BACKGROUND: Chronic liver disease (CLD), mainly non-alcoholic fatty liver disease (NAFLD), is a significant public health concern worldwide. This study aims to quantify the burden of NAFLD in CLD globally and within China, using data from the Global Burden of Disease (GBD) Study 2021, providing crucial insights for global and local health policies. METHODS: The study used comprehensive data from the GBD study 2021. It included estimates of prevalence, incidence, mortality, and disability-adjusted life years (DALYs). Age-standardized rates and average annual percent change (AAPC) from 2011 to 2021 were reported. A meticulous decomposition analysis was conducted. RESULTS: In 2021, there were 1582.5 million prevalent cases, 47.6 million incident cases, 1.4 million deaths, and 44.4 million DALYs attributable to CLD, globally. Among these, NAFLD has emerged as the predominant cause, accounting for 78.0% of all prevalent CLD cases (1234.7 million) and 87.2% of incident cases (41.5 million). Correspondingly, NAFLD had the highest age-standardized prevalence (15,017.5 per 100,000 population) and incidence (876.5 per 100,000 population) rates among CLDs. In addition, China's CLD age-standardized prevalence rate was 21,659.5 per 100,000 population, and the age-standardized incidence rate was 752.6 per 100,000 population, higher than the global average. From 2011 to 2021, the global prevalence rate of CLD increased slowly (AAPC = 0.17), consistent with the trend in China (AAPC = 0.23). Furthermore, the prevalence rate of NAFLD rose significantly in China (AAPC = 1.30) compared with the global average (AAPC = 0.91). Decomposition analysis also showed the worldwide increase in deaths and DALYs for NAFLD, which were primarily attributable to population growth and aging. CONCLUSIONS The burden of CLD and NAFLD remains substantial globally and within China in terms of high prevalence and incidence. As such, this underscores the need for targeted prevention and treatment strategies. These findings emphasize the importance of continued surveillance and research to mitigate the growing impact of liver diseases on global and Chinese health systems.
Humans ; Non-alcoholic Fatty Liver Disease/mortality* ; Global Burden of Disease ; China/epidemiology* ; Prevalence ; Male ; Disability-Adjusted Life Years ; Female ; Incidence ; Middle Aged ; Chronic Disease ; Adult ; Quality-Adjusted Life Years ; Liver Diseases/epidemiology* ; Aged

BACKGROUND: The heterogeneity of histological findings in preclinical diet-induced nonalcoholic fatty liver disease (NAFLD) animal models is highly challenging. Here, we aimed to evaluate the feasibility and stability of repeated liver biopsy in NAFLD animal models. METHODS: Heterogeneity of diet-induced NAFLD was evaluated at different time points in 52 high-fat diet (HFD), 35 methionine choline-deficiency diet (MCD), and 166 western diet (WD) induced NAFLD mice. Serial liver biopsies (left lateral, right medial, and left medial lobes) were performed monthly for up to 3 months. Mortality rates and changes in food intake, body weight, and liver enzymes were assessed. RESULTS: At 12 weeks, of the HFD animals, 14% and 30% did not develop steatosis and lobular inflammation, respectively; of the MCD animals, 7% did not develop lobular inflammation; and of the WD animals, 14% and 51% did not develop steatosis and lobular inflammation, respectively. The mortality rate of repeated liver biopsy was 1.62% (2/123 mice died). Repeated liver biopsy can be used to trace disease progression. Although body weight, food intake, and liver enzymes slightly changed after biopsy, all recovered within a week. Repeated liver biopsy did not affect the degrees of inflammation and steatosis of the other liver lobes. CONCLUSION: The diet-induced NAFLD models were quite heterogeneous. Our results suggest that the repeated liver biopsy before treatment was applicable and stable in this NAFLD animal study.
Animals ; Biopsy* ; Body Weight ; Diet ; Diet, High-Fat ; Diet, Western ; Disease Progression ; Eating ; Inflammation ; Liver* ; Methionine ; Mice ; Models, Animal ; Mortality ; Non-alcoholic Fatty Liver Disease* ; Population Characteristics

Nonalcoholic fatty liver disease (NAFLD), together with metabolic syndrome and obesity, has shown a rapid increase in prevalence worldwide and is emerging as a major cause of chronic liver disease and liver transplantation. Among the various phenotypes of NAFLD, nonalcoholic steatohepatitis (NASH) is highly likely to progress to development of end-stage liver disease and cardiometabolic disease, resulting in liver-related and non-liver–related mortality. Nonetheless, there is no standardized pharmacotherapy against NASH and many drugs are under development in ongoing clinical trials. To develop a successful anti-NASH drug, it is necessary to select an appropriate target population and treatment outcomes depending on whether the mode of action is anti-metabolic, anti-inflammatory or anti-fibrotic. Recently, innovative surrogate markers have been investigated to replace hard outcomes such as liver histology and mortality and reduce the clinical trial duration. Currently, several drugs with fast track designation are being tested in phase III clinical trials, and many other drugs have moved into phase II clinical trials. Both lean NAFLD and typical obese NAFLD have been extensively studied and genetic variants such as PNPLA3 and TM6SF2 have been identified as significant risk factors for lean NAFLD. In the near future, noninvasive biomarkers and effective targeted therapies for NASH and associated fibrosis are required to develop precision medicine and tailored therapy according to various phenotypes of NAFLD.
Biomarkers ; Drug Therapy ; Fibrosis ; Health Services Needs and Demand ; Liver ; Liver Diseases ; Liver Transplantation ; Mortality ; Non-alcoholic Fatty Liver Disease ; Obesity ; Phenotype ; Precision Medicine ; Prevalence ; Risk Factors

