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Relationship of sodium intake with obesity among Korean children and adolescents: Korea National Health and Nutrition Examination Survey

Published online by Cambridge University Press:  13 January 2016

Soo-Kyung Lee
Affiliation:
Department of Food and Nutrition, Inha University, Incheon 402-751, Korea
Mi Kyung Kim*
Affiliation:
National Cancer Center, Division of Cancer Epidemiology and Management, Goyang, Gyeonggi 411-769, Korea
*
*Corresponding author: M. K. Kim, fax +82 31 920 2006, email [email protected]
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Abstract

We investigated whether dietary and urinary Na is associated with adiposity in Korean children and adolescents (10–18 years), a population with a high salt intake. Study subjects were Korean children and adolescents who participated in the cross-sectional nationally representative Korea National Health and Nutrition Examination Survey (2010–2011). This study used measures of dietary (24-h dietary recall) and urinary Na (Na:creatinine ratio) and three methods to determine obesity (BMI, waist circumference (WC) and total body per cent fat (TBPF)). Higher Na intake was significantly associated with obesity, adjusting for the covariates. Subjects in the highest tertile of urinary Na excretion had a significantly higher OR for higher adiposity compared with those in the lowest tertile (multivariate-adjusted OR 3·13 (95 % CI 1·81, 5·50) for BMI, 2·15 (95 % CI 1·27, 3·66) for WC and 1·92 (95 % CI 1·29, 2·86) for TBPF, respectively). Na intake estimated by the 24-h recall method also showed significant association with adiposity (multivariate-adjusted OR 2·79 (95 % CI 1·66, 4·68) for BMI and 2·14 (95 % CI 1·25, 3·67) for WC, respectively). The significant associations between Na and adiposity remained significant after additionally adjusting for sugar-sweetened beverage (SSB) consumption. Our results revealed a significant positive association between urinary and dietary Na and adiposity in Korean children and adolescents, independent of SSB consumption.

Type
Full Papers
Copyright
Copyright © The Authors 2016 

High Na intake has been linked to a variety of increased health risks such as hypertension( Reference He, Li and Macgregor 1 , Reference Vollmer, Sacks and Ard 2 ), CVD( Reference Nagata, Takatsuka and Shimizu 3 , Reference Tuomilehto, Jousilahti and Rastenyte 4 ), stomach cancer( 5 Reference Tsugane and Sasazuki 7 ) and type 2 diabetes( Reference Hu, Jousilahti and Peltonen 8 ). In addition to the traditionally recognised health effects of high Na intake, obesity has recently gained much interest as another possible related health outcome( 5 ).

Although several studies including a longitudinal study have reported significant associations between Na intake and obesity among adults( Reference Dahl, Silver and Christie 9 Reference Larsen, Angquist and Sorensen 14 ), relatively limited evidence is available among children and adolescents( Reference Ellison, Sosenko and Harper 15 Reference Zhu, Pollock and Kotak 18 ). Investigation of the associations between Na intake and obesity, however, has been limited by weakness of assessment methods of both Na intake and obesity. Quantification of dietary salt intake is imperfect because of the limitations in dietary assessment methods and food databases( Reference Caggiula, Wing and Nowalk 19 , Reference Willett 20 ). The 24-h urinary Na excretion measurement, generally considered as the gold standard( Reference Willett 20 ), is also limited by the difficulty of urine collection for 24 h. Spot urine or half-day urine measurements have been proposed as substitutes for the 24-h urine measurement in an effort to overcome the difficulty( Reference Kawasaki, Itoh and Uezono 21 Reference Watson and Langford 23 ). For obesity measures, most studies, except one study( Reference Jain, Minhajuddin and Neeland 13 ), used either BMI or waist circumference (WC). Although both BMI and WC are valid and widely used measures, they have their own limitations such as not being able to control for muscle mass or total fat mass( Reference Prentice and Jebb 24 ).

Although mechanisms of the association between Na intake and obesity have not been well established, the role of soft drink consumption has been explored and shown to be significant among children and adolescents in the Western food culture( Reference He, Marrero and MacGregor 25 ). This hypothesis indicates that higher energy intake from sugar-sweetened beverages (SSB) consumed to quench thirst caused by high Na intake would contribute to obesity( Reference Grimes, Wright and Liu 26 , Reference Grimes, Riddell and Campbell 27 ). Whether this pathway would also be important in non-Western food cultures has not been examined, however, Koreans are reported to have approximately three times more salt intake than the recommended level, affording a large variation of exposure level( 28 , Reference Powles, Fahimi and Micha 29 ). Korean food culture is strongly preserved with wide-range influences of Western food culture, which makes it an interesting population to investigate for an association between Na and obesity.

