- Research article
- Open Access
Association of Cardiovascular Risk Factors and Metabolic Syndrome with non-alcoholic and alcoholic fatty liver disease: a retrospective analysis
BMC Endocrine Disorders volume 21, Article number: 91 (2021)
Although many studies on non-alcoholic fatty liver disease (NAFLD) are underway worldwide, and several existing studies have investigated the association between NAFLD and cardiovascular risk factors, studies comparing NAFLD and alcoholic fatty liver disease (AFLD) are scarce. This study aimed to evaluate differences between the incidence of cardiovascular risk factors and metabolic syndrome in NAFLD and AFLD.
A retrospective analysis of 913 patients who underwent abdominal computed tomography (CT) was performed to compare the incidence of cardiovascular risk factors and metabolic syndrome between NAFLD and AFLD. Subjects were divided into three groups based on criteria: healthy (n = 572), NAFLD (n = 295), and AFLD (n = 46). The healthy group had no liver disease. NAFLD was defined as fatty liver diagnosed on CT and drinking less than 140 g/week for men or 70 g/week for women. AFLD was defined as fatty liver diagnosed on CT and drinking more than 140 g/week for men or 70 g/week for women. We compared the incidence of cardiovascular risk factors and metabolic syndrome between the three groups. The relationship between each group and the metabolic syndrome risk was analyzed through multivariate logistic regression analysis.
No significant differences in several cardiovascular risk factors were observed between the NAFLD and AFLD groups. Upon analyzing the metabolic syndrome status in each group after making appropriate adjustments, the odds ratios (ORs) in the NAFLD (OR = 2.397, P = 0.002) and AFLD groups (OR = 4.445, P = 0.001) were found to be significantly higher than that in the healthy group; the incidence rate of metabolic syndrome was similar in the NAFLD and AFLD groups.
Both the NAFLD and AFLD groups had more cardiovascular risk factors and higher metabolic syndrome risk than the healthy group. Thus, the prevention of fatty liver disease, regardless of the specific type, should involve the identification of cardiovascular and metabolic syndrome risk factors. If abdominal CT reveals a fatty liver, whether NAFLD or AFLD, the risk of cardiovascular disease and metabolic syndrome should be assessed.
Fatty liver disease is defined as the accumulation of fat (mainly triglycerides [TG]) in hepatocytes that accounts for > 5% of the total liver weight. It includes benign steatosis and steatohepatitis, which can cause cirrhosis . Fatty liver disease is largely divided into alcoholic fatty liver disease (AFLD) and non-alcoholic fatty liver disease (NAFLD), depending on the drinking status of the patient. Distinguishing between the two types cannot be done clinically, biochemically, or by liver tissue biopsy, but only by determining the quantity of alcohol intake .
Fatty liver disease can be diagnosed using imaging techniques such as ultrasonography, computed tomography (CT), and magnetic resonance imaging (MRI) . Although the most accurate method for diagnosis is liver tissue biopsy, it is clinically difficult to perform. Therefore, assessment of the severity of fatty liver disease in clinical practice is mostly dependent on the clinical experience of the diagnosing physician .
Alcoholic fatty liver is caused by excessive drinking. This is due to increased TG synthesis and increased influx of fatty acids from peripheral tissues into the liver during drinking, when the release of lipoproteins into the blood and the oxidation of fatty acids are poor . While the condition can be alleviated by abstinence from alcohol, it can also progress to hepatitis, cirrhosis, and hepatocellular carcinoma . Meanwhile, NAFLD has pathological characteristics similar to those of AFLD but occurs in nondrinkers and can progress to chronic liver diseases .
As the number of health screening examinees has been increasing in recent years, along with an increased interest in health, the number of people diagnosed with fatty liver disease has also increased. Patients should be informed of the risks associated with fatty liver disease and the relationship of the disease with cardiovascular diseases, in order to help them understand the lifestyle changes needed to reduce risk factors, and should be provided with information about the treatment of this disease.