No abstract available.
Liver Diseases ; Liver ; Mortality ; Non-alcoholic Fatty Liver Disease ; Risk Factors

Childhood obesity increases the risk of morbidity and mortality in adulthood. The epidemic of childhood obesity has become an important public health issue in Korea. Currently, the overall prevalence of obesity among Korean children and adolescents is approximately 10%, which is 5 times higher than in the late 1970s. In most cases, a positive energy balance (from excessive calorie intake and limited physical activity) combined with a genetic predisposition is considered the major cause of childhood obesity. The evaluation of obese children should focus on possible causes of weight gain, including lifestyle factors and underlying endocrine or genetic abnormalities. The assessment of obesity-related comorbidities, such as hyperglycemia, dyslipidemia, hypertension, and non-alcoholic fatty liver disease, is often needed in obese children, especially those who have a family history of comorbidities. Family-based lifestyle interventions including goal-setting, guidelines for eating habits and physical activity, self-monitoring, and stimulus control are fundamental to the management of childhood obesity. Medications and bariatric surgery are possible choices for patients with severe obesity and comorbidities, although the data on the long-term efficacy and safety of these treatments are limited. This article reviews practical assessments and interventions for childhood obesity.
Adolescent ; Bariatric Surgery ; Child ; Comorbidity ; Dyslipidemias ; Eating ; Genetic Predisposition to Disease ; Humans ; Hyperglycemia ; Hypertension ; Korea ; Life Style ; Mortality ; Motor Activity ; Non-alcoholic Fatty Liver Disease ; Obesity ; Obesity, Morbid ; Pediatric Obesity* ; Prevalence ; Public Health ; Weight Gain

Obesity is closely associated with hepatocellular carcinoma (HCC) as well as other malignancies. Obesity is an important risk factor for cancer development and overall mortality in HCC. Molecular mechanisms of hepatocarcinogenesis in obesity are adipose tissue remodeling, dysregulation of adipokines, increased reactive oxygen species, insulin resistance or hyperinsulinemia, alteration of gut microbiota, and dysregulation of microRNA. Obesity is the most common cause of non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steatohepatitis (NASH). NAFLD or NASH leads to HCC as well as liver cirrhosis. Hepatitis C virus regulates lipid homeostasis in liver. Obesity and its’ related factors (metabolic syndrome and diabetes mellitus) are significantly related to the risk of HCC development in chronic hepatitis C. However, it is not clear whether obesity is a risk factor for HCC in chronic hepatitis B. The relationship between obesity and HCC seems to be different according to etiology of background liver disease. Further studies are needed to clarify the effect of obesity on HCC in different etiologies of chronic liver disease.
Adipokines ; Adipose Tissue ; Carcinoma, Hepatocellular* ; Fatty Liver ; Gastrointestinal Microbiome ; Hepacivirus ; Hepatitis B, Chronic ; Hepatitis C, Chronic ; Homeostasis ; Hyperinsulinism ; Insulin Resistance ; Liver ; Liver Cirrhosis ; Liver Diseases ; MicroRNAs ; Mortality ; Non-alcoholic Fatty Liver Disease ; Obesity* ; Reactive Oxygen Species ; Risk Factors

Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in both developed and developing countries and is an important risk factor for both hepatic and cardiometabolic mortality. Despite decades of clinical trials, effective treatment options for NAFLD are limited, requiring novel therapeutic approaches to prevent disease development and progression to cirrhosis and cancer. Recently, bile acids have emerged as signaling molecules and metabolic regulators that can activate signaling mediated by nuclear receptors and G protein-coupled receptors to regulate hepatic lipid, glucose, and energy homeostasis, as well as its own synthesis and transport in the liver and intestine. Many recent studies have reported that the activation or modulation of bile acid signaling mediated by bile acid receptors favorably affects both insulin sensitivity and NAFLD pathogenesis at multiple levels, suggesting that these approaches hold promise as novel therapies. In this review, we provide an overview of the role of bile acids, in particular, their signaling related to the nuclear receptor farnesoid X receptor in NAFLD and new insights into the possible approach of targeting bile acid-related pathways in the treatment of this serious disease.
Bile Acids and Salts ; Bile ; Developing Countries ; Fibrosis ; Gastrointestinal Microbiome ; Glucose ; Homeostasis ; Insulin Resistance ; Intestines ; Liver ; Liver Diseases ; Metabolism ; Mortality ; Non-alcoholic Fatty Liver Disease ; Receptors, Cytoplasmic and Nuclear ; Risk Factors