Abstract
Non-alcoholic fatty liver disease (NAFLD) is replacing hepatitis B as the leading cause of chronic liver disease in China. The purpose of this study is to select good tools to identify NAFLD from the body composition, anthropometry and related routine clinical parameters. A total of 5076 steelworkers, aged 22–60 years, was included in this study. Body fat mass was measured via bioelectrical impedance analysis (BIA) and fat mass index (FMI) was derived. Ultrasonography method was used to detect hepatic steatosis. Random forest classifier and best subset regression were used to select useful parameters or models that can accurately identify NAFLD. Receiver operating characteristic (ROC) curves were used to describe and compare the performance of different diagnostic indicators and algorithms including fatty liver index (FLI) and hepatic steatosis index (HSI) in NAFLD screening. ROC analysis indicated that FMI can be used with high accuracy to identify heavy steatosis as determined by ultrasonography in male workers [area under the curve (AUC) 0.95, 95% CI 0.93–0.98, sensitivity 89.0%, specificity 91.4%]. The ability of single FMI to identify NAFLD is no less than that of combination panels, even better than the combination panel of HSI. The best subset regression model that including FMI, waist circumference, and serum levels of triglyceride and alanine aminotransferase has moderate accuracy in diagnosing overall NAFLD (AUC 0.83). FMI and the NAFLD best subset (BIC) score seem to be good tools to identify NAFLD in Chinese steelworkers.
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Discover the latest articles, news and stories from top researchers in related subjects.Introduction
Non-alcoholic fatty liver disease (NAFLD) is increasingly a cause of chronic liver disease worldwide and affects about 30% of population in Mainland China1. It is estimated that the total NAFLD cases in China will reach 314.58 million by 20302. To make matters worse, China has the youngest median age of NAFLD worldwide, which implies that China will have to bear the burden of NAFLD progression and related complications in the coming decades2. Since the availability of liver biopsy in routine physical examination is limited by its invasive nature, there is a pressing need to develop noninvasive NAFLD biomarkers for health monitoring in China. At present, there are several noninvasive tests and scores used to evaluate hepatic steatosis, including fatty liver index (FLI)3, hepatic steatosis index (HSI)4, NAFLD liver fat score5, SteatoTest6, and NAFLD ridge score7. Although all of the above scores have moderate or good accuracy to diagnose fatty liver, there are some limitations. The inclusion of unconventional indicators, the absence of anthropometric measurements, and the reliability in different populations all limit the wider clinical use of these scores8.
Although obesity is a known risk factor for NAFLD, only a few studies have evaluated the value of obesity indices in screening for NAFLD9,10. It should be noted that body mass index (BMI) and waist circumference (WC) are the most frequently used predictors in the assessment of NAFLD10. However, BMI does not have the ability to distinguish between body fat mass and lean mass. Notably, the excess accumulation of body fat was felt to play a key role in most obesity-associated adverse health outcomes11. The prevalence of lean NAFLD (BMI < 25 kg/m2) in the Chinese population was reported to be 10.8%12, which implies that BMI may not be the best predictor to identify NAFLD, at least in China. In addition, emerging evidence has shown that body fat distribution may be a more important risk factor, which is responsible for NAFLD and metabolic syndrome9,10,13. Moreover, a finding that lends support to the idea that percentage of body fat (BF%) and fat mass index (FMI, the fat mass in kilograms divided by the square of the height in meters) seem to be good tools to identify metabolic syndrome14. After body size normalization, FMI can eliminate the effect of height on BF%, which can then be used to describe the distribution of body fat15. However, there have been no reports to evaluate the potential of FMI in screening for NAFLD.