Obesity, diabetes, and hyperlipidemia are known factors that increase the risk of AFLD , which is known to increase the prevalence rate of metabolic syndrome and disorders [8, 9]. Although many studies on NAFLD are underway worldwide, and several existing studies have investigated the association between NAFLD and cardiovascular risk factors, studies comparing NAFLD and AFLD are scarce. Therefore, in this study, we investigated the morbidity rate of AFLD and NAFLD in male health-screening examinees, while assessing their pathological and behavioral characteristics. We performed a comparative analysis of the association between each cardiovascular risk indicator, and the differences between these indicators, by dividing the subjects into healthy, AFLD, and NAFLD groups.
This study investigated the morbidity rate of AFLD and NAFLD in male health-screening examinees, while assessing their pathological and behavioral characteristics.
Study subjects older than 19 years of age were selected from among male and female city residents who underwent examinations at a university hospital health promotion center between March 2013 and March 2018. Based on the assumption of a significant difference in drinking habits between urban residents and the relatively fewer rural residents (Eop or Myon), the latter were excluded to keep the study conditions relatively homogeneous. The medical records of examinees who underwent CT were retrospectively reviewed in this study. Those who met the following criteria were also excluded from the study: incomplete records, leukocyte count > 10.0 × 103/μL, acute hepatitis-related test findings, hepatitis B surface antigen or hepatitis C virus antibody positive, abnormal thyroid function test findings, abdominal ultrasonography findings suggestive of diffuse or local liver diseases, creatinine level > 1.3 mg/dL, or a history of cancer. In addition, those with hypertension, diabetes, rheumatoid arthritis, asthma, rhinitis, ischemic heart diseases and myocardial infarction, cerebral infarction and hemorrhage, and thyroid diseases, or those receiving hormone replacement therapy were also excluded. Participants with high-sensitivity C-reactive protein (hsCRP) levels > 10 mg/dL were excluded because they were suspected of having active inflammation or tissue damage, such as acute infection or systemic inflammation . In addition, patients with normal abdominal ultrasonographic findings, but with aspartate aminotransferase (AST), alanine aminotransferase (ALT), and gamma-glutamyl transpeptidase (ϓ-GT) levels > 100 IU/L were excluded. As a result, 913 participants were included in the final analysis. This study followed the ethical standards laid out in the Declaration of Helsinki. The study was approved by the Clinical Trial Screening Committee of Wonkwang University Hospital (institutional review board approval number: 201609-HR-097), and informed consent was obtained verbally from all participants.
Through self-administered questionnaires and interviews with the attending physicians at the health promotion center, factors such as disease history, ongoing treatments and medications for existing diseases, drinking and smoking habits, and exercise habits were investigated. The types of alcohol and the average amount consumed per week were surveyed. By dividing the participants into current smokers and nonsmokers, the smoking status of the participants was also surveyed. The average weekly exercise frequency was also recorded.
Anthropometric measurements and blood pressure
Height and weight were measured using an automatic height scale, and body mass index (BMI) was calculated by dividing weight by the square of height (kg/m2). Waist circumference was measured according to the level recommended by the World Health Organization at the middle (halfway) point between the lowest rib and iliac crest on the CT image. Blood pressure was measured using an automatic blood pressure monitor after maintaining stable pressure for > 10 min, and the average of two measurements was recorded.
Venous blood was collected at 10:00 AM, after more than 12 h of fasting. Fasting plasma glucose, total cholesterol, high-density lipoprotein cholesterol, TG, low-density lipoprotein cholesterol, AST, ALT, ϓ-GT, and hsCRP levels were measured.
In order to avoid examiner bias, all of the data were reconfirmed by one medical imaging specialist who was blinded to the patients’ characteristics and study aims. CT examinations of the abdomen were performed using the Somatom Definition (Siemens Medical Solutions, Forchheim, Germany). Steatosis was confirmed by either a liver attenuation < 40 Hounsfield Units (HU) or a liver attenuation of at least 10 HU less than that of the spleen [11, 12].
