Longitudinal association of dietary acid load with kidney function decline in an older adult population with metabolic syndrome

Background: Diets high in acid load may contribute to kidney function impairment. This study aimed to investigate the association between dietary acid load and 1-year changes in glomerular filtration rate (eGFR) and urine albumin/creatinine ratio (UACR).

Methods: Older adults with overweight/obesity and metabolic syndrome (mean age 65 ± 5 years, 48% women) from the PREDIMED-Plus study who had available data on eGFR (n = 5,874) or UACR (n = 3,639) at baseline and after 1 year of follow-up were included in this prospective analysis. Dietary acid load was estimated as potential renal acid load (PRAL) and net endogenous acid production (NEAP) at baseline from a food frequency questionnaire. Linear and logistic regression models were fitted to evaluate the associations between baseline tertiles of dietary acid load and kidney function outcomes. One year-changes in eGFR and UACR were set as the primary outcomes. We secondarily assessed ≥ 10% eGFR decline or ≥10% UACR increase.

Results: After multiple adjustments, individuals in the highest tertile of PRAL or NEAP showed higher one-year changes in eGFR (PRAL, β: –0.64 ml/min/1.73 m²; 95% CI: –1.21 to –0.08 and NEAP, β: –0.56 ml/min/1.73 m²; 95% CI: –1.13 to 0.01) compared to those in the lowest category. No associations with changes in UACR were found. Participants with higher levels of PRAL and NEAP had significantly higher odds of developing ≥10% eGFR decline (PRAL, OR: 1.28; 95% CI: 1.07–1.54 and NEAP, OR: 1.24; 95% CI: 1.03–1.50) and ≥10 % UACR increase (PRAL, OR: 1.23; 95% CI: 1.04–1.46) compared to individuals with lower dietary acid load.

Conclusions: Higher PRAL and NEAP were associated with worse kidney function after 1 year of follow-up as measured by eGFR and UACR markers in an older Spanish population with overweight/obesity and metabolic syndrome.

Introduction

Impaired renal function is a common condition in older individuals with comorbidities as diabetes, hypertension or obesity that usually predicts the onset of Chronic Kidney Disease (CKD) (1). In the last few years, there has been a growing concern about this disease since it has a huge impact worldwide affecting around 700 million people (2). In addition, CKD is linked to several complications, such as cardiovascular events, hospitalization and/or premature death (2, 3). Consequently, appropriate and affordable prevention measures are required to preserve renal function, especially in high-risk populations (1). Prevention measures could also reduce the severe impact of CKD on the wellbeing of individuals and health systems (3–5).

Dietary habits appear to be one of the major modifiable risk factors markedly influencing renal impartment and its progression to CKD (5, 6). Additionally, the role of diet in preserving the acid-base balance of the body has recently become more relevant, given the emerging evidence linking dietary acid load with the development of different chronic diseases (7, 8), including CKD (9). It has been previously documented that healthy dietary patterns provide an alkaline environment in the body (10, 11) since plant-based food such as vegetables, fruit and some nuts or legumes have the capacity of inducing a basic environment (12). However, red and processed meats as well as ultra-processed foods are acid-producing (9, 12). Thus, these foods might be implied in the onset of a low-grade metabolic acidosis state, thereby, resulting in faster progression of kidney disease (11, 13). Overall, potential renal acid load (PRAL) and net endogenous acid production (NEAP) are the most common and suitable indexes used to estimate the acid load of the diet (9, 11). Considering the aforementioned evidence, following a healthy diet characterized by a low acid load may be a useful preventive strategy against kidney dysfunction.

To date, results from epidemiological studies focused on dietary acid load and kidney function or CKD development are inconsistent (9) and this relationship needs to be further explored. In some studies, an association between higher levels of PRAL and/or NEAP indexes and an estimated-glomerular filtration rate (eGFR) decline or higher risk of incident CKD (14–18) has been reported, but others have observed no such associations (19, 20). Also, the quality of evidence is moderate as most of the studies were mainly cross-sectional (14–17, 21, 22), and only a few were longitudinal studies (18–20). Furthermore, since most research has been conducted in healthy young or middle-aged individuals or in patients with advanced CKD, little is known about the potentially harmful association between dietary acid load and kidney function of older populations with underlying comorbid conditions. In addition, analyses assessing dietary acid load on kidney function have rarely been conducted in Mediterranean populations at high cardiovascular risk. Hence, as more scientific evidence and longitudinal studies in this field are required, we prospectively investigated the association between PRAL and NEAP and 1-year changes in two markers of kidney function decline, eGFR and Urine Albumin/Creatinine Ratio (UACR), in a large Spanish cohort of older adults with overweight/obesity and metabolic syndrome (MetS).

Materials and methods

Study population and design

The present study is a prospective analysis of baseline and 1-year data within the framework of the PREvención con DIeta MEDiterránea (PREDIMED)-Plus trial. Briefly, the PREDIMED-Plus is an ongoing, parallel-group, randomized and controlled clinical trial aiming to assess the effect of an intensive weight loss intervention on cardiovascular disease (CVD) morbidity and mortality. An energy-restricted Mediterranean diet (MedDiet), physical activity promotion and behavioral support are compared to usual care advice in 6,874 older adults enrolled between 2013 and 2016 by 23 Spanish recruitment centers. Eligible participants were men aged 55–75 years and women aged 60–75 years with overweight or obesity [Body Mass Index (BMI) 27–40 kg/m²], who satisfied at least 3 criteria for the MetS (23). Further details of the inclusion and exclusion criteria and the study design have been described elsewhere (24). A detailed explanation of the protocol is also available at https://www.predimedplus.com. This trial was registered on the International Standard Randomized Controlled Trial registry (https://www.isrctn.com/ISRCTN89898870) with number 89898870 in July of 2014. The final study protocol and procedures were approved following the standards of the Declaration of Helsinki by the Institutional Review Boards of participating centers and all participants provided written informed consent.