In terms of the body fat, dual-energy X-ray absorptiometry (DXA) or computed tomography (CT) are still the gold standards for measuring such indicators16. Nevertheless, the above-mentioned gold standards are difficult to be used in large-scale population studies or health monitoring due to factors such as radiation and high costs. In fact, bioelectrical impedance analysis (BIA) method is widely used in clinical practice and epidemiological studies to assess body composition, given its convenience, fast, low cost and excellent correlation with magnetic resonance imaging (MRI) and DXA17. In addition, the high accuracy of a BIA device (TANITA BC-532) for predicting BF% in health Chinese adults has been confirmed and the same brand of the device (TANITA BC-420) has been used in the China National Health Survey (CNHS)17,18. Therefore, we examined the application value of FMI via BIA method in screening for NAFLD among Chinese steelworkers in north China.
Methods
Study design and population
This cross-sectional study reported results from the baseline survey of a Chinese occupational cohort conducted among steelworkers in Tangshan City, Hebei Province in north China. The study design and population have been described in detail in our previous studies19,20. The main exclusion criteria were diagnosed or suspected secondary causes of hepatic fat accumulation such as excess alcohol intake, or serum hepatitis B surface antigen-positivity. Those who did not complete the ultrasound examination and (or) blood biochemical test and (or) body composition measurement were excluded. Eventually, a total of 5076 participants were included in the present study. All participants provided written informed consent before taking part in this study. This research was approved by the Ethics Committee of North China University of Science and Technology (No.16040).
Assessment of NAFLD
The diagnosis of NAFLD have been described in detail in one of our previous studies19. In brief, ultrasonography method was used to detect hepatic steatosis21. Subsequently, according to the ultrasound imaging criteria22, the fatty liver was divided into three grades: grade 1 (light), grade 2 (moderate), and grade 3 (heavy). The final assessment of NAFLD excluded secondary hepatic steatosis, including excess alcohol intake (over 140 g/week for men and 70 g/week for women), hepatitis B infection, hepatitis C infection, autoimmune, celiac disease, genetic disorders such as Wilson’s disease, alpha-1-antitrypsin deficiency liver diseases, hepatic malignancies, hepatobiliary infections, biliary tract, and related medications (tamoxifen, amiodarone, methotrexate, glucocorticoids) based on the above ultrasonography results23,24.
Anthropometric measurements
The values of fat mass and BF% were measured by the Body Composition Analyzer (TANITA BC-420, Japan). The manufacturer’s protocols18 and the intra-rater reliability20 of the body composition analyzer of the same brand and model have been described in detail elsewhere. The measurement criteria of height, weight, waist circumference and hip circumference (HC) in this study were shown in our previous study20. The detailed definitions of BF%, FMI, BMI, waist-to-hip ratio (WHR) and waist-to-height ratio (WHtR) have been elaborated in our previous study20. Blood pressure measurements were performed three times five-minute intervals using an electronic sphygmomanometer (OMRON, HBP-1100, China), and the participants were required to rest for more than ten minutes. Finally, the mean was obtained for analysis.
Measurement of laboratory parameters
Overnight fasting blood samples were drawn for determination of fasting plasma glucose (FPG), total cholesterol (TC), triglycerides (TG), low-density lipoprotein (LDL-C), high-density lipoprotein (HDL-C), alanine aminotransferase (ALT), aminotransferase (AST), γ-glutamyl transferase (GGT), platelet count (PLT), serum uric acid, and albumin. All blood samples were tested in the central laboratory of Tangshan Hongci Hospital Laboratory using automatic biochemical analysers (mindrary, BS-800, China) within four hours.
Assessment of metabolic comorbidities and alcohol consumption
Metabolic comorbidities mainly include diabetes, hyperuricemia, dyslipidaemia, and hypertension. Drinking status was evaluated from self-reported information, mainly including the amount and frequency of alcohol consumed per week. Those who usually consumed some alcohol at least once a week over the past 12 months were defined as current drinkers. For current drinkers, the frequency of drinking status (days/week), usually the average amount of alcohol consumed (g), and types of beverages were recorded. The definition of diabetes, hyperuricemia, dyslipidaemia and hypertension, and the amount of pure alcohol (g/week) consumed per week are provided in the supplementary materials.