Classification of study groups
The healthy group comprised examinees who showed normal liver echo on abdominal CT; whose AST, ALT, and ϓ-GT values were normal in the liver function tests; and who drank alcohol at a rate of less than 140 g/week for men or 70 g/week for women . The NAFLD group comprised examinees who were diagnosed with fatty liver disease according to abdominal CT results and drank less than 140 g/week for men and 70 g/week for women, regardless of the liver function test values [14, 15]. Meanwhile, the AFLD group comprised participants who drank more than 140 g/week for men or 70 g/week for women and were not obese (Fig. 1).
SPSS for Windows version 26.0 (SPSS Inc., Chicago, IL, USA) was used for statistical analysis. A comparative analysis between non-continuous variables was performed using the chi-square test. The comparative analysis between continuous variables was performed using one-way analysis of variance. The Scheffe test was used for post hoc testing of differences between the groups. The analysis of covariance was used to analyze the average difference between the groups for the following factors: waist circumference, blood pressure, fasting plasma glucose, total cholesterol, high-density lipoprotein cholesterol, TG, low-density lipoprotein cholesterol, and hsCRP levels, after adjusting for age, BMI, daily smoking quantity, and weekly exercise frequency. The differences between the groups were confirmed using a simple and repeated method of contrast testing. The relationship between each group and the metabolic syndrome was analyzed through multivariate logistic regression analysis after adjusting for age, daily smoking quantity, and weekly exercise frequency. Statistical significance was set at P < 0.05.
General patient characteristics
The total numbers of involved participants were as follows: 572 (62.7%), healthy group; 295 (32.3%), NAFLD group; and 46 (5.0%), AFLD group. The average ages were 52.5 ± 10.4 in the healthy group, 52.7 ± 9.7 in the NAFLD group, and 47.4 ± 9.1 in the AFLD group. The numbers of male subjects were 298 (52.1%) in the healthy group, 210 (71.2%) in the NAFLD group, and 39 (84.8%) in the AFLD group. The average BMI was higher in the AFLD group than in both the NAFLD and healthy groups. Significant differences in AST, ALT, and ϓ-GT levels were observed between the groups; the AST and ϓ-GT levels in the NAFLD group were higher than those in the healthy group. The ALT level was higher in the NAFLD and AFLD groups than in the healthy group. Both the AFLD and NAFLD groups had a larger waist circumference than the healthy group, whereas no significant difference was found between the AFLD and NAFLD groups. Significant differences were found in the average weekly exercise frequency in the following decreasing order: the AFLD, healthy, and NAFLD groups (Table 1).
Comparison of cardiovascular risk indicators
Significant differences were found between the groups in terms of average systolic blood pressure, diastolic blood pressure, fasting plasma glucose level, total cholesterol level, TG level, high-density lipoprotein level, low-density lipoprotein level, and hsCRP level. In the comparative analysis between the groups through post hoc tests, no significant difference was found between the NAFLD and AFLD groups in terms of systolic blood pressure, diastolic blood pressure, fasting plasma glucose level, total cholesterol level, high-density lipoprotein level, TG level, low-density lipoprotein level, and hsCRP, but the values from either group were higher than those of the healthy group.
Systolic blood pressure was higher in the NAFLD group than in the healthy group, and the diastolic blood pressure was higher in the NAFLD and AFLD groups than in the healthy group. The fasting plasma glucose level was highest in the AFLD group, followed by the NAFLD group, and lowest in the healthy group. High-density cholesterol was lower in the NAFLD group than in the healthy group. TG levels were higher in the NAFLD and AFLD groups than in the healthy group. Low-density cholesterol was higher in the NAFLD group than in the healthy group. The hsCRP level was higher in the AFLD group than in the healthy and NAFLD groups (Table 2).
Association with metabolic syndrome
In the analysis to determine the association of metabolic syndrome status with each group after adjusting for age, smoking, and exercise frequency, the odds ratios (ORs) in the NAFLD group (OR = 2.397, P = 0.002) and AFLD group (OR = 4.445, P = 0.001) were significantly higher than that in the healthy group (Table 3), but no significant difference was found between the NAFLD and AFLD groups (Table 4).