For the current study, participants without completed food frequency questionnaire (FFQ) information and reporting implausible total energy intake (men < 800 and >4,000 kcal/day and women < 500 and >3,500 kcal/day) at baseline were excluded (n = 227) from the analyses (25). We also excluded participants who died (n = 11) or were lost to follow-up (n = 16) during the first year. Moreover, participants with missing data on eGFR (n = 746) or UACR (n = 2,981) at baseline and/or at the 1-year assessment were excluded when eGFR or UACR were the outcomes, respectively. Therefore, a final sample of 5,874 participants for eGFR and 3,639 participants for UACR were analyzed (Supplementary Figure 1).

Assessment of dietary intake and dietary acid load

To evaluate dietary intake, trained dieticians administered a 143-item FFQ, based on a previously validated one for the Spanish population (26), in face-to-face interviews at baseline. Each participant was asked about their frequency of consumption during the preceding year of each specific item, which had nine possible answers ranging from never to more than 6 times per day. The typical portion size of each item was subsequently transformed into grams or milliliters per day, as appropriate. Two Spanish food composition databases were referenced to calculate total daily energy and nutrient intake (27, 28).

Dietary acid load was estimated at baseline using individual nutritional data obtained from the FFQ. Previously published methods proposed by Remer and Manz (29) and Frassetto et al. (8) were applied for the calculation of PRAL and NEAP scores, respectively. PRAL (mEq/day) = 0.4888 × protein intake (g/day) + 0.0366 × phosphorus (mg/day) – 0.0205 × potassium (mg/day) – 0.0125 × calcium (mg/day) – 0.0263 × magnesium (mg/day). NEAP (mEq/day) = 54.5 × protein (g/day)/potassium (mEq/day) – 10.2.

Ascertainment of the outcome

Serum creatinine (SCr) levels and urinary creatinine and albumin concentrations were determined using routine laboratory methods from blood and spot morning urine samples collected at baseline and 1-year following overnight fasting. For the current study, 1-year changes in eGFR and UACR were considered our primary outcomes. We indirectly determined eGFR from SCr using the Chronic Kidney Disease Epidemiology Collaboration equation for Caucasian individuals (CKD-EPI) (30) and the UACR was calculated by dividing urine albumin (mg/l) by urine creatinine concentrations (mg/l). UACR values were truncated at 500 mg/g to minimize the influence of outliers. There were 21 observations > 500 mg/g at baseline and 24 at 1 year that were >500 mg/g and subsequently set to 500 mg/g. One-year changes in both eGFR and UACR were calculated by subtracting values at 1 year minus values at baseline. Secondary outcomes were ≥10% eGFR decline and ≥10% UACR increase following a 1-year follow-up. These were estimated by applying the formula: [(1-year eGFR or UACR – baseline eGFR or UACR)/baseline eGFR or UACR]^*100. Participants were categorized as those with a ≥10% or <10% eGFR decline (31) or with a ≥10% or <10% increase in UACR.

Covariate assessment

At baseline, trained PREDIMED-Plus staff collected socio-demographic and lifestyle information including age, sex, educational level, physical activity, smoking status, as well as medication use and history of disease using several questionnaires or reviewing medical records. Moreover, adherence to the energy-reduced MedDiet was evaluated using a validated 17-item MedDiet questionnaire (32). Compliance with each item of the MedDiet questionnaire was scored with one point and non-compliance with 0. Thereafter, a cut-off point based on the median of the score was determined by dividing individuals into those with high adherence to a MedDiet (≥9 points) or a low adherence (<9 points). Moreover, other cut-off points were tested arbitrarily and defined as the highest tertiles or quartiles (in both cases high adherence was observed to be ≥12 points). Total daily energy intake and sodium intake were estimated according to data from the FFQ. Anthropometric variables were measured in duplicate and resting blood pressure was measured in triplicate using an automated digital device (Omron-HEM297705C). BMI was calculated as weight in kilograms divided by the square of height in meters. In our analysis, white blood cell count was used to assess inflammation (leucocytes > 10 × 10⁹/L).

Statistical analyses

For the present report, we used the PREDIMED-Plus database generated in December 2020. Participants were categorized into tertiles of PRAL and NEAP. One-way ANOVA and chi-square tests were used to evaluate differences among tertiles of PRAL and NEAP for the baseline characteristics of the study population. Descriptive data were expressed as means ± SD for continuous variables and percentages (%) and numbers for categorical variables.

Multivariate linear regression models were performed to examine the associations between tertiles of PRAL and NEAP at baseline and 1-year changes in eGFR (ml/min/1.73 m²) and UACR (mg/g). For these associations, PRAL and NEAP were also analyzed as continuous variables (both for each 1-SD increase). β-coefficients and 95% confidence intervals (CIs) were assessed using two different models: Model 1 was adjusted for sex and age; and Model 2 was further adjusted for study center (categorized into quartiles by number of participants), intervention group (treatment/control), BMI (kg/m²), smoking status (never/current/former smoker), educational level (primary education/secondary education/graduate), leisure-time physical activity (METs/min/week, tertiles), diabetes prevalence (yes/no), hypertension prevalence (yes/no), hypercholesterolemia prevalence (yes/no), angiotensin-converting enzyme inhibitors (ACEis) (yes/no), angiotensin II receptor blockers (ARBs) (yes/no), MedDiet adherence (high/low adherence), energy intake (kcal/day, tertiles), sodium intake (mg/day, tertiles) and high leukocyte levels (yes/no). Moreover, odds ratios (OR) and their 95% CIs were calculated for the association between tertiles of NEAP and PRAL and ≥10% eGFR decline and ≥10% UACR increase at 1-year of follow-up adjusting for the same confounders as mentioned in model 2. The first tertile was used as a reference category in all regression models. Additionally, linear regression models were further adjusted for baseline eGFR (ml/min/1.73 m²) or baseline UACR (mg/g) depending on the main outcome. Variance inflation factors (VIFs) were used to assess collinearity for the multivariable models and, as VIFs were <2.5, none of the covariates needed to be removed. All analyses were conducted with robust estimates of the variance to correct for possible intra-cluster correlation. Intra-cluster was defined as the participants who shared the same household. To assess the linear trend, the median value of each tertile of PRAL and NEAP were modeled as continuous variables.