Therefore, this study examined whether urinary and dietary Na exposure showed independent associations with obesity across multiple obesity measures – obesity measured by BMI, abdominal obesity measured by WC and per cent body fat measured by dual-energy X-ray absorptiometry (DEXA) – in a nationally representative sample of Korean children and adolescents aged from 10 to 18 years.

Methods

Study design

This study analysed the Korea National Health and Nutrition Examination Survey (KNHANES). The KNHANES is an annually conducted and nationally representative survey, consisting of a health interview, behaviour and nutrition surveys and a medical examination. This cross-sectional survey utilised a stratified, multistage, cluster probability sampling design with the National Census Registry. More details of the survey design and methods are available elsewhere( 30 ). This study chose to use data from 2010 to 2011 because urinary Na excretion data were collected only during these 2 years( 31 ).

The KNHANES is conducted in accordance with the Helsinki Declaration. Written informed consent was obtained from parents or guardians. Data without personal identifiable information were provided for this analysis.

Study participants

Among children aged between 10 and 18 years (n 1873), whose body weight, height and WC were recorded in the KNHANES 2010–2011, we excluded children with missing diet information (n 195) and extreme energy intake (n 12); the final analytical sample consisted of 1467 children and adolescents. Extreme energy intake was defined as <1673 kJ/d (400 kcal/d) or >23 848 kJ/d (5700 kcal/d) for 10–11-year-old boys, <2510 kJ/d (600 kcal/d) or >33 890 kJ/d (8100 kcal/d) for 12–18-year-old boys, <1569 kJ/d (375 kcal/d) or >21 338 kJ/d (5100 kcal/d) for 10–11-year-old girls and <2092 kJ/d (500 kcal/d) or >25 104 kJ/d (6000 kcal/d) for 12–18-year-old girls, respectively( Reference Kim, Kim and Lee 32 ). For the analysis of per cent body fat measured by DEXA, we only included subjects (n 1019) whose DEXA measurements were available. The age of 10 years had to be used as the lowest age because urine samples were available of individuals aged 10 years or above.

Measures

KNHANES utilises mobile examination centres where health interviews and medical examinations are conducted. The nutrition survey was conducted approximately 1 week after the health examination. This study used socio-demographic and health behaviour information from the health interviews, urinary Na, body fat and anthropometric information from the medical examination and dietary information from the nutrition survey.

Sodium intake

Na intake was assessed using two different methods: (1) dietary Na intake per 4184 kJ (1000 kcal) from a 24-h recall and (2) urinary Na:creatinine ratio. Dietary Na intake was calculated from 24-h recalls conducted by trained nutritionists with tools to help portion size estimation. To control for the reported tendency that higher food intake is naturally associated with higher Na intake( Reference Brown, Tzoulaki and Candeias 33 ), dietary Na density (dietary Na intake (mg)/4184 kJ (1000 kcal)) was calculated and used in the analyses. The KNHANES provided urinary Na and creatinine values from the overnight spot urine samples. From these values, we calculated the urinary Na:creatinine ratio.

Adiposity was also assessed by measuring three different parameters: (1) BMI, (2) WC and (3) total body per cent fat (TBPF). BMI was selected because it is one of the most widely used and recommended methods to determine the obesity status of children and adolescents( Reference Krebs, Himes and Jacobson 34 ). Height and weight were measured in the mobile examination centre following standardised measurement protocols. BMI was calculated by dividing body weight by the squared body height. The age- and sex-adjusted BMI Z score was obtained using a Korean growth chart( 35 ). Children and adolescents were considered to be obese if their BMI was of the 95th percentile or greater for their age and sex or if their BMI was 25 kg/m2 or higher, and overweight was defined as having 85th≤BMI<95th percentile for age and sex( 35 , Reference Moon, Lee and Nam 36 ). This study used WC as a measure of abdominal adiposity( Reference Taylor, Jones and Williams 37 ). WC was measured at the narrowest area between the lowest rib and the uppermost lateral border of the right iliac crest, and a WC of the 90th percentile for age and sex or greater was used as a cut-off value for abdominal adiposity( 35 , Reference Barlow 38 , Reference Seo, Cho and Kang 39 ). TBPF was obtained by DEXA using a QDR Discovery fan beam densitometer (Hologic Inc.) according to the recommended procedures from the manufacturer. DEXA examinations were included as a part of the medical examination in 2010 and 2011; therefore, analyses of TBPF were carried out in a smaller sample (n 1019). The DEXA method proved to be a valid assessment tool to measure body fat( Reference Prior, Cureton and Modlesky 40 ). Adiposity was also defined as having a TPBF >25 % for boys, >30 % for girls younger than 11 years and >35 % for girls aged 11 years or older( Reference Asayama, Ozeki and Sugihara 41 ).

