Abstract
Objectives
The present study aimed to investigate the relationship between male hormones and metabolic dysfunction-associated fatty liver disease (MAFLD) in males.
Methods
Data from the Fangchenggang Area Male Health and Examination Survey (FAMHES) were used to analyze the male hormone levels between MAFLD patients and controls. Univariate and multivariate logistic regression analyses were performed to identify risk factors for MAFLD. Receiver operating characteristic curve analysis was used to assess the diagnostic performance of male hormones for MAFLD.
Result
A total of 1578 individuals were included, with 482 individuals (30.54%) of MAFLD, including 293 (18.57%) with mild disease and 189 (11.98%) with moderate-to-severe disease. The MAFLD patients were significantly older than those without MAFLD. The LH, FSH, and SHBG levels in the MAFLD patients were significantly greater than those in the control group. Age, FSH, LH, SHBG, and estradiol were all risk factors for MAFLD. Age, FSH, and LH were risk factors for moderate-to-severe MAFLD. FSH was an independent risk factor for MAFLD and moderate-to-severe MAFLD. FSH showed an excellent diagnostic value, with an AUC of 0.992 alone and 0.996 after adjusting age.
Conclusions
Our findings indicate that FSH may be a potential diagnostic and predictive biomarker for MAFLD.
Introduction
Metabolic dysfunction-associated fatty liver disease (MAFLD), formerly known as nonalcoholic fatty liver disease (NAFLD), is the most common cause of chronic liver disease worldwide and can progress to liver fibrosis, cirrhosis, and even hepatocellular carcinoma [1,2,3,4]. Therefore, MAFLD is a major public health issue. A meta-analysis conducted in 2016 revealed that the prevalence of MAFLD in the general population is 25.24%, with the highest prevalence in the Middle East (31.79%) and South America (30.45%), and the lowest in Africa (13.48%) [5]. Another meta-analysis conducted in 2019 reported that the pooled prevalence of MAFLD in China is 29.2%, and it has been increasing rapidly, from 25.4% in 2008–2010 to 32.3% in 2015–2018 [6]. With the rising incidence of obesity worldwide, the prevalence of MAFLD is also growing rapidly [3, 7]. Currently, a liver biopsy is regarded as the gold standard for clinically diagnosing and staging MAFLD [7, 8]. However, its invasive nature makes it challenging to perform in routine clinical practice. Therefore, the identification of novel biomarkers associated with MAFLD has become crucial for the early detection and assessment of MAFLD severity [9].
MAFLD is clinically highly associated with metabolic syndrome [10]. Besides causing significant pathological changes in the liver, MAFLD also affects the function of other organs and systems, especially the endocrine system [11, 12]. MAFLD is a sex-dimorphic disease, with a generally greater prevalence in men [13, 14]. Gender and sex hormones have a significant impact on various factors associated with MAFLD, such as genetic variants, cytokines, stress, and environmental factors, which can modify the risk profiles and phenotypes of MAFLD in individuals [14, 15].
