Front. Nutr.Frontiers in NutritionFront. Nutr.2296-861XFrontiers Media S.A.10.3389/fnut.2022.851280NutritionOriginal ResearchThe Association Between Total Percent Fat and Serum Uric Acid in AdultsSunJuan1†YueChenyang2†LiuZhen1LiJie1KangWeiming1*1Division of General Surgery, Department of Surgery, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China2Department of Biology, York University, Toronto, ON, Canada
Edited by: Thea Magrone, University of Bari Aldo Moro, Italy
Reviewed by: Simiao Tian, Affiliated Zhongshan Hospital of Dalian University, China; Changhao Sun, Harbin Medical University, China
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Background
Serum uric acid (SUA) has been proven to be closely associated with metabolic abnormalities, including obesity. This study aimed to investigate the detailed relationship between total percent fat (TPF) and SUA among adults.
Methods
Briefly, 23,715 adults aged 18–59 years in the National Health and Nutrition Examination Survey (NHANES) 1999–2018 were included in this study. Multivariable linear regression models were used to examine the association between TPF and SUA. Subgroup analyses stratified by sex and obesity status were also performed by multivariable linear regression. Then, fitted smoothing curves and generalized additive models were also applied to address the non-linear relationship between TPF and SUA. Finally, a recursive algorithm was used to calculate the inflection point in the non-linear relationship and a two-segment piecewise linear regression model was used to analyze the relationship between TPF and SUA on both sides of the inflection point.
Results
There were 15,808 (66.7%) obese individuals in all 23,715 participants. In the fully adjusted model, there was a positive association between TPF and SUA (β = 0.99, 95% CI: 0.73–1.26). Besides, this positive association remained statistically significant in subgroup analyses stratified by sex and obesity status. Interestingly, in males, the association of TPF and SUA was an inverted U-shaped curve (inflection point: 34.3%).
Conclusion
Our study revealed a significant positive relationship between TPF and SUA among adults and this association remained statistically significant when stratified by sex and obesity status, but the shape of the smoothing curve in males differed from that in females.
total percent fatserum uric acidobesityhyperuricemiaNHANESIntroduction
Obesity has gradually become a major public health concern owing to its increased risk of various diseases. The negative impacts on quality of life and overall life expectancy in the obese populations, as well as the extra healthcare expenditures on obesity-related comorbidities, emphasize the need for a more detailed clinical assessment to allow effective obesity management (1, 2). Characterized by an increase in the number and/or the size of fat cells and the unusual distribution of fat mass, obesity cannot be accurately measured by body mass index (BMI) because it has difficulty differentiating lean mass from fat mass, and peripheral fat from central fat. This limitation makes BMI unable to identify normal weight obesity (NWO), a phenomenon associated with increased cardiovascular mortality and a high risk of developing metabolic abnormalities, making BMI an imprecise indicator of these negative events (3, 4). Compared with other techniques, dual-energy X-ray absorptiometry (DXA) not only evaluates body fat mass and its distribution with high precision, but also distinguishes fat mass from bone mass and lean mass (5). Notably, visceral adipose tissue measured by DXA has been confirmed to be associated with metabolic characteristics (6–8). In addition, the minimal radiation exposure and strong clinical feasibility also make DXA the preferred method for body composition assessment (5).
Hyperuricemia (HUA), defined as serum uric acid (SUA) levels >415 μmol/L in males and >340 μmol/L in females (9), is associated with a wide range of health outcomes, such as cardiovascular diseases, metabolic syndrome, and cancer (10). The prevalence of HUA is increasing worldwide, affecting approximately one out of five adults in the United States (11). A large-scale longitudinal study found that obese patients had a higher risk of developing HUA (12). Though many other studies indicated that SUA was closely related to obesity (13–15), the obesity mentioned in these studies were mainly measured by BMI. Since it was shown that SUA was more significantly correlated with fat mass (16, 17), the relationship between TPF and SUA seems to be much more meaningful.
The purpose of this study is to evaluate the detailed relationship between TPF and SUA using a large nationally representative sample of US adults. Furthermore, due to the male-female differences in TPF and SUA, subgroup analyses were carried out following the STROBE guidelines (18) to illustrate the associations in different subgroups.
Materials and MethodsStudy Population
Data were from the 1999–2018 National Health and Nutrition Examination Survey (NHANES), a continuous surveillance survey to assess the health and nutritional status of a representative sample of the United States civilians. Data of 40,117 participants aged 18–59 years were retrieved from the database. After excluding participants with incomplete TPF and SUA data (n = 16,402), participants with complete TPF and SUA data were included in our subsequent analyses (n = 23,715). The NHANES was reviewed and approved by the National Centre for Health Statistics Research Ethics Review Board and the informed consents were obtained from all participants in each year’s survey.
