Department of Medical Education, Medical Innovation and Research Office, Clinical Innovation Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Faculty of Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Sci Rep. 2023 Aug 11;13(1):13048. doi: 10.1038/s41598-023-40088-7.
The development of acute kidney injury (AKI) and hepatorenal syndrome-acute kidney injury (HRS-AKI) in cirrhosis has been associated with intestinal barrier dysfunction and gut-kidney crosstalk. We use the related markers such as zonulin, lipopolysaccharides (LPS), and lipopolysaccharide-binding protein (LBP) to predict AKI and HRS-AKI in cirrhotic patients and evaluate their in vitro effects on intestinal (Caco-2) cells and renal tubular (HK-2) cells. From 2013 to 2020, we enrolled 70 cirrhotic patients and developed prediction models for AKI and HRS-AKI over a six-month period. There were 13 (18.6%) and 8 (11.4%) cirrhotic patients developed AKI and HRS-AKI. The prediction models incorporated zonulin, LPS, LBP, C-reactive protein, age, and history of hepatitis B for AKI, and zonulin, LPS, LBP, total bilirubin, and Child-Pugh score for HRS-AKI. The area under curve (AUC) for the prediction of AKI and HRS-AKI was 0.94 and 0.95, respectively. Furthermore, the conditioned medium of LPS+hrLBP pre-treated Caco-2 cells induced apoptosis, necrosis, and zonulin release in HK-2 cells, demonstrating the communication between them. This study found that zonulin, LPS, and LBP are potential practical markers for predicting AKI and HRS-AKI in cirrhotic patients, which may serve as potential targets for renal outcomes in cirrhotic patients.
肝硬化患者急性肾损伤(AKI)和肝肾综合征-急性肾损伤(HRS-AKI)的发展与肠道屏障功能障碍和肠-肾相互作用有关。我们使用相关标志物,如紧密连接蛋白、脂多糖(LPS)和脂多糖结合蛋白(LBP),来预测肝硬化患者的 AKI 和 HRS-AKI,并评估它们对肠道(Caco-2)细胞和肾小管(HK-2)细胞的体外作用。2013 年至 2020 年,我们共纳入 70 例肝硬化患者,建立了 6 个月内 AKI 和 HRS-AKI 的预测模型。13 例(18.6%)和 8 例(11.4%)患者发生 AKI 和 HRS-AKI。AKI 预测模型包括紧密连接蛋白、LPS、LBP、C 反应蛋白、年龄和乙型肝炎病史,HRS-AKI 预测模型包括紧密连接蛋白、LPS、LBP、总胆红素和 Child-Pugh 评分。AKI 和 HRS-AKI 的预测曲线下面积(AUC)分别为 0.94 和 0.95。此外,LPS+hrLBP 预处理 Caco-2 细胞的条件培养基可诱导 HK-2 细胞凋亡、坏死和紧密连接蛋白释放,表明两者之间存在相互作用。本研究发现,紧密连接蛋白、LPS 和 LBP 是预测肝硬化患者 AKI 和 HRS-AKI 的潜在实用标志物,可能成为肝硬化患者肾脏结局的潜在治疗靶点。