Testosterone is the major male hormone and is responsible for regulating many metabolic processes, such as fat metabolism, insulin sensitization, and suppression of lipogenesis, besides maintaining normal sexual function and reproductive ability [16]. Several studies have investigated the relationship between testosterone levels and MAFLD, but the results are inconsistent. Some studies have reported that a lower total testosterone (TT) level is associated with a high prevalence of MAFLD and adverse clinical outcomes [17,18,19], while other studies have shown that there is no significant association between the testosterone level and MAFLD [20, 21]. Luteinizing hormone (LH) and sex hormone-binding globulin (SHBG) are two key regulatory factors that regulate testosterone levels [ This study was conducted using the data from the Fangchenggang Area Male Health and Examination Survey (FAMHES), which is a population-based survey conducted from September 2009 to December 2009 among noninstitutionalized Chinese males aged 17–88 years old in Guangxi, China, and has been used in many previous studies [30,31,32,33,34]. The aim of FAMHES was to investigate the impact of environmental and genetic factors, as well as their interactions, on the development of age-related chronic diseases. A comprehensive population and health questionnaire was provided to 4303 male participants at the Medical Center of the First People’s Hospital of Fangchenggang, and extensive physical examinations were conducted. Written informed consent was obtained from all participants. This human data is in accordance with the Declaration of Helsinki. and the study was approved by the Guangxi ethics committee. All participants were requested for follow-up, which included another health questionnaire and biochemical analysis of a fasting blood sample collected in the morning. A trained expert measured the height and weight of the participants using standard procedures. Participants were excluded from this study if any of the following conditions were met: (I) currently diagnosed with diabetes, coronary heart disease, stroke, hyperthyroidism, rheumatoid arthritis, inflammatory disease of the reproductive system, urinary diseases (infection, stone, hematuria, or hematospermia), prostatitis or history of any cancers; (II) taking any medication; (III) with impaired liver function (alanine aminotransferase >2.0 times the upper limit of normal); (IV) with a history of excessive alcohol consumption (>40 mL/d); or (V) with impaired kidney function (serum creatinine >178 mmol/L). After excluding participants who did not undergo complete clinical and laboratory tests or ultrasound examinations, a total of 1951 participants were available for analysis. It was found that 310 participants were positive for hepatitis B virus (determined by hepatitis B surface antigen detection), 45 participants were excessive alcohol drinkers (>40 mL/d), 11 participants had at least one potential cause of chronic liver disease, and seven participants were taking medications known to cause fatty liver imaging. After excluding these participants, 1578 males were finally included in this study (Fig. 1). Two experienced ultrasound doctors [Cohen’s kappa of 0.621 (95% CI 0.352–0.876)] performed abdominal ultrasound examinations on all patients using a portable ultrasound device (GE, LOGIQ, 5.0 MHz transducer, USA). The size, contour, echogenicity, structure, and posterior attenuation of the liver were assessed for each participant. The ultrasound criteria for diagnosing a fatty liver included increased liver echogenicity (bright), liver parenchymal echogenicity greater than that of the renal parenchyma, and blurring and narrowing of the hepatic vein lumen [35, 36]. According to the criteria described by Saadeh et al. [36], all participants were divided into two groups (mild and moderate-to-severe). In the laboratory tests of FAMHES, all participants were required to fast overnight. Samples containing approximately 10 mL of venous blood were collected from 8 am to 11 am the next day, frozen (~2 h), and sent to the testing center of the First Affiliated Hospital of Guangxi Medical University in Nanning. The samples were centrifuged within 15–25 min and then stored at −80 °C until analysis. The serum samples were thawed at room temperature for 1 h and then analyzed by inverting the test tube ten times. All analyses were performed by the same operator using the same batch of reagents. The blood lipid parameters were measured on an automated analyzer (Dade Behring, USA) in the laboratory at the Fangchenggang. The FSH, LH, SHBG, estradiol (E2), and testosterone levels were determined using the COBAS 6000 system E601 (Elecsys module) and an immunoassay analyzer (Roche Diagnostics GmbH, Mannheim, Germany). The inter-assay coefficients of variation were 3.6% for E2, 4.4% for SHBG, 4.3% for FSH, and 3.6% for LH. The lower limit of detection for the assay was 0.05 pg/mL. Hormones were measured in nonfasting blood samples that were collected within 4 h after waking up, thus balancing the diurnal variation of hormone levels. All measurements were performed according to the manufacturer’s instructions. Statistical analysis was performed