Efficacy and safety of a low-sodium diet and spironolactone in patients with stage 1-3a chronic kidney disease: a pilot study

Chronic kidney disease (CKD) incidence is growing worldwide. The USRDS in 2018 revealed that CKD prevalence in adults reached 14.8% in 2013–2016 [1]. An epidemiological survey in China in 2012 indicated a CKD prevalence of 10.8% in adults over 18 years old [2]. For patients with CKD, early intervention is of great importance in controlling CKD progression and reducing mortality.

High salt intake is closely associated with the progression of CKD. When the urine sodium-to-creatinine ratio increases by 100 mmol/L, the risk of CKD developing into end-stage renal disease (ESRD) increases by 1.61 times [3, 4]. High salt intake leads to renal impairment in various ways, including increasing transforming growth factor (TGF)-β1 production and enhancing oxidative stress and inflammatory response in the kidney [5‐7]. Salt restriction reduces the effects of the above adverse factors, protecting the kidney and enhancing the antiproteinuric and antihypertensive effects of the renin-angiotensin-aldosterone system (RAAS) antagonists such as angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs) [8, 9]. Heeg et al. [9] found that the effectiveness of the ACEI lisinopril in reducing albuminuria greatly depends on dietary sodium intake. The ACEI could not decrease albuminuria when sodium intake from food increased from 50 to 200 mmol/d, while the decreasing effect of the ACEI on albuminuria recovered accordingly when sodium intake was reduced back to 50 mmol/d. Vogt et al. [10] showed that proteinuria was reduced by 30% with losartan monotherapy alone. The reduction increased to 55% with the addition of salt restriction and to 56% with the addition of hydrochlorothiazide (HCT). The enhancing effects of salt restriction on ARB activity appeared similar to the addition of diuretics. Slagman et al. [11] reported that moderate dietary sodium restriction is more effective than the maximal dose of angiotensin receptor blocker in controlling proteinuria and blood pressure in patients with renal disease on a maximal dose of ACEI.

Aldosterone is a steroid hormone with mineralocorticoid activity. Historically, aldosterone has been shown to act mainly on the distal convoluted tubules of the kidney, regulating extracellular fluid capacity and potassium metabolism. However, in the past 20 years, studies have revealed an extensive role played by aldosterone [12‐16]. Mounting evidence has been observed that aldosterone could affect the heart, blood vessels, the central nervous system, and the kidney, promoting vascular remodeling, collagen formation, and endothelial dysfunction [15, 16]. These interactions play important roles in the pathophysiology of progressive renal dysfunction. Moreover, aldosterone/mineralocorticoid receptor (MR) could also damage podocytes. The enhanced MR effect is closely associated with protein leakage in the kidney [17‐20], leading to CKD progression. With these new insights, mineralocorticoid receptor antagonists (MRAs) as a new treatment strategy are of particular interest. The discovery of the “aldosterone escape” phenomenon has made MRAs even more attractive for the treatment of CKD [21]. Multiple studies have evaluated the effects of MRAs on blood pressure control and proteinuria reduction, as well as their possible role in delaying the progression of CKD [14, 22, 23].

Aldosterone has been recognized as an independent risk factor mediating renal injury. However, another important parameter, sodium intake, cannot be ignored. More than 70 years ago, a pioneering study by Hans Selye showed that when desoxycorticosterone acetate (DOCA) is used in a rodent model of partial nephrectomy, improper salt intake (3% saltwater) is required for inducing significant vasculitis changes in the heart and kidney [24]. A study of Dahl salt-sensitive rats also showed that high salt could induce oxidative stress and promote MR activation in the kidney [20]. These studies helped to understand the pathogenesis of MR-induced renal injury and establish reasonable treatment plans in CKD. Relevant research data also demonstrated that salt intake could affect the balance of beneficial and adverse effects of aldosterone [25]. In case of improper salt intake, acute administration of aldosterone reduces the levels of phosphorylated extracellular nitric oxide synthase (eNOS; vascular protection), increases the amounts of phosphorylated extracellular signal-regulated kinases 1 and 2 (ERK1/2) and protein kinase C (adverse to blood vessels). Conversely, salt intake reduction increases phosphorylated eNOS levels, reduces ERK1/2 and protein kinase C amounts, and minimizes or reverses the response to acute aldosterone administration. Plasma aldosterone levels unsuitable for intake of diet salt would amplify the above phenomenon. Hattori et al. [26] found that under low-salt conditions, MRA can completely suppress the expression of RAS-related genes in the myocardium of rats, alleviate myocardial oxidative stress and inflammatory response, and delay myocardial hypertrophy and fibrosis; meanwhile, MRA is only partly effective under high-salt conditions.

Based on the above, salt restriction is not only beneficial for renal protection but also can enhance the proteinuria-reducing effect of ACEI/ARB while alleviating aldosterone-associated renal damage. So far, the main treatment delaying CKD progression and reducing the risk of end-stage renal disease is RAAS antagonists, including ACEI and ARB medications, as well as direct renin inhibitors. These medications are the current standard treatment options for CKD patients with proteinuria [27‐31]. However, these medications only decrease the risk of proteinuria and ESRD by 20–30%. Additional new therapies are needed given the huge cost burden of CKD as well as the associated physiological and psychological damage to patients [32, 33]. Therefore, this study aims to investigate the renal protective effects and safety of a low-sodium diet combined with an MRA, spironolactone (SPL), in patients with stage 1-3a CKD.