We also conducted subgroup analyses for the 1-year changes in eGFR and UACR stratifying by baseline categories of eGFR (≥90; 60–90; <60 ml/min/1.73 m²) and UACR (<30; ≥30 mg/g). Interaction between tertiles of PRAL and NEAP with categories of eGFR, UACR, and energy-reduced MedDiet adherence (high/low), as well as the intervention/control group were checked in the fullest multivariable model using likelihood ratio tests and non-significant results were observed. In a sensitivity analysis, we repeated our main analysis investigating the association between PRAL and NEAP with 1-year changes in eGFR and UACR after excluding individuals with eGFR < 60 ml/min/1.73 m² or with UACR > 300 mg/g at baseline. In addition, as a supplementary analysis, we evaluated the association between dietary acid load and ≥5% eGFR decline and ≥5% UACR increase following the same procedure mentioned previously. Statistical analyses were conducted using Stata/SE software, version 14.0 (StataCorp, College Station, TX) and significance level was set at a 2-tailed p < 0.05.

Results

Table 1 shows the baseline characteristics of the study population according to tertiles of PRAL and NEAP. In general, participants with higher values of PRAL and NEAP at baseline were more likely to be younger, men, have a higher BMI, smoke, have a higher educational level, and were less likely to exercise. Participants in the highest tertiles of PRAL and NEAP also had higher levels of creatinine and eGFR than those in the lowest tertile. In terms of mediations, participants in the highest tertiles of PRAL and NEAP were more likely to have used insulin, ACEis treatment, and took less antihypertensive and ARB drugs. Furthermore, individuals in the highest tertile of NEAP were more likely to have type 2 diabetes. However, no significant differences were observed between tertiles of PRAL nor NEAP regarding the UACR or CKD. Concerning dietary assessment, adherence to an energy-reduced MedDiet was lower in individuals with higher dietary acid load levels than those in the lowest tertile of PRAL and NEAP. Moreover, participants in the highest tertile of PRAL and NEAP had a lower intake of vegetable/animal protein ratio, carbohydrates and fiber while they had a higher energy, protein and fat consumption than those with low values of both dietary acid load indexes. Similar trends were observed when baseline consumption of food groups across tertiles of PRAL and NEAP were analyzed (Supplementary Table 1). Supplementary Table 2 presents further information regarding macronutrient and micronutrient intake, especially those related to dietary acid load, at 1-year of follow-up. Baseline characteristics according to included and excluded participants from the eGFR or UACR analyses are described in Supplementary Table 3.

TABLE 1

Table 1. Baseline characteristics of the study population with data on eGFR at 1-year follow-up by tertiles of PRAL and NEAP (n = 5,874).

The association (β-coefficient; 95% CI) between tertiles of PRAL and NEAP and 1-year changes in eGFR and UACR are displayed in Table 2. In the most adjusted model, PRAL showed a significant inverse association with 1-year changes in eGFR (β: −0.17 ml/min/1.73 m²; 95% CI: −0.71 to 0.36 for T2 vs. T1, β: −0.64 ml/min/1.73 m²; 95% CI: −1.21 to −0.08 for T3 vs. T1). We found similar results when PRAL and NEAP were analyzed as continuous variables (PRAL: β: −0.25 ml/min/1.73 m²; 95% CI: −0.47 to −0.03 for each 1-SD increment. NEAP: β: −0.28 ml/min/1.73 m²; 95% CI: −0.51 to −0.05 for each 1-SD increment). Results remained essentially the same after adding 1-year BMI change to the most adjusted model (data not shown). PRAL and NEAP were not significantly associated with UACR changes after 1-year of follow-up after modeling them as tertiles, nor as continuous variables. In the sensitivity analyses, excluding individuals with <60 ml/min/1.73 m² of eGFR or with >300 mg/g of UACR did not modify the main findings for both outcomes (data not shown). When we repeated the principal analyses, stratifying by baseline categories of eGFR (≥90; 60–90; < 60 ml/min/1.73 m²) and UACR (<30; ≥30 mg/g), the results presented a similar tendency (Supplementary Table 4). In participants with eGFR ≥ 90 ml/min/1.73 m², significant associations were observed with eGFR changes when both dietary acid load indexes were modeled as continuous variables (PRAL: β: −0.28 ml/min/1.73 m²; 95% CI: −0.56 to −0.01 for each 1-SD increment. NEAP: β: −0.31 ml/min/1.73 m²; 95% CI: −0.58 to −0.03 for each 1-SD increment). The main analysis was repeated using other cut-offs points for the MedDiet score confounding factor (i.e., ≥12 points for high adherence) and similar results were found (Supplementary Table 5). We also explored the interactions between tertiles of PRAL and NEAP and the adherence to energy-reduced MedDiet, categories of eGFR and UACR, as well as intervention/control group, and no statistically significant findings were observed (all interactions, p > 0.05).

TABLE 2

Table 2. Multivariable-adjusted β-coefficients and 95% CI of 1-year changes in eGFR (ml/min/1.73 m²) or in UACR (mg/g) across tertiles and per 1-SD increment of baseline PRAL and NEAP.