Variables
The exposure variable, TPF, was measured by whole body DXA scan using QDR-4500 Hologic Scanner (Bedford, MA, United States). The outcome variable, SUA, was measured by 704 Multichannel Analyzer or Roche Hitachi Model 917 from 1999 to 2001, Beckman Synchron LX20 from 2002 to 2007, Beckman Coulter UniCel® DxC800 from 2008 to 2016, and Roche Cobas 6000 (c501 module) in 2017 and 2018.
Other variables included age, sex, race, BMI, ratio of family income to poverty, education level, dietary intakes of energy and nutrients (protein, carbohydrate, and fat), prescription medication use, smoking status (whether smoked at least 100 cigarettes in life), heavy alcohol consumption (ever had 4/5 or more drinks every day), hypertension (mean systolic blood pressure ≥130 mmHg, mean diastolic blood pressure ≥80 mmHg, current use of antihypertensive medications, or self-reported physician-diagnosed hypertension) (19, 20), diabetes (self-reported physician-diagnosed diabetes or glycohemoglobin (HbA1c) ≥6.5% in those without a self-reported diagnosis) (21), weak/failing kidneys (self-reported physician-diagnosed weak/failing kidneys or estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m2) (22), vigorous work activity and laboratory variables (blood urea nitrogen, cholesterol, triglycerides). These data can be found on the NHANES website.1
Statistical Analyses
The baseline characteristics were shown as means ± SDs (standard deviation) and percentages for continuous variables and categorical variables, respectively. In our study, obesity was defined as TPF >25% in males and >35% in females according to the American Association of Clinical Endocrinologists (AACE) and the American College of Endocrinology (ACE) (23). Multivariable linear regression models were used to estimate βs and their 95% CIs for the relationship between TPF and SUA. No covariate was adjusted in Model 1. Model 2 analysis was adjusted for age, sex, and race to account for potential demographic confounders. Model 3 analysis was additionally adjusted for health-related behaviors (smoking status, heavy alcohol consumption, and vigorous work activity), hypertension, diabetes, weak/failing kidneys, BMI, blood urea nitrogen, cholesterol, triglycerides, education level, ratio of family income to poverty, dietary intakes of energy and nutrients (protein, carbohydrate, and fat), and prescription medication use. Subgroup analyses stratified by sex and obesity status were also performed by multivariable regression. Furthermore, the non-linear relationship between TPF and SUA was addressed by smoothing and generalized additive models. When non-linearity was detected, a recursive algorithm was used to calculate the inflection point. Then, a two-segment piecewise linear regression model was used to analyze the relationship between TPF and SUA on both sides of the inflection point. All analyses were performed using R2 and EmpowerStats,3p-values less than 0.05 were considered to indicate statistical significance.
Results
The weighted characteristics of study samples based on obesity status are shown in Table 1. Overall, there were 15,808 (66.7%) obese individuals in all 23,715 participants. Compared with the non-obese group, the obese group showed older age, higher measurements of SUA, cholesterol, triglycerides, BMI, but lower dietary intakes of energy and nutrients (protein, carbohydrate, and fat). Additionally, there were higher proportions of Hispanics, females, hypertension, diabetes, prescription medication use, but lower proportion of vigorous work activity in the obese group compared with the non-obese group.
Weighted characteristics of study samples based on obesity status.
Non-obese (n = 7,907)
Obese (n = 15,808)
p-value
Total percent fat (%)
24.89 ± 5.89
36.71 ± 7.08
<0.01
Serum uric acid (μmol/L)
296.98 ± 75.70
325.33 ± 82.98
<0.01
Age (years)
34.41 ± 11.65
40.33 ± 11.51
<0.01
Blood urea nitrogen (mmol/L)
4.49 ± 1.56
4.47 ± 1.48
0.29
Cholesterol (mmol/L)
4.73 ± 0.97
5.16 ± 1.08
<0.01
Triglycerides (mmol/L)
1.24 ± 1.35
1.83 ± 1.73
<0.01
BMI (kg/m2)
22.99 ± 3.19
30.85 ± 6.28
<0.01
Ratio of family income to poverty
2.98 ± 1.69
3.00 ± 1.65
0.30
Energy intake (kcal)
2417.24 ± 1016.61
2171.35 ± 900.03
<0.01
Protein intake (g)
91.74 ± 44.16
83.42 ± 37.89
<0.01
Carbohydrate intake (g)
292.55 ± 134.04
259.98 ± 117.61
<0.01
Fat intake (g)
89.53 ± 44.87
83.92 ± 42.22
<0.01
Sex (%)
<0.01
Males
56.20
47.69
Females
43.80
52.31
Race (%)
<0.01
Hispanic
12.88
17.60
Non-Hispanic White
66.68
64.93
Non-Hispanic Black
12.44
10.64
Others
8.00
6.83
Education level (%)
0.93
Less than high school
15.79
15.84
High school and above
84.21
84.16
Smoking status (%)
0.09
Yes
45.42
44.22
No
54.58
55.78
Heavy alcohol consumption (%)
0.89
Yes
16.04
15.97
No
83.96
84.03
Hypertension (%)
<0.01
Yes
25.36
45.11
No
74.64
54.89
Diabetes (%)
<0.01
Yes
2.92
9.54
No
97.08
90.46
Weak/failing kidneys (%)
<0.01
Yes
2.68
2.12
No
97.32
97.88
Vigorous work activity (%)
<0.01
Yes
41.92
30.31
No
58.08
69.69
Prescription medication use (%)
<0.01
Yes
37.70
51.12
No
62.30
48.88
Mean ± SD for continuous variables and p-value was calculated by weighted linear regression model.% for categorical variables and p-value was calculated by weighted chi-square test.
