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将常规新生儿筛查中的血清瓜氨酸浓度用作坏死性小肠结肠炎的生物标志物。

Use of serum citrulline concentrations from routine newborn screen as a biomarker for necrotizing enterocolitis.

作者信息

Babu Sharmila, Prasad Malavika, Miller Malki, Morrissey Mark, Bhutada Alok, Rojas Mary, Rastogi Shantanu

机构信息

Maimonides Medical Center, Maimonides Infant and Children's Hospital, 4802 Tenth Ave, F-119, Brooklyn, NY, 11219, USA.

Morgan Stanley Children's Hospital of New York, Columbia University, New York, NY, USA.

出版信息

Pediatr Surg Int. 2019 Jun;35(6):715-722. doi: 10.1007/s00383-019-04470-9. Epub 2019 Mar 9.

DOI:10.1007/s00383-019-04470-9
PMID:30852646
Abstract

PURPOSE

Necrotizing enterocolitis (NEC), a leading cause of mortality and morbidity in preterm neonates, lacks a reliable biomarker. Citrulline is primarily produced by enterocytes and correlates with intestinal function. Serum citrulline concentration (CIT) is routinely measured in routine newborn screening (NBS). The purpose of the study is to test if CIT from NBS may predict the occurrence of NEC and whether it correlates with the time to full feeds (TTFF) and length of stay (LOS), serving as a biomarker of NEC and intestinal health.

METHODS

In a retrospective case control study conducted on neonates with gestational age of 26-32 weeks, we compared CIT levels between cases (neonates with NEC) and controls (next-born neonate). NBS was collected within first 24 h, at day 5 and when the neonates achieved full feeds and were compared using non-parametric tests.

RESULTS

There was no difference in CIT between the controls and cases on day 1 [11.42 (7.42-14.84 vs. 11.93 (6.85-18.8) µmol/L, p = 0.55], on day 5 [11.99 (7.99-16.55) vs. 13.70 (7.42-26.83) µmol/L, p = 0.05], or at full feeds [14.86 (6.85-25.69) vs. 15.7 (7.42-26.26) µmol/L, p = 0.87]. CIT on day 1 did not correlate with TTFF (r = 0.08, p = 0.53) or LOS (r = 0.23, p = 0.06), respectively).

CONCLUSIONS

CIT from routine NBS does not serve as a biomarker to predict NEC in preterm neonates.

摘要

目的

坏死性小肠结肠炎(NEC)是早产新生儿死亡和发病的主要原因,目前缺乏可靠的生物标志物。瓜氨酸主要由肠上皮细胞产生,与肠道功能相关。血清瓜氨酸浓度(CIT)在常规新生儿筛查(NBS)中常规检测。本研究的目的是检验NBS中的CIT是否可预测NEC的发生,以及它是否与完全经口喂养时间(TTFF)和住院时间(LOS)相关,作为NEC和肠道健康的生物标志物。

方法

在一项对胎龄为26 - 32周的新生儿进行的回顾性病例对照研究中,我们比较了病例组(患有NEC的新生儿)和对照组(下一个出生的新生儿)的CIT水平。NBS在出生后24小时内、第5天以及新生儿完全经口喂养时采集,并使用非参数检验进行比较。

结果

第1天对照组和病例组的CIT无差异[11.42(7.42 - 14.84)对11.93(6.85 - 18.8)µmol/L,p = 0.55],第5天[11.99(7.99 - 16.55)对13.70(7.42 - 26.83)µmol/L,p = 0.05],或完全经口喂养时[14.86(6.85 - 25.69)对15.7(7.42 - 26.26)µmol/L,p = 0.87]。第1天的CIT分别与TTFF(r = 0.08,p = 0.53)或LOS(r = 0.23,p = 0.06)均无相关性。

结论

常规NBS中的CIT不能作为预测早产新生儿NEC的生物标志物。

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Arch Dis Child Fetal Neonatal Ed. 2018 Mar;103(2):F182-F189. doi: 10.1136/archdischild-2017-313880. Epub 2018 Jan 9.
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Nutritional strategies and gut microbiota composition as risk factors for necrotizing enterocolitis in very-preterm infants.营养策略和肠道微生物群组成作为极早产儿坏死性小肠结肠炎的危险因素
Am J Clin Nutr. 2017 Sep;106(3):821-830. doi: 10.3945/ajcn.117.152967. Epub 2017 Jun 28.
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Reduced early dried blood spot citrulline levels in preterm infants with meconium obstruction of prematurity.
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Early Hum Dev. 2015 Dec;91(12):777-81. doi: 10.1016/j.earlhumdev.2015.09.004. Epub 2015 Oct 1.
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Trends in Care Practices, Morbidity, and Mortality of Extremely Preterm Neonates, 1993-2012.1993 - 2012年极早产儿的护理实践、发病率及死亡率趋势
JAMA. 2015 Sep 8;314(10):1039-51. doi: 10.1001/jama.2015.10244.
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Acta Paediatr. 2014 Nov;103(11):1143-7. doi: 10.1111/apa.12750. Epub 2014 Aug 15.
6
Reduced plasma citrulline levels in low birth weight infants with necrotizing enterocolitis.低出生体重儿坏死性小肠结肠炎时血浆瓜氨酸水平降低。
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7
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Early Hum Dev. 2012 Jul;88(7):563-6. doi: 10.1016/j.earlhumdev.2011.11.008. Epub 2012 Jan 31.
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Plasma citrulline concentration as a biomarker for bowel loss and adaptation in hospitalized pediatric patients requiring parenteral nutrition.血浆瓜氨酸浓度作为需要肠外营养的住院儿科患者肠丢失和适应的生物标志物。
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Acute intestinal failure in critically ill patients: is plasma citrulline the right marker?危重症患者的急性肠衰竭:瓜氨酸是否是合适的标志物?
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