Skip to main content


Springer Nature is making SARS-CoV-2 and COVID-19 research free. View research | View latest news | Sign up for updates

Sweetened beverage consumption and the risk of hyperuricemia in Mexican adults: a cross-sectional study



The prevalence of hyperuricemia has doubled worldwide during the last few decades. The substantial increase in sweetened beverage (SB) consumption has also coincided with the secular trend of hyperuricemia. Recent studies do show that the consumption of SB can induce hyperuricemia. However, the association between SB and hyperuricemia remains unclear. The aim of this study was to evaluate the association between SB consumption and levels of uric acid in Mexican adults.


We performed a cross-sectional analysis of data from selected adults participating in the baseline assessment of the Health Workers Cohort Study. A total of 6,705 participants of both sexes between ages 18 and 70 years were included. SB intake was estimated using a validated semi-quantitative food frequency questionnaire. Biochemical and anthropometric information was collected using standard procedures. Hyperuricemia was defined as uric acid levels ≥ 7.0 mg/dL in men and ≥ 5.8 mg/dL in women. The association of interest was assessed by multiple logistic regression models.


The odds ratios (OR) for hyperuricemia in men who consume 0.5-1 SB/day was 1.59 (95% CI; 1.05-2.40) and 2.29 (95% CI; 1.55-3.38) for those who consume ≥3 SB/day when compared to men who consume less than half a SB/day. In women, the OR for hyperuricemia for those who consume >1.0- < 3.0 SB/day was 1.33 (95% CI; 1.04-1.70) and 1.35 (95% CI; 1.04-1.75) for those who consume ≥3 SB/day when compared to women who consume less than half a SB/day, independent of other covariables. Men and women with high SB consumption and a body mass index (BMI) ≥ 25 Kg/m2 had greater risk for hyperuricemia than men and women with low SB consumption and normal BMI < 25 Kg/m2.


Our findings suggest that the consumption of SB is associated with an increased risk of hyperuricemia in Mexican adults. However, longitudinal research is needed to confirm the association between SB intake and hyperuricemia.

Peer Review reports


The prevalence of hyperuricemia, defined as increased serum uric acid levels [1], has doubled worldwide during the last few decades [2]. Hyperuricemia is the precursor of gout, which is the principal cause of inflammatory arthritis among adult men and older women [3]. Hyperuricemia is furthermore recognized as an independent risk factor for metabolic and cardiorenovascular conditions including metabolic syndrome, type 2 diabetes (T2DM) and insulin resistance [47]. In addition, epidemiological evidence suggests that hyperuricemia may play a role in epidemics of hypertension and coronary heart disease [8, 9]; however, recent evidence suggests no causal association between uric acid and ischemic heart disease and blood pressure [10]. The worldwide population-level increase in serum uric acid levels over the past few decades correlates with pronounced changes in the most prevalent health risk factors known to be associated with hyperuricemina including: an increased prevalence of obesity and metabolic syndrome as well as changes in dietary patterns [11]. Studies suggest that foods such as alcohol, meat and seafood play an important role in the development of hyperuricemia [1214]. In general, a purine-rich diet has been long recognized as a risk factor for hyperuricemia. Since uric acid is the end product of purine degradation, gout patients are advised to avoid purine-rich foods [15]. In contrast, dairy products and foods rich in vitamin C have been shown to be protective against hyperuricemia [16]. Although it is believed that diet plays an important role in the development of hyperuricemia, the association between other specific dietary factors or foods and hyperuricemia remains unclear.

Recent studies do show that the consumption of sugar-sweetened beverages (SB) can induce hyperuricemia [1, 17, 18]. Although these beverages do not contain purines, they do contain large quantities of sweeteners including sucrose (composed of 50% glucose and 50% fructose), fructose and high fructose corn syrup (typically composed of 45% glucose and 55% fructose) [19]. Both fructose and high fructose corn syrup have been associated with increased serum uric acid levels [20, 21], since uric acid production is upregulated by fructose, unlike glucose and other monosaccharides [21]. The potential mechanisms underlying the detrimental effects of sucrose, fructose and high fructose corn syrup are under debate. Some studies have suggested insulin resistance as one of the mechanisms involved in hyperuricemia [22, 23]. One recent study suggests that long-term consumption of fructose and high fructose corn syrup could be a source of reactive dicarbonyls that increases risk of metabolic disorders including hyperuricemia [24].

