金属蛋白酶-2和胰岛素样生长因子结合蛋白7的组织抑制剂作为产科患者急性肾损伤的预测因子

Rekha Sachan, Munna Lal Patel, Himani Chaudhary, Radhey Shyam, Wahid Ali
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引用次数: 0

摘要

背景:本研究旨在评估细胞周期阻滞尿液生物标志物、金属蛋白酶-2组织抑制剂(TIMP2)和胰岛素样生长因子结合蛋白7 (IGFBP7)联合应用在产科危重患者AKI早期预测中的作用。方法:本前瞻性观察研究在产科重症监护病房进行。在入院当天抽取产科危重病人的血液和尿液样本,并在48小时后抽取第二次尿液样本。入院后,测定APACHE 2评分。根据制造商的说明,使用ELISA试剂盒进行[TIMP2]*[IGFBP7]的最终估计。AKI的诊断和分期是按照KDIGO 2012指南进行的。结果:入院时,符合研究纳入要求的131名危重产科患者均未出现AKI。131名患者中只有127名进行了分析,4名患者被排除在外,3名患者在48小时内死亡,1名患者不遵医嘱离开。妊娠相关高血压疾病是AKI的主要危险因素(57.1%),其次是出血(48.1%),其中包括早剥(19.5%)、前置胎盘/增生胎盘/percreta胎盘(10.4%)和PPH(14.3%)。发生AKI的患者在入院当天的平均[TIMP2]*[IGFBP7](3.47±3.66 (ng/ml)2/1000)明显高于未发生AKI的患者(0.22±0.12 ng/ml)2/1000)。采用ROC曲线分析确定第1天[TIMP2]*[IGFBP7]水平的诊断准确性。[TIMP2]*[IGFBP7]在临界值≥0.41(ng/ml)2/1000时预测AKI的敏感性为94.8%,特异性为94%,置信区间为95%,AUC为0.990。结论:尿生物标志物[TIMP-2]*[IGFBP7]能准确预测患者发生AKI的风险。它也具有良好的预后价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tissue inhibitor of metalloproteinase-2 and insulin-like growth factor binding protein 7 as a predictor of acute kidney injury in obstetric patients.

Tissue inhibitor of metalloproteinase-2 and insulin-like growth factor binding protein 7 as a predictor of acute kidney injury in obstetric patients.

Background: This study seeks to evaluate the role of the combination of cell cycle arrest urine biomarkers, Tissue inhibitor of metalloproteinase-2 (TIMP2) and insulin-like growth factor binding protein 7 (IGFBP7) for early prediction of AKI in critically ill obstetrics patients.

Methodology: This prospective observational study was conducted at Obstetrics Intensive Care Unit. Blood and urine samples were taken from critically sick obstetric patients on the day of admission, and the second urine sample was taken after 48 hours. Following admission, the APACHE 2 score was determined. According to the manufacturer's instructions, an ELISA kit was used to perform the final estimation of [TIMP2]*[IGFBP7]. AKI was diagnosed and staged as per KDIGO 2012 guidelines.

Results: At the time of admission, AKI was not present in any of the 131 critically ill obstetric patients who met the study's inclusion requirements. Only 127 out of the 131 patients were analysed, four patients were excluded, 3 patients died within 48 hours, and 1 patient left against medical advice. Pregnancy-related hypertensive disorders accounted for the majority of AKI as risk factors (57.1%), followed by haemorrhage (48.1%), which included abruption in 19.5%, placenta previa/accreta/percreta (10.4%), and PPH (14.3%).Patients who developed AKI had a substantially higher mean [TIMP2]*[IGFBP7] on the day of admission (3.47±3.66 (ng/ml)2/1000) than those who did not (0.22±0.12 ng/ml)2/1000). ROC curve analysis was used to determine the diagnostic accuracy of [TIMP2]*[IGFBP7] levels on Day 1. [TIMP2]*[IGFBP7] exhibited a sensitivity of 94.8% and specificity of 94% for predicting AKI at a cutoff value of ≥0.41(ng/ml)2/1000, with a 95% confidence interval and an AUC of 0.990.

Conclusion: Patient risk of developing AKI was accurately predicted by the urine biomarker [TIMP-2]*[IGFBP7]. It also has good prognostic value.

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