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生长分化因子15(GDF - 15)水平与新冠肺炎慢性肾脏病患者较低的生存率相关。

Growth Differentiation Factor 15 (GDF-15) Levels Associate with Lower Survival in Chronic Kidney Disease Patients with COVID-19.

作者信息

Galassi Andrea, Ciceri Paola, Bono Valeria, Magagnoli Lorenza, Sala Matteo, Artioli Luisa, Rovito Roberta, Hadla Mohamad, Yellenki Vaibhav, D'Arminio Monforte Antonella, Tincati Camilla, Cozzolino Mario, Marchetti Giulia

机构信息

Department of Health Sciences, Renal Division, University of Milan, ASST Santi Paolo e Carlo, 20142 Milan, Italy.

Department of Health Sciences, Clinic of Infectious Diseases, University of Milan, ASST Santi Paolo e Carlo, 20142 Milan, Italy.

出版信息

Biomedicines. 2022 Dec 14;10(12):3251. doi: 10.3390/biomedicines10123251.

Abstract

A cytokine storm drives the pathogenesis of severe COVID-19 infection and several biomarkers have been linked to mortality. Chronic kidney disease (CKD) emerged as a risk factor for severe COVID-19. We investigated the association between selected biomarkers and mortality in 77 patients hospitalized for COVID-19, and whether they differ in patients with eGFR higher and lower than 45 mL/min. The association between patients’ characteristics, plasma biomarkers and mortality was conducted by univariate logistic regression models and independent predictors of mortality were then used to create a multivariate prediction model through Cox regression. Patients with lower eGFR had a significant increase of GDF-15, CD-25 and RAGE, with higher plasma levels in non-survivors and in patients who needed ventilation. At univariate analysis, low and mid-low GDF-15 quartiles (<4.45 ng/mL) were associated with lower mortality risk, while mid-high and high quartiles (>4.45 ng/mL) were associated with higher mortality risk. Independent association between GDF-15 quartiles and mortality risk was confirmed in the Cox model and adjusted for eGFR, age, fever and dyspnea (HR 2.28, CI 1.53−3.39, p < 0.0001). The strength of the association between GDF-15 quartiles and mortality risk increased in patients with lower compared to higher eGFR (HR 2.53, CI 1.34−4.79 versus HR 1.99, CI 1.17−3.39). Our findings may suggest a further investigation of the effect of GDF-15 signaling pathway inhibition in CKD.

摘要

细胞因子风暴驱动了重症新型冠状病毒肺炎(COVID-19)感染的发病机制,且有几种生物标志物与死亡率相关。慢性肾脏病(CKD)已成为重症COVID-19的一个危险因素。我们调查了77例因COVID-19住院患者中选定生物标志物与死亡率之间的关联,以及估算肾小球滤过率(eGFR)高于和低于45 mL/min的患者之间这些生物标志物是否存在差异。通过单因素逻辑回归模型分析患者特征、血浆生物标志物与死亡率之间的关联,然后使用死亡率的独立预测因子通过Cox回归创建多变量预测模型。eGFR较低的患者中生长分化因子15(GDF-15)、CD-25和晚期糖基化终末产物受体(RAGE)显著升高,非幸存者和需要机械通气的患者血浆水平更高。在单因素分析中,低和中低四分位数的GDF-15(<4.45 ng/mL)与较低的死亡风险相关,而中高和高四分位数(>4.45 ng/mL)与较高的死亡风险相关。在Cox模型中证实了GDF-15四分位数与死亡风险之间的独立关联,并对eGFR、年龄、发热和呼吸困难进行了校正(风险比[HR] 2.28,95%置信区间[CI] 1.53 - 3.39,p < 0.0001)。与eGFR较高的患者相比,eGFR较低的患者中GDF-15四分位数与死亡风险之间的关联强度增加(HR 2.53,CI 1.34 - 4.79对比HR 1.99,CI 1.17 - 3.39)。我们的研究结果可能提示进一步研究GDF-15信号通路抑制在CKD中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6629/9775159/1faa7eb51ecc/biomedicines-10-03251-g001.jpg

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