Fatty liver disease has the highest prevalence rate among liver diseases not only worldwide but also in South Korea. According to a recent study conducted in South Korea, the prevalence rate of fatty liver disease diagnosed using ultrasonography was 30%, accounting for 69.7% of liver disease cases . Similarly, the morbidity rate of fatty liver disease in this study was 32.3%. The worldwide prevalence rate of NAFLD varies between studies . In the United States, one-third have been diagnosed with NAFLD, and in the United Kingdom it is reported as 29 cases per 100,000 person-years, which is clearly on a globally increasing trend [17, 18].
Because it is a standard commonly used in the diagnosis of NAFLD, the weekly alcohol consumption among patients diagnosed with NAFLD ranges from 0 to 140 g for men or 0 to 70 g for women [14, 15]. In this study, we defined nondrinkers as individuals who consumed < 140 g per week, according to the standard proposed by Choi et al. . In addition, while the total drinking quantity was measured through the questionnaire, 350 mL of beer, 120 mL of wine, 25 mL of brandy, or 50 mL of soju was considered to contain 10 g of alcohol by surveying the type of alcohol and the number of bottles consumed.
There was no difference between the NAFLD and AFLD groups for each of the indicators of cardiovascular risk factors. Importantly, however, these indicators differed between those two groups and the healthy group. This conclusion suggests that the risk factors are more related to the presence or absence of fatty liver, regardless of the cause of the occurrence of fatty liver. Systolic blood pressure, diastolic blood pressure, fasting plasma glucose level, total cholesterol level, and TG level were higher, whereas high-density cholesterol was lower in the NAFLD group than in the healthy group, indicating an increase in cardiovascular risk indicators in the NAFLD group. NAFLD is reportedly accompanied by obesity (30–100%), diabetes (10–75%), or dyslipidemia (20–92%) . In a study on the association between NAFLD and cardiovascular disease, blood pressure, fasting plasma glucose level, total cholesterol level, and TG level were higher in the NAFLD group than in the healthy group. In another study , systolic blood pressure, fasting plasma glucose level, total cholesterol level, and TG level were higher in the NAFLD group than in the healthy group, although sex-related differences in the values were found. The previous results are similar to the results of this study.
Diastolic blood pressure, fasting plasma glucose level, total cholesterol level, TG level, and hsCRP level were all higher in the AFLD group than in the healthy group. That is, except for high-density cholesterol levels, the values of the cardiovascular indicators in the AFLD group, as in the NAFLD group, were higher than those in the healthy group. Studies on the relationship between high-density cholesterol levels and fatty liver disease reported that high-density cholesterol levels were decreased in fatty liver [20, 21], though one study reported a contradictory result . Additionally, other studies reported that low-density cholesterol levels were decreased in NAFLD [23, 24]. In this study, low-density cholesterol levels were higher in the NAFLD group than in the healthy group. Several studies that investigated TG levels reported, as found in this study, that TG increased in both the NAFLD and AFLD groups [20,21,22, 25]. Although no difference was found in the hsCRP level, one of the cardiovascular risk indicators, in both the healthy and NAFLD groups, was lower than that in the AFLD group. Among the many studies that support the association between fatty liver disease and inflammation indicators, one identified that high hsCRP levels were independently associated with fatty liver disease, obesity, and metabolic syndrome , whereas another reported that hsCRP level was a strong predictor of NAFLD .
While the metabolic syndrome rate was higher in the NAFLD and AFLD groups than in the healthy group, no significant difference was observed between the NAFLD and AFLD groups. A previous study reported that the fatty acid content in the liver was increased in patients with metabolic syndrome regardless of age, sex, or BMI , and an association between several metabolic disorders and serious liver diseases was identified [28, 29].
