outcomes of bariatric surgery in patients with cirrhosis. Obes Surg. 2019;29(2):585–92.
Younus H, Sharma A, Miquel R, Quaglia A, Kanchustambam SR, Carswell KA, et al. Bariatric surgery in cirrhotic patients: is it safe? Obes Surg. 2020;30(4):1241–8.
Frey S, Petrucciani N, Iannelli A. Bariatric surgery in the setting of liver cirrhosis with portal hypertension: the confection and particularities of roux-en-Y gastric bypass in a high-risk patient. Obes Surg. 2020;30(10):4165–6.
Quezada N, Maturana G, Irarrázaval MJ, Muñoz R, Morales S, Achurra P, et al. Bariatric surgery in cirrhotic patients: a matched case-control study. Obes Surg. 2020;30(12):4724–31. https://doi.org/10.1007/s11695-020-04929-y.
Kaul A, Singla V, Baksi A, Aggarwal S, Bhambri A, Shalimar A, et al. Safety and efficacy of bariatric surgery in advanced liver fibrosis. Obes Surg. 2020;30:4359–65.
Salman MA, Mikhail HMS, Nafea MA, Sultan A, Elshafey HE, Tourky M, et al. Impact of laparoscopic sleeve gastrectomy on fibrosis stage in patients with child-a NASH-related cirrhosis. Surg Endosc. 2021;35(3):1269–77. https://doi.org/10.1007/s00464-020-07498-4.
Vuppalanchi R, McCabe MET, Tandra SR, Parcha SP, Ghafoor A, Schuh L, et al. Safety and efficacy of bariatric surgery in cirrhosis patients with extreme obesity. Ann Surg. 2022;275(1):e174–80. https://doi.org/10.1097/SLA.0000000000003891.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Pouwels, S., Sakran, N., Graham, Y. et al. Non-alcoholic fatty liver disease (NAFLD): a review of pathophysiology, clinical management and effects of weight loss. BMC Endocr Disord 22, 63 (2022). https://doi.org/10.1186/s12902-022-00980-1
- Non-alcoholic fatty liver disease
- Weight management
- Bariatric surgery
- Metabolic surgery
- Conservative therapy