The key observations of this study are as follows. First, no further benefit exists from the addition of SPL in patients with a low sodium diet (3.0 g/d salt). Second, small doses of SPL may benefit patients with poor sodium restriction.

Few clinical studies have assessed the relationship between salt intake and MRA administration, and a literature review found no related randomized controlled trials. A post hoc analysis of MRA efficacy stratified by urinary sodium excretion of the Eplerenone Combination Versus Conventional Agents to Lower Blood Pressure on Urinary Antialbuminuric Treatment Effect (EVALUATE) trial was recently conducted [35]. In this study, the population included patients with CKD and hypertension but without diabetes, and the basic treatment was ACEI and/or ARB. The results showed that eplerenone-treated patients in the highest sodium excretion tertile exhibited significantly greater reduction in urinary albumin to creatinine ratio (UACR) compared with the placebo subjects in the same tertile (− 22.5% vs. + 21.8%, p = 0.02). While this disparity was not observed neither in the lowest tertile (− 10.2% vs. -0.84%, p = 0.65) nor in the middle tertile (− 19.5% vs. + 9.5%, p = 0.22). These authors concluded that the therapeutic effect of MRA is related to salt intake. In patients with high urinary sodium, the antiproteinuric effect of MRA was more significant than that of a placebo, while in patients with low urinary sodium, the antiproteinuric effect was not significantly different [35]. This conclusion corroborated our findings. The possible mechanism is as follows. Salt loading could enhance the renal MR activation pathway by activating Rac1 without increasing circulating aldosterone, causing hypertension and renal damage; meanwhile, MRA blocks this pathway, inhibits high-salt intake associated renal injury, overcomes salt-associated resistance to routine RAS blockade treatment, and plays a role of renal protection [36]. Similar results have been found in patients with refractory hypertension. The higher the salt intake level, the greater the blood pressure response to SPL treatment, suggesting that MRA could antagonize the increase of blood pressure caused by high salt intake [37].

As a simple and cost-effective treatment, dietary salt restriction delays CKD progression. However, patients with CKD show poor adherence to a low-salt diet in their daily life. Data showed that average 24 h urine sodium excretion in patients with CKD ranges between 144 and 200 mmol/d [3, 38‐41]. It is challenging to achieve salt restriction even in clinical trials. Average daily salt consumption is 9–13 g/d in reported CKD clinical studies up to now [42]. Adding SPL to the treatment regimen may be a potential new strategy in patients with CKD that are unable to achieve the ideal salt restriction goal.

Hyperkalemia is the main adverse side effect in patients taking MRA, especially in combination with ACEI and/or ARB. Previous studies have shown that the risk of hyperkalemia after treatment with MRA combined with ACEI and/or ARB is elevated compared with ACEI and/or ARB alone [22, 23, 43‐46]. Epstein et al. carefully evaluated hyperkalemia incidence in 268 patients, and blood potassium levels showed no significant change in MRA combined with ACEI compared to ACEI alone [47]. During the 12 week intervention period in this study, there was no hyperkalemia in medium-sodium+SPL and low-sodium+SPL groups. Even in patients with ESRD, previous research has suggested that treatment is safe provided that the medication indication is accurate and strict monitoring parameters are applied [48].

Gynecomastia resulting from the combination of aldosterone with androgen and progesterone receptors is often reported as a side effect of SPL, thereby limiting its clinical usefulness. In the RALES study, gynecomastia incidence in patients treated with SPL was 9% versus 1% in the placebo arm [49]. The use of the selective MRA EPL could reduce these risks and other side effects [50]. In addition, finerenone, a nonsteroidal, selective mineralocorticoid receptor antagonist, reduced the risks of CKD progression and cardiovascular events in patients with CKD and type 2 diabetes compared with placebo in the FIDELIO-DKD trial; meanwhile, the overall rates of adverse events were similar in both groups [51]. In this study, the non-selective MRA SPL was administered at 20 mg/day, and no significant adverse events were found in the medium-sodium+SPL and low-sodium+SPL groups throughout the study.

Several limitations in this clinical trial are noted as follows. First, although this was a prospective, randomized controlled study (medication administration was performed in a blinded manner), salt intake could not be blinded. Secondly, based on ethical principles, a high salt group (oral salt tablet) was not established in this study due to the proven high salt-associated renal damage. Thirdly, low-dose ARB was administered to most patients, and the independent effect of salt restriction alone or salt restriction combined with MRA could not be explained. Fourthly, this was a single-center pilot study, with a relatively small sample size, relatively normal kidney function, and short follow-up, which limited the evaluation of the efficacy and long-term safety profile. Fifthly, long-term data for various endpoints were not obtained. Based on these limitations, larger multicenter clinical trials with longer follow-up are required to further evaluate the effects and safety of sodium restriction and MRAs.

Under low sodium intake conditions, ARB combined with SPL has no additional benefits on lowering urine protein compared with ARB alone. It is unnecessary to add on SPL for patients with satisfying sodium restriction, thus avoiding the adverse events of SPL. In patients with poor sodium restriction, supplementation of low-dose SPL might show a therapeutic benefit on lowering 24-h urine protein. The combination of short-term low-dose SPL and ARB is safe in patients with stage 1-3a CKD, but blood potassium must be carefully monitored.