Department of Internal Medicine Section of Nephrology Amsterdam UMC University of AmsterdamAmsterdam Cardiovascular Sciences Amsterdam The Netherlands.
Amsterdam UMC University of AmsterdamCenter for Experimental and Molecular Medicine Amsterdam The Netherlands.
J Am Heart Assoc. 2022 Jul 5;11(13):e023727. doi: 10.1161/JAHA.121.023727. Epub 2022 Jun 22.
Background Experimental studies show that high-sodium intake affects the innate immune system, among others with increased circulating granulocytes. Whether this relationship exists on a population level and whether this relates to disease outcomes is unclear. We aimed to test the hypotheses that (1) sodium intake is associated with granulocytes on a population level; (2) granulocytes are associated with the presence of hypertension and both cardiovascular and renal outcomes; and (3) the relation between high-sodium intake and these outcomes is mediated by granulocytes. Methods and Results We performed an analysis in 13 804 participants from the prospective EPIC (European Prospective Investigation into Cancer)-Norfolk cohort, with a mean age of 58 years and median follow-up of 19.3 years. Analyses were carried out using calculated estimated sodium intake and sodium-to-potassium ratios from spot urines at baseline. The main outcomes were hypertension at baseline, and composite cardiovascular (mortality or cardiovascular events) and renal (mortality or renal events) outcomes during follow-up. Sodium intake and urine sodium-to-potassium ratio were positively associated with circulating granulocyte concentrations after adjustment for confounders (β=0.03; =0.028 and β=0.06; <0.001, respectively). Granulocytes significantly mediated the associations of, respectively, sodium intake and urine sodium-to-potassium ratio with hypertension at baseline, and cardiovascular and renal outcomes. Conclusions Sodium intake is positively associated with circulating granulocyte concentrations, and higher granulocyte concentrations associate with worse long-term cardiovascular and renal outcomes. Given the recently established immune-modulating effects of sodium and the role of immune cells in both cardiovascular and renal disease, causality for this pathway may need consideration in further studies.
实验研究表明,高钠摄入除其他外会影响先天免疫系统,导致循环中的粒细胞增多。这种关系在人群中是否存在,以及这是否与疾病结局相关尚不清楚。我们旨在检验以下假设:(1)人群中钠摄入量与粒细胞有关;(2)粒细胞与高血压以及心血管和肾脏结局的发生有关;(3)高钠摄入与这些结局之间的关系是通过粒细胞介导的。
我们对前瞻性 EPIC(欧洲癌症前瞻性调查)-诺福克队列中的 13804 名参与者进行了分析,平均年龄为 58 岁,中位随访时间为 19.3 年。分析使用基线时的点尿计算得出的估计钠摄入量和钠钾比进行。主要结局是基线时的高血压,以及随访期间的复合心血管(死亡或心血管事件)和肾脏(死亡或肾脏事件)结局。钠摄入量和尿钠钾比与调整混杂因素后的循环粒细胞浓度呈正相关(β=0.03;P=0.028 和 β=0.06;P<0.001)。粒细胞显著介导了钠摄入量和尿钠钾比分别与基线时高血压以及心血管和肾脏结局的关联。
钠摄入量与循环粒细胞浓度呈正相关,较高的粒细胞浓度与较差的长期心血管和肾脏结局相关。鉴于最近确定的钠的免疫调节作用以及免疫细胞在心血管和肾脏疾病中的作用,在进一步的研究中可能需要考虑这一途径的因果关系。