Sugar-sweetened beverages

SSB were obtained using a single 24-h recall questionnaire, and included energetic sweeteners such as sugar-sweetened soda, soft drinks, fruit drinks, sport drinks, energy drinks, sugar-sweetened tea or sweetened milk( 42 ). The KNHANES food-group classification system was used to identify food groups that fell within the definition of SSB. These food codes were used to aggregate data to calculate the SSB (g/d).

Adjusting variables

Adjusting variables included age, sex and household income obtained from the Health Interview and Behavior Surveys, which were obtained through face-to-face interviews by trained interviewers. Household income quartile was used in the analyses. Physical activity was assessed by a pre-validated questionnaire in the Health Interview and Behavior Survey. The subjects specified how many hours of a day they spent doing vigorous, moderate and light activities for a usual 1 week. Subsequently, metabolic equivalents (MET)-h/week was estimated for each subject by multiplying together the number of hours per week a woman spent in a particular activity and the estimated MET score for that activity. Total energy intake was calculated using the 24-h recall data from the Nutrition Survey.

Statistical analysis

All the analyses were carried out using the survey procedures provided in SAS software 9.2, accounting for the complex survey design used, and following the analytical guidelines for KNHANES data from the Korea Center for Disease Control and Prevention( 30 ) to estimate nationally representative values and to extrapolate the findings to the entire Korean population. Distributions of general characteristics are presented as mean values with their standard errors or weighted percentages. Differences between groups were analysed using survey means or weighted percentages for survey design. We checked the normality of urinary and dietary Na variables, which were not normally distributed. These exposure variables were then log-transformed, and we carried out further analysis. In addition, logistic regression analyses were carried out for tertiles of Na variables. A survey logistic regression was used to test the associations between tertile of Na measurements and adiposity and to calculate the crude and multivariate-adjusted OR along with 95 % CI for each tertile compared with the lowest tertile. Two multivariate models were tested to explore the roles of Na in relation to adiposity. Model 1 adjusted for age, sex (only for analysis of sex combined), household income, total daily energy intake (only for urinary Na variables) and physical activity (MET). To examine the effect of soft drink consumption, model 2 additionally adjusted for soft drink consumption in addition to all the mentioned variables in model 1. Separate analyses for each sex were also carried out. The P values used to test for linear trends were calculated using Na measurements as continuous variables after adjustment for confounding factors. The significance level of 0·05 was used for all statistical tests.

Results

Characteristics of the participants

Basic characteristics of socio-demographic factors, Na intake, adiposity, soft drink consumption and adjusting variables are presented in Table 1. The participants were 1467 children and adolescents with an average age of 13·4 years, and 43·6 % of the participants were girls. The daily Na intake assessed by 24-h recalls was 4305 mg. The average Na excretion estimated by morning spot urine analysis was 138 mg. Boys excreted Na significantly more than girls (P=0·0007), and the difference remained significant after controlling for muscle mass by dividing the Na value with creatinine. The children showed an average BMI of 20·7 kg/m2 and a WC of 69·5 cm. The average TBPF was 26·6 %. Although average values of WC were significantly higher in boys than in girls (P<0·0001), adiposity rate by WC was higher in girls than in boys (P=0·0254). Approximately 59 % of the participants reported soft drink consumption, and soft drink consumers drank on average 398 g/d of soft drinks. Boys showed higher soft drink consumption than girls (P=0·0059). The average MET was 31·4 h/d, and boys reported significantly higher MET than girls (P<0·0001).

Table 1 Characteristics of the participants (Mean values with their standard errors; percentages)

WC, waist circumference; TBPF, total body per cent fat; SSB, sugar-sweetened beverages; MET, metabolic equivalents.

* Categorical variables were analysed using the χ 2 test; continuing variables were analysed using the t test.