In model 1 with no covariate adjusted and model 2 with age, sex, and race adjusted, TPF was positively associated with SUA (model 1: β = 3.38, 95% CI: 3.25–3.51; model 2: β = 3.55, 95% CI: 3.41–3.68). When fully adjusted for age, sex, race, health-related behaviors (smoking status, heavy alcohol consumption, vigorous work activity), hypertension, diabetes, weak/failing kidneys, BMI, blood urea nitrogen, cholesterol, triglycerides, education level, ratio of family income to poverty, dietary intakes of energy and nutrients, and prescription medication use, TPF was still positively associated with SUA (model 3: β = 0.99, 95% CI: 0.73–1.26), suggesting a 1% increase in TPF was accompanied by a 0.99 μmol/L increase in SUA. Additionally, subgroup analyses stratified by sex in these three models showed the same trend in both males and females (Males, model 1: β = 3.35, 95% CI: 3.15–3.56; model 2: β = 3.73, 95% CI: 3.52–3.93; model 3: β = 1.72, 95% CI: 1.32–2.12. Females, model 1: β = 3.40, 95% CI: 3.23–3.57; model 2: β = 3.40, 95% CI: 3.23–3.57; model 3: β = 0.38, 95% CI: 0.03–0.72). When stratified by obesity status, the positive association remained statistically significant in the adjusted models. The results of these models are presented in Table 2.
The association between total percent fat (%) and serum uric acid (μmol/L).
Model 1 β (95% CI) p-value
Model 2 β (95% CI) p-value
Model 3 β (95% CI) p-value
Total
3.38 (3.25, 3.51) < 0.0001
3.55 (3.41, 3.68) < 0.0001
0.99 (0.73, 1.26) < 0.0001
Sex
Males
3.35 (3.15, 3.56) < 0.0001
3.73 (3.52, 3.93) < 0.0001
1.72 (1.32, 2.12) < 0.0001
Females
3.40 (3.23, 3.57) < 0.0001
3.40 (3.23, 3.57) < 0.0001
0.38 (0.03, 0.72) 0.03
Obesity status
Non-obese
–5.45 (–5.71, –5.20) < 0.0001
2.97 (2.57, 3.38) < 0.0001
1.43 (0.84, 2.02) < 0.0001
Obese
–3.69 (–3.86, –3.51) < 0.0001
3.81 (3.56, 4.07) < 0.0001
0.62 (0.19, 1.05) 0.0051
No covariate was adjusted in Model 1. Model 2 indicates that analysis was adjusted for age, sex, and race. Model 3 indicates model 2 adjustment plus the adjustment for health-related behaviors (smoking status, heavy alcohol consumption, vigorous work activity), hypertension, diabetes, weak/failing kidneys, body mass index, blood urea nitrogen, cholesterol, triglycerides, education level, ratio of family income to poverty, dietary intakes of energy and nutrients (protein, carbohydrate, and fat), and prescription medication use. Sex was not adjusted in the sex-stratified subgroup analyses.
The non-linear relationship between TPF and SUA was further captured by smooth curve fittings and generalized additive models (Figures 1A,B). In the subgroup analysis, an inverted U-shaped relationship between TPF and SUA was observed in males (Figure 1C), with the inflection point at 34.3% TPF which was identified by a two-segment piecewise linear regression model. Moreover, in males with TPF < 34.3%, every 1% increase in TPF was accompanied by a 1.97 μmol/L increase in SUA (95% CI: 1.55–2.38). By contrast, in males with TPF > 34.3%, a 1% increase in TPF was accompanied by a 0.96 μmol/L decrease in SUA, but the P-value indicated no statistical significance (95% CI: -2.24 to 0.33). The results are shown in Table 3. The subgroup analysis stratified by obesity status is shown in Figure 1D.