Figure 1 depicts the OR and 95% CI for ≥10% eGFR decline and ≥10% UACR increase according to tertiles of PRAL and NEAP. After multiple adjustments, participants in the highest tertile of PRAL and NEAP were significantly more likely to have a ≥10% eGFR decline after 1 year of follow up compared to those in the lowest tertile, with ORs of 1.28 (95% CI: 1.07–1.54) for PRAL and 1.24 (95% CI: 1.03–1.0) for NEAP. When PRAL and NEAP were modeled as continuous variables (per each 1-SD increment) higher ORs were also observed. Compared to participants with low PRAL values at baseline, participants with the highest levels had a 23% (95% CI: 1.04–1.46) higher odds of ≥10% UACR increase after 1 year of follow-up after adjusting for potential confounders. No significant associations were found between NEAP and the odds of ≥10% UACR increase or for 1-SD increment of PRAL and NEAP. When a ≥5% eGFR decline and a ≥5% UACR increase were assessed, the same results were found (Supplementary Table 6).

FIGURE 1

Figure 1. (A) Multivariable-adjusted OR (95% CIs) for ≥10% eGFR decline by tertiles of baseline PRAL and NEAP and per 1-SD increment. (B) Multivariable-adjusted OR (95% CIs) for ≥10% UACR increase by tertiles of baseline PRAL and NEAP and per 1-SD increment. eGFR, Estimated glomerular filtration rate; NEAP, Net Endogenous Acid Production; T, tertile; PRAL, Potential Renal Acid Load; UACR, Urine albumin/creatinine ratio. Percentage of participants with eGFR decline (>10%): tertile 1 of PRAL (n = 296; % = 15.1), tertile 2 of PRAL (n = 304; % = 15.5), tertile 3 of PRAL (n = 346; % = 17.7); tertile 1 of NEAP (n = 297; % = 15.2), tertile 2 of NEAP (n = 312; % = 15.9). tertile 3 of NEAP (n = 337; % = 17.2). Percentage of participants with UACR increase (>10%): tertile 1 of PRAL (n = 539; % = 44.4), tertile 2 of PRAL (n = 547; % = 45.1), tertile 3 of PRAL (n = 597; % = 49.2); tertile 1 of NEAP (n = 550; % = 45.3), tertile 2 of NEAP (n = 539; % = 44.4), tertile 3 of NEAP (n = 594; % = 49.0). All models were adjusted for age (years), sex, participating center (categorized into quartiles by number of participants), intervention group (treatment/control), body mass index (kg/m²), smoking habits (never, current or former smoker), educational level (primary, secondary education or graduate), leisure-time physical activity (METS/min/week in tertiles), diabetes prevalence (yes/no), hypertension prevalence (yes/no) and hypercholesterolemia prevalence (yes/no), ARBs (yes/no), ACEis (yes/no), Mediterranean diet adherence (high/low adherence), energy intake (kcal/day in tertiles), sodium intake (mg/g in tertiles), and high leukocytes levels (yes/no). **one SD = 15.6 mEq/d in PRAL and 8.1 mEq/d in NEAP.

Discussion

The results of this prospective study conducted in older Spanish adults at high cardiovascular disease risk suggest that PRAL and NEAP are inversely associated with 1-year changes in eGFR, but not with 1-year UACR changes. Furthermore, participants with higher levels of both estimates of dietary acid load had higher odds of a ≥10% eGFR decline, and those in the highest tertile of PRAL had 23% higher odds of a ≥10% UACR increase. GFR and albuminuria are the main complementary biomarkers used in epidemiological studies to assess kidney function (3). As far as we know, this is the first study to prospectively evaluate the association between dietary acid load and kidney function concurrently assessing eGFR and UACR in a population of older adults with underlying comorbidities.

A large body of evidence has linked dietary acid load with kidney outcomes in several studies (9). However, to the best of our knowledge, there are only four cross-sectional studies and one longitudinal study investigating the potential relationship of dietary acid load with renal function defined by eGFR and/or CKD in older adults without CKD. These cross-sectional studies conducted in different cohorts of adults reported that higher dietary acid load was associated with higher odds of CKD and/or impaired kidney function as indicated by low eGFR after adjusting for multiple confounders (14, 16, 17, 33). Our observations are in accordance with these cross-sectional studies since we observed a greater eGFR decline at 1 year with higher PRAL and NEAP scores, even after adjusting for baseline eGFR and other essential confounding factors. Interestingly, our supplementary stratified analyses according to categories of eGFR, which have seldom been performed in previous studies, revealed a similar non-significant tendency to worsen kidney function with increased dietary acid load. Consistent with our findings, the prospective analysis from the cohort of the Atherosclerosis Risk in Communities (ARIC) study of 15,055 apparently healthy middle-aged participants with preserved kidney function showed that higher levels of PRAL were associated with a 13% higher risk of CKD incidence over 21 years of follow-up (18).

Regarding albuminuria, which is considered a reliable marker of kidney damage (3), preceding studies have assessed its cross-sectional association with dietary acid load obtaining inconclusive findings. In The Jackson Heart Study, there was no association between estimated Net Acid Excretion (NAE_es) and albuminuria (16). In contrast, the NHANES study reported a positive association between dietary acid load and albuminuria in 12,293 healthy American adults (17). Additionally, the researchers from The Uonuma CKD Cohort Study also found that higher NEAP was associated with a higher UACR and risk of albuminuria among 6,684 middle-aged Japanese adults (21). To date, no large prospective cohort study has focused on the relationship between dietary acid load and albuminuria in vulnerable older adults. In the current study, we report no association between PRAL and NEAP scores and 1-year changes in UACR. This could suggest that high dietary acid load may promote tubule-interstitial injury rather than glomerular damage. Nevertheless, we were not able to check this tubular damage hypothesis since spot/24 h total proteinuria data were not available in our dataset (34). However, it is worthwhile to mention that when UACR was also assessed as an increase ≥10% after 1 year of follow-up, which is a more clinical approach, we found a significant association with PRAL. Consequently, future longitudinal studies and clinical trials would be helpful to clarify these observations related to albuminuria and dietary acid load.