Mexico has one of the highest rates of SB consumption in the world [4]. Reports indicate that SB consumption among Mexican adults has increased to 21% of total caloric consumption from 1996 to 2006 [25, 26], meaning SB consumption is a significant component of the current Mexican diet. For these reasons, a better understanding of how fructose can affect plasma urate concentrations is important if effective dietary recommendations are to be formulated. Current recommendations include restriction of alcohol, meat and other purine-rich foods, but planning recommendations concerning SB should also be considered [27].

In this study we assess the potential health impact of SB consumption by examining the relationship between SB intake and uric acid levels in Mexican adults participating in the Health Workers Cohort Study. Because earlier evidence [28] has suggested that body mass index (BMI) may modify the effect of sweetened beverage on gout or hyperuricemia, we also examined this relationship stratifying by BMI and age.


Study population

A cross-sectional analysis was performed using data from adults participating in the baseline evaluation of the ¨Health Workers Cohort Study¨ (2004–2006). The methodology and participant characteristics have been detailed previously [29]. Of the 8,977 adults formally enrolled, for the present analysis we used data from 8,514 participants aged 18 to 70 years, of which the following were excluded: pregnant women (n = 186), those with a diagnosis of gout (n = 67), those taking medications to control uric acid (n = 20), those taking diuretics (n = 79), those without uric acid values (n = 693), subjects that responded to less than 85% of questions or did not complete all the diet related questions (n = 525), subjects with extreme values of caloric intake (<600, > 7000 Kcal/day) (n = 87) using the standard deviation method (>3.86SD) [30], subjects with outlying values of energy consumption from SB (n = 74), subjects not providing information on tobacco use (n = 74) and subjects with incomplete anthropometric data (n = 4). Ultimately, a total of 6,705 subjects were included in the analysis.

This study was planned and performed according to the guidelines of the Declaration of Helsinki. All participating institutions’ research ethics committees [Comité de Ética en Investigación, Instituto Mexicano del Seguro Social (No. 12CEI 09 006 14); Comité de Ética en Investigación, Instituto Nacional de Salud Pública (No. 13CEI 17 007 36); Comité de Ética, Centro de Investigación en Ciencias Médicas (No. 1233008X0236)], approved the study protocol and informed consent forms. Written informed consent was obtained from all participants.

Assessment of sugar- and artificially-sweetened beverage consumption and other dietary intake

To assess diet, a validated semi-quantitative food frequency questionnaire (FFQ) was used [31]. To test the FFQ’s reproducibility, it was administered twice, at a 1-year interval, to 134 women residing in Mexico city and the validity results were then compared with those from the set of 4 recall tests given at 3 month intervals. The questionnaire includes data describing the frequency of consumption of 116 foods during the previous year. This FFQ collects information about the consumption of soft drinks, such as: sugar-sweetened soft drinks (colas and other carbonated beverages with sugar), flavored water with sugar (such as lemon or orange water prepared with artificial flavorings) and diet soft drinks (low-calorie colas and other low-calorie beverages), using a standard serving size of 355 ml. We also assessed consumption of orange juice. The amount of energy intake from the ingestion of these beverages (Kcal/serving) was determined using the Evaluation System of Eating Habits and Nutrient Consumption (SNUT) [32]. For this study, we summed the intakes of single items to create totals for SB (sugar sweetened soft drinks and flavored water with sugar) and diet beverages (low-calorie colas and other low-calorie beverages). In addition, SB intake was divided into four categories: (I) < 0.5 servings of SB/day, (II) ≥0.5 – 1.0 servings of SB/day, (III) >1.0 - < 3 servings of SB/day, and (IV) ≥ 3 servings of SB/day. Total energy, energy from other carbohydrates, nutrient intakes and alcohol consumption were similarly estimated with this questionnaire.

Biological measures

A fasting venous blood sample was collected from the antecubital vein; fasting time was ≥8 hours. Serum uric acid levels were determined with the enzymatic colorimetric method using the SYNCHRON CX® system [33]. Hyperuricemia was defined as uric acid levels ≥ 7.0 mg/dL in men and ≥ 5.8 mg/dL in women [1].