The association between total percent fat (%) and serum uric acid (μmol/L). (A) Each black point represents a sample. (B) Solid red line represents the smooth curve fit between variables. Blue bands represent the 95% confidence bands derived from the fit. (C) Stratified by sex. (D) Stratified by obesity status. Age, sex, race, smoking status, heavy alcohol consumption, vigorous work activity, hypertension, diabetes, weak/failing kidneys, body mass index, blood urea nitrogen, cholesterol, triglycerides, education level, ratio of family income to poverty, dietary intakes of energy and nutrients (protein, carbohydrate, and fat), and prescription medication use were adjusted (C was not sex-adjusted).
Threshold effect analysis of total percent fat (%) and serum uric acid (μmol/L) using the two-segment piecewise linear regression model.
Males β (95% CI) p-value
Fitting by standard linear model
1.72 (1.32, 2.12) <0.0001
Fitting by two-segment piecewise linear model
Inflection point
34.3
TPF < Inflection point
1.97 (1.55, 2.38) <0.0001
TPF > Inflection point
–0.96 (–2.24, 0.33) 0.1452
Log-likelihood ratio
<0.001
Discussion
Our study demonstrated that TPF was positively and significantly related to SUA in adults aged 18–59 years in all three models analyzing the NHANES 1999–2018 data. Sex- and obesity-stratified analyses revealed that TPF was still positively and significantly associated with SUA in the adjusted models. Additionally, the inverted U-shaped non-linear relationship between TPF and SUA was identified in males with the inflection point at 34.3% TPF.
In the past few decades, several epidemiological studies have shown the positive association between obesity and SUA. However, the majority of them used the BMI approach to measure obesity, and very few of them focused on the association between TPF and SUA. For example, Chen et al. (14), Dai et al. (24), and Tanaka et al. (25), all observed the strong positive correlation between BMI and SUA in different groups of individuals. However, the primary concern of the BMI approach was that it could not identify normal weight obesity, which is defined as the combination of high percentage of body fat and normal BMI (26). Thus, more assessment methods of obesity were developed to explore the relationship between obesity and SUA. In early 1997, Takahashi et al. showed that in a cohort of 50 healthy males, the accumulation of visceral fat measured by abdominal computed tomography (CT) at the level of the umbilicus may have a greater adverse effect on UA metabolism than BMI (27). In 1998, Matsuura et al. investigated the relationship between body fat distribution measured by CT and UA metabolism in 36 obese males. They found that the frequency of hyperuricemia (HUA) was markedly higher in the visceral fat obesity group compared with the subcutaneous fat obesity group, suggesting the crucial role of fat distribution pattern in UA metabolism (28). Subsequently, some large-scale cross-sectional studies were carried out to investigate this relationship. For instance, a study involving 508 males found a close relationship between the increased CT-measured visceral adiposity and the high risk of HUA after adjusting for BMI, blood pressure and other confounders (29). Additionally, a cohort containing 699 individuals with diabetes showed the same findings and it further found a 2.33-fold increased risk of HUA in subjects with high visceral adiposity (30). A recent study showed that in patients with type 2 diabetes, the waist circumference (WC) and visceral adipose tissue (VAT) mass were independent risk factors for HUA (16). It was also shown that the adipokines released from VAT had potential effects on SUA production (31), and the reduction of VAT may contribute to the significant decline in SUA (32).
Furthermore, not only was obesity associated with a higher risk of HUA, an elevated SUA was also proven to be independently linked to the development of obesity (17, 33). Studies have shown that SUA can increase fat storage, elevate triglyceride levels (34), and predict subsequent weight gain in humans (33, 35). An in vivo study further showed that an SUA-lowering drug (allopurinol) can both prevent HUA and weight gain in rats (36). Besides, HUA was also suspected to cause obesity through accelerating hepatic and peripheral lipogenesis (37). In addition, lowering SUA can prevent fructose-induced fat accumulation in HepG2 cells and reduce hepatic steatosis in a mouse model of metabolic syndrome (38). Recently, a cross-sectional study demonstrated a strong association between SUA and VAT (measured by magnetic resonance imaging) after adjustment for BMI or WC (39). We also noticed that in a study of 7,544 participants ≥ 40 years from the NHANES III, the highest SUA group (>8 mg/dL) participants were twice as likely to show sarcopenia compared to the lowest SUA group (<6 mg/dL) participants (40). Moreover, there seemed to be a vicious circle between SUA and fat mass accumulation since the secretion of SUA from adipose tissue may be enhanced in obese individuals (41, 42). Additionally, a strong association with metabolic syndrome was also found in children and adolescents with high adiposity index or high SUA (43, 44).
