Kaliuresis and Intracellular Uptake of Potassium with Potassium Citrate and Potassium Chloride Supplements A Randomized Controlled Trial

被引:1
|
作者
Wouda, Rosa D. [1 ]
Gritter, Martin [2 ]
Karsten, Micky [1 ]
Michels, Erik H. A. [1 ]
Nieuweboer, Tamar M. [1 ]
Danser, A. H. Jan [3 ]
de Borst, Martin H. [4 ]
Hoorn, Ewout J. [2 ]
Rotmans, Joris I. [5 ]
Vogt, Liffert [1 ,6 ]
机构
[1] Univ Amsterdam, Dept Internal Med, Sect Nephrol, Amsterdam Cardiovasc Sci,Med Ctr, Amsterdam, Netherlands
[2] Erasmus MC, Dept Internal Med, Div Nephrol & Transplantat, Rotterdam, Netherlands
[3] Univ Med Ctr Rotterdam, Erasmus Med Ctr, Dept Internal Med, Vasc Med & Pharmacol, Rotterdam, Netherlands
[4] Univ Med Ctr Groningen, Div Nephrol, Dept Internal Med, Groningen, Netherlands
[5] Leiden Univ, Dept Internal Med, Div Nephrol, Med Ctr, Leiden, Netherlands
[6] Univ Amsterdam, Dept Internal Med, Sect Nephrol, Amsterdam UMC,Amsterdam Cardiovasc Sci, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
关键词
ACE inhibitors; acidosis; clinical trial; electrolytes; potassium (K) channels; renin-angiotensin system; fluid; electrolyte; and acid-base disorders; ELECTROLYTE DISORDERS; DISTAL NEPHRON; URINARY SODIUM; PH-DEPENDENCE; K-ATPASE; EXCRETION; TRANSPORT; ALDOSTERONE; LOCALIZATION; MODULATION;
D O I
10.2215/CJN.0000000000000228
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background A potassium replete diet is associated with lower cardiovascular risk but may increase the risk of hyperkalemia, particularly in people using renin-angiotensin-aldosterone system inhibitors. We investigated whether intracellular uptake and potassium excretion after an acute oral potassium load depend on the accompanying anion and/or aldosterone and whether this results in altered plasma potassium change. Methods In this placebo-controlled interventional cross-over trial including 18 healthy individuals, we studied the acute effects of one oral load of potassium citrate (40 mmol), potassium chloride (40 mmol), and placebo in random order after overnight fasting. Supplements were administered after a 6-week period with and without lisinopril pretreatment. Linear mixed effect models were used to compare blood and urine values before and after supplementation and between the interventions. Univariable linear regression was used to determine the association between baseline variables and change in blood and urine values after supplementation. Results During the 4-hour follow-up, the rise in plasma potassium was similar for all interventions. After potassium citrate, both red blood cell potassium-as measure of the intracellular potassium-and transtubular potassium gradient (TTKG)-reflecting potassium secretory capacity-were higher than after potassium chloride or potassium citrate with lisinopril pretreatment. Baseline aldosterone was significantly associated with TTKG after potassium citrate, but not after potassium chloride or potassium citrate with lisinopril pretreatment. The observed TTKG change after potassium citrate was significantly associated with urine pH change during this intervention (R50.60, P, 0.001). Conclusions With similar plasma potassium increase, red blood cell potassium uptake and kaliuresis were higher after an acute load of potassium citrate as compared with potassium chloride alone or pretreatment with lisinopril.
引用
收藏
页码:1260 / 1271
页数:12
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