As for the limitations of this study, the study results cannot be generalized because all the patients included in the study were hospitalized at the same health promotion center. Moreover, achieving reliability was difficult because the alcohol consumption level, smoking habit, and exercise frequency were surveyed through a self-administered questionnaire. In addition, NAFLD was determined by CT with no histologic confirmation of fatty liver. However, the fact that the AST/ALT ratio in most NAFLD patients was below 1 rationalizes the selection method of patients for the NAFLD group in this study . Another limitation is as follows. NAFLD was renamed metabolic dysfunction associated fatty liver disease (MAFLD) [31,32,33]. Because NAFLD is an “exclusive” disease, it is insufficient to explain its pathogenesis and management. The diagnostic criteria for MAFLD better reflect disease mechanisms than those for NAFLD [31,32,33]. However, we designed this study before MAFLD was termed. In the future, there is a need to develop this research on the subject using MAFLD.
This is a comparative study on not only NAFLD, which has been previously studied extensively, but also on AFLD, and patients taking medications for hypertension, diabetes, hyperlipidemia, ischemic heart disease, myocardial infarction, cerebral infarction, and hemorrhage were excluded. Therefore, this study is significant in that it provided a pure association between the cardiovascular risk indicators and the NAFLD or AFLD group.
The values of the cardiovascular risk indicators were significantly higher in the NAFLD and AFLD groups than in the healthy group in this study. Ultimately, considering that the patients in both the NAFLD and AFLD groups have the same cardiovascular disease risks, patients diagnosed with fatty liver disease should be examined for risk factors of cardiovascular diseases and should undergo management and treatment of such diseases. Although this study demonstrated that cardiovascular risk indicators and the severity of fatty liver are not associated, additional studies in this area are necessary.
Availability of data and materials
Alcoholic fatty liver disease
Non-alcoholic fatty liver disease
Magnetic resonance imaging
high-sensitivity C-reactive protein
Body mass index
Bedogni G, Bellentani S. Fatty liver: how frequent is it and why? Ann Hepatol. 2004;3(2):63–5. https://0-doi-org.brum.beds.ac.uk/10.1016/S1665-2681(19)32110-6.
Van Hoek B. Non-alcoholic fatty liver disease: a brief review. Scand J Gastroenterol. 2004;241:56–9.
Sanyal AJ. Nonalcoholic steatohepatitis. Clin Perspect Gastroenterol. 2000;3:129–39.
Crabb DW. Pathogenesis of alcoholic liver disease: newer mechanisms of injury. Keio J Med. 1999;48(4):184–8. https://0-doi-org.brum.beds.ac.uk/10.2302/kjm.48.184.
Sorensen TI, Orholm M, Bentsen KD, Hoybye G, Eghoje K, Christoffersen P. Prospective evaluation of alcohol abuse and alcoholic liver injury in men as predictors of development of cirrhosis. Lancet. 1984;2(8397):241–4. https://0-doi-org.brum.beds.ac.uk/10.1016/s0140-6736(84)90295-2.
Yeon JE. The clinical implication of non-alcoholic fatty liver disease. J Korean Acad Fam Med. 2003;24:510–5.
Seo SH, Lee HW, Park HW, Jang BG, Chung WJ, Park KS, et al. Prevalence and associated factors of nonalcoholic fatty liver disease in the health screen examinees. Korean J Med. 2006;70:26–32.
Kang JH, Lee SW, Lee HS, Cho CY, Yu BY. The relation of nonalcoholic fatty liver disease to metabolic syndrome. J Korean Acad Fam Med. 2004;25:746–53.
Lee SY, Kim SK, Kwon CI, Kim MJ, Kang MS, Ko KH, et al. Clinical characteristics of health screen examinees with nonalcoholic fatty liver and normal liver function test. Korean J Gastroenterol. 2008;52:161–70.
Gabay C, Kushner I. Acute-phase proteins and other systemic responses to inflammation. N Engl J Med. 1999;340(6):448–54. https://0-doi-org.brum.beds.ac.uk/10.1056/NEJM199902113400607.
Lawrence DA, Oliva IB, Israel GM. Detection of hepatic Steatosis on contrast-enhanced CT images: diagnostic accuracy of identification of areas of presumed focal fatty sparing. Am J Roentgenol. 2012;199(1):44–7. https://0-doi-org.brum.beds.ac.uk/10.2214/AJR.11.7838.
