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血清肠脂肪酸结合蛋白水平对坏死性小肠结肠炎的早期诊断和严重程度预测。

Serum intestinal fatty acid binding protein level for early diagnosis and prediction of severity of necrotizing enterocolitis.

机构信息

Department of Neonatology, Zekai Tahir Burak Maternity Hospital, Ankara, Turkey.

出版信息

Early Hum Dev. 2011 Oct;87(10):659-61. doi: 10.1016/j.earlhumdev.2011.05.004. Epub 2011 Jun 8.

Abstract

BACKGROUND/AIM: Intestinal fatty acid binding protein (I-FABP) is found within cells at the tip of the intestinal villi, an area commonly injured in necrotizing enterocolitis (NEC). In this study, we aimed to investigate the value of serum I-FABP in early diagnosis and predicting severity of NEC.

METHODS

This prospective study was conducted between April 2009 and November 2009. The preterm infants with suspected NEC were included in the study. These infants were divided into two groups according to their final diagnoses; Group 1: Stage 1 NEC and Group 2: Stages 2-3 NEC (Group 2a: Stage 2 NEC, Group 2b: Stage 3 NEC). Healthy preterms were assigned to control group (Group 3). Serial blood samples were obtained from the patients at symptom onset, 24h and 72 h later. One blood sample was taken from the controls. Serum I-FABP levels were compared among the groups.

RESULTS

Initial serum I-FABP concentrations were 324.0±165.8 pg/ml, 764.7±465.1 pg/ml, and 360.2±439.5 pg/ml in Group 1, Group 2a, and Group 2b, respectively, and all were significantly higher than those of the control group (76.9±115.9 pg/ml) (p<0.001). The serum I-FABP levels gradually decreased from the onset of the disease to 72nd hour in Group 1 and Group 2a (p=0.001). In Group 2b I-FABP concentrations slightly decreased at 24th hour of the disease and increased thereafter, but the difference was not significant (p=0.06).

CONCLUSION

Serial measurements of I-FABP levels may be a useful marker for early diagnosis and prediction of disease severity in NEC.

摘要

背景/目的:肠脂肪酸结合蛋白(I-FABP)存在于肠绒毛尖端的细胞内,该区域是坏死性小肠结肠炎(NEC)常见的损伤部位。在本研究中,我们旨在探讨血清 I-FABP 在 NEC 的早期诊断和预测严重程度中的价值。

方法

本前瞻性研究于 2009 年 4 月至 2009 年 11 月进行。将疑似 NEC 的早产儿纳入研究。根据最终诊断,这些早产儿分为两组;第 1 组:NEC 1 期,第 2 组:NEC 2-3 期(第 2a 组:NEC 2 期,第 2b 组:NEC 3 期)。健康早产儿被分配到对照组(第 3 组)。在症状出现时、24 小时和 72 小时后从患者采集连续血样。对照组采集 1 份血样。比较各组间血清 I-FABP 水平。

结果

第 1 组、第 2a 组和第 2b 组的初始血清 I-FABP 浓度分别为 324.0±165.8pg/ml、764.7±465.1pg/ml 和 360.2±439.5pg/ml,均明显高于对照组(76.9±115.9pg/ml)(p<0.001)。第 1 组和第 2a 组的血清 I-FABP 水平从疾病发作到第 72 小时逐渐下降(p=0.001)。第 2b 组 I-FABP 浓度在疾病发作后 24 小时略有下降,此后有所增加,但差异无统计学意义(p=0.06)。

结论

连续测量 I-FABP 水平可能是 NEC 早期诊断和预测疾病严重程度的有用标志物。

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