Statistical analysis
Continuous variables were presented as means and standard deviation (SD) and between-group comparisons were performed using analysis of variance (ANOVA) or Student’s t-test if the data were normally distributed. Otherwise, the median (upper quartile–lower quartile) and Kruskal–Wallis test (or Wilcoxon rank sum test) were used to describe and compare these continuous variables among the various groups. The classification data were presented as numbers and percentages, and the χ2 test was used to compare differences among groups. The receiver operating characteristic (ROC) curve analyses were performed to determine the appropriate cutoff points for FMI, WC, WHtR, WHR, BF% and BMI in identifying NAFLD. The area under the receiver operating characteristic curves (AUCs) were used to describe the diagnostic abilities of the different anthropometric measurements, and a nonparametric approach described by DeLong et al. was performed to compare the differences between areas25. The random forest classifier was used to rank the relative importance of anthropometric indicators and related routine clinical parameters in identifying NAFLD. The variance inflation factor (VIF) and the conditional index were used to diagnose the collinearity of the candidate variables. After finding serious multicollinearity among candidate variables, cluster analysis was used to cluster the variables. Finally, variables with high representativeness (according to cluster analysis) and relative importance (according to random forest classifier) were used as candidates for the best subset regression. To obtain a linear logit, the linearity of logits of all continuous candidate predictors was ascertained using the Box–Tidwell procedure26. According to the results of the procedure, a natural logarithmic conversion of GGT and TG was recommended. Information criteria including Akaike information criterion (AIC) and Bayesian information criterion (BIC) were used to determine the best fit in the best subset regression. The tenfold cross-validation method was used to evaluate the generalization ability of different models. The machine learning library (Python 3) scikit-learn (sklearn) was used for model fitting and evaluation. In order to preliminarily explore the relationship between FMI and liver fibrosis, the restricted cubic spline (RCS) models were used to examine the association of FMI with Fibrosis-4 (FIB-4), and NAFLD fibrosis score (NFS). P < 0.05 was regarded as significant for two-sided tests. P value for pairwise comparisons was adjusted by Bonferroni correction.
Ethics approval and consent to participate
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. This research was approved by the Ethics Committee of North China University of Science and Technology (No. 16040). All participants gave informed consent before taking part in this study.
Results
General characteristics of the participants
The general characteristics of the included 5076 participants according to NAFLD status are summarized in Table 1. The general demographic characteristics, including age and sex differed significantly by NAFLD status. No significant differences in ethnicity were observed according to different grades of hepatic steatosis. As for anthropometric indicators, participants with heavy hepatic steatosis (Grade 3) tend to have higher BMI, WC, HC, WHR, WHtR, BF% and FMI. The distribution characteristics of the above indicators in different NAFLD grades are shown in Fig. 1. All of the related routine clinical parameters, including systolic blood pressure (SBP), diastolic blood pressure (DBP), FPG, HDL-C, LDL-C, TG, TC, AST, ALT and GGT differed significantly by grades of hepatic steatosis. With the increase of the degree of hepatic steatosis, the prevalence of diabetes, hypertension, hyperuricemia, and dyslipidaemia also showed an increasing trend. Supplementary Table S1 shows the general characteristics of the study participants according to sex. There were no significant sex discrepancies in age, ethnicity and TC. Compared with female workers, male workers tend to have higher levels of BMI, WC, HC, WHR, WHtR, SBP, DBP, FPG, LDL-C, TG, TC, AST, ALT and GGT, but lower levels of BF%, FMI and HDL-C.
As shown in Supplementary Table S2, in both genders, all the six anthropometric indicators, including BMI, WC, WHR, WHtR, BF% and FMI were positively correlated with NAFLD. After adjustment for diabetes, dyslipidaemia, hypertension, and hyperuricemia, these estimates were attenuated but remained robust (unadjusted model). Specifically, for per 1 SD increase of FMI, the odds of NAFLD in men and women increased by 2.07-fold (OR 3.07, 95% CI 2.80–3.36) and 1.92-fold (OR 2.92, 95% CI 2.13–4.00), respectively (adjusted model).
