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用低钠盐替代物(LSSS)代替盐以促进成年人、儿童和孕妇的心血管健康。

Replacing salt with low-sodium salt substitutes (LSSS) for cardiovascular health in adults, children and pregnant women.

机构信息

Centre for Evidence-based Health Care, Division of Epidemiology and Biostatistics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.

出版信息

Cochrane Database Syst Rev. 2022 Aug 10;8(8):CD015207. doi: 10.1002/14651858.CD015207.

Abstract

BACKGROUND

Elevated blood pressure, or hypertension, is the leading cause of preventable deaths globally. Diets high in sodium (predominantly sodium chloride) and low in potassium contribute to elevated blood pressure. The WHO recommends decreasing mean population sodium intake through effective and safe strategies to reduce hypertension and its associated disease burden. Incorporating low-sodium salt substitutes (LSSS) into population strategies has increasingly been recognised as a possible sodium reduction strategy, particularly in populations where a substantial proportion of overall sodium intake comes from discretionary salt. The LSSS contain lower concentrations of sodium through its displacement with potassium predominantly, or other minerals. Potassium-containing LSSS can potentially simultaneously decrease sodium intake and increase potassium intake.  Benefits of LSSS include their potential blood pressure-lowering effect and relatively low cost. However, there are concerns about potential adverse effects of LSSS, such as hyperkalaemia, particularly in people at risk, for example, those with chronic kidney disease (CKD) or taking medications that impair potassium excretion.

OBJECTIVES

To assess the effects and safety of replacing salt with LSSS to reduce sodium intake on cardiovascular health in adults, pregnant women and children.

SEARCH METHODS

We searched MEDLINE (PubMed), Embase (Ovid), Cochrane Central Register of Controlled Trials (CENTRAL), Web of Science Core Collection (Clarivate Analytics), Cumulative Index to Nursing and Allied Health Literature (CINAHL, EBSCOhost), ClinicalTrials.gov and WHO International Clinical Trials Registry Platform (ICTRP) up to 18 August 2021, and screened reference lists of included trials and relevant systematic reviews. No language or publication restrictions were applied.

SELECTION CRITERIA

We included randomised controlled trials (RCTs) and prospective analytical cohort studies in participants of any age in the general population, from any setting in any country. This included participants with non-communicable diseases and those taking medications that impair potassium excretion. Studies had to compare any type and method of implementation of LSSS with the use of regular salt, or no active intervention, at an individual, household or community level, for any duration.

DATA COLLECTION AND ANALYSIS

Two review authors independently screened titles, abstracts and full-text articles to determine eligibility; and extracted data, assessed risk of bias (RoB) using the Cochrane RoB tool, and assessed the certainty of the evidence using GRADE. We stratified analyses by adults, children (≤ 18 years) and pregnant women. Primary effectiveness outcomes were change in diastolic and systolic blood pressure (DBP and SBP), hypertension and blood pressure control; cardiovascular events and cardiovascular mortality were additionally assessed as primary effectiveness outcomes in adults. Primary safety outcomes were change in blood potassium, hyperkalaemia and hypokalaemia.