Several pathophysiological and metabolic mechanisms have been proposed to explain the abovementioned association between adipose tissue and SUA. On the one hand, UA secreted from the adipose tissue was enhanced through the increased production of xanthine oxidoreductase (XOR) in obese individuals (45). Additionally, the obesity-linked insulin resistance can also inhibit the excretion and promote the reabsorption of SUA (46, 47). On the other hand, SUA may also induce insulin resistance via inhibiting the availability of nitric oxide and decreasing insulin-mediated glucose uptake in skeletal muscles (48, 49), and the elevated SUA may damage islet B cells directly to aggravate insulin resistance (50). In addition, the accumulated insulin can inhibit the decomposition of visceral fat, leading to the development of obesity (51). And it was also indicated that SUA might take part in stimulating the secretion of inflammatory markers such as C-reactive protein (CRP), interleukin (IL)-6, IL-18, and tumor necrosis factor (TNF)-alpha which are crucial to the development of metabolic syndrome (52, 53).
Interestingly, an earlier study showed that estrogen can lower SUA in postmenopausal women (54) and trans-sexual men (55), which can be explained by the possible enhancement of SUA excretion by estrogen (56). Specifically, estrogen was found to decrease urate reabsorptive transporter expression at the posttranscriptional level, resulting in increased UA excretion and decreased SUA levels (57). Thus, estrogen may account for the different patterns of association between TPF and SUA in different sexes, but the detailed mechanisms still need to be further investigated. In our study, the non-linear relationships between TPF and SUA differed in males and females. With the increase of TPF, a steady increase in SUA was observed in females, while an inflection point was identified in males. Moreover, other studies showed that the relationship between SUA and the incidence of coronary heart disease, hypertension and renal dysfunction was stronger in females than in males (58–60), suggesting that females might be more vulnerable to organ damage caused by UA, which was consistent with the observation that females had lower UA levels than males (61). Thus, it would be desirable to take into account sex-related differences while implementing measures to prevent HUA caused by obesity.
There are some strengths and limitations of our study. First, it was a large-scale study involving nationally representative American adults with complete TPF and SUA data (n = 23,715), which made it possible for us to conduct subgroup analysis to further illustrate the different patterns of association between TPF and SUA in males and females. Second, the TPF data in our study were measured by DXA, which offered a more accurate measurement of adipose tissue compared with the traditional BMI-based approach. The limitations of this study are also worthy of note. First and foremost, it was the nature of cross-sectional study that the outcomes and exposures were ascertained at the same time that limited the inference of a causal relationship between TPF and SUA. Thus, large-sample prospective studies are further needed to explore this causality. Second, the TPF data of participants ineligible for DXA scan (e.g., excess body weight or height) were not included in the original survey. Thus, the selection bias cannot be avoided. Third, some covariates in our study such as hypertension and diabetes status, smoking and drinking status, as well as physical activity level were all based on self-report data, which may introduce the recall bias. Finally, little was known about the potential biases caused by other unrecognized confounding factors, leaving them unadjusted in this study.
Conclusion
In conclusion, our results supported a significant positive association between TPF and SUA, even after the adjustment for a wide range of potential confounders. And this association remained statistically significant when stratified by sex and obesity status. However, the underlying mechanisms of the different patterns of this relationship in males and females still need further investigation.
Data Availability Statement
Publicly available datasets were analyzed in this study. These data can be found here: http://www.cdc.gov/nchs/nhanes.
Author Contributions
JS and CY contributed to data collection, statistical analysis, and writing of the manuscript. ZL and JL contributed to data collection and statistical analysis. WK supervised the study and contributed to polishing and reviewing of the manuscript. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Funding
This work was supported by 2017 Beijing Municipal Science and Technology Project (D171100006517004), 2019 Li Jieshou Intestinal Barrier Research Fund (Z-2017-24-2009), Wu Jieping Medical Foundation (320.6750.2020-08-32), and the CAMS Innovation Fund for Medical Sciences (No. 2020-I2M-C&T-B-027).
We thank the staff members and the participants of the NHANES study for their valuable contributions.