ROC analyses of different anthropometric indicators and combination panels for the screening of NAFLD
Supplementary Figure S1 presents the ROC curves of FMI, WC, WHtR, WHR, BF% and BMI in the total study population, male and female workers respectively, which were used to identify subjects with non-NAFLD from overall NAFLD or different grades of hepatic steatosis. As shown in Supplementary Fig. S1, all the curves were significantly above the diagonal line (all P < 0.001). The accuracy of FMI in diagnosing NAFLD was superior to WHtR, WHR, BF%, and BMI [compared with FMI, all P values for the difference between AUCs < 0.05/7 (Bonferroni adjusted alpha level)], when the severity of steatosis and sex were not taken into consideration (Table 2). For male workers, FMI remains the optimal anthropometric indicator for the screening of overall NAFLD, with a moderate AUC (95% CI) of 0.78 (0.77–0.80). For female workers, FMI was not superior to abdominal obesity measurements, including WC, WHtR, and WHR, in identifying NAFLD, but it was superior to BMI (P = 0.005). When the grades of steatosis was taken into account, the accuracy of FMI in identifying grade 2 or grade 3 steatosis improved in both men and women (women with grade 2 or grade 3 steatosis were combined into one group because of small numbers). In male workers, the optimal cutoff point of FMI in identifying subjects with grade 3 steatosis from non NAFLD was 9.3 kg/m2 (according to Youden J-index), with the sensitivity of 89.0%, the specificity of 91.4%, the positive likelihood ratio (+LR) of 10.3, the negative likelihood ratio (−LR) of 0.1, and the AUC (95% CI) of 0.95 (0.93–0.98). The accuracy of FMI in screening for grade 3 steatosis among male workers was superior to WHR (AUC = 0.82, P < 0.0001), BF% (AUC = 0.92, P < 0.0001) and BMI (AUC = 0.88, P = 0.0041), but not superior to WC (AUC = 0.92, P = 0.0438, Bonferroni adjusted alpha level was 0.05/7) and WHtR (AUC = 0.90, P = 0.0083, Bonferroni adjusted alpha level was 0.05/7). For female workers, the accuracy of FMI in screening for grade 2 or grade 3 steatosis was superior to BF%. The accuracy of FMI in screening for overall NAFLD was superior to the combination panel of HSI (AUC = 0.75, P = 0.0026), but not superior to the combination panel of FLI (AUC = 0.79, P = 0.3012). For male workers, the accuracy of FMI in identifying overall NAFLD, grade 2 or grade 3 steatosis remained superior to the combination panel of HSI (All P for pairwise comparison 0.05/7).
Anthropometric indicators combined with related routine clinical parameters for NAFLD prediction
The grid search method was used to determine the parameters of the random forest model. Figure 2 shows the relative importance of anthropometric and related routine clinical parameters for classification of NAFLD from random forest model. FMI ranked first in relative importance, followed by WC, WHtR, ALT, BF%, BMI, TG, WHR, HDL, GGT, TC, LDL, SBP, FPG, AST and DBP, respectively. As shown in Supplementary Table S3, collinearity diagnosis results showed severe multicollinearity among the 16 variables in Fig. 2 (conditional index 327.6). Subsequently, cluster analysis was conducted on these 16 variables, and the results were shown in Supplementary Table S4 and Supplementary Fig. S2. Seven variables, including FMI, WC, ALT, TC, SBP, TG, and FPG were selected from each cluster as candidates for the best subset model based on their relative importance to the NAFLD. When age, sex and the above seven variables were included as the candidate variables into the best subset generalized linear model (the information criterion was BIC), the results shown that the model including WC, FMI, ln (TG), and ln (ALT) was the best model (Supplementary Table S5). Supplementary Figure S3 shows the partial nomogram that can be used to manually obtain predicted values of NAFLD from the best subset regression model.