MAIN RESULTS

We included 26 RCTs, 16 randomising individual participants and 10 randomising clusters (families, households or villages). A total of 34,961 adult participants and 92 children were randomised to either LSSS or regular salt, with the smallest trial including 10 and the largest including 20,995 participants. No studies in pregnant women were identified. Studies included only participants with hypertension (11/26), normal blood pressure (1/26), pre-hypertension (1/26), or participants with and without hypertension (11/26). This was unknown in the remaining studies. The largest study included only participants with an elevated risk of stroke at baseline. Seven studies included adult participants possibly at risk of hyperkalaemia. All 26 trials specifically excluded participants in whom an increased potassium intake is known to be potentially harmful. The majority of trials were conducted in rural or suburban settings, with more than half (14/26) conducted in low- and middle-income countries. The proportion of sodium chloride replacement in the LSSS interventions varied from approximately 3% to 77%. The majority of trials (23/26) investigated LSSS where potassium-containing salts were used to substitute sodium. In most trials, LSSS implementation was discretionary (22/26). Trial duration ranged from two months to nearly five years.  We assessed the overall risk of bias as high in six trials and unclear in 12 trials. LSSS compared to regular salt in adults: LSSS compared to regular salt probably reduce DBP on average (mean difference (MD) -2.43 mmHg, 95% confidence interval (CI) -3.50 to -1.36; 20,830 participants, 19 RCTs, moderate-certainty evidence) and SBP (MD -4.76 mmHg, 95% CI -6.01 to -3.50; 21,414 participants, 20 RCTs, moderate-certainty evidence) slightly.  On average, LSSS probably reduce non-fatal stroke (absolute effect (AE) 20 fewer/100,000 person-years, 95% CI -40 to 2; 21,250 participants, 3 RCTs, moderate-certainty evidence), non-fatal acute coronary syndrome (AE 150 fewer/100,000 person-years, 95% CI -250 to -30; 20,995 participants, 1 RCT, moderate-certainty evidence) and cardiovascular mortality (AE 180 fewer/100,000 person-years, 95% CI -310 to 0; 23,200 participants, 3 RCTs, moderate-certainty evidence) slightly, and probably increase blood potassium slightly (MD 0.12 mmol/L, 95% CI 0.07 to 0.18; 784 participants, 6 RCTs, moderate-certainty evidence), compared to regular salt.  LSSS may result in little to no difference, on average, in hypertension (AE 17 fewer/1000, 95% CI -58 to 17; 2566 participants, 1 RCT, low-certainty evidence) and hyperkalaemia (AE 4 more/100,000, 95% CI -47 to 121; 22,849 participants, 5 RCTs, moderate-certainty evidence) compared to regular salt. The evidence is very uncertain about the effects of LSSS on blood pressure control, various cardiovascular events, stroke mortality, hypokalaemia, and other adverse events (very-low certainty evidence). LSSS compared to regular salt in children: The evidence is very uncertain about the effects of LSSS on DBP and SBP in children. We found no evidence about the effects of LSSS on hypertension, blood pressure control, blood potassium, hyperkalaemia and hypokalaemia in children.

AUTHORS' CONCLUSIONS: When compared to regular salt, LSSS probably reduce blood pressure, non-fatal cardiovascular events and cardiovascular mortality slightly in adults. However, LSSS also probably increase blood potassium slightly in adults. These small effects may be important when LSSS interventions are implemented at the population level. Evidence is limited for adults without elevated blood pressure, and there is a lack of evidence in pregnant women and people in whom an increased potassium intake is known to be potentially harmful, limiting conclusions on the safety of LSSS in the general population. We also cannot draw firm conclusions about effects of non-discretionary LSSS implementations. The evidence is very uncertain about the effects of LSSS on blood pressure in children.

摘要

背景

高血压是全球可预防死亡的主要原因。高钠(主要是氯化钠)和低钾的饮食会导致血压升高。世卫组织建议通过有效和安全的策略来减少平均人口的钠摄入量,以降低高血压及其相关疾病负担。将低钠盐替代品(LSSS)纳入人群策略已越来越被认为是一种可能的减钠策略,特别是在相当一部分总钠摄入量来自随意摄入盐的人群中。LSSS 通过主要用钾或其他矿物质替代其含钠量,从而降低其钠浓度。含钾的 LSSS 可以同时降低钠的摄入量并增加钾的摄入量。LSSS 的益处包括其潜在的降压作用和相对较低的成本。然而,人们对 LSSS 的潜在不良反应存在担忧,例如高钾血症,特别是在有风险的人群中,例如患有慢性肾脏病(CKD)或正在服用影响钾排泄的药物的人群。

目的

评估用 LSSS 替代盐以减少钠摄入量对成年人、孕妇和儿童心血管健康的影响和安全性。

检索方法

我们检索了 MEDLINE(PubMed)、Embase(Ovid)、Cochrane 对照试验中心注册库(CENTRAL)、Web of Science 核心合集(Clarivate Analytics)、护理与联合健康文献累积索引(CINAHL,EBSCOhost)、临床试验.gov 和世卫组织国际临床试验注册平台(ICTRP),截至 2021 年 8 月 18 日,并筛选了纳入试验的参考文献列表和相关系统评价。未对语言或出版情况进行任何限制。

选择标准

我们纳入了任何年龄的一般人群中的参与者、任何设置的任何国家的参与者的随机对照试验(RCT)和前瞻性分析队列研究。这包括患有非传染性疾病和正在服用影响钾排泄药物的参与者。研究必须比较任何类型和实施方法的 LSSS 与常规盐的使用,或在个体、家庭或社区层面上不进行任何积极干预,持续任何时间。

