尿法检测疑似坏死性小肠结肠炎新生儿肠黏膜细胞损伤

Fady Elgendy, Nouran Aboelkhair, Nesma El-Desokyc, Hanan Z El-Sayed
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引用次数: 0

摘要

目的探讨尿肠脂肪酸结合蛋白(iFABP)在新生儿坏死性小肠结肠炎(NEC)早期的诊断价值。背景NEC是一种影响早产儿的严重急性胃肠道疾病。iFABP与NEC常见的肠黏膜损伤有关。患者和方法本横断面研究纳入40例早产儿,分为两组:ⅰ组20例根据NEC改良Bell分期标准疑似NEC的早产儿,ⅱ组20例非NEC的早产儿。所有纳入的参与者都进行了完整的病史记录、全面检查、常规实验室调查和尿iFABP评估。结果尿中iFABP水平ⅰ组为17.26±3.69 ng/dl,ⅱ组为8.39±2.49 ng/ml。在疑似NEC组中,这一差异明显更高(P = 0.001)。iFABP在9.25 ng/ml以上的临界值对早期NEC病例具有显著的鉴别能力(P = 0.001),敏感性为96.0%,特异性为71.0%。线性回归显示,采样时间是预测iFABP的重要指标(P = 0.001)。结论尿中iFABP水平升高与NEC存在相关性,提示iFABP可作为NEC早期诊断的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Urine-based detection of intestinal mucosal cell damage in neonates with suspected necrotizing enterocolitis
Objectives To assess the diagnostic value of the urinary intestinal fatty acid-binding protein (iFABP) in neonatal necrotizing enterocolitis (NEC) in the early stage of the disease. Background NEC is a severe acute gastrointestinal disease affecting preterm newborns. iFABP has been associated with injury to the intestinal mucosa common to NEC. Patients and methods This cross-sectional study included 40 preterm neonates divided into two groups: group I included 20 preterm neonates with suspected NEC according to Modified Bell Staging Criteria for NEC and group II included 20 preterm neonates with non-NEC. All the included participants underwent full history taking, full examination, routine laboratory investigations, and assessment of urinary iFABP. Results The mean urinary iFABP level was 17.26 ± 3.69 ng/dl in group I and 8.39 ± 2.49 ng/ml in group II. This difference was significantly higher in the suspected NEC group (P = 0.001). The iFABP level at a cutoff more than 9.25 ng/ml had significant power of discrimination of NEC cases at an early stage (P = 0.001) with a sensitivity of 96.0% and specificity of 71.0%. Linear regression revealed that the sampling time was a significant measure for prediction of iFABP (P = 0.001). Conclusion There was an association between elevated iFABP levels in urine and NEC, suggesting that iFABP may be useful as a diagnostic biomarker for earlier identification of NEC.
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