Model evaluation
We randomly divided 5076 subjects in the present study into training (70%) and validation (30%) groups. Four predicting parameters [WC, FMI, ln (TG), and ln (ALT)] selected from the best subset model were used to fit the model in the training group. The AUCs of the fitted model in training and validation groups to diagnose NAFLD were 0.826 and 0.823, respectively. In the subsequent analysis, we replace the information criterion from BIC to AIC to fit the best subset model. In addition, variables in FLI and HSI were used to fit the logistic regression model (Supplementary Table S5). The model comparison results shown that the accuracy of the best subset model (AUC 0.826, 95% CI 0.815–0.836) (AIC) was superior to FLI model (AUC 0.797, 95% CI 0.786–0.808) and HSI model (AUC 0.750, 95% CI 0.738–0.762), with P values for pairwise comparisons < 0.0001 (Supplementary Table S4). No significant difference was observed between the AUCs of the two best subset models (BIC and AIC). In addition, we performed tenfold cross-validation on the above four models. The results shown that the AUCs of the best subset (BIC), best subset (AIC), FLI, and HSI model were 0.823, 0.824, 0.789, and 0.751, respectively, which were comparable with the results in Supplementary Table S5. The best subset (BIC) model was selected as the optimal model in this study, due to its higher accuracy and feasibility in diagnosing NAFLD. According to the regression coefficients summarized in Supplementary Table S5, the equation to calculate NAFLD best subset (BIC) score was the following:
Supplementary Figure S4 shows the calibration curve of the best subset (BIC) model. No serious deviation from the calibration results was observed, with the Brier score of 0.16. In order to maximize the corresponding specificity and sensitivity respectively, dual cut-offs were selected to achieve 90% sensitivity and 90% specificity to rule out and rule in NAFLD patients. Dual cut-offs of 0.19 and 0.53 were determined for NAFLD best subset (BIC) score to achieve 90% (88–91%) sensitivity and 90% (88–91%) specificity, with meaningful negative predictive value (NPV) of 91% (90–92%) and positive predictive value (PPV) of 72% (69–74%). The dual cut-offs ruled in and ruled out NAFLD in 3211 (63%) subjects. The diagnosis of NAFLD was indeterminate in 1865 (37%) subjects with NAFLD best subset (BIC) scores ranging from 0.19 to 0.53.
The association of FMI and NAFLD best subset (BIC) score with existing noninvasive biomarkers or panels associated with hepatic steatosis and fibrosis
The lack of invasive liver biopsy made it difficult to identify nonalcoholic steatohepatitis (NASH) in the present study population, an active histological phenotype of NAFLD with hepatic inflammation and faster fibrosis progression. As for liver fibrosis, FIB-4 index and the NFS are the 2 most popular noninvasive panels for widespread fibrosis screening. In this study, the values of the continuous variables FIB-4 index and NFS were used as proxies to measure the stage of liver fibrosis, and the RCS models showed a significant positive correlation of FMI and NAFLD best subset (BIC) score with NFS (P for overall association < 0.05) (Fig. 3). Finally, we calculated the HSI and FLI scores of the present study population separately, following the published algorithms, and compared the screening performance of a single FMI with the combination panels of liver steatosis HSI and FLI. Supplementary Figure S5 presents the ROC curves of FMI, HSI and FLI to identify subjects with non-NAFLD from overall NAFLD or light (grade 1) to heavy (grade 3) degree of hepatic steatosis. As shown in Supplementary Table S6, the performance of FMI and FLI was almost comparable in identifying hepatic steatosis (P for pairwise comparison > 0.05/3). While, the single FMI performs better than the combination panel of HSI in identifying hepatic steatosis (P for pairwise comparison < 0.05/3).
In subsequent analyses, we separately analyzed the performance of FMI in identifying hepatic steatosis in different BMI subgroups. The results showed that FMI was better at identifying hepatic steatosis in subjects with a BMI of less than 25 kg/m2 than in those with a BMI of 25 to 30 kg/m2 (Supplementary Table S7).
