Suppr超能文献

机械通气的足月儿和早产儿呼吸窘迫综合征及支气管肺发育不良风险患儿的克拉拉细胞蛋白表达:一项初步研究

Clara Cell Protein Expression in Mechanically Ventilated Term and Preterm Infants with Respiratory Distress Syndrome and at Risk of Bronchopulmonary Dysplasia: A Pilot Study.

作者信息

Guzmán-Bárcenas José, Calderón-Moore Antonio, Baptista-González Héctor, Irles Claudine

机构信息

Department of Perinatal Hematology, Instituto Nacional de Perinatología Isidro Espinoza de los Reyes, Montes Urales 800, 11000 Lomas de Virreyes, CDMX, Mexico.

Neonatal Intensive Care Unit, Hospital Infantil de México, Dr. Márquez No. 162, Cuauhtémoc, 06720 Doctores, CDMX, Mexico.

出版信息

Can Respir J. 2017;2017:8074678. doi: 10.1155/2017/8074678. Epub 2017 Apr 11.

Abstract

The aim of this pilot study was to determine Clara cell protein (CC16) concentration in bronchoalveolar lavages (BAL) fluid from full-term and preterm (<37 weeks' gestational age) neonates requiring respiratory support, having symptoms of neonatal respiratory distress syndrome, and at risk of bronchopulmonary dysplasia (BPD). We hypothesized that CC16 may be predictive of BPD diagnosis regardless of gestational age. BAL fluid CC16 was measured by ELISA at birth and at day 7 of life. Both groups that developed BPD showed significantly decreased BAL fluid CC16 levels compared to those infants that did not develop the disease. CC16 positively correlated with diagnosis of BPD and negatively with the severity of the disease. These results suggest that BAL fluid CC16 levels may have a diagnostic value at day 7 for BPD in both term and preterm infants. This study demonstrates the potential utility of BAL fluid CC16 levels as a biomarker for BPD in term infants.

摘要

这项初步研究的目的是测定来自足月和早产(胎龄<37周)新生儿的支气管肺泡灌洗(BAL)液中克拉拉细胞蛋白(CC16)的浓度,这些新生儿需要呼吸支持,有新生儿呼吸窘迫综合征的症状,且有支气管肺发育不良(BPD)的风险。我们假设CC16可能是BPD诊断的预测指标,而与胎龄无关。在出生时和出生后第7天通过酶联免疫吸附测定法(ELISA)测量BAL液中的CC16。与未患该疾病的婴儿相比,两组患BPD的婴儿BAL液中CC16水平均显著降低。CC16与BPD诊断呈正相关,与疾病严重程度呈负相关。这些结果表明,BAL液中CC16水平在出生后第7天对足月儿和早产儿的BPD可能具有诊断价值。本研究证明了BAL液中CC16水平作为足月儿BPD生物标志物的潜在效用。

相似文献

2
Cord blood Clara cell protein CC16 predicts the development of bronchopulmonary dysplasia.
Eur J Pediatr. 2008 Nov;167(11):1305-12. doi: 10.1007/s00431-008-0713-2. Epub 2008 Jun 3.
3
Clara cell secretory protein (CC16) as a peripheral blood biomarker of lung injury in ventilated preterm neonates.
Eur J Pediatr. 2008 Nov;167(11):1297-303. doi: 10.1007/s00431-008-0712-3. Epub 2008 Jun 3.
4
Club cell secretory protein (CC16) in gastric fluid at birth and subsequent lung disease in preterm infants.
Pediatr Pulmonol. 2018 Oct;53(10):1399-1406. doi: 10.1002/ppul.24128. Epub 2018 Jul 10.
8
Respiratory burst activity in bronchopulmonary dysplasia and changes with dexamethasone.
Pediatr Pulmonol. 2003 May;35(5):392-9. doi: 10.1002/ppul.10279.
9

引用本文的文献

本文引用的文献

1
Biomarkers for Bronchopulmonary Dysplasia in the Preterm Infant.
Front Pediatr. 2016 Mar 31;4:33. doi: 10.3389/fped.2016.00033. eCollection 2016.
2
Univariate description and bivariate statistical inference: the first step delving into data.
Ann Transl Med. 2016 Mar;4(5):91. doi: 10.21037/atm.2016.02.11.
3
Bronchopulmonary dysplasia - an overview about pathophysiologic concepts.
Mol Cell Pediatr. 2015 Dec;2(1):2. doi: 10.1186/s40348-015-0013-7. Epub 2015 Feb 26.
4
Depletion of bone marrow CCSP-expressing cells delays airway regeneration.
Mol Ther. 2015 Mar;23(3):561-9. doi: 10.1038/mt.2014.223. Epub 2014 Nov 20.
7
Predictors of bronchopulmonary dysplasia.
Clin Perinatol. 2012 Sep;39(3):585-601. doi: 10.1016/j.clp.2012.06.014.
8
Clara cell protein expression in human neonates during respiratory distress syndrome.
Cell Physiol Biochem. 2012;29(5-6):753-60. doi: 10.1159/000264417. Epub 2012 May 11.
9
Early postnatal surge of serum Clara cell secretory protein in newborn infants.
Neonatology. 2012;101(2):125-31. doi: 10.1159/000329557. Epub 2011 Sep 23.
10
Bronchopulmonary dysplasia.
Respir Care. 2009 Sep;54(9):1252-62.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验