Anthropometric measures

Body weight was measured with a previously calibrated electronic scale (model BC-533; Tanita, Tokyo, Japan), with participants wearing minimal clothing. Height was measured using a conventional stadiometer (SECA brand), on barefoot subjects standing with their shoulders in a normal position; measurements were taken with the tape in a horizontal plane perpendicular to the vertical scale, touching the top of the head at the moment of inspiration. Waist circumference was measured at the high point of the iliac crest at the end of normal expiration, to the nearest 0.1 cm, with a conventional steel measuring tape (SECA brand). Abdominal obesity was defined as a waist circumference > 102 cm for men and > 88 cm for women [34]. Body mass index was classified as: normal (18.5 to < 25 kg/m2), overweight (≥25 to < 30 kg/m2), or obese (≥30 kg/m2) [35]. The proportion of body fat was determined by dual X-ray absorptiometry (DEXA) using a Lunar densitometer (model: DPX-GE 73735, serial number: 638405U77) (Lunar Radiation Corporation, Madison, WI, USA; software version .35, fast scan mode). Excess body fat was defined as >35% in women and >25% in men [36]. All measurement procedures were performed by trained personnel using standardized procedures.

Assessment of other variables

Demographic information was collected using a self-administered questionnaire. Physical activity level was determined using a survey used in similar follow-up studies [37, 38]. The participants reported the time they spent each week on activities such as running, walking, etc. during a typical week in the previous year. The physical activity variable was categorized into: inactive <30 min/day and active ≥30 min/day, in accordance with previous studies [39]. Finally, participants were asked about weight changes they experienced during the previous year, and this information was categorized as: no weight change, weight loss, or weight gain in the past year. Participants who gained or lost less than 5 kg were categorized have experienced no weight change.

Statistical analysis

We performed an exploratory analysis by sex and SB intake considering the variables of age, body mass index, body fat proportion, tobacco use, physical activity, levels of uric acid, SB consumption and other dietary variables. We used Student t tests for continuous variables and Chi2 tests for categorical variables to test for differences between sexes. When continuous variables did not show a normal distribution, non-parametric tests for trends across ordered groups were performed.

We assessed trends of acid uric levels, hyperuricemia, and other variables across categories of SB intake. Differences between groups were computed with the test for linear trend.

The effect of SB consumption on uric acid levels was determined using linear regression models. In this case, the increments of uric acid levels were considered across categories of SB intake, using the lowest category of consumption (<0.5 SB/day) as a reference.

To estimate the association between SB intake and levels of uric acid, we computed odds ratios (OR) and 95% confidence intervals (CI 95%) using multiple logistic regression models, adjusting for different covariables in several models. The first model was adjusted for age, the second added tobacco use, physical activity (min/day), and body weight changes, the third model added energy intake (kcal/day), alcohol consumption (g/day), percentage of energy from carbohydrates (quintiles), total meats (servings/day), seafood (servings/day), total fruits (servings/day), dairy products (servings/day), coffee (cups/day), and vitamin C intake (mg/day), and finally the fourth model added BMI (kg/m2) to determine whether or not the relationship was the result of a BMI classified as overweight or obese. In all the multivariate models, the reference category of energy intake from SB was defined as < 0.5 SB/day.

To assess possible effect modification, we explored analyses stratified by age (two categories: < 50 years vs. ≥ 50 years), and BMI (two categories: <25 kg/m2 vs. ≥25 kg/m2). We tested the significance of the interaction with a likelihood ratio test by comparing a model with the main effects of each intake and the stratifying variable and the interaction terms with a reduced model with only the main effects. All p values presented are two sided; p < 0.05 was considered statistically significant. All the statistical analyses were performed using the STATA statistical software package, version 9.2 for Windows (Stata Corp. LP: College Station, TX).


The study population was made up of mainly middle-aged participants; most (70.8%) were women with a mean age of 43 years, and the rest were men with a mean age of 42.6 years. Their average uric acid level was 5.9 mg/dL in men and 4.4 mg/dL in women (p < 0.001). A total of 20.6% of men had hyperuricemia as compared to 13.5% of women (p < 0.001). Men consumed an average of 225 kcal/day from SB, whereas women consumed 186 Kcal/day (p < 0.001) (Table 1).

Table 1 Characteristics of Mexican adults from the baseline assessment of the Health Workers Cohort Study

Men with the highest SB intake (≥3 servings of SB/day) were younger, had higher caloric and total carbohydrate intakes and were more frequently smokers. Additionally, the male participants with the highest SB intake had higher average BMIs, proportions of obesity, and percentages of body fat than men in the category with the lowest SB intake (<0.5 servings of SB/day). Finally, serum uric acid concentrations and hyperuricemia prevalence were higher in men with the highest levels of SB intake (p for trend <0.001). For the female participants, women in the highest category of SB consumption were more frequently smokers and were less active than women in the lowest category of SB consumption (Table 2).