Obesity was defined as having a BMI ≥95th percentile for age and sex or ≥25 kg/m2; overweight was defined as having 85th≤BMI<95th percentile for age and sex; abdominal adiposity as a WC ≥90th percentile for age and sex in the study sample; as a TPBF >25 % for boys, >30 % for girls younger than 11 years and >35 % for girls aged 11 years or older.

Analysis was conducted (n 1019) in a subsample of the subjects with dual-energy X-ray absorptiometry, the TBPF.

§ Analysis was completed in a subsample of SSB consumers only.

Association between urinary sodium excretion and adiposity

The spot urinary Na:creatinine ratio (Table 2), used to estimate dietary Na intake, showed significant associations with BMI, WC and TBPF (P<0·05). Using BMI, risk of ‘overweight’ was not significantly associated with urinary Na:creatinine ratio, but risk of ‘obesity’ showed consistent and significant association with higher multivariate OR around three than OR of WC or TBPF. Significant dose–response relationships were also found in associations between urinary Na:creatinine ratio and risk of obesity assessed by BMI in both boys and girls (P<0·05).

Table 2 Risk of adiposityFootnote * by urinary sodium:creatinine ratio (Odds ratios and 95 % confidence intervals)

WC, waist circumference; TBPF, total body per cent fat; MET, metabolic equivalents.

* Adiposity was defined as having a BMI ≥95th percentile for age and sex or ≥25 kg/m2; overweight was defined as having 85th≤BMI<95th percentile for age and sex; abdominal adiposity as a WC ≥90th percentile for age and sex in the study sample; as a TPBF >25 % for boys, >30 % for girls younger than 11 years and >35 % for girls aged 11 years or older.

The tertiles of urinary Na:creatinine ratio were based on the distribution of values among subjects after log-transformation.

Test for linear trends used the median value in each tertile as a continuous variable in linear regression.

§ Reference group of BMI was defined as having BMI<85th percentile for age and sex.

|| Multiple logistic regression model 1: adjusted for age (continuous), sex (not adjusted for in the stratified models), household income, physical activity (MET) and total daily energy intake (kJ/d (kcal/d)).

Multiple logistic regression model 2: same as model 1 and additionally adjusted for sugar-sweetened beverages.

** Reference group of WC was defined as a WC <90th percentile for age and sex in the study sample.

†† Analysis was conducted (n 1019) in a subsample of the subjects with dual-energy X-ray absorptiometry, the TBPF.

‡‡ Reference group of TPBF was defined as a TPBF ≤25 % for boys, ≤30 % for girls younger than 11 years and ≤35 % for girls aged 11 years or older.

The urinary Na:creatinine ratio showed significant association with risk of adiposity assessed by WC only in boys in the highest tertile group with OR of 2·26 (95 % CI 1·02, 4·99). The dose–response relationship was also significant at P<0·05. The multivariate-adjusted OR for adiposity risk assessed by TBPF in children of the highest tertile of urinary Na:creatinine ratio in model 1, compared with the lowest tertile, were 2·13 (95 % CI 1·15, 3·97; P for trend=0·0166) for boys and 1·75 (95 % CI 0·96, 3·24; P for trend=0·0662) for girls, respectively.

The addition of soft drink consumption into the multivariate logistic model (model 2) did not create any statistically significant differences in the patterns of the association between urinary Na excretion and adiposity (Table 2). Soft drink consumption itself was not significantly associated with the risk of adiposity (data not shown).

Association between dietary sodium intake and adiposity

Table 3 shows varying degrees of associations between dietary Na density (Na/4184 kJ (1000 Kcal) of E) estimated from 24-h recalls and the three adiposity measures. The multivariate-adjusted OR for overweight risk assessed by BMI, obesity risk assessed by BMI and adiposity risk assessed by WC in children of the highest tertile of dietary Na density in model 1, compared with the lowest tertile, were 2·11 (95 % CI 1·14, 3·90), 2·73 (95 % CI 1·65, 4·51) and 1·95 (95 % CI 1·17, 3·26), respectively. Significant dose–response relationships were found with overweight risk assessed by BMI, adiposity risk assessed by BMI and adiposity risk assessed by WC (P for trend=0·0207, <0·001 and 0·0086, respectively). Although girls showed a significant association of dietary Na intake with overweight risk assessed by BMI and obesity risk assessed by BMI (P<0·05), boys reported a significant association with obesity risk assessed by BMI. Significant associations between adiposity risk assessed by WC and dietary Na intake were only found in the total sample, but no consistently significant associations were found for each sex. We found no significant associations between adiposity risk assessed by TBPF and dietary Na intake.