Discussion
In the present study, we showed that FMI and NAFLD best subset (BIC) score were useful tools for the assessment of NAFLD. For male workers, FMI had very good accuracy to distinguish subjects with heavy hepatic steatosis from non-NAFLD subjects. The NAFLD best subset (BIC) score that combines anthropometric indicators and common clinical parameters which can be easily available in the regular health check-up, showed a moderate performance in screening for overall NAFLD. At the dual cut-offs of 0.19 and 0.53, NAFLD best subset (BIC) score achieved 90% sensitivity and 90% specificity in the study population with 91% NPV and 72% PPV, respectively.
Several studies have evaluated the role of body composition and abdominal obesity indicators in screening for NAFLD9,10. In line with previous studies, we showed that the simple anthropometric parameter WC is a useful tool for identifying NAFLD9,10,27. In addition, a previous study on the relationship between body composition variables and NAFLD indicated that intra-abdominal adipose tissue (diagnosed by ultrasound) was also a potential predictor of NAFLD10. The BF% and FMI (measured by bioelectrical impedance analysis) have been reported as good tools to identify metabolic syndrome14,28, which is closely associated with NAFLD29. However, evidence regarding the performance of BF% and FMI in identifying NAFLD remains sparse. Several prediction index and scores have been developed to identify NAFLD8. Given the accessibility of electronic health records, many existing NAFLD prediction models make full use of laboratory parameters as predictors, while anthropometric measurements are often missing. For example, NAFLD liver fat score5 and NAFLD ridge score7 were only dependent on laboratory biomarkers, which may limit their ability to identify NAFLD. Aside from that, some parameters, such as insulin and glycosylated haemoglobin (HbA1c) are not always routinely measured, which will lead to their limited availability. Notably, among those models that involved both laboratory and anthropometric parameters, BMI was the most commonly used anthropometric index3,4,6. Although about 80% of patients with NAFLD are obese (BMI > 30 kg/m2), BMI does not differentiate between body lean mass and body fat mass30. Moreover, the prevalence of lean NAFLD (BMI < 25 kg/m2) in the Chinese population was reported to be 10.8%12, which implies that the accuracy of BMI in predicting NAFLD may be limited. Stranges et al.13 concluded that BMI was not a reliable marker of fatty liver. While, FMI, an alternative simple and inexpensive approach for assessing body fat distribution, has been reported as a surrogate marker of cardiovascular risk and metabolic syndrome14,15. Our present study aligns with the idea that the distribution of fat tissue (assessed by FMI) plays a greater role in NAFLD than the BMI30. Furthermore, this study adds to the evidence that FMI is not only strongly associated with overall NAFLD, but also with the degree of steatosis. The results of model comparison shown that the accuracy of the best subset model in the diagnosis of NAFLD was better than that of FLI and HSI models in our study population. The main difference between the current model and the previous models is the inclusion of FMI as a predictive indicator, which indirectly supports the important role of FMI in identifying NAFLD, at least among Chinese steelworkers in north China.