Table 2 Characteristics, according to categories of sugar-sweetened beverage intake by sex in a Mexican adult population

The results of a multivariate regression analysis evaluating the effect of sweetened beverage intake on uric acid levels are presented in Table 3. In the adjusted model, we found that uric acid levels in men who consumed more than 3 servings of sweetened beverages per day increased 0.38 mg/dL (P < 0.001); whereas in women these levels increased to 0.21 mg/dL, in comparison with subjects who consumed less than 0.5 servings of SB/day.

Table 3 Differences in serum uric acid levels (mg/dL) according to categories of sugar-sweetened beverage intake

Results of the multiple logistic regression analysis show a positive association between SB consumption and the presence of hyperuricemia in men and women. In men consuming ≥0.5 - 1.0 servings of SB/day, the multivariate odds ratio for hyperuricemia was 1.59 (95% CI: 1.05–2.40), as compared with the reference consumption level of SB (<0.5 servings of SB/day). For men consuming >1.0 - <3.0 servings of SB/day, this was 1.68 (95% CI: 1.14–2.49), and men consuming ≥ 3.0 SB/day was 2.29 (95% CI: 1.55–3.38; p for trend <0.001). For women, the ORs for hyperuricemia across categories of SB consumption were: 1.19 (95% CI: 0.92-1.53), 1.33 (95% CI: 1.04-1.70) and 1.35 (95% CI: 1.04-1.75) p for trend 0.015 (Table 4).

Table 4 Odds ratios (95% CI) for hyperuricemia according to categories of energy of sweetened beverage intake

We examined the joint effect of SB intake and body mass index by cross classifying the study population by both variables. The odds ratio from these stratified analyses was 4.71 (95% CI: 2.64-8.36; p for interaction 0.007) when men with high SB consumption and overweight/obesity were compared with men with a low consumption of sweetened beverage and body mass index < 25 kg/m2 (Figure 1A). In women (Figure 2A), the OR for the combination of a high consumption of SB and BMI ≥ 25 kg/m2 compared with women in the opposite extreme was 3.77 (95% CI: 2.53-5.35, p for interaction 0.007).

Figure 1

Multivariate odds ratio of hyperuricemia in men, according to the tertiles of sweetened beverage intake. *Analyses of effect modification: (A) stratified by body mass index (BMI: < 25 kg/m2 vs ≥ 25 kg/m2), (B) stratified by age (< 50 years vs ≥ 50 years. Reference group for comparisons was men in lowest tertile of sweetened beverage intake and (A) with body mass index < 25 kg/m2, and (B) with age < 50 years. Odds ratio were adjusted for: age (years), tobacco use (current smoker, ex-smoker y non-smoker), physical activity (active ≥ 30 min/day, inactive < 30 min/day), weight change (did not gain, gained, lost), calorie intake (quintiles), percentage of energy from total carbohydrate (quintiles), percentage of energy from protein (quintiles), alcohol intake (gr/day), vitamin C intake (mg/day), and body mass index.

Figure 2

Multivariate odds ratio of hyperuricemia in women, according to the tertiles of sweetened beverage intake. *Analyses of effect modification: (A) stratified by body mass index (BMI: < 25 kg/m2 vs. ≥ 25 kg/m2), (B) stratified by age (< 50 years vs. ≥ 50 years. Reference group for comparisons was women in lowest tertile of sweetened beverage intake and (A) with body mass index < 25 kg/m2, and (B) with age < 50 years. Odds ratio were adjusted for: age (years), tobacco use (current smoker, ex-smoker y non-smoker), physical activity (active ≥ 30 min/d, inactive < 30 min/d), weight change (did not gain, gained, lost), calorie intake (quintiles), percentage of energy from total carbohydrate (quintiles), percentage of energy from protein (quintiles), alcohol intake (g/d), vitamin C intake (mg/d), and body mass index.


Our results suggest that a considerable portion of our male participants’ energy consumption came from SB (9.5%). This result is consistent with previous reports that estimate the daily energy intake from SB among Mexican adults (10%) [4, 26]. We found that men consumed an average of 225 Kcal/day and women consumed 186 Kcal/day from SB. These findings suggest that excessive SB consumption is contributing to excess calorie intake [25], supporting recommendations to minimize daily SB consumption. These recommendations are further supported given that our study population exceeded the recommended calorie intake limit (220 Kcal/day for men and 180 Kcal/day for women) established for the Mexican population by a committee of experts [26].