ReferencesBleichSVercammenKZatzLFrelierJEbbelingCPeetersA. Interventions to prevent global childhood overweight and obesity: a systematic review.Lancet Diabete Endocrinol. (2018) 6:332–46. 10.1016/S2213-8587(17)30358-329066096WithrowDAlterD. The economic burden of obesity worldwide: a systematic review of the direct costs of obesity.Obes Rev. (2011) 12:131–41. 10.1111/j.1467-789X.2009.00712.x20122135OliverosESomersVSochorOGoelKLopez-JimenezF. The concept of normal weight obesity.Prog Cardiovasc Dis. (2014) 56:426–33. 10.1016/j.pcad.2013.10.00324438734LuYCLinYCYenMFChanWP. Dual-energy x-ray absorptiometry-assessed adipose tissues in metabolically unhealthy normal weight asians.Sci Rep. (2019) 9:17698. 10.1038/s41598-019-53557-931776349KaulSRothneyMPPetersDMWackerWKErgunDL. Dual-energy X-ray absorptiometry for quantification of visceral fat.Obesity. (2012) 20:1313–8. 10.1038/oby.2011.39322282048Eriksson HoglingDBäckdahlJThorellARydénMAnderssonD. Metabolic impact of body fat percentage independent of body mass index in women with obesity remission after gastric bypass.Obes Surg. (2020) 30:1086–92. 10.1007/s11695-019-04304-631832934ScottDCummingRNaganathanVBlythFLe CouteurDHandelsmanDAssociations of sarcopenic obesity with the metabolic syndrome and insulin resistance over five years in older men: the concord health and ageing in men project.Exp Gerontol. (2018) 108:99–105. 10.1016/j.exger.2018.04.00629649572OkoroduduDJumeanMMontoriVRomero-CorralASomersVErwinPDiagnostic performance of body mass index to identify obesity as defined by body adiposity: a systematic review and meta-analysis.Int J Obes. (2010) 34:791–9. 10.1038/ijo.2010.520125098De BeckerBBorghiCBurnierMvan de BorneP. Uric acid and hypertension: a focused review and practical recommendations.J Hypertens. (2019) 37:878–83. 10.1097/HJH.000000000000198030620339LiXMengXTimofeevaMTzoulakiITsilidisKIoannidisJSerum uric acid levels and multiple health outcomes: umbrella review of evidence from observational studies, randomised controlled trials, and Mendelian randomisation studies.BMJ (Clin Res ed). (2017) 357:j2376. 10.1136/bmj.j237628592419ZhuYPandyaBChoiH. Prevalence of gout and hyperuricemia in the US general population: the National Health and Nutrition Examination Survey 2007-2008.Arthritis Rheum. (2011) 63:3136–41. 10.1002/art.3052021800283DongHYangXZhangXTianS. Visceral adiposity index is strongly associated with hyperuricemia independently of metabolic health and obesity phenotypes.Sci Rep. (2017) 7:8822. 10.1038/s41598-017-09455-z28821853VayáARiveraLHernández-MijaresABautistaDLaizB. Association of metabolic syndrome and its components with hyperuricemia in a Mediterranean population.Clin Hemorheol Microcirc. (2015) 60:327–34. 10.3233/CH-14188725261431ChenMYZhaoCCLiTTZhuYYuTPBaoYQSerum uric acid levels are associated with obesity but not cardio-cerebrovascular events in Chinese inpatients with type 2 diabetes.Sci Rep. (2017) 7:40009. 10.1038/srep4000928051185DuanY. Association between serum uric acid levels and obesity among university students (China).Nutr Hosp. (2015) 31:2407–11. 10.3305/nh.2015.31.6.873426040345ZongJSunYZhangYYuanJGuY. Correlation between serum uric acid level and central body fat distribution in patients with type 2 diabetes.Diabetes Metab Syndr Obes. (2020) 13:2521–31. 10.2147/DMSO.S26089132765031KimTLeeSYooJKimSYooSSongHThe relationship between the regional abdominal adipose tissue distribution and the serum uric acid levels in people with type 2 diabetes mellitus.Diabetol Metab Syndr. (2012) 4:3. 10.1186/1758-5996-4-322301198Von ElmEAltmanDEggerMPocockSGøtzschePVandenbrouckeJ. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies.Lancet (Lond Engl). (2007) 370:1453–7.WheltonPKCareyRMAronowWSCaseyDEWrightJT. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA guideline for the prevention, detection, evaluation, and management of high blood pressure in adults. a report of the American college of cardiology/American heart association task force on clinical pra.Hypertension. (2017) 19:213–21.YangHLiuHLSunJYKongXQSunWXiongYQ. Association between serum calcium and the prevalence of hypertension among US adults.Front Cardiovasc Med. (2021) 8:719165. 