In our NAFLD best subset (BIC) score, anthropometric indicators include WC in addition to FMI. This is consistent with previous studies showing that abdominal fat accumulation can be an independent predictor of hepatic steatosis13. In particular, a study in Korean reported that WC was as useful as DXA and CT in screening for NAFLD9. However, WC suffered from a key limitation in that it cannot differentiate between visceral and subcutaneous fat. While, what we already known is that visceral adipose tissue is directly associated with the development and progression of hepatic steatosis30. Therefore, the role of FMI cannot be completely replaced. Interestingly, pairwise comparison of ROC show that the performance of single FMI to identify hepatic steatosis is no less than that of combination panels and even better than the combination panel of HSI. Overall, the role of FMI in identifying liver steatosis may be more practical in terms of practical availability and feasibility. As for the laboratory indicators, the logarithmic conversion values of TG and ALT are included in our best subset model. In theory, excess free fatty acids are considered to be one of the most important factors contributing to the development and progression of NAFLD. NAFLD arises when the uptake of fatty acids and TG from circulation and de novo lipogenesis saturate the rate of fatty acids β-oxidation and very-low density lipoprotein (VLDL)-TG export31. Therefore, it seems logical to use serum levels of TG to screen for NAFLD. Evidence is particularly extensive with regard to the link between liver enzymes and NAFLD. Elevated liver enzymes were reported in about 20% of patients with NAFLD32. The liver enzymes included in previous models for predicting NAFLD were mainly ALT, AST, GGT and AST/ALT ratio. Among these liver enzymes, ALT serves as a specific marker of liver inflammation and hepatocellular injury33. Differences in composition of NAFLD subtypes between different studies were thus more likely to contribute to the discrepancy in selection of liver enzymes in different NAFLD screening models.
On the basis of disease severity, NAFLD is divided into nonalcoholic fatty liver (NAFL) and NASH. NASH is the active form of NAFLD characterized by histological lobular inflammation and hepatocyte ballooning and is associated with cirrhosis, hepatocellular carcinoma, liver transplantation, and death. Although FMI performs better in identifying liver steatosis, the significance of detecting liver inflammation and fibrosis in clinical practice may be of greater concern34. Unfortunately, the lack of liver biopsy made it difficult to diagnose NASH directly. However, to achieve better diagnostic of liver fibrosis through noninvasive methods, many biomarkers and panels have been developed, among which FIB-4 index and the NFS are the 2 most popular noninvasive panels for fibrosis screening35. We observed that FMI was positively associated with NFS, but not FIB4-4. For FIB-4, dual cutoffs of < 1.45 and of > 3.25 were used to rule-out and rule-in elevated liver stiffness36. In other words, individuals with FIB-4 values inside 1.45–3.25 would not be correctly classified. Therefore, the relationship between FMI and FIB-4 may be affected by individuals with FIB-4 values inside 1.45–3.25. Given that indirect biomarkers are in general less accurate than biomarkers directly measuring fibrogenesis or fibrinolysis, the reproducibility of FIB-4 in different populations needs to be further verified. It is noteworthy, however, that the NFS was specifically derived and validated in patients with biopsy-proven NAFLD, and thus may have a higher accuracy. In addition, NFS has been well validated in Chinese populations37. Although this study failed to directly define the role of FMI in the detection of liver fibrosis, the relationship between FMI and NFS, a proxy of fibrosis, supports the potential research value of FMI in this area.
The major strengths of our study include the large sample size, good availability and inexpensive screening indicators. To our knowledge, this is the first study to explore the usefulness of FMI in screening for NAFLD. However, our study also has certain limitations. First, although FMI and NAFLD best subset (BIC) score can be good for detecting NAFLD in cross-sectional study, their accuracy in assessing changes in liver fat over time is still unknown. Second, BIA is a predictive method that requires assumptions based on population mean values. An improved standardization of protocols for measurement is essential38. Third, the sample size of females in this study was small, so it was difficult for us to identify sex differences. Although our understanding of sex differences in NAFLD remains insufficient, adequate consideration of sex differences are needed to implement precision medicine for patients with NAFLD. Previous evidence has shown that the prevalence and severity of NAFLD are higher in men than in women during the reproductive age, whereas NAFLD occurs at a higher rate in postmenopausal women, suggesting a protective effect of estrogen39. The sex difference may be due to differences in hormone levels. In addition, according to the results in Supplementary Table S1, sex differences may also be related to the discrepancy distribution of general characteristics of male and female workers, despite the limited sample size. Future studies should include sufficient and comparable female subjects to identify sex differences. Fourth, although the dual cut-offs can maximize both sensitivity and specificity in ruling out and ruling in NAFLD patients, the NAFLD best subset (BIC) score has a somewhat low PPV (72%). Fifth, our survey population consisted of steelworkers in north China, which limits our ability to generalize these results to the general population. It seems that FMI and the NAFLD best subset (BIC) score need external validation to widely use. Sixth, the assessment of NAFLD by ultrasound may be subjective and inconsistent. At present, tissue biopsy is still the gold standard for diagnosing NAFLD. However, this method is not feasible in large-scale epidemiological investigations, since most people affected by NAFLD are likely to be asymptomatic, so other noninvasive methods like ultrasonography, is advised and might be preferred40,41. Seventh, due to the lack of liver biopsy, it is difficult to directly determine the performance of FMI in screening for liver inflammation and fibrosis. However, the relationship between FMI and proxy metrics of liver inflammation and fibrosis also indirectly supports the potential research value of FMI.