According to our results, increased SB intake is positively associated with increased risk of hyperuricemia in Mexican adults, independent of other covariables. The prevalence of hyperuricemia in our study (20.6% of men, 13.5% of women) is similar to that reported in a cross-sectional analysis completed by Choi et al. (19% of men, 17% of women) in the US using information from the Third US National Health and Nutrition Examination Survey, in which the association between SB consumption and levels of uric acid was analyzed [1].

In this study, Choi et al. reports that the subjects consuming more than 4 SB/day had an 82% increased risk of hyperuricemia (OR = 1.82; p = 0.003) in comparison with those that did not consume SB [1]. In our results, the risk of hyperuricemia increased significantly with an intake of SB greater than 3 SB/day, leading to 129% increased odds of hyperuricemia in men and 35% increased odds of hyperuricemia in women compared with participants who consumed less than 0.5 servings of SB/day.

In this study, we observed that men and women with high SB consumption and a body mass index ≥ 25 Kg/m2 are respectively at approximately 5.0 and 4.0 times greater risk for hyperuricemia than men and women with low SB consumption and normal body mass index, independent of dietary and other risk factors. Obesity is associated with hyperuricemia [40], and also positively and independently associated with clinical conditions commonly related to hyperuricemia including insulin resistance, hypertension, and inflammation [41].

The effect of SB consumption on uric acid levels may be explained by changes resulting from the ingestion of sucrose and fructose. During the metabolism of fructose, it is phosphorylated to fructose-1-phosphate (F1P) by fructokinase. The depletion of adenosine triphosphate (ATP) inhibits the oxidative phosphorylation of adenosine diphosphate (ADP) by creating a shortage of inorganic phosphate (Pi). As a result, F1P is sequestered and the ADP produced during this metabolic cycle is converted into adenosine monophosphate (AMP) by adenylate kinase, which can also serve as a substrate for the production of uric acid. Moreover, the depletion of ATP and Pi during the metabolism of fructose decreases feedback inhibition for the generation of uric acid. Indeed, experimental studies in humans and animals show a short term rise in acid uric concentrations with subsequent fructose ingestion or infusion [20, 21]. Fructose may also indirectly increase serum levels of uric acid by increasing insulin resistance, leading to impaired glucose tolerance, and elevated circulating insulin levels [18, 20, 21, 42, 43].

Our findings have important implications for the prevention of hyperuricemia. Our results provide evidence that SB poses an increased risk for hyperuricemia. This casts doubt on the adequacy of the current dietary recommendations of the Mexican public health system aimed at reducing SB consumption. New health policies are necessary. While obesity is an important risk factor for T2DM, and other metabolic complications, there is new evidence suggesting that elevated uric acid levels is one of the most important risk factors for cardiovascular disease and also plays an important role in the development of renal disease [5], T2DM metabolic syndrome, and insulin resistance [44, 45], which are important public health problems in Mexico.

There are some potential limitations of our study. First, the cross-sectional design of the study does not allow for identification of a causal relationship between SB intake and the occurrence of hyperuricemia, since the temporal relationship of these events cannot be determined. The relationship between high SB consumption and hyperuricemia is, however, biologically plausible, and will need to be confirmed in future longitudinal studies. Second, this cohort population cannot be considered representative of the Mexican population as a whole, but instead only representative of adults living in urban areas in central Mexico. Finally, even though many studies, including ours, used ≥ 7 mg/dL for men and ≥ 5.8 mg/dL for women as a cut-off to identify hyperuricemia, there is no consensus on the acid uric level cut-off point for identifying hyperuricemia. In spite of these limitations, the main strength of this study was the large number of participants.


Our findings support a positive association between SB intake and serum uric acid levels in Mexican adults. If this relationship is causal, it could inform approaches for preventing chronic diseases such as T2DM, hypertension, gout, and cardiovascular disease. This evidence furthermore suggests the need to implement health policies for reducing SB consumption in Mexico. Longitudinal research is needed to confirm the association between SB intake and hyperuricemia. Further studies are also required to elucidate the risk of hyperuricemia among high SB consuming overweight/obese individuals and the elderly.



Type 2 diabetes mellitus


Sweetened beverages


Body mass index


Food frequency questionnaire


Evaluation system of eating habits and nutrient composition


Dual X-ray absorptiometry


Odds ratio

CI 95%:

Confidence intervals




Adenosine triphosphate


Adenosine diphosphate


Inorganic phosphate


Adenosine monophosphate.


  1. 1.