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 Association for the Study of Liver Diseases, American College of Gastroenterology, and the American Gastroenterological Association. Hepatology. 2012;55(6):2005–23. https://0-doi-org.brum.beds.ac.uk/10.1002/hep.25762.
Choi SY, Kim D, Kang JH, Park MJ, Kim YS, Lim SH, et al. Nonalcoholic fatty liver disease as a risk factor of cardiovascular disease: relation of non-alcoholic fatty liver disease to carotid atherosclerosis. Korean J Hepatol. 2008;14(1):77–88. https://0-doi-org.brum.beds.ac.uk/10.3350/kjhep.2008.14.1.77.
Angulo P. Nonalcoholic fatty liver disease. N Engl J Med. 2002;346(16):1221–31. https://0-doi-org.brum.beds.ac.uk/10.1056/NEJMra011775.
Adams LA, Angulo P. Recent concepts in non-alcoholic fatty liver disease. Diabet Med. 2005;22(9):1129–33. https://0-doi-org.brum.beds.ac.uk/10.1111/j.1464-5491.2005.01748.x.
Lee MY, Jung HR, Lim CH. Comparative analysis per area of the liver diseases in ultrasound diagnosis of healthcare center. J Korea Contents Assoc. 2009;9(3):278–87. https://0-doi-org.brum.beds.ac.uk/10.5392/JKCA.2009.9.3.278.
Whalley S, Puvanachandra P, Desai A, Kennedy H. Hepatology outpatient service provision in secondary care: a study of liver disease incidence and resource costs. Clin Med. 2007;7(2):119–24. https://0-doi-org.brum.beds.ac.uk/10.7861/clinmedicine.7-2-119.
Stepanova M, Younossi ZM. Independent association between nonalcoholic fatty liver disease and cardiovascular disease in the US population. Clin Gastroenterol Hepatol. 2012;10(6):646–50. https://0-doi-org.brum.beds.ac.uk/10.1016/j.cgh.2011.12.039.
Al Rifai M, Silverman MG, Nasir K, Budoff MJ, Blankstein R, Szklo M, et al. The association of nonalcoholic fatty liver disease, obesity, and metabolic syndrome, with systemic inflammation and subclinical atherosclerosis: the multi-ethnic study of atherosclerosis (MESA). Atherosclerosis. 2015;239(2):629–33. https://0-doi-org.brum.beds.ac.uk/10.1016/j.atherosclerosis.2015.02.011.
Baraona E, Lieber CS. Effects of ethanol on lipid metabolism. J Lipid Res. 1979;20(3):289–315. https://0-doi-org.brum.beds.ac.uk/10.1016/S0022-2275(20)40613-3.
Hannuksela ML, Rämet ME, Nissinen AE, Liisanantti MK, Savolainen MJ. Effects of ethanol on lipids and atherosclerosis. Pathophysiology. 2004;10(2):93–103. https://0-doi-org.brum.beds.ac.uk/10.1016/j.pathophys.2003.10.009.
Turecky L, Kupcova V, Szantova M, Uhlikova E. Plasma lipid parameters in patients with alcoholic fatty liver after treatment with essential phospholipids. Bratisl Lek Listy. 2003;104(7-8):227–31.
Ferrannini E, Balkau B, Coppack SW, Dekker JM, Mari A, Nolan J, et al. Insulin resistance, insulin response, and obesity as indicators of metabolic risk. J Clin Endocrinol Metab. 2007;92(8):2885–92. https://0-doi-org.brum.beds.ac.uk/10.1210/jc.2007-0334.
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. https://0-doi-org.brum.beds.ac.uk/10.1056/NEJMra0912063.
Riquelme A, Arrese M, Soza A, Morales A, Baudrand R, Perez-Ayuso RM, et al. Non-alcoholic fatty liver disease and its association with obesity, insulin resistance and increased serum levels of C-reactive protein in Hispanics. Liver Int. 2009;29(1):82–8. https://0-doi-org.brum.beds.ac.uk/10.1111/j.1478-3231.2008.01823.x.
