Lipiec Katarzyna, Adamczyk Piotr, Świętochowska Elżbieta, Ziora Katarzyna, Szczepańska Maria
Department of Pediatric Nephrology with Dialysis Division for Children, Zabrze, Poland.
Department and Clinic of Pediatrics, SMDZ in Zabrze, SUM in Katowice, Poland.
Adv Clin Exp Med. 2018 Jul;27(7):955-962. doi: 10.17219/acem/70567.
Hemolytic-uremic syndrome (HUS) is a form of thrombotic microangiopathy, in the course of which some patients may develop chronic kidney disease (CKD). From a clinical point of view, it is important to search for markers that allow for early identification of patients at risk of a poor prognosis.
The study evaluated the serum and urine levels of liver-type fatty acid binding protein (L-FABP) and interleukin 6 (IL-6).
The study was conducted in 29 children with a history of HUS. The relationship between L-FABP and IL-6 and anthropometric measurements, the value of estimated glomerular filtration rate (eGFR) and albuminuria were additionally evaluated.
In children after HUS, L-FABP and IL-6 concentration in both serum and urine was significantly higher in comparison to the control group. No differences in L-FABP and IL-6 concentration in serum and urine depending on the type of HUS and gender were noted. Correlation between L-FABP and IL-6 in serum and urine with eGFR and urine albumin-creatinine ratio (ACR) in the total group of patients after HUS was not detected. In the group of children after 6 month observation after HUS, a negative correlation of L-FABP concentration with eGFR was found.
The results indicate that the higher concentration of L-FABP in serum and urine of children with a history of HUS can be the result of protracted injury initiated during the acute phase of the disease. Lack of correlation of L-FABP concentration with the ACR may be associated with a short (less than 6 months) observation after acute renal failure or merely temporary renal tubular damage in the acute phase of the disease. In contrast, higher levels of IL-6 in serum and urine in children after HUS compared to healthy children and the negative correlation of L-FABP concentration and eGFR in children after 6 month observation after HUS may confirm their participation in CKD. Thus, L-FABP and IL-6 seem to be good biomarkers of chronic kidney damage in survivors of the acute phase of HUS.
溶血尿毒综合征(HUS)是血栓性微血管病的一种形式,在此过程中一些患者可能会发展为慢性肾脏病(CKD)。从临床角度来看,寻找能够早期识别预后不良风险患者的标志物很重要。
本研究评估了肝型脂肪酸结合蛋白(L-FABP)和白细胞介素6(IL-6)的血清和尿液水平。
对29例有HUS病史的儿童进行了研究。此外,还评估了L-FABP和IL-6与人体测量指标、估计肾小球滤过率(eGFR)值和蛋白尿之间的关系。
与对照组相比,HUS患儿血清和尿液中的L-FABP和IL-6浓度显著更高。未发现血清和尿液中L-FABP和IL-6浓度因HUS类型和性别而异。在HUS后患者的总体组中,未检测到血清和尿液中L-FABP和IL-6与eGFR和尿白蛋白-肌酐比值(ACR)之间的相关性。在HUS后6个月观察的儿童组中,发现L-FABP浓度与eGFR呈负相关。
结果表明,有HUS病史儿童血清和尿液中L-FABP浓度较高可能是疾病急性期引发的持续性损伤的结果。L-FABP浓度与ACR缺乏相关性可能与急性肾衰竭后观察时间短(少于6个月)或疾病急性期仅为暂时性肾小管损伤有关。相比之下,HUS后儿童血清和尿液中IL-6水平高于健康儿童,以及HUS后6个月观察的儿童中L-FABP浓度与eGFR呈负相关,可能证实它们参与了CKD的发生。因此,L-FABP和IL-6似乎是HUS急性期幸存者慢性肾损伤的良好生物标志物。