Background
There is much evidence from epidemiological studies and animal experiments have shown that dietary sodium plays an important role in the regulation of blood pressure [
1]. A positive relationship between sodium intake and blood pressure has been documented both in hypertensive and normotensive individuals [
2,
3]. The INTERSALT study was an observational study showed an association between dietary salt intake and blood pressure. Of the study populations, four centres with low sodium excretion had low median blood pressures, low prevalence of hypertension, and either a decrease or only a small increase of blood pressure with age [
4].
In a randomized double-blind crossover trial of salt restriction among mild hypertensive patients, with reductions in salt intake, there were significant falls in BP in all three ethnic groups including whites, blacks, and Asians [
5]. Furthermore, a meta-analysis of 13 studies revealed that a higher salt intake was associated with greater risk of stroke (pooled relative risk 1.23, 95 % confidence interval 1.06 to 1.43;
P = 0.007) and cardiovascular disease (1.14, 0.99 to 1.32;
P = 0.07) [
6]. The potential BP-independent increased CVD risk under a high salt diet may be related to vascular structural and functional changes, through alterations in endothelial function [
7].
Retinal blood vessels are the only human microvessels that can be directly observed and quantitatively detected by many methods. Retinal microvascular lesion indicates the status of small vascular diseases in the body, and is an important indicator for predicting cardio-cerebrovascular complications [
8]. The urinary albumin reflects endothelial dysfunction and renal vascular lesions, it is a risk factor of cardiovascular events in the general population, particularly in patients with hypertension [
9,
10]. The risk of renal and cardiovascular events can be decreased after reducing albuminuria.
Several large cohort studies used 24 h urinary sodium excretion to estimate sodium intake, However, this method involved a considerable burden on subjects and it is difficult to collect complete and accurate 24-h urine samples [
11,
12]. The urinary sodium-creatinine ratio of causal urine specimens may be an alternative method for estimating population mean levels of 24 h urinary sodium excretion, and were available for comparing different populations, as well [
13].
In most of areas of China, sodium intake is above 12 g per person per day. Our study using urinary sodium-creatinine ratio of a single early morning urine to estimate 24-h urinary sodium excretion which can be used to evaluate sodium intake, aims to explore the association between sodium excretion, blood pressure and arterial injury in a Chinese population on high-sodium diets.
Methods
Study population
A cross-sectional survey using random and cluster sampling was performed from July 2011 through November 2011. The clusters were the individual administrative coastal villages in Fujian province of China, and we sought to obtain 7 sampling units in 14 villages for two specified townships. Invitations to participate in the survey were sent to 4616 subjects who were sampled from the 8947 inhabitants, aged 30 years and above. A total of 3343 subjects participated in the survey. We excluded 887 subjects from the analysis due to incomplete data (133 subjects), affliction with infectious disease (C-reactive protein level >10 mg/L; 39 subjects), took diuretics and angiotension converting enzyme inhibitors (25 subjects) and unqualified or unclear fundus photographs that affected the analysis (675 subjects). In the final analysis, only 2456 subjects were involved. This study was approved by the ethics committee of the Fujian Provincial Hospital, China. Written informed consent was obtained from all participants following a detailed description of the potential benefits and risks associated with the study.
Data collection
The questionnaire survey covered the information including age, sex, occupation, smoking,alcohol habits, medical history (such as hypertension, coronary heart disease, heart failure, diabetes, stroke, or liver disease), drug use, and a family history of hypertension.
Physical examination
Body mass index (BMI) was calculated as weight (kg)/height (m) 2. Blood pressure was measured on the right upper arm using a mercury sphygmomanometer by two trained internists with an appropriately sized cuff after 10 min in a sitting position without intaking tea or coffee in 30 min. The first appearance (phase I) and disappearance (phase V) of Korotkoff sounds were used to defined systolic and diastolic blood pressure (SBP, DBP). Three consecutive measurement were taken in 5 min intervals, and the average was used in the analysis.
Blood and urine sampling and sample detection
Blood samples were collected after 8 h of overnight fasting to determine the plasma levels of triglyceride, total cholesterol, high-density lipoprotein cholesterol (HDL- C), low-density lipoprotein cholesterol (LDL- C), serum glucose, C-reactive protein (hs-CRP). Urine sample was collected in the morning. We did not ask the participants to change their dietary patterns during the collection so that the urine sodium excretion amount could be considered as a marker for usual intake. Spot urinary sodium (SUNa) by, Spot urinary creatinine (SUCr) and albumin in the urine were measured by ion-selective electrode, picric acid (LX20 automatic biochemical analyzer, USA), and Immunonephelometry (Dade Behring BN II specific protein analyzer, Germany), respectively.
