Plewes Katherine, Kingston Hugh W F, Ghose Aniruddha, Maude Richard J, Herdman M Trent, Leopold Stije J, Ishioka Haruhiko, Hasan Md Mahtab Uddin, Haider Md Shafiul, Alam Shamsul, Piera Kim A, Charunwatthana Prakaykaew, Silamut Kamolrat, Yeo Tsin W, Faiz Md Abul, Lee Sue J, Mukaka Mavuto, Turner Gareth D H, Anstey Nicholas M, Jackson Roberts L, White Nicholas J, Day Nicholas P J, Hossain Md Amir, Dondorp Arjen M
Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
BMC Infect Dis. 2017 Apr 27;17(1):313. doi: 10.1186/s12879-017-2373-1.
Intravascular hemolysis is an intrinsic feature of severe malaria pathophysiology but the pathogenic role of cell-free hemoglobin-mediated oxidative stress in severe malaria associated acute kidney injury (AKI) is unknown.
As part of a prospective observational study, enrolment plasma cell-free hemoglobin (CFH), lipid peroxidation markers (F-isoprostanes (F-IsoPs) and isofurans (IsoFs)), red cell deformability, and serum creatinine were quantified in Bangladeshi patients with severe falciparum malaria (n = 107), uncomplicated malaria (n = 80) and sepsis (n = 28). The relationships between these indices and kidney function and clinical outcomes were examined.
AKI was diagnosed at enrolment in 58% (62/107) of consecutive patients with severe malaria, defined by an increase in creatinine ≥1.5 times expected baseline. Severe malaria patients with AKI had significantly higher plasma cell-free hemoglobin (geometric mean CFH: 8.8 μM; 95% CI, 6.2-12.3 μM), F-isoprostane (56.7 pg/ml; 95% CI, 45.3-71.0 pg/ml) and isofuran (109.2 pg/ml; 95% CI, 85.1-140.1 pg/ml) concentrations on enrolment compared to those without AKI (CFH: 5.1 μM; 95% CI, 4.0-6.6 μM; P = 0.018; F-IsoPs: 27.8 pg/ml; 95% CI, 23.7-32.7 pg/ml; P < 0.001; IsoFs: 41.7 pg/ml; 95% CI, 30.2-57.6 pg/ml; P < 0.001). Cell-free hemoglobin correlated with markers of hemolysis, parasite burden (P. falciparum histidine rich protein 2 (PfHRP2)), and F-IsoPs. Plasma F-IsoPs and IsoFs inversely correlated with pH, positively correlated with creatinine, PfHRP2 and fractional excretion of sodium, and were higher in patients later requiring hemodialysis. Plasma F-IsoP concentrations also inversely correlated with red cell deformability and were higher in fatal cases. Mixed effects modeling including an interaction term for CFH and time showed that F-IsoPs, IsoFs, PfHRP2, CFH, and red cell rigidity were independently associated with increasing creatinine over 72 h. Multivariable logistic regression showed that admission F-IsoPs, IsoFs and red cell deformability were associated with the need for subsequent hemodialysis.
Cell-free hemoglobin and lipid peroxidation are associated with acute kidney injury and disease severity in falciparum malaria, suggesting a pathophysiological role in renal tubular injury. Evaluation of adjunctive therapies targeting cell-free hemoglobin-mediated oxidative stress is warranted.
血管内溶血是重症疟疾病理生理学的一个内在特征,但游离血红蛋白介导的氧化应激在重症疟疾相关急性肾损伤(AKI)中的致病作用尚不清楚。
作为一项前瞻性观察性研究的一部分,对孟加拉国重症恶性疟患者(n = 107)、非重症疟疾患者(n = 80)和脓毒症患者(n = 28)的入院血浆游离血红蛋白(CFH)、脂质过氧化标志物(F-异前列腺素(F-IsoPs)和异呋喃(IsoFs))、红细胞变形性和血清肌酐进行了定量分析。研究了这些指标与肾功能及临床结局之间的关系。
在连续的重症疟疾患者中,58%(62/107)在入院时被诊断为AKI,定义为肌酐升高≥预期基线值的1.5倍。与无AKI的重症疟疾患者相比,发生AKI的重症疟疾患者入院时血浆游离血红蛋白(几何平均CFH:8.8 μM;95% CI,6.2 - 12.3 μM)、F-异前列腺素(56.7 pg/ml;95% CI,45.3 - 71.0 pg/ml)和异呋喃(109.2 pg/ml;95% CI,85.1 - 140.1 pg/ml)浓度显著更高(CFH:5.1 μM;95% CI,4.0 - 6.6 μM;P = 0.018;F-IsoPs:27.8 pg/ml;95% CI,23.7 - 32.7 pg/ml;P < 0.001;IsoFs:41.7 pg/ml;95% CI,30.2 - 57.6 pg/ml;P < 0.001)。游离血红蛋白与溶血标志物、疟原虫负荷(恶性疟富含组氨酸蛋白2(PfHRP2))和F-IsoPs相关。血浆F-IsoPs和IsoFs与pH呈负相关,与肌酐、PfHRP2和钠分数排泄呈正相关,且在后来需要血液透析的患者中更高。血浆F-IsoP浓度也与红细胞变形性呈负相关,在死亡病例中更高。包含CFH和时间交互项的混合效应模型显示,F-IsoPs、IsoFs、PfHRP2、CFH和红细胞刚性与72小时内肌酐升高独立相关。多变量逻辑回归显示,入院时的F-IsoPs、IsoFs和红细胞变形性与后续血液透析的需求相关。
游离血红蛋白和脂质过氧化与恶性疟急性肾损伤及疾病严重程度相关,提示在肾小管损伤中起病理生理作用。有必要评估针对游离血红蛋白介导的氧化应激的辅助治疗。