Table 3 Risk of adiposityFootnote * by dietary sodium intake (Odds ratios and 95 % confidence intervals)

WC, waist circumference; TBPF, total body per cent fat; MET, metabolic equivalents.

* Adiposity was defined as having a BMI ≥95th percentile for age and sex or ≥25 kg/m2; overweight was defined as having 85th≤BMI<95th percentile for age and sex; abdominal adiposity as a WC ≥90th percentile for age and sex in the study sample; as a TPBF >25 % for boys, >30 % for girls younger than 11 years and >35 % for girls aged 11 years or older.

The tertiles of dietary Na intake were based on the distribution of values among subjects after log-transformation.

Test for linear trend used the median value in each tertile as a continuous variable in linear regression.

§ Reference group of BMI was defined as having BMI<85th percentile for age and sex.

|| Multiple logistic regression model 1: adjusted for age (continuous), sex (not adjusted for in the stratified models), household income, total daily energy intake and physical activity (MET).

Multiple logistic regression model 2: same as model 1 and additionally adjusted for sugar-sweetened beverages.

** Reference group of WC was defined as a WC <90th percentile for age and sex in the study sample.

†† Analysis was conducted (n 1019) in a subsample of the subjects with dual-energy X-ray absorptiometry, the TPBF.

‡‡ Reference group of TPBF was defined as a TPBF ≤25 % for boys, ≤30 % for girls younger than 11 years and ≤35 % for girls aged 11 years or older.

Adding soft drink consumption to the model (model 2) did not alter the general pattern of the associations described above (model 1). Overall, the association between BMI-obesity and dietary Na density appeared to be the strongest in terms of size of OR and consistency of significant dose–response relationships in both models 1 and 2 (Table 3).

Discussion

This study found that higher Na intake was significantly associated with adiposity in children and adolescents, after adjusting for energy intake, SSB intake, physical activity and socio-demographic variables. The results showed generally consistent patterns of association regardless of the assessment methods of Na intake or measure of adiposity. Risk of obesity assessed by BMI was consistently and significantly associated with urinary Na:creatinine ratio and dietary Na intake, whereas risk of overweight assessed by BMI, risk of abdominal adiposity assessed by WC and TBPF showed relatively weaker and less consistent association with Na intake. Along with consistently significant dose–response relationships between Na intake and obesity, findings of this study suggest that higher Na intake was related to obesity and abdominal adiposity to a lesser degree.

This study also explored a possible role of SSB consumption, using soft drink consumption as a proxy variable, in the association between Na intake and obesity in Korean children and adolescents. The addition of soft drink consumption into the multivariate logistic regression models did not make meaningful differences across assessment methods and sex, which means there appears to be Na intake effects independent of soft drink consumption in this population. This finding is not in agreement with previously reported findings from the US population( Reference Grimes, Wright and Liu 26 ) and the Australian population( Reference Grimes, Riddell and Campbell 27 ). Approximately 59 % of Korean children and adolescents in this study reported consuming SSB, whereas the US and Australian counterparts reported 64 and 62 %, respectively. This study found the average SSB consumption level per consumer to be 398 (se 18·2) g/d, which is lower than the consumption of SSB among US children and adolescents (631 g/d) and higher than that of Australian children and adolescents (248 g/d). The link between Na intake and SSB consumption and its impact on obesity should be explored further.

One can also propose that individuals with high Na intake would also practise bad health behaviours leading to adiposity – that is, the association between Na intake and adiposity is an outcome of clustering of unhealthy behaviours( Reference Buck and Frosini 43 ). This study controlled for physical activity and consumption of SSB and still found significant associations between Na intake and adiposity independent of physical activity. This finding indicates a possibility of an independent relationship between Na intake and adiposity.

Another possible mechanism between Na intake and obesity is that higher Na intake would result in higher water retention leading to higher body weight. This study used TBPF in an effort to exclude Na-related water retention as a possible reason for the association between Na intake and adiposity. This study found significant associations between urinary Na:creatinine ratio and TBPF among boys in a full model, whereas the association was relatively weaker among girls (model 2, Table 2). The association of TBPF with dietary Na intake was found to be weaker (Table 3). This possible mechanism appears to be worth further examination.

