Abstract

BackgroundAldosterone is elevated in chronic kidney disease (CKD) and may be involved in hypertension. Surprisingly, the determinants of the plasma aldosterone concentration (PAC) and its role in hypertension are not well studied in CKD. Therefore, we studied the determinants of aldosterone and its association with blood pressure in CKD patients. We also studied this during renin-angiotensin-aldosterone system inhibition (RAASi) to establish clinical relevance, as RAASi is the treatment of choice in CKD with albuminuria.MethodsWe performed a post-hoc analysis on data from a randomized controlled double blind cross-over trial in non-diabetic CKD patients (n = 33, creatinine clearance (CrCl) 85 (75–95) ml/min, proteinuria 3.2 (2.5–4.0) g/day). Patients were treated with losartan 100 mg (ARB), and ARB + hydrochlorothiazide 25 mg (HCT), during both a regular (200 ± 10 mmol Na+/day) and low (89 ± 8 mmol Na+/day) dietary sodium intake, in 6-week study periods. PAC data at the end of each study period were analyzed. The association between PAC and blood pressure was analyzed continuously, and according to PAC above or below the median.ResultsLower CrCl was correlated with higher PAC during placebo as well as during ARB (β = −1.213, P = 0.008 and β = −1.090, P = 0.010). Higher PAC was not explained by high renin, illustrated by a comparable association between CrCl and the aldosterone-to-renin ratio. The association between lower CrCl and higher PAC was also found in a second study with single RAASi with ACE inhibition (ACEi; lisinopril 40 mg/day), and dual RAASi (lisinopril 40 mg/day + valsartan 320 mg/day). Higher PAC was associated with a higher systolic blood pressure (P = 0.010) during different study periods. Only during maximal treatment with ARB + HCT + dietary sodium restriction, blood pressure was no longer different in subjects with a PAC above and below the median.ConclusionsIn CKD patients with a standardized regular sodium intake, worse renal function is associated with a higher aldosterone, untreated and during RAASi with either ARB, ACEi, or both. Furthermore, higher aldosterone is associated with higher blood pressure, which can be treated with the combination of RAASi, HCT and dietary sodium restriction.The first study was performed before it was standard to register trials and the study was not retrospectively registered. The second study was registered in the Netherlands Trial Register on the 5th of May 2006 (NTR675).

Highlights

  • Aldosterone is elevated in chronic kidney disease (CKD) and may be involved in hypertension

  • Systolic blood pressure dropped stepwise with the lowest value on Angiotensin II receptor blocker (ARB) + hydrochlorothiazide mg (HCT) + low dietary sodium intake (LS), whereas diastolic blood pressure was lowest on ARB + HCT on either sodium intake

  • We show for the first time that in CKD, high aldosterone levels are associated with higher blood pressure, even despite RAAS inhibition (RAASi)

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Summary

Introduction

Aldosterone is elevated in chronic kidney disease (CKD) and may be involved in hypertension. The determinants of the plasma aldosterone concentration (PAC) and its role in hypertension are not well studied in CKD. We studied the determinants of aldosterone and its association with blood pressure in CKD patients. We studied this during renin-angiotensin-aldosterone system inhibition (RAASi) to establish clinical relevance, as RAASi is the treatment of choice in CKD with albuminuria. Aldosterone is involved in sodium and volume homeostasis, and regulation of extracellular volume and blood pressure It has a main role in the homeostatic response to volume depletion, where higher aldosterone levels contribute to renal retention of sodium and water, and followingly restoration of the extracellular volume. Whether RAAS inhibition (RAASi) ameliorates the high aldosterone levels associated with CKD, has not been systemically assessed

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