Overall, our findings in conjunction with the evidence available to date, suggests that following a diet with a low acid load could be an appropriate measure to improve renal function and, accordingly, decrease the risk of CKD development and progression among older individuals from middle-aged to elderly with underlying comorbid conditions.

The potential mechanisms by which high dietary acid load may induce kidney dysfunction are unclear, though possible mechanisms have been proposed for consideration. Acid retention has been proposed to activate the intracellular renin-angiotensin system, through the previous stimulation of aldosterone production, which might be implicated in the onset or progression of kidney damage (35, 36). Moreover, metabolic acidosis appears to contribute to endothelin-1 production, which in turn could be related to tubulointerstitial injury (37–39). Besides, high dietary acid load would also induce tubular toxicity activating the complement pathway and increasing renal medullary ammonia concentrations (40–42). There is also a high probability that acid retention increases the production of oxygen-free radicals and oxidative stress (43, 44). Consequently, it is crucial for kidney health to maintain appropriate levels of acid load, and diet may play an important role in this respect (11). It should be noted that in our study individuals with high levels of dietary acid load reported higher intakes of some food groups which have been directly or indirectly implicated in kidney function damage, such as total and animal protein intake (33, 45) or sugar and sweetened products (46). By contrast, as dietary acid load increased there was a lower consumption of fiber-rich foods, including fruits, vegetables, whole-grain cereals, and nuts. Thus, the potential beneficial effects of fiber on the kidney (47) could be lacking in those individuals with high dietary acid load.

This study has some limitations that deserve to be mentioned. First, the population consisted of older Spanish individuals at high cardiovascular risk, meaning the findings may not be generalizable to other populations. Furthermore, the Mediterranean lifestyle could imply healthier habits which, at the same time, may result in different macro- and micronutrients intake related to kidney function, such as potassium-rich or low-sodium dietary intakes. Second, as PREDIMED-Plus is a randomized controlled trial, though, all the analyses were adjusted for the intervention group, the lifestyle advice that participants received could be affecting our findings. Third, dietary acid load was calculated using PRAL and NEAP from dietary nutrient intake information obtained from FFQ data. Although this questionnaire was validated and carefully administered by trained dietitians, potential measurement errors and reporting bias could be present. Fourth, while SCr-based eGFR was used as a biomarker of kidney function, as is common in most epidemiologic studies, there are other more optimal markers such as inulin, iothalamate or 24-h urinary creatinine clearance. Nevertheless, these procedures are expensive, time-consuming, and difficult measure in large populations. Finally, as in any observational study, although a substantial number of confounding factors were considered, confounding bias could not be completely ruled out and direct causality cannot be inferred. However, our study also has several strengths. Analyses were conducted using data from a large cohort, which has a wide selection of different variables to adjust the models for kidney function related-potential confounders. Moreover, it is important to highlight the prospective design that we performed and the joint assessment of two commonly used biomarkers of renal function. Another novel aspect of this study is the sensitivity and supplementary analyses conducted which gave robustness to the main results.

Conclusion

In conclusion, the current study conducted in a population of older Spanish adults with overweight/obesity and MetS shows that higher dietary acid load is associated with changes toward a worse eGFR and higher odds of ≥10% eGFR decline and ≥10% UACR increase. Nevertheless, further longitudinal and interventional studies are needed to clarify and confirm the consistency of these associations before considering a reduction in dietary acid load as part of strategies for preventing kidney function decline.

Data availability statement

There are restrictions on the availability of data for the PREDIMED-Plus trial, due to the signed consent agreements around data sharing, which only allow access to external researchers for studies following the project purposes. Requestors wishing to access the PREDIMED-Plus trial data used in this study can make a request to the PREDIMED-Plus trial Steering Committee chair: cHJlZGltZWRfcGx1c19zY29tbWl0dGUmI3gwMDA0MDtnb29nbGVncm91cHMuY29t. The request will then be passed to members of the PREDIMED-Plus Steering Committee for deliberation.

Ethics statement

The studies involving human participants were reviewed and approved by the ethical standards of the Declaration of Helsinki by the Institutional Review Boards (IRBs). The patients/participants provided their written informed consent to participate in this study.

Author contributions

CV-H, NB-T, AD-L, ZV-R, IM, DC, AG, JM, ÁA-Gó, JW, JVio, DR, JL-M, RE, FT, JL, LS-M, AB-C, JT, VM-S, XP, JG, PM-M, JVid, AA-Ga, LD, ER, AG-A, RB, MF, PP-O, AA-A, EG-G, DM-U, MM, RC, EMG-G, LT-S, MD-F, EG, CO-A, OC, AG-R, CG-S, CS-O, HS, JS-S, and NB designed and conducted the research. CV-H and AD-L analyzed the data. CV-H, NB-T, AD-L, and NB wrote the article. CV-H and AD-L are the guarantors of this work and, as such, had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. All authors revised the manuscript for important intellectual content and read and approved the final manuscript.