Previous studies have reported sex differences in the associations between Na intake and obesity. Song et al. ( Reference Song, Cho and Lee 11 ) analysed the data of adults from KNHANES 2007–2009 and found significant associations between Na intake and obesity in men but not in women. Jain et al. ( Reference Jain, Minhajuddin and Neeland 13 ) found the opposite in the US population – that is, significant associations after controlling for covariates in women but not in men. This study found that different adiposity measures showed more apparent associations with Na intake in different sexes. Risk of overweight assessed by BMI was significantly associated with dietary Na intake only in girls, whereas adiposity risk assessed by WC was significantly associated with dietary Na intake only in boys. Risks of adiposity assessed by BMI and TBPF were in general consistent in both sexes. These inconsistent sex differences need to be further explored.

This study was limited by the cross-sectional nature of KNHANES; therefore, temporal relationship between Na intake and adiposity could not be established. Morning spot urine rather than 24-h urine samples were used in this study. Although the 24-h urine measurement is the gold standard for assessing salt intake through urinary Na excretion in individuals and in populations, it is often deemed inconvenient for repeated use in large population studies. There are concerns that a high participation burden, a lack of completeness and a high cost will affect the response rate and the practicality of using the test. Alternative methods such as spot and timed urine samples have been derived in an attempt to overcome this concern( Reference Brown, Tzoulaki and Candeias 33 ). The validity of spot urine samples, however, remains controversial. A recent review showed that the correlations between mean Na amount from 24-h urine samples and that from overnight urine samples ranged from 0·62 to 0·95 among children and adolescents, although the authors concluded reliability of alternative methods to replace the 24-h urine Na test( Reference Ji, Sykes and Paul 44 ). Although an equation has been developed to convert Na from spot urine samples to 24-h urine samples among adults( Reference Kawasaki, Itoh and Uezono 21 ), no such equation exists for children. Therefore, this study utilised urinary Na:creatinine ratio value from spot urine samples without converting it to that of 24-h urine samples. Valid and reliable methods to replace 24-h urine Na, including developing equations to convert Na from spot urine to 24-h Na in children, are much needed. Finally, adjustment with urinary K has been recommended in using urinary Na excretion( 5 ); however, this study was not able to do so because KNHANES did not test for urinary K.

One of the most meaningful contributions of this study was testing multiple assessment methods of not only Na intake but also adiposity. Na intake was assessed by dietary Na intake from 24-h recalls and urinary Na excretion, and significant associations with adiposity were found. For the outcome variable, adiposity, three different assessment methods (BMI, WC and TBPF) were used. This study found that associations with risk of obesity assessed by BMI were most consistent and stronger than other measures, whereas TBPF showed relatively weak association, showing no significant association with dietary Na intake. Using the DEXA method, one of the better assessment methods for total body fat, was a particular strength of this study. The significant findings regardless of assessment methods strongly support the associations between Na intake and adiposity, with suggestions for further studies on mechanisms of the association between Na intake and adiposity and needs of valid and easier assessment methods for Na intake among children.

In conclusion, this study demonstrated the significant associations between Na intake and adiposity in children and adolescents, independent of SSB consumption. The sex difference in this association warrants more research along with further investigations to establish mechanisms for the association. The findings of this study strongly support the worldwide campaign for Na intake reduction and suggest that the campaign would help decrease not only the traditionally discussed Na-related diseases such as hypertension, CVD and stroke but also adiposity.

Acknowledgements

The authors thank the members of the Korea Center for Disease Control who conducted the national survey.

This study was financially supported by an Inha University Research Grant (S.-K. L. 39208) and grants from the National Cancer Center in Korea (M. K. K. NCC-1310361).

The authors’ contributions are as follows: M. K. K. designed and conducted the present study, arranged the data and performed the statistical analyses; S.-K. L. was involved in the interpretation of the results and drafted the paper. All the authors contributed to the development of the manuscript.

The authors declare that there are no conflicts of interest.