using SPSS 20.0. Data distribution was analyzed by the Kolmogorov–Smirnov and Shapiro–Wilk tests. Continuous data with a normal distribution were expressed as the mean ± standard derivation, while continuous data with a non-abnormal distribution were expressed as the median (range). Univariate logistic regression analysis was performed to identify risk factors for MAFLD or moderate-to-severe MAFLD in all collected factors. Parameters with a P value less than 0.1 in univariate analysis entered multivariate logistic regression analysis to identify independent risk factors for MAFLD or moderate-to-severe MAFLD. The variance inflation factor was calculated to analyze the multicollinearity and variables with multicollinearity were excluded from the multivariate logistic regression. The receiver operating characteristic (ROC) curve was plotted, and the area under the curve (AUC) with 95% confidence interval (CI) was used to assess the diagnostic performance of male hormones for MAFLD. A P value less than 0.05 was considered statistically significant. Of the included 1578 subjects, 482 individuals (30.54%) were diagnosed with MAFLD, with 293 (18.57%) having mild disease and 189 (11.98%) having moderate-to-severe disease (Table 1). Therefore, these participants were divided into three groups: control (1096 cases), mild MAFLD (293 cases), and moderate-to-severe MAFLD (189 cases). The MAFLD patients was significantly older than those without MAFLD (P < 0.001), and the patients with moderate-to-severe MAFLD were older than those with mild MAFLD (P < 0.05). The LH, FSH, and SHBG were significantly greater in the MAFLD patients compared to the control group (P < 0.001). In addition, the LH, and FSH levels were greater in the patients with moderate-to-severe MAFLD compared to those with mild MAFLD (P < 0.05), while there was no significant difference in the SHBG levels between the patients with moderate-to-severe MAFLD and those with mild MAFLD (Table 1). Moreover, the levels of LH, FSH, and SHBG were all significantly greater in the MAFLD patients than in the control group among different age groups and increased in an age-dependent manner (P < 0.05, Table 2). Since age was a confounder for MAFLD, the parameters with a p value less than 0.05 in Table 1 was further analyzed using age as a covariate. After adjusting age, LH, FSH, and SHBG remained significantly higher in the MAFLD patients compared to the control group (Table 1). Univariate logistic regression analysis showed that age, waist–hip ratio (WHR), systolic blood pressure (SBP), diastolic blood pressure (DBP), blood glucose (GLU), cholesterol (CHOL), high-density lipoprotein (HDL), low-density lipoprotein (LDL), FSH, LH, SHBG, and E2 were all risk factors for the occurrence of MAFLD (all P < 0.05) (Table 3). Multivariate logistic regression analysis identified that only FSH was an independent risk factor for MAFLD (P < 0.001) (Table 3). According to the univariate regression analysis comparing the severe MAFLD patients with the mild MAFLD patients, age, FSH, and LH were found to be risk factors for severe MAFLD (all P < 0.05). Compared to the patients aged >45 years old, those aged <35 years old (OR = 0.341, 95% CI: 0.197–0.589) or 35–45 years old (OR = 0.598, 95% CI: 0.398–0.898) had a reduced risk of moderate-to-severe MAFLD (P < 0.05) (Table 4). Further multivariate regression analysis revealed that only FSH was an independent risk factor for moderate-to-severe MAFLD (P < 0.001) (Table 4). We also analyzed the diagnostic values of LH, FSH, TT, SHBG, and E2 for MAFLD. As shown in Fig. 2A, FSH showed an excellent diagnostic value, with an AUC of 0.992 (95% CI: 0.985–0.999); LH had an AUC of 0.710 (95% CI: 0.682–0.738); while TT, SHBG, and E2 only had AUC values of 0.446–0.597. After adjusting the age confounder, AUCs of all hormones were increased, with FSH presenting an AUC of 0.996 (95% CI: 0.991–1.000) and LH presenting an AUC of 0.788 (0.764–0.811) (Fig. 2B). In the present study, we found that age, WHR, SBP, DBP, GLU, CHOL, HDL, LDL, FSH, LH, SHBG, and E2 were all risk factors for MAFLD (all P < 0.05). Moreover, the severity of MAFLD was correlated with age, FT, LH, and SHBG. Multivariate regression analysis revealed that FSH was an independent risk factor for MAFLD as well as moderate-to-severe MAFLD. FSH showed an excellent diagnostic value, with an AUC value of 0.992. Age-adjusted FSH presents an AUC value of 0.996. Univariate logistic regression analysis determined that LH and SHBG, but not TT affected the occurrence of MAFLD. Many studies have shown that serum testosterone concentrations decrease with age, which is partly due to a decrease in the number and function of interstitial cells in the testes and a decrease in the pulsatile secretion of LH that stimulates interstitial cells [37]. SHBG is a sex hormone-binding globulin synthesized by liver cells that protects sex hormones from adhesion as well as biological and chemical degradation [38]. The SHBG level in adult males gradually increases with age, leading to more testosterone binding to SHBG [38]. Several previous studies have demonstrated that a lower TT level is associated with a high prevalence of MAFLD [17,18,19], while other