Funding

This work was supported by the official Spanish Institutions for funding scientific biomedical research, CIBER Fisiopatología de la Obesidad y Nutrición (CIBEROBN) and Instituto de Salud Carlos III (ISCIII), through the Fondo de Investigación para la Salud (FIS), which is co-funded by the European Regional Development Fund (six coordinated FIS projects leaded by JS-S and JVid, including the following projects: PI13/00673, PI13/00492, PI13/00272, PI13/01123, PI13/00462, PI13/00233, PI13/02184, PI13/00728, PI13/01090, PI13/01056, PI14/01722, PI14/00636, PI14/00618, PI14/00696, PI14/01206, PI14/01919, PI14/00853, PI14/01374, PI14/00972, PI14/00728, PI14/01471, PI16/00473, PI16/00662, PI16/01873, PI16/01094, PI16/00501, PI16/00533, PI16/00381, PI16/00366, PI16/01522, PI16/01120, PI17/00764, PI17/01183, PI17/00855, PI17/01347, PI17/00525, PI17/01827, PI17/00532, PI17/00215, PI17/01441, PI17/00508, PI17/01732, PI17/00926, PI19/00957, PI19/00386, PI19/00309, PI19/01032, PI19/00576, PI19/00017, PI19/01226, PI19/00781, PI19/01560, PI19/01332, PI20/01802, PI20/00138, PI20/01532, PI20/00456, PI20/00339, PI20/00557, PI20/00886, and PI20/01158); the Especial Action Project entitled: Implementación y evaluación de una intervención intensiva sobre la actividad física Cohorte PREDIMED-Plus grant to JS-S; the European Research Council (Advanced Research Grant 2014–2019; agreement #340918) granted to ÁA-Gó; the Recercaixa (Number: 2013ACUP00194) grant to JS-S; grants from the Consejería de Salud de la Junta de Andalucía (PI0458/2013, PS0358/2016, and PI0137/2018); the PROMETEO/2017/017 and PROMETEO/2021/021 grants from the Generalitat Valenciana; Generalitat Valenciana AICO/2021/347 grant to JVid; the SEMERGEN grant; the Boosting young talent call grant program for the development of IISPV research projects 2019–2021 (Ref.: 2019/IISPV/03 grant to AD-L); the Societat Catalana d'Endocrinologia i Nutrició (SCEN) Clinical-Research Grant 2019 (IPs: JS-S and AD-L). Collaborative Nutrition and/or Obesity Project for Young Researchers 2019 supported by CIBEROBN entitled: Lifestyle Interventions and Chronic Kidney Disease: Inflammation, Oxidative Stress and Metabolomic Profile (LIKIDI study) grant to AD-L. Jordi Salas-Salvadó, gratefully acknowledges the financial support by ICREA under the ICREA Academia programme. CV-H receives a predoctoral grant from the Generalitat de Catalunya (2022 FI_B100108). None of the funding sources took part in the design, collection, analysis, interpretation of the data, or writing the report, or in the decision to submit the manuscript for publication.

Acknowledgments

The authors would especially like to thank the PREDIMED-Plus participants for their enthusiastic collaboration, the PREDIMED-Plus personnel for their outstanding support and the personnel of affiliated primary care centers for their exceptional effort. CIBEROBN, CIBERESP, and CIBERDEM are initiatives of ISCIII, Madrid, Spain. We also thank the PREDIMED-Plus Biobank Network, part of the National Biobank Platform of the ISCIII for storing and managing the PREDIMED-Plus biological samples.

Conflict of interest

Author JS-S reported receiving research support from the Instituto de Salud Carlos III (ISCIII), Ministerio de Educación y Ciencia, Departament de Salut Pública de la Generalitat de Catalunya, the European Commission, the California Walnut Commission, Patrimonio Comunal Olivarero, La Morella Nuts, and Borges S.A; receiving consulting fees or travel expenses from California Walnut Commission, Eroski Foundation, Instituto Danone, Abbott Laboratories and Mundifarma, receiving non-financial support from Hojiblanca, Patrimonio Comunal Olivarero, and Almond Board of California; serving on the board of and receiving grant support through his institution from the International Nut and Dried Foundation and the Eroski Foundation; and grants and personal fees from Instituto Danone. Author ER reported receiving grants, personal fees, and non-financial support from the California Walnut Commission during the conduct of the study and grants, personal fees, non-financial support from Alexion; personal fees from Amarin; and non-financial support from the International Nut Council outside the submitted work. Author RE reported receiving grants from Instituto de Salud Carlos III and olive oil for the trial from Fundacion Patrimonio Comunal Olivarero/during the conduct of the study and personal fees from Brewers of Europe, Fundación Cerveza y Salud, Interprofesional del Aceite de Oliva, Instituto Cervantes, Pernaud Richar, Fundación Dieta Mediterránea, Wine and Culinary International Forum; non-financial support from Sociedad Española de Nutrición and Fundación Bosch y Gimpera; and grants from Uriach Laboratories outside the submitted work. Author XP reported receiving grants from ISCIII during the conduct of the study; receiving consulting fees from Sanofi Aventis, Amgen, and Abbott laboratories; receiving lecture personal fees from Esteve, Lacer and Rubio laboratories.

The remaining 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.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnut.2022.986190/full#supplementary-material

Abbreviations

BMI, Body Mass Index; CKD, Chronic Kidney Disease; CI, Confidence Interval; E, Energy; FFQ, Food Frequency Questionnaire; GFR, Glomerular Filtration Rate; MedDiet, Mediterranean Diet; MetS, Metabolic Syndrome; METS, Metabolic Equivalent Task; NEAP, Net Endogenous Acid Production; PRAL, Potential Renal Acid Load; PREDIMED, Prevención con Dieta Mediterránea; SCr, Serum Creatinine; CKD-EPI, Chronic Kidney Disease Epidemiology Collaboration equation for Caucasian individuals; OR, Odds Ratios; UACR, Urine Albumin/Creatinine Ratio.