10.3389/fcvm.2021.71916534912855American Diabetes Association.2. Classification and diagnosis of diabetes: standards of medical care in diabetes-2019.Diabetes Care. (2019) 42(Suppl. 1):S13–28. 10.2337/dc19-S00230559228TuotDSZhuYVelasquezAEspinozaJMendezCDBanerjeeTVariation in patients’ awareness of CKD according to how they are asked.Clin J Am Soc Nephrol. (2016) 11:1566–73. 10.2215/CJN.0049011627340288DickeyRABartuskaDGBrayGWCallawayWKennedyFP.AACE/ACE Position Statement on the Prevention, Diagnosis, and Treatment Of Obesity (1998 Revision). (1997).DaiXYuanJYaoPYangBGuiLZhangXAssociation between serum uric acid and the metabolic syndrome among a middle- and old-age Chinese population.Eur J Epidemiol. (2013) 28:669–76. 10.1007/s10654-013-9829-423864233TanakaKOgataSTanakaHOmuraKHondaCHayakawaK. The relationship between body mass index and uric acid: a study on Japanese adult twins.Environ Health Prev Med. (2015) 20:347–53. 10.1007/s12199-015-0473-326037073KaravaVDotisJKondouAChristoforidisALiakopoulosVTsioniKAssociation between relative fat mass, uric acid, and insulin resistance in children with chronic kidney disease.Pediatric Nephrol. (2021) 36:425–34. 10.1007/s00467-020-04716-y32767109TakahashiSYamamotoTTsutsumiZMoriwakiYYamakitaJHigashinoK. Close correlation between visceral fat accumulation and uric acid metabolism in healthy men.Metab Clin Exp. (1997) 46:1162–5. 10.1016/s0026-0495(97)90210-99322800MatsuuraFYamashitaSNakamuraTNishidaMNozakiSFunahashiTEffect of visceral fat accumulation on uric acid metabolism in male obese subjects: visceral fat obesity is linked more closely to overproduction of uric acid than subcutaneous fat obesity.Metabolism. (1998) 47:929–33. 10.1016/s0026-0495(98)90346-89711987HikitaMOhnoIMoriYIchidaKYokoseTHosoyaT. Relationship between hyperuricemia and body fat distribution.Intern Med. (2007) 46:1353–8. 10.2169/internalmedicine.46.004517827832KimTHLeeSSJiHYKimSRYongKK. The relationship between the regional abdominal adipose tissue distribution and the serum uric acid levels in people with type 2 diabetes mellitus.Diabetol Metab Syndr. (2012) 4:3. 22301198KahlSGanchevaSStraburgerKHerderCRodenM. Empagliflozin effectively lowers liver fat content in well-controlled type 2 diabetes: a randomized, double-blind, phase 4, placebo-controlled trial.Diabetes Care. (2019) 42:dc190641. 10.2337/dc19-064131540903TambaSNishizawaHFunahashiTOkauchiYOgawaTNoguchiMRelationship between the serum uric acid level, Visceral fat accumulation and serum adiponectin concentration in Japanese men.Intern Med. (2009) 48:1493–1493. 10.2169/internalmedicine.47.060318591837MasuoKKawaguchiHMikamiHOgiharaTTuckML. Serum Uric Acid and Plasma Norepinephrine Concentrations Predict Subsequent Weight Gain and Blood Pressure Elevation.Hypertension. (2003) 42:474–80. 10.1161/01.HYP.0000091371.53502.D312953019BeckerBDBorghiCBurnierMBornePVD. Uric acid and hypertension: a focused review and practical recommendations.J Hypertens. (2018) 37:1. 30620339KuwabaraMNiwaKHisatomeINakagawaTCarlosA. Asymptomatic hyperuricemia without comorbidities predicts cardiometabolic diseases: five-year Japanese cohort study.Hypertension. (2017) 69:1036–44. 10.1161/HYPERTENSIONAHA.116.0899828396536NakagawaTHuHZharikovSTuttleKRJohnsonRJ. A causal role for uric acid in fructose-induced metabolic syndrome.Am J Physiol Renal Physiol. (2006) 290:F625. 10.1152/ajprenal.00140.200516234313HanTSMengXShanRQ. Temporal relationship between hyperuricemia and obesity, and its association with future risk of type 2 diabetes.Int J Obes (Lond). (2018) 42:1336–44. 10.1038/s41366-018-0074-529717279LanaspaMASanchez-LozadaLGChoiYJCicerchiCKanbayMRoncal-JimenezCAUric acid induces hepatic steatosis by generation of mitochondrial oxidative stress: potential role in fructose-dependent and -independent fatty liver.J Biol Chem. (2012) 287:40732. 10.1074/jbc.M112.39989923035112RospleszczSDermyshiDMüller-PeltzerKStrauchKBambergFPetersA. Association of serum uric acid with visceral, subcutaneous and hepatic fat quantified by magnetic resonance imaging.Sci Rep. (2020) 10:442. 10.1038/s41598-020-57459-z31949261BeaversKBeaversDSerraMBowdenRWilsonR. Low relative skeletal muscle mass indicative of sarcopenia is associated with elevations in serum uric acid levels: findings from NHANES III.J Nutr Health Aging. (2009) 13:177–82. 