References

1. He, FJ, Li, J & Macgregor, GA (2013) Effect of longer-term modest salt reduction on blood pressure: Cochrane systematic review and meta-analysis of randomized trials. BMJ 346, f1325.CrossRefGoogle Scholar
2. Vollmer, WM, Sacks, FM, Ard, J, et al. (2001) Effects of diet and sodium intake on blood pressure: subgroup analysis of the DASH-sodium trial. Ann Intern Med 135, 10191028.CrossRefGoogle ScholarPubMed
3. Nagata, C, Takatsuka, N, Shimizu, N, et al. (2004) Sodium intake and risk of death from stroke in Japanese men and women. Stroke 35, 15431547.Google Scholar
4. Tuomilehto, J, Jousilahti, P, Rastenyte, D, et al. (2001) Urinary sodium excretion and cardiovascular mortality in Finland: a prospective study. Lancet 357, 848851.Google Scholar
5. Committee on the Consequences of Sodium Reduction in Populations (2013) Sodium Intake in Populations: Assessment of Evidence. Washington, DC: National Academy of Sciences.Google Scholar
6. Shikata, K, Kiyohara, Y, Kubo, M, et al. (2006) A prospective study of dietary salt intake and gastric cancer incidence in a defined Japanese population: the Hisayama study. Int J Cancer 119, 196201.Google Scholar
7. Tsugane, S & Sasazuki, S (2007) Diet and the risk of gastric cancer: review of epidemiological evidence. Gastric Cancer 10, 7583.Google Scholar
8. Hu, G, Jousilahti, P, Peltonen, M, et al. (2005) Urinary sodium and potassium excretion and the risk of type 2 diabetes: a prospective study in Finland. Diabetologia 48, 14771483.CrossRefGoogle ScholarPubMed
9. Dahl, LK, Silver, L & Christie, RW (1958) The role of salt in the fall of blood pressure accompanying reduction in obesity. N Engl J Med 258, 11861192.Google Scholar
10. Venezia, A, Barba, G, Russo, O, et al. (2010) Dietary sodium intake in a sample of adult male population in southern Italy: results of the Olivetti Heart Study. Eur J Clin Nutr 64, 518524.CrossRefGoogle Scholar
11. Song, HJ, Cho, YG & Lee, HJ (2013) Dietary sodium intake and prevalence of overweight in adults. Metabolism 62, 703708.Google Scholar
12. Yoon, YS & Oh, SW (2013) Sodium density and obesity: the Korea National Health and Nutrition Examination Survey 2007–2010. Eur J Clin Nutr 67, 141146.Google Scholar
13. Jain, N, Minhajuddin, AT, Neeland, IJ, et al. (2014) Association of urinary sodium-to-potassium ratio with obesity in a multiethnic cohort. Am J Clin Nutr 99, 992998.Google Scholar
14. Larsen, SC, Angquist, L, Sorensen, TI, et al. (2013) 24h urinary sodium excretion and subsequent change in weight, waist circumference and body composition. PLOS ONE 8, e69689.Google Scholar
15. Ellison, RC, Sosenko, JM, Harper, GP, et al. (1980) Obesity, sodium intake, and blood pressure in adolescents. Hypertension 2, 7882.CrossRefGoogle ScholarPubMed
16. Libuda, L, Kersting, M & Alexy, U (2012) Consumption of dietary salt measured by urinary sodium excretion and its association with body weight status in healthy children and adolescents. Public Health Nutr 15, 433441.Google Scholar
17. Woodruff, SJ, Fryer, K, Campbell, T, et al. (2014) Associations among blood pressure, salt consumption and body weight status of students from south-western Ontario. Public Health Nutr 17, 11141119.Google Scholar
18. Zhu, H, Pollock, NK, Kotak, I, et al. (2014) Dietary sodium, adiposity, and inflammation in healthy adolescents. Pediatrics 133, e635e642.Google Scholar
19. Caggiula, AW, Wing, RR, Nowalk, MP, et al. (1985) The measurement of sodium and potassium intake. Am J Clin Nutr 42, 391398.Google Scholar
20. Willett, W (2013) Nutritional Epidemiology, 3rd ed. New York, NY: Oxford University Press.Google Scholar
21. Kawasaki, T, Itoh, K, Uezono, K, et al. (1993) A simple method for estimating 24h urinary sodium and potassium excretion from second morning voiding urine specimen in adults. Clin Exp Pharmacol Physiol 20, 714.Google Scholar
22. Liu, K, Dyer, AR, Cooper, RS, et al. (1979) Can overnight urine replace 24-hour urine collection to asses salt intake? Hypertension 1, 529536.Google Scholar
23. Watson, RL & Langford, HG (1970) Usefulness of overnight urines in population groups. Pilot studies of sodium, potassium, and calcium excretion. Am J Clin Nutr 23, 290304.Google Scholar
24. Prentice, AM & Jebb, SA (2001) Beyond body mass index. Obes Rev 2, 141147.CrossRefGoogle ScholarPubMed