References

1. O'Sullivan ED, Hughes J, Ferenbach DA. Renal aging: causes and consequences. J Am Soc Nephrol. (2017) 28:407–20. doi: 10.1681/ASN.2015121308

PubMed Abstract | CrossRef Full Text | Google Scholar

2. GBD Chronic Kidney Disease Collaboration. Global, regional, and national burden of chronic kidney disease, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. (2020) 395:709–33. doi: 10.1016/S0140-6736(20)30045-3

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Levin A, Stevens PE, Bilous RW, Coresh J, De Francisco ALM, De Jong PE et al. Kidney disease: Improving global outcomes (KDIGO) CKD work group. KDIGO 2012 clinical practice guideline for the evaluation and management of chronic kidney disease. Kidney Int Suppl. (2013) 3:1–150. doi: 10.1038/kisup.2012.73

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Levey AS, Eckardt KU, Tsukamoto Y, Levin A, Coresh J, Rossert J, et al. Definition and classification of chronic kidney disease: a position statement from Kidney Disease: Improving Global Outcomes (KDIGO)z. Kidney Int. (2005) 67:2089–100. doi: 10.1111/j.1523-1755.2005.00365.x

PubMed Abstract | CrossRef Full Text | Google Scholar

5. van Westing AC, Küpers LK, Geleijnse JM. Diet and kidney function: a literature review. Curr Hypertens Rep. (2020) 22:1–9. doi: 10.1007/s11906-020-1020-1

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Abbate M, Mascaró CM, Montemayor S, Barbería-Latasa M, Casares M, Gómez C, et al. Energy expenditure improved risk factors associated with renal function loss in nafld and mets patients. Nutrients. (2021) 13:1–24. doi: 10.3390/nu13020629

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Murakami K, Sasaki S, Takahashi Y, Uenishi K, Yamasaki M, Hisatomi Y, et al. Association between dietary acid-base load and cardiometabolic risk factors in young Japanese women. Br J Nutr. (2008) 100:642–51. doi: 10.1017/S0007114508901288

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Frassetto LA, Todd KM, Morris RC, Sebastian A. Estimation of net endogenous noncarbonic acid production in humans from diet potassium and protein contents. Am J Clin Nutr. (1998) 68:576–83. doi: 10.1093/ajcn/68.3.576

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Mofrad MD, Daneshzad E, Azadbakht L. Dietary acid load, kidney function and risk of chronic kidney disease: a systematic review and meta-analysis of observational studies. Int J Vitam Nutr Res. (2021) 91:343–55. doi: 10.1024/0300-9831/a000584

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Bach KE, Kelly JT, Campbell KL, Palmer SC, Khalesi S, Strippoli GFM. Healthy dietary patterns and incidence of CKD: a meta-analysis of cohort studies. Clin J Am Soc Nephrol. (2019) 14:1441–9. doi: 10.2215/CJN.00530119

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Scialla JJ, Anderson CAM. Dietary acid load: a novel nutritional target in chronic kidney disease? Adv Chronic Kidney Dis. (2013) 20:141–9. doi: 10.1053/j.ackd.2012.11.001

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Remer T. Influence of diet on acid-base balance. (2000) 13:221–6. doi: 10.1046/j.1525-139x.2000.00062.x

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Kanda E, Ai M, Kuriyama R, Yoshida M, Shiigai T. Dietary acid intake and kidney disease progression in the elderly. Am J Nephrol. (2014) 39:145–52. doi: 10.1159/000358262

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Mirmiran P, Yuzbashian E, Bahadoran Z, Asghari G, Azizi F. Dietary acid-base load and risk of chronic kidney disease in adults: Tehran lipid and glucose study. Iran J Kidney Dis. (2016) 10:119–25.

PubMed Abstract | Google Scholar

15. Ko BJ, Chang Y, Ryu S, Kim EM, Lee MY, Hyun YY, et al. Dietary acid load and chronic kidney disease in elderly adults: protein and potassium intake. PLoS ONE. (2017) 12:1–10. doi: 10.1371/journal.pone.0185069

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Banerjee T, Tucker K, Griswold M, Wyatt SB, Harman J, Young B, et al. Dietary potential renal acid load and risk of albuminuria and reduced kidney function in the Jackson heart study. J Ren Nutr. (2018) 28:251–8. doi: 10.1053/j.jrn.2017.12.008

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Banerjee T, Crews DC, Wesson DE, Tilea A, Saran R, Rios Burrows N, et al. Dietary acid load and chronic kidney disease among adults in the United States. BMC Nephrol. (2014) 15:1–12. doi: 10.1186/1471-2369-15-137

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Rebholz CM, Coresh J, Grams ME, Steffen LM, Anderson CAM, Appel LJ, et al. Dietary acid load and incident chronic kidney disease: results from the ARIC study. Am J Nephrol. (2015) 42:427–35. doi: 10.1159/000443746

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Scialla JJ, Appel LJ, Astor BC, Miller ER, Beddhu S, Woodward M, et al. Net endogenous acid production is associated with a faster decline in GFR in African Americans. Kidney Int. (2012) 82:106–12. doi: 10.1038/ki.2012.82

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Scialla JJ, Asplin J, Dobre M, Chang A, Lash J, Kallem RR, et al. Higher net acid excretion is associated with lower risk of kidney disease progression in patients with diabetes. Kidney Int. (2018) 91:204–15. doi: 10.1016/j.kint.2016.09.012

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Kabasawa K, Hosojima M, Takachi R, Nakamura K, Ito Y, Saito A, et al. Association of estimated dietary acid load with albuminuria in Japanese adults: a cross-sectional study. BMC Nephrol. (2019) 20:1–10. doi: 10.1186/s12882-019-1352-8

PubMed Abstract | CrossRef Full Text | Google Scholar

22. So R, Song S, Lee JE, Yoon HJ. The association between renal hyperfiltration and the sources of habitual protein intake and dietary acid load in a general population with preserved renal function: the KoGES study. PLoS ONE. (2016) 11:e0166495. doi: 10.1371/journal.pone.0166495

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Alberti KGMM, Eckel RH, Grundy SM, Zimmet PZ, Cleeman JI, Donato KA, et al. Harmonizing the metabolic syndrome: a joint interim statement of the international diabetes federation task force on epidemiology and prevention; National heart, lung, and blood institute; American heart association; World heart federation; International. Circulation. (2009) 120:1640–5. doi: 10.1161/CIRCULATIONAHA.109.192644

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Martínez-González MA, Buil-Cosiales P, Corella D, Bulló M, Fitó M, Vioque J, et al. Cohort profile: design and methods of the PREDIMED-Plus randomized trial. Int J Epidemiol. (2019) 48:387–8o. doi: 10.1093/ije/dyy225

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Willett WC, Howe R, Kushi LH. Adjustment for total energy intake in epidemiologic studies. Am J Clin Nutr. (1997) 65:1220S−8S. doi: 10.1093/ajcn/65.4.1220S

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Fernández-Ballart JD, Piñol JL, Zazpe I, Corella D, Carrasco P, Toledo E, et al. Relative validity of a semi-quantitative food-frequency questionnaire in an elderly Mediterranean population of Spain. Br J Nutr. (2010) 103:1808–16. doi: 10.1017/S0007114509993837

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Moreiras O, Carvajal A, Cabrera L CC. Tablas de composición de alimentos” Food Composition Tables” Pirámide. Madrid: Pirámide (2005).