10.1007/s12603-009-0054-519262948OliveiraEBuriniRC. High plasma uric acid concentration: causes and consequences.Diabetol Metab Syndr. (2012) 4:12. 10.1186/1758-5996-4-1222475652TsushimaYNishizawaHTochinoY. Uric acid secretion from adipose tissue and its increase in obesity.J Biol Chem. (2013) 288:27138–49. 10.1074/jbc.M113.48509423913681FordELiCCookSChoiH. Serum concentrations of uric acid and the metabolic syndrome among US children and adolescents.Circulation. (2007) 115:2526–32. 10.1161/CIRCULATIONAHA.106.65762717470699MirandaJAlmeidaGGMartinsRCunhaMBBeloVASantosJThe role of uric acid in the insulin resistance in children and adolescents with obesity.Rev Paul Pediatr. (2015) 33:431–6. 10.1016/j.rpped.2015.03.00926300523TsushimaYNishizawaHTochinoYNakatsujiHSekimotoRNagaoHUric acid secretion from adipose tissue and its increase in obesity.J Biol Chem. (2013) 288:27138–49. 23913681HuangGXuJBZhangTJNieXLLiQLiuYHyperuricemia is associated with cardiovascular diseases clustering among very elderly women - a community based study in Chengdu. China.Sci Rep. (2017) 7:996. 10.1038/s41598-017-01042-628428538FuruhashiMKoyamaMMatsumotoMMuraseTNakamuraTHigashiuraYAnnual change in plasma xanthine oxidoreductase activity is associated with changes in liver enzymes and body weight.Endocr J. (2019) 66:777–86. 10.1507/endocrj.EJ19-005331130575JohnsonRJNakagawaTSanchez-LozadaLGShafiuMSundaramSLeMSugar, uric acid, and the etiology of diabetes and obesity.Diabetes. (2013) 62:3307–15. 10.2337/db12-181424065788RoyDPerreaultMMaretteA. Insulin stimulation of glucose uptake in skeletal muscles and adipose tissues in vivo is NO dependent.Am J Physiol. (1998) 274:E692–9. 10.1152/ajpendo.1998.274.4.E6929575831AdnanERahmanIAFaridinHP. Relationship between insulin resistance, metabolic syndrome components and serum uric acid.Diabetes Metab Syndr. (2019) 13:2158–62. 10.1016/j.dsx.2019.04.00131235151ObeidatAAAhmadMNHaddadFHAzzehFS. Leptin and uric acid as predictors of metabolic syndrome in jordanian adults.Nutr Res Pract. (2016) 10:411–7. 10.4162/nrp.2016.10.4.41127478548RuggieroCCherubiniABleABosAJMaggioMDixitVDUric acid and inflammatory markers.Eur Heart J. (2006) 27:1174–81. 10.1093/eurheartj/ehi87916611671KanellisJWatanabeSLiJHKangDHLiPNakagawaTUric acid stimulates monocyte chemoattractant protein-1 production in vascular smooth muscle cells via mitogen-activated protein kinase and cyclooxygenase-2.Hypertension. (2003) 41:1287–93. 10.1161/01.HYP.0000072820.07472.3B12743010SuminoHIchikawaSKandaTNakamuraTSakamakiT. Reduction of serum uric acid by hormone replacement therapy in postmenopausal women with hyperuricaemia.Lancet (Lond Engl). (1999) 354:650. 10.1016/S0140-6736(99)92381-410466673NichollsAScottJT. Effect of weight-loss on plasma and urinary levels of uric acid.Lancet. (1973) 2:1223–4. 10.1016/s0140-6736(72)92271-4LiuHPengLMaJHeLLongKOuyangXLow expression of estrogen receptor β in renal tubular epithelial cells may cause hyperuricemia in premenopausal patients with systemic lupus erythematosus.Lupus. (2021) 30:560–7. 10.1177/096120332098423133407049TakiueYHosoyamadaMKimuraMSaitoH. The effect of female hormones upon urate transport systems in the mouse kidney.Nucleosides Nucleotides Nucleic Acids. (2011) 30:113–9. 10.1080/15257770.2010.55164521360409KimSYGuevaraJPKimKMChoiHKHeitjanDFAlbertDA. Hyperuricemia and coronary heart disease: a systematic review and meta-analysis.Arthritis Care Res (Hoboken). (2010) 62:170–80.WangJQinTQChenJRLiTLWangLHuangHHyperuricemia and risk of incident hypertension: a systematic review and meta-analysis of observational studies.PLoS One. (2014) 9:e114259. 10.1371/journal.pone.011425925437867IsekiKIsekiCKinjoK. Changes in serum uric acid have a reciprocal effect on eGFR change: a 10-year follow-up study of community-based screening in Okinawa, Japan.Hypertens Res. (2013) 36:650–4. 10.1038/hr.2013.1123486166NagasawaYYamamotoRShojiTShinzawaMHasuikeYNagatoyaKSerum uric acid level predicts progression of Iga nephropathy in females but not in males.PLoS One (2016) 11:e0160828. 10.1371/journal.pone.016082827560997