The 24-h dietary sodium excretion was estimated by the following equations [
13]
$$ 24 hUNa\ \left( mmol/ day\right)= 1. 2929\times {\left[ SUNa/ SUCr\times \left(\mathit{\hbox{-}} 2.04\times age+ 1 4.89\times weight\ (kg)+ 1 6.14\times height\ (cm)\mathit{\hbox{-}} 2244.45\right)/ 88\right]}^{0.392} $$
Fundus photography
High-resolution fundus photography using a digital non-mydriatic camera was performed on both eyes (Topcon NW-8 and Nikon D90, Japan) with a capturing range of 45° using the optic disk as the center. The central retinal arteriolar equivalent (CRAE) was measured using the modified Knudtson-Parr-Hubbard formula [
14] in the range of 0.5–1 DD from the disc margin. We used a semi-automated computer-based program (Singapore I Vessel Assessment [SIVA] version 3.0, jointly developed by Singapore National University and Singapore Eye Research Institute) for CRAE. A double-blind analysis of the photographs was performed by two professionally trained ophthalmologists, and high-quality fundus photographs were used for analysis.
Diagnostic criteria and related definitions
According to the JNC7 [
15], a systolic blood pressure of ≥140 mmHg or a diastolic blood pressure of ≥90 mmHg were defined as diagnostic indicators of hypertension. In addition, the patients with a hypertension history or those taking antihypertensive drugs were regarded as the population with hypertension. The lowest quartile of CRAE was defined as the central retinal artery narrowing [
16]. The Estimated Glomerular filtration rate (eGFR) was calculated using the MDRD formula:
$$ eGFR\ \left( ml.mi{n}^{\mathit{\hbox{-}} 1}. 1. 7{3}^{\mathit{\hbox{-}} 1}.{m}^{\mathit{\hbox{-}} 2}\right)= 1 86. 3\times serum\ creatinine\ \left( mg.d{l}^{\mathit{\hbox{-}} 1}\right)\mathit{\hbox{-}} 1. 1 54\times Age\mathit{\hbox{-}} 0. 2 0 3\times \left( 0.742,\ if\ female\right) $$
Urinary albumin-creatinine ratio (UACR) was was calculated as \( UACR\ \left( mg.{g}^{\mathit{\hbox{-}} 1}\right)= urinary\ albumin\ \left( mg.{L}^{\mathit{\hbox{-}} 1}\right)/ urine\ creatinine\ \left(g.{L}^{\mathit{\hbox{-}} 1}\right) \)
Sodium excretion was divided into quartiles: the lowest quartile (Q1) corresponding to <9.04 g, the second quartile (Q2) corresponding to 9.04 g-10.73 g the third quartile (Q3) corresponding to 10.74 g-12.61 g, the highest quartile (Q4) corresponding to >12.61 g. There were all 614 cases in quartiles Q1, Q2, Q3, and Q4, respectively.
Statistical analysis
All the data were analyzed by the SPSS 17.0 statistical software (SPSS, Inc., Chicago, IL, USA), with a P value <0.05 indicative of statistical significance.
The normally distributed data are shown as mean ± SD, while Skewed distributed variables are described by median (upper and lower quartile). Skewed distributed variables were taken as approximately normal distribution after logarithmic transformation for analysis. Differences in measurement data were using t-Test, one-way analysis of variance (ANOVA) and Wilconxon Rank Sum Test while the count data were analyzed by Chi-Square Test. Age-and sex-adjusted comparisons of UACR and CRAE according to the quartile of sodium excretion were made using analysis of covariance (ANCOVA). The sequential linear trend test was used for analyzing the intergroup relationships of the categorical data. Logistic regressions were used for the relationship analysis between sodium excretion, and UACR or CRAE, respectively. The factors such as age, BMI, CRAE(in the model of UACR), UACR(in the model of CRAE), total cholesterol, LDL-cholesterol, SBP, and DBP were adjusted for the regression. The chi-square test for trend was used for analyzing prevalence of hypertension within the quartiles.
Discussion
Epidemiological studies confirmed that excessive sodium intake could cause high blood pressure, and that a high sodium diet could be an important risk factor for hypertension [
17]. In general, the accurate estimation of sodium content in the diet is difficult. With normal renal function, an individual can excrete 90.4–95 % of the sodium intake in the urine by the kidneys. Therefore, for an individual with stable diet, the 24-h urinary sodium excretion basically reflects the level of sodium intake without taking medication which could interfere sodium intake such as diuretics, and is also a reliable method to index the sodium intake [
18,
19]. A high urinary sodium reflects a high sodium diet to some extent [
13,
18]. The urinary sodium-creatinine ratio of causal urine specimens [
13] and second morning voiding urine collecting [
20] were correlated with the 24-h urinary sodium excretion, which could represent the 24-h urinary sodium excretion. A single urine collection is simple, easy, and suitable for the epidemiological study of a large number of samples. Hence, this study used the first morning urine samples and evaluated 24-h urinary sodium excretion to illustrate the level of sodium intake based on the urinary sodium-creatinine ratio.