Conclusion
FMI and NAFLD best subset (BIC) score seem to be good tools for screening of liver steatosis. The NAFLD best subset (BIC) score that combines anthropometric indicators and common clinical parameters which can be easily available in the regular health check-up, is a simple and robust reference to identify overall NAFLD patients among steelworkers in north China.
Data availability
The data that support the findings of this study are available from [Institute of basic medicine, Chinese academy of medical sciences] but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. Data are however available from the authors upon reasonable request. For data request, please contact professor Yuan Juxiang (email address: yuanjx@ncst.edu.cn).
Abbreviations
- NAFLD:
-
Non-alcoholic fatty liver disease
- BIA:
-
Bioelectrical impedance analysis
- FMI:
-
Fat mass index
- ROC:
-
Receiver operating characteristic
- OR:
-
Odds ratio
- CI:
-
Confidence interval
- AUC:
-
Area under the curve
- FLI:
-
Fatty liver index
- HSI:
-
Hepatic steatosis index
- BMI:
-
Body mass index
- WC:
-
Waist circumference
- BF%:
-
Percentage of body fat
- DXA:
-
Dual-energy X-ray absorptiometry
- CT:
-
Computed tomography
- HC:
-
Hip circumference
- WHR:
-
Waist-to-hip ratio
- WHtR:
-
Waist-to-height ratio
- FPG:
-
Fasting plasma glucose
- TC:
-
Total cholesterol
- TG:
-
Triglycerides
- LDL-C:
-
Low-density lipoprotein
- HDL-C:
-
High-density lipoprotein
- ALT:
-
Alanine aminotransferase
- AST:
-
Aminotransferase
- GGT:
-
γ-Glutamyl transferase
- SD:
-
Standard deviation
- ANOVA:
-
Analysis of variance
- AIC:
-
Akaike information criterion
- BIC:
-
Bayesian information criterion
- SBP:
-
Systolic blood pressure
- DBP:
-
Diastolic blood pressure
- +LR:
-
Positive likelihood ratio
- −LR:
-
Negative likelihood ratio
- NASH:
-
Nonalcoholic steatohepatitis
- FIB-4:
-
Fibrosis-4 index
- NFS:
-
Nonalcoholic fatty liver disease fibrosis score
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Acknowledgements
The authors would like to acknowledge all the participants and institutions involving the collection of the baseline data.
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This work was supported by the National Key R&D Program of China (No. 2016YFC0900605). The funders had no role in study design, data collection, and analysis, decision to publish, or preparation of the manuscript.
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S.Z. and J.Y. planned the study. S.Z. carried out the statistical analyses, and drafted the manuscript. L.W. and M.Y. interpreted the data. S.Z. contributed to the data collection and data cleaning. W.G. supervised the fieldwork of this project. S.Z. and J.Y. revised drafts critically. All authors approved the final version of the manuscript.
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Zhang, S., Wang, L., Yu, M. et al. Fat mass index as a screening tool for the assessment of non-alcoholic fatty liver disease. Sci Rep 12, 20219 (2022). https://doi.org/10.1038/s41598-022-23729-1
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DOI: https://doi.org/10.1038/s41598-022-23729-1
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