Yeniova AO, Küçükazman M, Ata N, Dal K, Kefeli A, Başyiğit S, et al. High-sensitivity C-reactive protein is a strong predictor of non-alcoholic fatty liver disease. Hepatogastroenterology. 2014;61(130):422–5.
Kotronen A, Westerbacka J, Bergholm R, Pietiläinen KH, Yki-Järvinen H. Liver fat in the metabolic syndrome. J Clin Endocrinol Metab. 2007;92(9):3490–7. https://0-doi-org.brum.beds.ac.uk/10.1210/jc.2007-0482.
Marchesini G, Bugianesi E, Forlani G, Cerrelli F, Lenzi M, Manini R, et al. Nonalcoholic fatty liver, steatohepatitis, and the metabolic syndrome. Hepatology. 2003;37(4):917–23. https://0-doi-org.brum.beds.ac.uk/10.1053/jhep.2003.50161.
Marchesini G, Marzocchi R. Metabolic syndrome and NASH. Clin Liver Dis. 2007;11(1):105–17. https://0-doi-org.brum.beds.ac.uk/10.1016/j.cld.2007.02.013.
Contos MJ, Sanyal AJ. The clinicopathologic spectrum and management of nonalcoholic fatty liver disease. Adv Anat Pathol. 2002;9(1):37–51. https://0-doi-org.brum.beds.ac.uk/10.1097/00125480-200201000-00005.
Eslam M, Sanyal AJ, George J, Sanyal A, Neuschwander-Tetri B, Tiribelli C, et al. MAFLD: a consensus-driven proposed nomenclature for metabolic associated fatty liver disease. Gastroenterology. 2020;158(7):1999–2014. https://0-doi-org.brum.beds.ac.uk/10.1053/j.gastro.2019.11.312.
Lin S, Huang J, Wang M, Kumar R, Liu Y, Liu S, et al. Comparison of MAFLD and NAFLD diagnostic criteria in real world. Liver Int. 2020;40(9):2082–9. https://0-doi-org.brum.beds.ac.uk/10.1111/liv.14548.
Eslam M, Sarin SK, Wong VWS, Fan JG, Kawaguchi T, Ahn SH, et al. The Asian Pacific Association for the Study of the liver clinical practice guidelines for the diagnosis and management of metabolic associated fatty liver disease. Hepatol Int. 2020;14(6):889–919. https://0-doi-org.brum.beds.ac.uk/10.1007/s12072-020-10094-2.
Thanks to Editage, a professional native-speaking proofreader for editing this manuscript in English.
This study was supported by Wonkwang University (2021). When this manuscript is published, researchers will receive a certain amount of research funding from Wonkwang University.
Ethics approval and consent to participate
This study followed the ethical standards laid out in the Declaration of Helsinki. The study was approved by the Clinical Trial Screening Committee of Wonkwang University Hospital (institutional review board [IRB] approval number: 201609-HR-097).
The name of the IRB is Wonkwang University Hospital Institutional Review Board, which belongs to Wonkwang University 3rd General Hospital, and its address is as follows: Wonkwang University Hospital, Sinyong-dong 344–2, Iksan, Jeollabuk-do.
Informed consent was obtained verbally from all participants. Since we only reviewed patient charts for this study, we pledged that we would not use the information for anything other than research purposes. This was approved by the ethics committee.
Consent for publication
Not applicable. This is because all patient information was investigated anonymously, and the manuscript did not reveal the patient’s personal clinical information or the patient’s image.
The author declares no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Han, A.L. Association of Cardiovascular Risk Factors and Metabolic Syndrome with non-alcoholic and alcoholic fatty liver disease: a retrospective analysis. BMC Endocr Disord 21, 91 (2021). https://0-doi-org.brum.beds.ac.uk/10.1186/s12902-021-00758-x
- Non-alcoholic fatty liver
- Alcoholic fatty liver
- Cardiovascular risk factor
- Metabolic syndrome