González-Lafuente Laura, Mercado-García Elisa, Vázquez-Sánchez Sara, González-Moreno Daniel, Boscá Lisardo, Fernández-Velasco María, Segura Julián, Kuro-O Makoto, Ruilope Luis M, Liaño Fernando, Ruiz-Hurtado Gema
Laboratorio Traslacional Cardiorrenal, Instituto de Investigación Imas12, Hospital Universitario 12 de Octubre, Madrid, Spain.
Instituto de Investigaciones Biomédicas Alberto Sols, CSIC-UAM Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBER-CV), Instituto de Salud Carlos III, Madrid, Spain.
Nefrologia (Engl Ed). 2024 Nov-Dec;44(6):818-829. doi: 10.1016/j.nefroe.2024.11.010. Epub 2024 Nov 29.
In acute kidney injury (AKI), a strong inflammatory component is activated in response to the renal damage, and one of the main mediators behind this process is the pro-inflammatory interleukin 6 or IL-6. Beside to this phenomenon, there are also alterations in different components of mineral metabolism, such as those dependent on fibroblast growth factor (FGF)23 and the anti-ageing cofactor klotho. The aim of this work was to explore the association between renal function and systemic levels of IL-6, as well as FGF23 and klotho in the early stages of AKI, analysing the predictive capacity of IL-6 in early mortality associated with AKI.
Plasma levels of IL-6, klotho and FGF23 were analysed in samples from 28 patients with AKI and related to renal function on hospital admission, and after 24 and 72 h. In addition, the predictive capacity of IL-6 on AKI-associated mortality was analysed at the three study time points. In an experimental nephrotoxic -AKI mouse model, systemic IL-6 and FGF23 values were also analysed 24 and 72 h after induction of kidney damage, as well as in mice overexpressing the anti-ageing protein, klotho.
Systemic IL-6 levels increased in AKI patients, especially in hospital admission time, and decreased in parallel with improving renal function. At the same time as IL-6 values increased, there was an increase in FGF23 and a decrease in klotho levels, with a significant and positive correlation between IL-6 and FGF23 levels. In addition, we obtained that systemic IL-6 levels were a good predictor of mortality in these patients, with an area under the curve equal to one at 72 h after AKI. In the experimental mouse AKI model, we also observed an increase in plasma levels in both IL-6 and FGF23 after 24 h of kidney damage. Nevertheless, in transgenic mice overexpressing klotho, there was no such increase in any of them.
There is an association between renal damage and increased levels of IL-6 and FGF23 in patients with AKI, especially on hospital admission time. Moreover, IL-6 levels are able to predict mortality in these patients, being a promising prognostic biomarker at any study time with a strong prediction at 72 h after patient admission. Maintaining adequate klotho levels could prevent the IL-6 mediated inflammatory response and therefore also reduce the degree and severity of renal damage after AKI.
在急性肾损伤(AKI)中,针对肾脏损伤会激活强烈的炎症反应,这一过程背后的主要介质之一是促炎性白细胞介素6(IL-6)。除此之外,矿物质代谢的不同成分也会发生改变,比如那些依赖成纤维细胞生长因子(FGF)23和抗衰老辅助因子α-klotho的成分。本研究旨在探讨AKI早期肾功能与IL-6、FGF23及α-klotho全身水平之间的关联,并分析IL-6对AKI相关早期死亡率的预测能力。
分析了28例AKI患者入院时、24小时及72小时后的样本中IL-6、α-klotho和FGF23的血浆水平,并将其与肾功能相关联。此外,在三个研究时间点分析了IL-6对AKI相关死亡率的预测能力。在实验性肾毒性AKI小鼠模型中,还分析了肾损伤诱导后24小时和72小时的全身IL-6和FGF23值,以及过表达抗衰老蛋白α-klotho的小鼠中的这些值。
AKI患者的全身IL-6水平升高,尤其是在入院时,并随着肾功能的改善而下降。与IL-6值升高的同时,FGF23升高而α-klotho水平下降,IL-6与FGF23水平之间存在显著正相关。此外,我们发现全身IL-6水平是这些患者死亡率的良好预测指标,在AKI后72小时曲线下面积等于1。在实验性小鼠AKI模型中,我们还观察到肾损伤24小时后IL-6和FGF23的血浆水平均升高。然而,在过表达α-klotho的转基因小鼠中,它们均未出现这种升高。
AKI患者的肾损伤与IL-6和FGF2