25. He, FJ, Marrero, NM & MacGregor, GA (2008) Salt intake is related to soft drink consumption in children and adolescents: a link to obesity? Hypertension 51, 629634.Google Scholar
26. Grimes, CA, Wright, JD, Liu, K, et al. (2013) Dietary sodium intake is associated with total fluid and sugar-sweetened beverage consumption in US children and adolescents aged 2-18 y: NHANES 2005–2008. Am J Clin Nutr 98, 189196.Google Scholar
27. Grimes, CA, Riddell, LJ, Campbell, KJ, et al. (2013) Dietary salt intake, sugar-sweetened beverage consumption, and obesity risk. Pediatrics 131, 1421.Google Scholar
28. Korea Center for Disease Control and Prevention (2013) Korea Health Statistics 2012: Korea National Health and Nutrition Examination Survey (KHNAES v-3). Seoul: KCDC.Google Scholar
29. Powles, J, Fahimi, S, Micha, R, et al. (2013) Global, regional and national sodium intakes in 1990 and 2010: a systematic analysis of 24h urinary sodium excretion and dietary surveys worldwide. BMJ Open 3, e003733.Google Scholar
30. Korea Center for Disease Control and Prevention (2012) Analytic Guidelines of the Fifth Korea National Health and Nutrition Examination Survey 2011. Seoul: KCDC.Google Scholar
31. Korea Center for Disease Control and Prevention (2012) Korean National Health and Nutrition Examination Survey 2009–2011. Seoul: KCDC.Google Scholar
32. Kim, YO, Kim, MK, Lee, SA, et al. (2009) A study testing the usefulness of a dish-based food-frequency questionnaire developed for epidemiological studies in Korea. Br J Nutr 101, 12181227.CrossRefGoogle ScholarPubMed
33. Brown, IJ, Tzoulaki, I, Candeias, V, et al. (2009) Salt intakes around the world: implications for public health. Int J Epidemiol 38, 791813.Google Scholar
34. Krebs, NF, Himes, JH, Jacobson, D, et al. (2007) Assessment of child and adolescent overweight and obesity. Pediatrics 120, Suppl. 4, S193S228.Google Scholar
35. Korea Center for Disease Control and Prevention (KCDC) and The Korean Pediatric Society (2008) 2007 Korean National Growth Charts. Seoul: Korea Center for Disease Control and Prevention and The Korean Pediatric Society.Google Scholar
36. Moon, JS, Lee, SY, Nam, CM, et al. (2008) 2007 Korean National Growth Charts: review of development process and an outlook. Korean J Pediatr 51, 125.Google Scholar
37. Taylor, RW, Jones, IE, Williams, SM, et al. (2000) Evaluation of waist circumference, waist-to-hip ratio, and the conicity index as screening tools for high trunk fat mass, as measured by dual-energy X-ray absorptiometry, in children aged 3-19 y. Am J Clin Nutr 72, 490495.Google Scholar
38. Barlow, SE (2007) Expert committee recommendations regarding the prevention, assessment, and treatment of child and adolescent overweight and obesity: summary report. Pediatrics 120, Suppl. 4, S164S192.Google Scholar
39. Seo, JY, Cho, YG, Kang, JH, et al. (2013) New diagnostic criteria for obesity and overweight in Korean children and adolescents using 2007 Korean National Growth Charts. Obes Res Clin Pract 7, e182e189.Google Scholar
40. Prior, BM, Cureton, KJ, Modlesky, CM, et al. (1997) In vivo validation of whole body composition estimates from dual-energy X-ray absorptiometry. J Appl Physiol (1985) 83, 623630.Google Scholar
41. Asayama, K, Ozeki, T, Sugihara, S, et al. (2003) Criteria for medical intervention in obese children: a new definition of ‘obesity disease’ in Japanese children. Pediatr Int 45, 642646.Google Scholar
42. US Department of Agriculture & US Department of Health and Human Services (2010) Dietary Guidelines for Americans, 2010. Washington, DC: US Department of Agriculture and US Department of Health and Human Services.Google Scholar
43. Buck, D & Frosini, F (2012) Clustering of Unhealthy Behaviors Over Time: Implications for Policy and Practice. London: The King’s Fund.Google Scholar
44. Ji, C, Sykes, L, Paul, C, et al. (2012) Systematic review of studies comparing 24-hour and spot urine collections for estimating population salt intake. Rev Panam Salud Publica 32, 307315.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Characteristics of the participants (Mean values with their standard errors; percentages)

Figure 1

Table 2 Risk of adiposity* by urinary sodium:creatinine ratio (Odds ratios and 95 % confidence intervals)

Figure 2

Table 3 Risk of adiposity* by dietary sodium intake (Odds ratios and 95 % confidence intervals)