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英文作者:Zhu Jiajia1 Zhang Ning1 Chen Liying1 Liu Baoli2
单位:1首都医科大学附属北京安贞医院心脏内科危重症中心,北京100029;2首都医科大学附属北京中医医院肾内科,北京100010
英文单位:1Critical Care Center of Department of Cardiology Beijing Anzhen Hospital Capital Medical University Beijing 100029 China; 2Department of Nephrology Beijing Hospital of Traditional Chinese Medicine Capital Medical University Beijing 100010 China
关键词:急性心肌梗死;急性肾损伤;肾损伤分子1;心肾综合征;早期检测;危险分层
英文关键词:Acutemyocardialinfarction;Acutekidneyinjury;Kidneyinjurymolecule-1;Cardiorenalsyndrome;Earlydetection;Riskstratification
目的 探讨血清肾损伤分子 1(KIM-1)对急性心肌梗死(AMI)患者发病后72 h内急性肾损伤(AKI)早期危险分层的潜在价值。方法 连续纳入2025年11月至2026年1月于首都医科大学附属北京安贞医院住院的30例AMI患者开展单中心前瞻性初步研究。依据是否发生AKI分为AKI组(10例)和非AKI组(20例)。于入院即刻(T0)、入院后 6~12 h(T1)、入院后24 h(T2)、入院后48 h(T3)、入院后72 h(T4)采集血清,检测KIM-1与血肌酐水平,采用受试者工作特征曲线分析其预测72 h内AKI的价值。本研究为探索性研究,样本量有限,结果仅用于提出假设并报告置信区间。结果 AKI组T0时点KIM-1水平显著高于非AKI组[0.150(0.095,0.305)μg/L比0.080(0.058,0.132)μg/L](P=0.019);T0时点KIM-1 预测72 h内AKI的曲线下面积(AUC)为0.77(95%置信区间:0.52~0.94),优于同期血肌酐(AUC=0.66,95%置信区间:0.45~0.88)。以0.100 μg/L为临界值,KIM-1预测AKI的敏感度为100%(95%置信区间:69%~100%)、特异度为60%(95%置信区间:36%~81%)。在2组从症状发作到入院的中位时间一致情况下,患者KIM-1于T0时点即表现组间差异,血肌酐直至T2时点才出现差异,二者时间差约24 h。结论 入院时血清KIM-1对AMI后AKI发生具有早期危险分层的潜在价值,检出时间早于血肌酐,但其探索性结果需大样本、多中心研究外部验证及临床实用性评估后,方可转化应用。
Objective To explore the potential value of serum kidney injury molecule-1 (KIM-1) in the early risk stratification of acute kidney injury (AKI) within 72 h after onset in patients with acute myocardial infarction (AMI). Methods A total of 30 consecutive AMI patients hospitalized in Beijing Anzhen Hospital, Capital Medical University from November 2025 to January 2026 were enrolled in this single-center prospective preliminary study. Patients were divided into AKI group (10 cases) and non-AKI group (20 cases) according to the occurrence of AKI. Serum samples were collected at admission immediately (T0), 6-12 h after admission (T1), 24 h after admission (T2), 48 h after admission (T3), and 72 h after admission (T4) to detect the levels of KIM-1 and serum creatinine. Receiver operating characteristic curve was used to analyze its value in predicting AKI within 72 h. As an exploratory study with a limited sample size, the results were only used to generate hypotheses and report confidence intervals. Results The level of KIM-1 at T0 in the AKI group was significantly higher than that in the non-AKI group [0.150(0.095, 0.305)μg/L vs 0.080(0.058, 0.132)μg/L](P=0.019). The area under the curve (AUC) of KIM-1 at T0 for predicting AKI within 72 h was 0.77 (95% confidence interval: 0.52-0.94), which was superior to serum creatinine at the same time point (AUC=0.66, 95% confidence interval: 0.45-0.88). Taking 0.100 μg/L as the cut-off value, the sensitivity of KIM-1 for predicting AKI was 100% (95% confidence interval: 69%-100%) and the specificity was 60% (95% confidence interval: 36%-81%). With the consistent median time from symptom onset to admission between the two groups, KIM-1 showed intergroup differences at T0, while serum creatinine did not show significant differences until T2, with a time difference of approximately 24 h. Conclusion sSerum KIM-1 at admission has potential value for early risk stratification of AKI after AMI, with an earlier detection time than serum creatinine. However, these exploratory findings need external verification by large-sample and multicenter studies as well as clinical practicability evaluation before clinical transformation and application.
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