对发生坏死性小肠结肠炎的极早产儿尿液 I-FABP 进行纵向分析。

IF 3.1 3区 医学 Q1 PEDIATRICS Pediatric Research Pub Date : 2024-11-16 DOI:10.1038/s41390-024-03737-9
Jennifer B Fundora, Darla R Shores, Allen D Everett, Lisa R Yanek, Frances J Northington, Maureen M Gilmore
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引用次数: 0

摘要

背景:肠脂肪酸结合蛋白(I-FABP)是一种可在患有坏死性小肠结肠炎(NEC)的婴儿体内检测到的肠上皮细胞蛋白。I-FABP 在 NEC 后的纵向行为或其与胃肠道或神经发育结果的关系尚不清楚:在早产儿促红细胞生成素神经保护试验的二次分析中,我们对患有和未患有 NEC 的婴儿进行了比较。使用酶联免疫吸附法对匹配婴儿(n = 70)的尿液 I-FABP 浓度进行连续测量,并使用配对分析法进行比较。在患有 NEC 的婴儿中,采用非参数分析法确定 I-FABP 水平与短期结果和 22-26 个月大时神经发育结果的关系:结果:NEC患儿更有可能出现胆汁淤积、死亡或严重神经发育障碍、脑瘫以及较低的Bayley-III运动评分。各组的基线尿I-FABP水平相似。与对照组相比,NEC 患儿在诊断时尿 I-FABP 浓度较高(中位数为 11 vs 2.6 ng/ml,p = 0.006),NEC 后尿 I-FABP 浓度较低(中位数为 1 vs 5 ng/ml,p = 0.002)。诊断时的 I-FABP 水平与 22-26 个月大时的胃肠道或神经发育结果无关:结论:与匹配的对照组相比,极早产儿在确诊 NEC 时尿 I-FABP 升高,NEC 后则降低。I-FABP水平与胃肠道或神经发育的不良后果无关:影响:极早产儿在确诊 NEC 时尿中的肠脂肪酸结合蛋白 (I-FABP) 水平会升高,NEC 后会降至基线以下。诊断 NEC 时的尿 I-FABP 水平与胆汁淤积症、肠道狭窄或梗阻、NEC 后是否需要额外的肠道手术或 22-26 个月大时的神经发育结果无关。尿 I-FABP 水平可能有助于 NEC 的诊断。诊断性 I-FABP 水平不能预测 NEC 后的短期胃肠道或神经发育结果。
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Longitudinal analysis of urinary I-FABP in extremely preterm infants that develop necrotizing enterocolitis.

Background: Intestinal fatty acid binding protein (I-FABP) is an intestinal epithelial protein detectable in infants with necrotizing enterocolitis (NEC). The longitudinal behavior of I-FABP following NEC or its association with gastrointestinal or neurodevelopmental outcomes is unknown.

Methods: In this secondary analysis of the Preterm Erythropoietin Neuroprotection Trial, we compared infants with and without NEC. Urine I-FABP concentrations in matched infants (n = 70) were measured serially using ELISA and compared using paired analysis. In infants with NEC, the associations of I-FABP levels with short-term outcomes and neurodevelopmental outcomes at 22-26 months corrected age were determined using non-parametric analysis.

Results: Infants with NEC were more likely to have cholestasis, death or severe neurodevelopmental impairment, cerebral palsy, and lower Bayley-III motor scores. Baseline urinary I-FABP levels were similar between groups. When compared to controls, infants with NEC had urinary I-FABP concentrations that were higher at diagnosis (median 11 vs 2.6 ng/ml, p = 0.006) and lower post-NEC (median 1 vs 5 ng/ml, p = 0.002). Diagnosis I-FABP levels were not associated with gastrointestinal or neurodevelopmental outcomes at 22-26 months corrected age.

Conclusions: In extremely preterm infants, urinary I-FABP was elevated at NEC diagnosis and lower post-NEC compared to matched controls. I-FABP levels were not associated with adverse gastrointestinal or neurodevelopmental outcomes.

Impact: Urinary intestinal fatty acid binding protein (I-FABP) levels are increased at diagnosis of NEC and fall to below baseline after NEC in extremely preterm infants. Urine I-FABP levels at NEC diagnosis are not associated with cholestasis, intestinal stricture or obstruction, need for additional intestinal surgery after NEC, or neurodevelopmental outcomes at 22-26 months corrected age. Urine I-FABP levels may be useful in the diagnosis of NEC. Diagnostic I-FABP levels do not predict short-term gastrointestinal or neurodevelopmental outcomes after NEC.

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来源期刊
Pediatric Research
Pediatric Research 医学-小儿科
CiteScore
6.80
自引率
5.60%
发文量
473
审稿时长
3-8 weeks
期刊介绍: Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of children''s diseases and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies
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