Google Scholar

28. Mataix Verdú J. Tabla de composición de alimentos [Food Composition Tables]. Granada: Universidad de Granada (2003).

Google Scholar

29. Remer T, Manz F. Potential renal acid load of foods and its influence on urine pH. J Am Diet Assoc. (1995) 95:791–7. doi: 10.1016/S0002-8223(95)00219-7

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Levey AS, Stevens LA, Schmid CH, Zhang Y, Castro AF, Feldman HI, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med. (2009) 150:604–12. doi: 10.7326/0003-4819-150-9-200905050-00006

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Levey AS, Inker LA, Matsushita K, Greene T, Willis K, Lewis E, et al. GFR decline as an end point for clinical trials in CKD: a scientific workshop sponsored by the national kidney foundation and the US food and drug administration. Am J Kidney Dis. (2014) 64:821–35. doi: 10.1053/j.ajkd.2014.07.030

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Schröder H, Zomeño MD, Martínez-González MA, Salas-Salvadó J, Corella D, Vioque J, et al. Validity of the energy-restricted mediterranean diet adherence screener. Clin Nutr. (2021) 40:4971–9. doi: 10.1016/j.clnu.2021.06.030

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Jee Ko G, Obi Y, Tortorici AR, Kalantar-Zadeh K. Dietary protein intake and chronic kidney disease. Curr Opin Clin Nutr Metab Care. (2017) 20:77–85. doi: 10.1097/MCO.0000000000000342

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Cravedi P, Remuzzi G. Pathophysiology of proteinuria and its value as an outcome measure in chronic kidney disease. Br J Clin Pharmacol. (2013) 76:516–23. doi: 10.1111/bcp.12104

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Ng HY, Chen HC, Tsai YC, Yang YK, Lee C Te. Activation of intrarenal renin-angiotensin system during metabolic acidosis. Am J Nephrol. (2011) 34:55–63. doi: 10.1159/000328742

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Remuzzi G, Perico N, Macia M, Ruggenenti P. The role of renin-angiotensin-aldosterone system in the progression of chronic kidney disease. Kidney Int. (2005) 68:57–65. doi: 10.1111/j.1523-1755.2005.09911.x

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Khanna A, Simoni J, Hacker C, Duran MJ, Wesson DE. Increased endothelin activity mediates augmented distal nephron acidification induced by dietary protein. J Am Soc Nephrol. (2004) 15:2266–2275. doi: 10.1097/01.ASN.0000138233.78329.4E

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Wesson DE, Simoni J, Broglio K, Sheather S. Acid retention accompanies reduced GFR in humans and increases plasma levels of endothelin and aldosterone. Am J Physiol Ren Physiol. (2011) 300:830–7. doi: 10.1152/ajprenal.00587.2010

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Phisitkul S, Khanna A, Simoni J, Broglio K, Sheather S, Rajab MH, et al. Amelioration of metabolic acidosis in patients with low GFR reduced kidney endothelin production and kidney injury, and better preserved GFR. Kidney Int. (2010) 77:617–23. doi: 10.1038/ki.2009.519

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Nath KA, Hostetter MK, Hostetter TH. Increased ammoniagenesis as a determinant of progressive renal injury. Am J Kidney Dis. (1991) 17:654–7. doi: 10.1016/S0272-6386(12)80344-1

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Nath KA, Hostetter MK, Hostetter TH. Pathophysiology of chronic tubulo-interstitial disease in rats. J Clin Investig. (1985) 76:667–75. doi: 10.1172/JCI112020

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Nagami GT, Hamm LL. Regulation of acid-base balance in chronic kidney disease. Adv Chronic Kidney Dis. (2017) 24:274–9. doi: 10.1053/j.ackd.2017.07.004

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Irazabal M, Torres V. ROS and redox signaling in chronic kidney disease. Ann Intern Med. (2020) 162:ITC1–ITC14. doi: 10.7326/AITC201506020

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Katholi RE, Woods WT, Taylor GJ, Deitrick CL, Womack KA, Katholi CR, et al. Oxygen free radicals and contrast nephropathy. Am J Kidney Dis. (1998) 32:64–71. doi: 10.1053/ajkd.1998.v32.pm9669426

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Lew QLJ, Jafar TH, Koh HWL, Jin A, Chow KY, Yuan JM, et al. Red meat intake and risk of ESRD. J Am Soc Nephrol. (2017) 28:304–12. doi: 10.1681/ASN.2016030248

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Karalius VP, Shoham DA. Dietary sugar and artificial sweetener intake and chronic kidney disease: a review. Adv Chronic Kidney Dis. (2013) 20:157–64. doi: 10.1053/j.ackd.2012.12.005

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Chiavaroli L, Mirrahimi A, Sievenpiper JL, Jenkins DJA, Darling PB. Dietary fiber effects in chronic kidney disease: a systematic review and meta-analysis of controlled feeding trials. Eur J Clin Nutr. (2015) 69:761–8. doi: 10.1038/ejcn.2014.237

PubMed Abstract | CrossRef Full Text | Google Scholar