数据收集和分析

两名综述作者独立筛选标题、摘要和全文文章以确定合格性;并提取数据、使用 Cochrane 偏倚风险工具评估偏倚风险(RoB),并使用 GRADE 评估证据的确定性。我们按成年人、儿童(≤ 18 岁)和孕妇进行分层分析。主要有效性结果是舒张压和收缩压(DBP 和 SBP)、高血压和血压控制的变化;心血管事件和心血管死亡率也是成年人的主要有效性结果。主要安全性结果是血钾变化、高钾血症和低钾血症。

主要结果

我们纳入了 26 项 RCT,其中 16 项随机分配个体参与者,10 项随机分配集群(家庭、家庭或村庄)。共有 34961 名成年参与者和 92 名儿童被随机分配到 LSSS 或常规盐组,最小的试验纳入了 10 名参与者,最大的试验纳入了 20995 名参与者。未发现孕妇的研究。研究仅包括高血压(11/26)、正常血压(1/26)、前期高血压(1/26)或高血压和无高血压(11/26)的参与者。在其余的研究中,这是未知的。最大的研究仅包括基线时中风风险升高的参与者。有 7 项研究包括可能有高钾血症风险的成年参与者。所有 26 项试验均特别排除了已知增加钾摄入可能有害的参与者。大多数试验是在农村或郊区环境中进行的,超过一半(14/26)是在中低收入国家进行的。LSSS 干预措施中的氯化钠替代比例从大约 3%到 77%不等。大多数试验(23/26)研究了使用含钾盐替代钠的 LSSS。在大多数试验中,LSSS 的实施是随意的(22/26)。试验持续时间从两个月到近五年不等。我们评估了六项试验的总体风险偏倚高,十二项试验的风险偏倚不确定。LSSS 与常规盐相比,LSSS 可能会使成年人的 DBP 平均降低(平均差值(MD)-2.43mmHg,95%置信区间(CI)-3.50 至-1.36;20830 名参与者,19 项 RCT,中等确定性证据)和 SBP(MD-4.76mmHg,95% CI-6.01 至-3.50;21414 名参与者,20 项 RCT,中等确定性证据)。平均而言,LSSS 可能会使非致命性中风(每 100000 人年的绝对效果(AE)减少 20 例,95%CI-40 至 2;21250 名参与者,3 项 RCT,中等确定性证据)、非致命性急性冠状动脉综合征(AE 减少 150 例/100000 人年,95%CI-250 至-30;20995 名参与者,1 项 RCT,中等确定性证据)和心血管死亡率(AE 减少 180 例/100000 人年,95%CI-310 至 0;23200 名参与者,3 项 RCT,中等确定性证据)略有减少,并且可能会使血钾略有升高(MD 0.12mmol/L,95%CI 0.07 至 0.18;784 名参与者,6 项 RCT,中等确定性证据),与常规盐相比。与常规盐相比,LSSS 可能在高血压(AE 减少 17 例/1000,95%CI-58 至 17;2566 名参与者,1 项 RCT,低确定性证据)和高钾血症(AE 增加 4 例/100000,95%CI-47 至 121;22849 名参与者,5 项 RCT,中等确定性证据)方面几乎没有差异。关于 LSSS 对血压控制、各种心血管事件、中风死亡率、低钾血症和其他不良反应的影响的证据非常不确定(极低确定性证据)。LSSS 与常规盐相比,儿童:LSSS 对儿童 DBP 和 SBP 的影响的证据非常不确定。我们没有发现关于 LSSS 对高血压、血压控制、血钾、高钾血症和低钾血症的影响的证据。

作者的结论

与常规盐相比,LSSS 可能会使成年人的血压、非致命性心血管事件和心血管死亡率略有降低。然而,LSSS 也可能会使成年人的血钾略有升高。这些小的影响在 LSSS 干预措施在人群层面实施时可能很重要。对于没有高血压的成年人,证据有限,对于已知增加钾摄入可能有害的成年人和孕妇,限制了 LSSS 在一般人群中的安全性的结论。我们也不能对非随意性 LSSS 实施的效果得出明确的结论。关于儿童血压的证据非常不确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f419/9363242/6378bf1bd500/nCD015207-FIG-01.jpg

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