    Choi JW, Ford ES, Gao X, Choi HK: Sugar-sweetened soft drinks, diet soft drinks, and serum uric acid level: the Third National Health and nutrition Examination Survey. Arthritis Rheum. 2008, 59: 109-116. 10.1002/art.23245.

  2. 2.

    Mikuls TR, Farrar JT, Bilker WB, Fernandes S, Schumacher HR, Saag KG: Gout epidemiology: results from de UK general practice research database 2000–2005. Ann Rheum Dis. 2005, 64: 267-272. 10.1136/ard.2004.024091.

  3. 3.

    Roubenoff R, Klag MJ, Mead LA, Liang KY, Seidler AJ, Hochberg MC: Incidence and risk factors for gout in white men. JAMA. 1991, 266: 3004-3007. 10.1001/jama.1991.03470210072035.

  4. 4.

    Denova-Gutiérrez E, Talavera JO, Huitrón-Bravo G, Méndez-Hernández P, Salmerón J: Sweetened beverage consumption and increased risk of metabolic syndrome in Mexican adults. Public Health Nutr. 2010, 13: 835-842. 10.1017/S1368980009991145.

  5. 5.

    Schulze MB, Manson JE, Ludwig DS, Colditz GA, Stampfer MJ, Willett WC, Hu FB: Sugar-sweetened beverages, weight gain, and incidence of type 2 diabetes in young and middle-aged women. JAMA. 2004, 292: 927-934. 10.1001/jama.292.8.927.

  6. 6.

    Choi HK, Curhan G: Independent impact of gout on mortality and risk for coronary heart disease. Circulation. 2007, 116: 894-900. 10.1161/CIRCULATIONAHA.107.703389.

  7. 7.

    Changgui L, Ming-Chia H, Shun-Jen C: Metabolic syndrome, diabetes and hyperuricemia. Curr Opin Rheumatol. 2013, 25: 210-216. 10.1097/BOR.0b013e32835d951e.

  8. 8.

    Grassi D, Ferri L, Desideri G, Di Giosia P, Cheli P, Del Pinto R, Properzi G, Ferri C: Chronic hyperuricemia, uric acid deposit and cardiovascular risk. Curr Pharm Des. 2013, 19: 2432-2438. 10.2174/1381612811319130011.

  9. 9.

    Feig DI, Kang D-H, Johnson RJ: Uric acid and cardiovascular risk. N Engl J Med. 2008, 359: 1811-1821. 10.1056/NEJMra0800885.

  10. 10.

    Palmer TM, Nordestgaard BG, Benn M, Tybjaerg-Hansen A, Davey Smith G, Lawlor DA, Timpson NJ: Association of plasma uric acid with ischaemic heart disease and blood pressure: mendelian randomization analysis of two large cohorts. BMJ. 2013, 347: f4262-10.1136/bmj.f4262.

  11. 11.

    Rho YH, Zhu Y, Choi HK: The epidemiology of uric acid and fructose. Semin Nephrol. 2011, 31: 410-419. 10.1016/j.semnephrol.2011.08.004.

  12. 12.

    Villegas R, Xiang YB, Xu WH, Cai H, Cai Q, Linton MF, Fazio S, Zheng W, Shu XO: Puri-rich foods, protein intake and the prevalence of hyperuricemia: the Shanghai Men’s Health Study. Nutr Metabol Cardiovasc Dis. 2012, 22: 409-416. 10.1016/j.numecd.2010.07.012.

  13. 13.

    Yu KH, See LC, Huang YC, Yang CH, Sun JH: Dietary factors associated with hyperuricemia in adults. Semin Arthritis Rheum. 2008, 37: 243-250. 10.1016/j.semarthrit.2007.04.007.

  14. 14.

    Choi HK, Liu S, Curhan G: Intake of purine-rich foods, protein, and dairy products and relationship to serum levels of uric acid. Arthritis Rheum. 2005, 52: 283-289. 10.1002/art.20761.

  15. 15.

    Jordan KM, Cameron JS, Snaith M, Zhang W, Doherty M, Seckl J, Hingorani A, Jaques R, Nuki G, British Society for Rheumatology and British Health Professionals in Rheumatology Standards, Guidelines and Audit Working Group (SGAWG): British Society for rheumatology and british health professionals in rheumatology guideline for the management of gout. Rheumatology. 2007, 46: 1372-1374. 10.1093/rheumatology/kem056a.

  16. 16.

    Choi HK, Willett W, Curhan G: Fructose-rich beverages and risk of gout in women. JAMA. 2010, 304: 2270-2278. 10.1001/jama.2010.1638.

