Safety and efficacy of salt substitution with a low sodium-potassium enriched dietary salt in patients with heart failure with reduced ejection fraction: A pilot study

被引:17
作者
Bistola, Vasiliki [1 ]
Arfaras-Melainis, Angelos [1 ]
Trogkanis, Efstratios [2 ]
Bakosis, Georgios [1 ]
Polyzogopoulou, Eftihia [3 ]
Karavidas, Ioannis-Nektarios [2 ]
Ikonomidis, Ignatios [1 ]
Parissis, John [1 ]
Karavidas, Apostolos [2 ]
机构
[1] Natl & Kapodistrian Univ Athens, Attikon Univ Hosp, Dept Cardiol, Heart Failure Unit, Athens, Greece
[2] Gennimatas Gen Hosp, Gen Hosp Dept Cardiol, Cardiol Clin, Athens, Greece
[3] Natl & Kapodistrian Univ Athens, Attikon Univ Hosp, Emergency Med Dept, Athens, Greece
关键词
Heart failure with reduced ejection fraction; Low sodium salt substitute; Safety; Exercise capacity; BLOOD-PRESSURE; RESTRICTION; GUIDELINES; MORTALITY; OUTCOMES;
D O I
10.1016/j.clnesp.2019.11.004
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background and aims: Increased sodium intake is associated with increased risk of decompensation in patients with heart failure. This non-randomized, open-label, controlled study aimed to examine the feasibility, preliminary safety and efficacy of a low sodium-potassium enriched salt substitute compared to regular table salt in patients with heart failure with reduced ejection fraction (HFREF). Methods: Fifty patients (68% male, NYHA I/II/III 6%/68%/26%, mean age 70 +/- 9 years, LVEF 31 +/- 5%, median BNP 112 pg/ml) were included. Of these, 30 patients received the salt substitute (maximum consumption of 2 g daily), who were prospectively compared to a control group of 20 age/sex/NYHA class-matched HFREF patients who consumed regular salt (maximum consumption of 2 g daily). Consumption of regular salt was prohibited in the salt substitution group. All patients were followed for 12 weeks. Results: Patient groups did not differ by sex, age, LVEF, NYHA class, 6MWD, and BNP at baseline. In primary safety analysis, no significant differences were detected between groups regarding SBP (p = 0.052), DBP (p = 0.159), HR (p = 0.246), serum potassium (p = 0.579), serum sodium (p = 0.125), and eGFR (p = 0.710) throughout the 12 weeks. Secondary efficacy analysis revealed a statistically significant difference in 6MWD at 12 weeks between the salt substitute and regular salt groups after adjustment for baseline 6MWD (mean difference +/- SEM, 4.7 +/- 2.1 m, F = 4.92, p = 0.031). Conclusions: In this pilot study, a low sodium-potassium enriched salt substitute was found to be safe compared to regular salt in HFREF patients, while it resulted in a small albeit significant improvement in exercise capacity, possibly justifying further investigation with randomized clinical studies. (c) 2019 European Society for Clinical Nutrition and Metabolism. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:90 / 94
页数:5
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