Previous studies have shown that with the increase of sodium intake, SBP and DBP were also significantly increased [
21]. Furthermore, it has been shown that reduction of dietary sodium intake lowered the SBP and DBP levels [
22,
23]. Consistent with the previous studies, the results of this study also showed that the SBP and DBP levels were significantly correlated with sodium excretion. As far as we know, the conclusion may be explained by the phenomenon of salt sensitivity of BP, which refers to the BP responses for changes in dietary salt intake to produce meaningful BP increases or decreases. Epidemiologic data demonstrate the role of high dietary salt intake in mediating cardiovascular and renal morbidity and mortality. Recent studys suggested that salt sensitivity seem to be related not only the kidney malfunction but also the endothelial dysfunction [
24].As such, it is necessary to take measures to reduce the sodium intake in the coastal areas of China in order to lower the blood pressure levels and reduce cardiovascular events in some individuals.
The typical diet may also effect sodium excretion, such as potassium: sodium ratio. The urinary potassium: sodium ratio in the INTERSALT study had a significant, inverse relation with blood pressure. This ratio bore a stronger statistical relationship to blood pressure than did either sodium or potassium excretion alone [
4]. In the DASH trial, a diet rich in fruits and vegetables, which were found forms of potassium that do not contain chloride, offered larger cellular entry in exchange for sodium and greater antihypertensive effects, as compared with the typical American diet [
25].
An increased urinary albumin excretion has been reported in the patients with hypertension or diabetes, as well as the individuals with a normal blood pressure [
20,
26]. Microalbuminuria could reflect the renal arteriolar damage, and is closely associated with cardiovascular events and mortality [
27].This study showed that with an increase in the urinary sodium excretion, the urinary albumin excretion along with the incidence of UACR abnormalities (greater than 30 mg g
−1) were increased. After the adjustment of factors, such as age and blood pressure, the incidence of UACR abnormalities still remained higher than normal with an increase in the urinary sodium excretion. This observation indicated that a high-sodium diet was an independent risk factor for the UACR anomalies. A high sodium diet increased the urinary albumin excretion along with the risk of cardiovascular events. Similarly, Verhave et al. [
28] reported that a high sodium diet exacerbated the high UACR-induced cardiovascular and renal damages. The related mechanism involved could be due to the sodium overload-induced neurohumoral reactions that could cause systolic and diastolic abnormalities of the renal afferent and efferent arterioles, which could further lead to abnormal glomerular filtration rate, vascular endothelial damage, and hemodynamic abnormalities [
29].
Retinal vascular and cardiovascular systems have a common anatomical and physiological characteristic. They are the only blood vessels that can be non-invasively observed in the body, and have attracted a great attention. The population-based epidemiological survey of the eye-fundus blood vessels demonstrated that retinal vascular abnormalities could increase cardiovascular mortality [
30]. These surveys included: the atherosclerosis risk in community, the cardiovascular health, the beaver dam eye, and the Blue Mountains eye studies. A prospective study [
31] revealed that the retinal vascular changes might occur before the onset of the cardio-cerebrovascular disease, and could be independent predictors of the occurrence and prognosis of systemic diseases. In this study, we found that the central retinal artery diameter was decreased with increasing urinary sodium excretion. After adjustment of factors such as age, sex, and blood pressure, the logistic regression showed that the risk of the central retinal artery diameter abnormalities was still significant in the participants with high sodium excretion. It further suggested that a high sodium diet was an independent risk factor for the central retinal arterial damage, which could increase the risk of cardiovascular disease.
However, we were aware of the limitations of this study. In our cross-sectional study, the exposure and outcome variables coexisted, which could have led to difficulty in clarifying the causal relationship between sodium excretion and vascular damage. In addition, some information on the participants was obtained through questionnaires, which could have led to an inevitable information bias. And according to the including criteria, we already excluded the population who have been on long-term usage of diuretics or ACEI/ARB which may affect the UACR. However, other antihypertensive treatment was not adjusted in the multivariable-adjusted models, which could have affected our results.
Acknowledgements
Our study was supported by the Fujian Major Program of Basic Science Project Foundation entitled “Epidemiologic survey of hypertension and prehypertension intervention research in HaiDao County of Fujian Province” (2010Y0013), “Predictive value of quantitative parameters of retinal vessel for subclinical atherosclerosis ischemic stroke and their relationship with Cognitive Impairment in Elderly Hypertensive Patients” (2014-CX-4) and the Fujian Medical Innovation Project entitled “The association of plasma apelin levels and apelin polymorphism with hypertension and hypertensive vascular injury” (2012-CX-1).