4.7 Article

RAASi Therapy Attenuates the Association between 24-h Urinary Potassium Excretion and Dietary Potassium Intake in CKD Patients

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NUTRIENTS
卷 15, 期 11, 页码 -

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MDPI
DOI: 10.3390/nu15112454

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diet; RAAS inhibitors; CKD; potassium; urine potassium

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The study aimed to assess the use of urinary potassium excretion as an indicator of dietary potassium intake in CKD patients with or without RAAS inhibitor therapy. A cohort of 138 CKD patients participated in the study, and there were no significant differences in dietary intakes, blood biochemistry, and urine excretion parameters between patients with or without RAAS inhibitor therapy. Urinary potassium showed a weak correlation with eGFR and dietary potassium intake, while serum potassium was inversely correlated with eGFR. In patients receiving RAAS inhibitor therapy, the correlation between urinary potassium excretion and dietary potassium intake was reduced.
The aim of this study was to evaluate urinary potassium (K) excretion as a reliable marker of dietary K intake, in a cohort of CKD patients with or without Renin-Angiotensin-Aldosterone System (RAAS) inhibitor therapy. One hundred and thirty-eight consecutive out-patients (51 f and 87 m) aged 60 +/- 13 years and affected by CKD stage 3-4, who were metabolically and nutritionally stable, entered the study between November 2021 and October 2022. No difference was observed between patients with (n = 85) or without (n = 53) RAAS inhibitor therapy, regarding dietary intakes, blood biochemistry, and 24-h urine excretion parameters. Considering all patients, urinary K showed a weak relationship with eGFR (r = 0.243, p < 0.01), and with dietary K intake (r = 0.184, p < 0.05). Serum K was not associated with dietary K intake, but an inverse relationship was observed with eGFR (r = -0.269, p < 0.01). When patients were examined depending on whether they were receiving RAAS inhibitor therapy, the weak inverse relationship between serum K and eGFR was maintained in both groups. Conversely, urinary K excretion remained positively associated with dietary K intake only in the no RAAS inhibitor group. In conclusion, 24-h urine K excretion may be used as a surrogate of K intake, but RAAS inhibitor therapy reduces the association between 24-h urine K excretion and dietary K intake in CKD patients.

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