Crouch Simone H, Botha-Le Roux Shani, Delles Christian, Graham Lesley A, Schutte Aletta E
Hypertension in Africa Research Team (HART), North-West University, Potchefstroom, South Africa.
MRC Research Unit: Hypertension and Cardiovascular Disease, North-West University, Potchefstroom, South Africa.
Eur J Nutr. 2021 Mar;60(2):873-882. doi: 10.1007/s00394-020-02292-3. Epub 2020 Jun 3.
Low-grade inflammation and a diet high in salt are both established risk factors for cardiovascular disease. High potassium (K) intake was found to counter increase in blood pressure due to high salt intake and may potentially also have protective anti-inflammatory effects. To better understand these interactions under normal physiological conditions, we investigated the relationships between 22 inflammatory mediators with 24-h urinary K in young healthy adults stratified by low, medium and high salt intake (salt tertiles). We stratified by ethnicity due to potential salt sensitivity in black populations.
In 991 healthy black (N = 457) and white (N = 534) adults, aged 20-30 years, with complete data for 24-h urinary sodium and K, we analysed blood samples for 22 inflammatory mediators.
We found no differences in inflammatory mediators between low-, mid- and high-sodium tertiles in either the black or white groups. In multivariable-adjusted regression analyses in white adults, we found only in the lowest salt tertile that K associated negatively with pro-inflammatory mediators, namely interferon gamma, interleukin (IL) -7, IL-12, IL-17A, IL-23 and tumour necrosis factor alpha (all p ≤ 0.046). In the black population, we found no independent associations between K and any inflammatory mediator.
In healthy white adults, 24-h urinary K associated independently and negatively with specific pro-inflammatory mediators, but only in those with a daily salt intake less than 6.31 g, suggesting K to play a protective, anti-inflammatory role in a low-sodium environment. No similar associations were found in young healthy black adults.
低度炎症和高盐饮食均为已确定的心血管疾病风险因素。研究发现,高钾(K)摄入可抵消高盐摄入导致的血压升高,并且可能还具有保护性抗炎作用。为了更好地了解正常生理条件下的这些相互作用,我们在按低盐、中等盐和高盐摄入量分层(盐三分位数)的年轻健康成年人中,研究了22种炎症介质与24小时尿钾之间的关系。由于黑人人群存在潜在的盐敏感性,我们按种族进行了分层。
在991名年龄在20 - 30岁、有完整24小时尿钠和钾数据的健康黑人(N = 457)和白人(N = 534)成年人中,我们分析了血液样本中的22种炎症介质。
我们发现,黑人或白人组中,低、中、高钠三分位数之间的炎症介质没有差异。在白人成年人的多变量调整回归分析中,我们仅在最低盐三分位数中发现钾与促炎介质呈负相关,即γ干扰素、白细胞介素(IL)-7、IL-12、IL-17A、IL-23和肿瘤坏死因子α(所有p≤0.046)。在黑人人群中,我们未发现钾与任何炎症介质之间存在独立关联。
在健康白人成年人中,24小时尿钾与特定促炎介质独立且呈负相关,但仅在每日盐摄入量低于6.31克的人群中如此,这表明钾在低钠环境中发挥着保护性抗炎作用。在年轻健康黑人成年人中未发现类似关联。