  17. 17.

    Gao X, Qi L, Qiao N, Choi HK, Curhan G, Tucker KL, Ascherio A: Intake of added sugar and sugar-sweetened drink and serum uric acid concentration in US men and women. Hypertension. 2007, 50: 306-312. 10.1161/HYPERTENSIONAHA.107.091041.

  18. 18.

    Angelopoulos TJ, Lowndes J, Zukley L, Melanson KJ, Nguyen V, Huffman A, Rippe JM: The effect of high-fructose corn syrup consumption on triglycerides and uric acid. J Nutr. 2009, 139: 1242S-1245S. 10.3945/jn.108.098194.

  19. 19.

    Welsh JA, Sharma A, Abramson JL, Vaccarino V, Gillespie C, Vos MB: Caloric sweetener consumption and dyslipidemia among US adults. JAMA. 2010, 303: 1490-1497. 10.1001/jama.2010.449.

  20. 20.

    Fox IH, Kelley WN: Studies of the mechanism of fructose-induced hiperuricemia in man. Metabolism. 1972, 21: 713-721. 10.1016/0026-0495(72)90120-5.

  21. 21.

    Dalbeth N, House ME, Gamble GD, Horne A, Pool B, Purvis L, Stewart A, Merriman M, Cadzow M, Phipps-Green A, Merriman TR: Population-specific influence of SLC2A9 genotype on the acute hyperuricaemic response to a fructose load. Ann Rheum Dis. 2013, 72: 1868-1873. 10.1136/annrheumdis-2012-202732.

  22. 22.

    White JS: Challenging the fructose hypothesis: new perspectives on fructose consumption and metabolism. Adv Nutr. 2013, 4: 246-256. 10.3945/an.112.003137.

  23. 23.

    Tappy L, Le KA, Tran C, Paquot N: Fructose and metabolic diseases: new findings, new questions. Nutrition. 2010, 26: 1044-1049. 10.1016/j.nut.2010.02.014.

  24. 24.

    Semchyshyn HM: Fructation in vivo: detrimental and protective effects of fructose. BioMed Res Int. 2013, 2013: 343914-

  25. 25.

    Barquera S, Hernandez-Barrera L, Tolentino ML, Espinosa J, Ng SW, Rivera JA, Popkin BM: Energy intake from beverages is increasing among Mexican adolescents and adults. J Nutr. 2008, 138: 2454-2461. 10.3945/jn.108.092163.

  26. 26.

    Rivera JA, Muñoz-Hernández O, Rosas-Peralta M, Aguilar-Salinas CA, Popkin BM, Willett WC: Beverage consumption for a healthy life: recommendations for the Mexican population. Salud Publica Mex. 2008, 50: 172-194.

  27. 27.

    Emerson BT: Effect of oral fructose on urate production. Ann Rheum Dis. 1974, 33: 276-280. 10.1136/ard.33.3.276.

  28. 28.

    Choi HK: Soft drinks, fructose consumption, and the risk of gout in men: prospective cohort study. BMJ. 2008, 336: 309-312. 10.1136/bmj.39449.819271.BE.

  29. 29.

    Denova-Gutiérrez E, Castañón S, Talavera JO, Flores M, Macías N, Rodríguez-Ramírez S, Flores YN, Salmerón J: Dietary patterns are associated with different indexes of adiposity and obesity in an urban Mexican population. J Nutr. 2011, 141: 921-927. 10.3945/jn.110.132332.

  30. 30.

    Rosner B: Percentage points for generalized ESD many-outlier procedure. Technometrics. 1983, 25: 165-172. 10.1080/00401706.1983.10487848.

  31. 31.

    Hernández-Avila M, Romieu I, Parra S, Hernández-Avila J, Madrigal H, Willett W: Validity and reproducibility of a food frequency questionnaire to assess dietary intake of women living in Mexico City. Salud Publica Mex. 1998, 40: 133-140. 10.1590/S0036-36341998000200005.

  32. 32.

    Hernández-Ávila M, Resoles M, Parra S: Sistema de Evaluación de Hábitos Nutricionales y Consumo de Nutrimentos (SNUT). 2000, Cuernavaca, México: INSP

  33. 33.

    Tietz NW: Textbook of Clinical Chemistry. Specimen Collection and Processing; Sources of Biological Variation. 1994, Philadelphia, PA: WB Saunders, 2

  34. 34.