studies have found no significant association between the testosterone level and MAFLD [20, 21]. Moreover, in this study, multivariate regression analysis revealed that only FSH was an independent risk factor. Many previous studies only compared the parameters between the MAFLD and control groups but did not adjust for confounders [17,18,19], which may explain the controversial results. In the current study, we found that FSH was an independent risk factor for MAFLD as well as moderate-to-severe MAFLD. FSH is a glycoprotein peptide hormone synthesized by the anterior pituitary gland that affects both the reproductive and nonreproductive systems. A recent study has demonstrated that FSH regulates hepatic lipid metabolism in mice [39]. Additionally, a cross-sectional study has reported that high FSH level is associated with MAFLD in men aged over 80 years old [40]. Moreover, a recent study in a Chinese elderly population (over 60 years old) consisting of both men and women has found that FSH is negatively associated with NAFLD in both men and women [41]. Our data were inconsistent with these reports, which may be due to the difference in study populations. The above studies enrolled an elderly population, while our study had a much younger population. Here, we also determined that FSH had an excellent diagnostic value for MAFLD, with an AUC of 0.992 alone and 0.996 after adjusting age confounder, indicating that FSH may be a potential diagnostic biomarker for MAFLD. Our data suggest that MAFLD is related to male hormones. Previous studies have suggested a link between metabolic dysfunction and male reproductive health [42, 43]. Metabolic syndrome was reported to be associated with a decline in TT while no alterations in gonadotropin levels, and it was associated with hypogonadism, poor sperm morphology, testis ultrasound inhomogeneity, and erectile dysfunction [44]. A meta-analysis of 21 studies revealed a J-shaped association between body mass index and abnormal sperm count [45]. Obesity is negatively correlated with TT, LH, and SHBG [46], and affects male-factor infertility [47]. Our findings and these studies confirmed that metabolic dysfunction may affect male reproduction health by regulating male hormones. However, further experiments are needed to uncover the underlying mechanism. This study has several limitations. First, this was a retrospective study and the inherent bias associated with such a study design cannot be avoided. Second, crucial data on marital or fertility status, and history of (in)fertility were not collected. Male sex hormones have been shown to correlate with male fertility status [48], which underscores the significance of these missing data. Therefore, our conclusion that FSH is a risk factor for MAFLD should be applied with caution due to the lack of male fertility data. Third, we did not collect data on semen parameters and testicular ultrasound. However, FSH plays a crucial role in the regulation of spermatogenesis [49]. and acts on Sertoli cells, the main component of the seminiferous tubules [50]. Increased levels of FSH may indicate abnormal spermatogenesis or testicular damage. Therefore, the findings of this study should be interpreted with careful consideration of these unexamined factors. In conclusion, the present study identified that FSH is an independent risk factor for both MAFLD and moderate-to-severe MAFLD and that it had a diagnostic value for MAFLD, with an AUC value of 0.992 alone and 0.996 after adjusting the age confounder. Therefore, FSH may be a potential diagnostic and predictive biomarker for MAFLD, which warrants further clinical studies.Materials and methods
Participants
Ultrasound examination
Laboratory tests
Statistical analysis
Results
Baseline characteristics of the included individuals
Logistic regression analysis for the risk factors of MAFLD
Diagnostic value of male hormones for MAFLD
Discussion
Data availability
All the data were included in this paper.
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Acknowledgements
This work was supported by grants from the National Natural Science Foundation of China (Grant number: 82002397), Natural Science Foundation of Hunan Province, (Grant Number: 2021JJ40868; 2023JJ60410), Scientific Research Project of Hunan Provincial Health Commission (202207012427,202206032424). Changsha Soft Science Project (Grant Number: kh2302010). Thanks for the support of National Traditional Chinese Medicine Advantage Specialist (Surgery) Funding.
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D.-H.B., F.L., K.P.-P. performed experiments, analyzed data, and reviewed manuscripts. M.Z., Y.T., Q.L., W.T., and Z.-N.M. organized the study and supervised experiments. G.-X.T. and X.-J.P. designed the project and prepared the manuscript.
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Bin, DH., Liu, F., Peng, KP. et al. The relationship between follicle-stimulating hormone and metabolic dysfunction-associated fatty liver disease in men. Nutr. Diabetes 14, 52 (2024). https://doi.org/10.1038/s41387-024-00314-1
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DOI: https://doi.org/10.1038/s41387-024-00314-1
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