Vaara Suvi T, Lakkisto Päivi, Immonen Katariina, Tikkanen Ilkka, Ala-Kokko Tero, Pettilä Ville
Division of Intensive Care Medicine, Department of Anaesthesiology, Intensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Minerva Institute for Medical Research, Helsinki, Finland.
PLoS One. 2016 Feb 26;11(2):e0149956. doi: 10.1371/journal.pone.0149956. eCollection 2016.
Apoptosis is a key mechanism involved in ischemic acute kidney injury (AKI), but its role in septic AKI is controversial. Biomarkers indicative of apoptosis could potentially detect developing AKI prior to its clinical diagnosis.
As a part of the multicenter, observational FINNAKI study, we performed a pilot study among critically ill patients who developed AKI (n = 30) matched to critically ill patients without AKI (n = 30). We explored the urine and plasma levels of cytokeratin-18 neoepitope M30 (CK-18 M30), cell-free DNA, and heat shock protein 70 (HSP70) at intensive care unit (ICU) admission and 24h thereafter, before the clinical diagnosis of AKI defined by the Kidney Disease: Improving Global Outcomes -creatinine and urine output criteria. Furthermore, we performed a validation study in 197 consecutive patients in the FINNAKI cohort and analyzed the urine sample at ICU admission for CK-18 M30 levels.
In the pilot study, the urine or plasma levels of measured biomarkers at ICU admission, at 24h, or their maximum value did not differ significantly between AKI and non-AKI patients. Among 20 AKI patients without severe sepsis, the urine CK-18 M30 levels were significantly higher at 24h (median 116.0, IQR [32.3-233.0] U/L) than among those 20 patients who did not develop AKI (46.0 [0.0-54.0] U/L), P = 0.020. Neither urine cell-free DNA nor HSP70 levels significantly differed between AKI and non-AKI patients regardless of the presence of severe sepsis. In the validation study, urine CK-18 M30 level at ICU admission was not significantly higher among patients developing AKI compared to non-AKI patients regardless of the presence of severe sepsis or CKD.
Our findings do not support that apoptosis detected with CK-18 M30 level would be useful in assessing the development of AKI in the critically ill. Urine HSP or cell-free DNA levels did not differ between AKI and non-AKI patients.
细胞凋亡是缺血性急性肾损伤(AKI)的关键机制,但其在脓毒症相关性AKI中的作用仍存在争议。能够指示细胞凋亡的生物标志物可能在AKI临床诊断之前检测到其发生发展。
作为多中心观察性FINNAKI研究的一部分,我们在发生AKI的重症患者(n = 30)和未发生AKI的重症患者(n = 30)中进行了一项初步研究。我们在重症监护病房(ICU)入院时及之后24小时,在根据肾脏病改善全球预后组织(KDIGO)的肌酐和尿量标准对AKI进行临床诊断之前,检测了尿和血浆中的细胞角蛋白18新表位M30(CK-18 M30)、游离DNA和热休克蛋白70(HSP70)水平。此外,我们在FINNAKI队列的197例连续患者中进行了一项验证研究,并在ICU入院时分析了尿样中的CK-18 M30水平。
在初步研究中,AKI患者和非AKI患者在ICU入院时、24小时时或其最大值时,所测生物标志物的尿或血浆水平无显著差异。在20例无严重脓毒症的AKI患者中,24小时时尿CK-18 M30水平(中位数116.0,IQR[32.3 - 233.0]U/L)显著高于20例未发生AKI的患者(46.0[0.0 - 54.0]U/L),P = 0.020。无论是否存在严重脓毒症,AKI患者和非AKI患者的尿游离DNA和HSP70水平均无显著差异。在验证研究中,无论是否存在严重脓毒症或慢性肾脏病(CKD),发生AKI的患者在ICU入院时的尿CK-18 M30水平与未发生AKI的患者相比无显著升高。
我们的研究结果不支持通过CK-18 M30水平检测细胞凋亡对评估重症患者AKI的发生发展有用。AKI患者和非AKI患者的尿HSP或游离DNA水平无差异。