    Barquera S, Flores M, Olaiz-Fernández G, Monterrubio E, Villalpando S, González C, Rivera-Dommarco J, Sepulveda J: Dyslipidemias and obesity in Mexico. Salud Publica Mex. 2007, 49 (suppl 3): S338-S347.

  35. 35.

    Olaiz-Fernández G, Rivera-Dommarco J, Shamah-Levy T, Rojas R, Villalpando-Hernández S, Hernández-Avila M: Encuesta Nacional de Salud y Nutrición 2006. 2006, Cuernavaca, México: Instituto Nacional de Salud Pública

  36. 36.

    Deurenberg P, Yap M, Staveren WA: Body mass index and percent body fat: a meta analysis among different ethnic groups. Int J Obes. 1998, 22: 1164-1171. 10.1038/sj.ijo.0800741.

  37. 37.

    Chasan-Taber S, Rimm EB, Stampfer MJ, Spiegelman D, Colditz GA, Giovannucci E, Ascherio A, Willett WC: Reproducibility and validity of a self-administered physical activity questionnaire for male health professionals. Epidemiology. 1996, 7: 81-86. 10.1097/00001648-199601000-00014.

  38. 38.

    Martínez-González MA, López-Fontana C, Varo JJ, Sánchez-Villegas A, Martinez JA: Validation of the Spanish version of the physical activity questionnaire used in the Nurses‘Health Study and the Health Professionals’ Follow-up Study. Public Health Nutr. 2005, 8: 920-927.

  39. 39.

    World Health Organization: Global Strategy on Diet, Physical Activity and Health. Global Recommendations on Physical Activity for Health. 2010,,

  40. 40.

    Hiroyuki S, Masatomo M: Obesity and hyperuricemia. Adiposcience. 2005, 2: 349-353.

  41. 41.

    Sánchez-Lozada LG, Nakagawa T, Kang DH, Feig DI, Franco M, Johnson RJ, Herrera-Acosta J: Hormonal and cytoquine effects of uric acid. Curr Opin Nephrol Hypertens. 2006, 15: 30-33. 10.1097/01.mnh.0000199010.33929.7f.

  42. 42.

    Hallfrisch J: Metabolic effects of dietary fructose. FASEB J. 1990, 4: 2652-2660.

  43. 43.

    Batt C, Phipps-Green A, Black MA, Cadzow M, Merriman ME, Topless R, Gow P, Harrison A, Highton J, Jones P, Stamp L, Dalbeth N, Merriman TR: Sugar-sweetened beverage consumption: a risk factor for prevalent gout with SLC2A9 genotype-specific effects on serum urate and risk of gout. Ann Rheum Dis. 2013, 0: 1-6.

  44. 44.

    Sui X, Church TS, Meriwether RA, Lobelo F, Blair SN: Uric acid and development of metabolic syndrome in women and men. Metabolism. 2008, 57: 845-852. 10.1016/j.metabol.2008.01.030.

  45. 45.

    Tomiyama H, Higashi Y, Takase B, Node K, Sata M, Inoue T, Ishibashi Y, Ueda S, Shimada K, Yamashina A: Relationships among hyperuricemia, metabolic syndrome and endotelial function. Am J Hypertens. 2011, 24: 770-774. 10.1038/ajh.2011.55.

Pre-publication history

  1. The pre-publication history for this paper can be accessed here:

Download references


Supported by Consejo Nacional de Ciencia y Tecnología (grant no. C01-7876/A-1), the Universidad Autónoma del Estado de México (grant. no. 1860/2004), and the Instituto Mexicano del Seguro Social (grant no. 2005-1-I-080).

Author information

Correspondence to Edgar Denova-Gutiérrez.

Additional information

Competing interest

We declare that there is no competing interest in submitting this manuscript for publication to BMC Public Health.

Authors’ contributions

ED-G and JS designed the study; JM-L, ED-G, JS, SC-R, BR-P, GH-B, MQ-T, collected the data; JM-L, ED-G, JS performed the statistical analyses, JM-L, MC-R, SR, ED-G, JS, drafted the manuscript. All authors reviewed and commented on the manuscript. All authors read and approved the final version of the paper.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Meneses-Leon, J., Denova-Gutiérrez, E., Castañón-Robles, S. et al. Sweetened beverage consumption and the risk of hyperuricemia in Mexican adults: a cross-sectional study. BMC Public Health 14, 445 (2014).

Download citation


  • Sweetened beverages
  • Hyperuricemia
  • Mexican adults
  • Obesity