• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

血浆脂质代谢物与胎龄相关,但与支气管肺发育不良无关。

Plasma lipid metabolites are associated with gestational age but not bronchopulmonary dysplasia.

机构信息

Department of Pediatrics, Center for Perinatal Research, The Research Institute at Nationwide Children's Hospital, The Ohio State University, Columbus, OH, USA.

出版信息

Acta Paediatr. 2012 Aug;101(8):e321-6. doi: 10.1111/j.1651-2227.2012.02694.x. Epub 2012 May 2.

DOI:10.1111/j.1651-2227.2012.02694.x
PMID:22497282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3693574/
Abstract

AIM

To test the hypothesis that plasma lipid metabolite levels in premature infants are associated with the development of bronchopulmonary dysplasia (BPD). The studies also tested a secondary hypothesis that plasma lipid metabolite levels were correlated with gestational age.

METHODS

Infants born <32 weeks' gestation were enrolled during the first 72 h of life. Plasma samples were obtained and lipid levels were measured by LC-MS/MS. Clinical data were collected to determine infant outcomes and BPD diagnosis.

RESULTS

Following adjustment for confounders, lipid levels were not associated with BPD; however, levels of specific lipid metabolites were correlated with gestational age.

CONCLUSION

Immature lipid metabolism pathways in premature infants may contribute to the pathogenesis of BPD and other diseases.

摘要

目的

验证早产儿血浆脂质代谢物水平与支气管肺发育不良(BPD)发展相关的假设。研究还检验了血浆脂质代谢物水平与胎龄相关的次要假设。

方法

在出生后 72 小时内,纳入胎龄<32 周的婴儿。采集血浆样本,通过 LC-MS/MS 测量脂质水平。收集临床数据以确定婴儿结局和 BPD 诊断。

结果

在调整混杂因素后,脂质水平与 BPD 无关;然而,特定脂质代谢物的水平与胎龄相关。

结论

早产儿不成熟的脂质代谢途径可能导致 BPD 和其他疾病的发病机制。

相似文献

1
Plasma lipid metabolites are associated with gestational age but not bronchopulmonary dysplasia.血浆脂质代谢物与胎龄相关,但与支气管肺发育不良无关。
Acta Paediatr. 2012 Aug;101(8):e321-6. doi: 10.1111/j.1651-2227.2012.02694.x. Epub 2012 May 2.
2
Developmental changes in polyunsaturated fetal plasma phospholipids and feto-maternal plasma phospholipid ratios and their association with bronchopulmonary dysplasia.胎儿血浆多不饱和磷脂及胎儿-母体血浆磷脂比率的发育变化及其与支气管肺发育不良的关联。
Eur J Nutr. 2016 Oct;55(7):2265-74. doi: 10.1007/s00394-015-1036-5. Epub 2015 Sep 12.
3
Early metabolic markers as predictors of respiratory complications in preterm infants with bronchopulmonary dysplasia.早期代谢标志物作为支气管肺发育不良早产儿呼吸并发症的预测指标
Early Hum Dev. 2024 Mar;190:105950. doi: 10.1016/j.earlhumdev.2024.105950. Epub 2024 Jan 28.
4
Role of antioxidant nutrients and lipid peroxidation in premature infants with respiratory distress syndrome and bronchopulmonary dysplasia.抗氧化营养素和脂质过氧化在呼吸窘迫综合征和支气管肺发育不良早产儿中的作用。
Am J Perinatol. 2003 Feb;20(2):97-107. doi: 10.1055/s-2003-38315.
5
Vitamin D and bronchopulmonary dysplasia in preterm infants.维生素D与早产儿支气管肺发育不良
J Perinatol. 2016 Oct;36(10):878-82. doi: 10.1038/jp.2016.115. Epub 2016 Jul 28.
6
Urinary leukotriene E(4) excretion during the first month of life and subsequent bronchopulmonary dysplasia in premature infants.早产儿出生后第一个月尿白三烯E(4)排泄量与随后发生的支气管肺发育不良
Chest. 2001 Jun;119(6):1749-54. doi: 10.1378/chest.119.6.1749.
7
Early clinical markers for the development of bronchopulmonary dysplasia: soluble E-Selectin and ICAM-1.支气管肺发育不良发生的早期临床标志物:可溶性E-选择素和细胞间黏附分子-1
Pediatrics. 1998 Oct;102(4 Pt 1):927-32. doi: 10.1542/peds.102.4.927.
8
Plasma 3-nitrotyrosine is elevated in premature infants who develop bronchopulmonary dysplasia.
Pediatrics. 1998 May;101(5):870-4. doi: 10.1542/peds.101.5.870.
9
Angiopoietin-1 and endostatin levels in cord plasma predict the development of bronchopulmonary dysplasia in preterm infants.脐血浆血管生成素-1 和内皮抑素水平预测早产儿支气管肺发育不良的发生。
J Trop Pediatr. 2011 Oct;57(5):385-8. doi: 10.1093/tropej/fmq112. Epub 2010 Dec 2.
10
Preeclampsia and the Risk of Bronchopulmonary Dysplasia in Preterm Infants Less Than 32 Weeks' Gestation.小于32周妊娠的早产儿子痫前期与支气管肺发育不良的风险
Am J Perinatol. 2017 May;34(6):585-592. doi: 10.1055/s-0036-1594017. Epub 2016 Dec 5.

引用本文的文献

1
Something Smells Fishy: How Lipid Mediators Impact the Maternal-Fetal Interface and Neonatal Development.有些可疑:脂质介质如何影响母胎界面和新生儿发育。
Biomedicines. 2023 Jan 10;11(1):171. doi: 10.3390/biomedicines11010171.
2
Umbilical cord blood metabolomics reveal distinct signatures of dyslipidemia prior to bronchopulmonary dysplasia and pulmonary hypertension.脐带血代谢组学揭示了支气管肺发育不良和肺动脉高压前血脂异常的独特特征。
Am J Physiol Lung Cell Mol Physiol. 2018 Nov 1;315(5):L870-L881. doi: 10.1152/ajplung.00283.2017. Epub 2018 Aug 16.
3
miR-29b supplementation decreases expression of matrix proteins and improves alveolarization in mice exposed to maternal inflammation and neonatal hyperoxia.补充miR-29b可降低基质蛋白的表达,并改善暴露于母体炎症和新生儿高氧环境下的小鼠的肺泡化。
Am J Physiol Lung Cell Mol Physiol. 2017 Aug 1;313(2):L339-L349. doi: 10.1152/ajplung.00273.2016. Epub 2017 May 4.
4
Of mice and men: correlations between microRNA-17∼92 cluster expression and promoter methylation in severe bronchopulmonary dysplasia.小鼠与人:重度支气管肺发育不良中微小RNA - 17∼92簇表达与启动子甲基化之间的相关性
Am J Physiol Lung Cell Mol Physiol. 2016 Nov 1;311(5):L981-L984. doi: 10.1152/ajplung.00390.2016. Epub 2016 Sep 30.
5
Attenuation of miR-17∼92 Cluster in Bronchopulmonary Dysplasia.支气管肺发育不良中miR-17∼92簇的衰减
Ann Am Thorac Soc. 2015 Oct;12(10):1506-13. doi: 10.1513/AnnalsATS.201501-058OC.
6
DHA suppresses chronic apoptosis in the lung caused by perinatal inflammation.二十二碳六烯酸可抑制围产期炎症引起的肺部慢性细胞凋亡。
Am J Physiol Lung Cell Mol Physiol. 2015 Sep 1;309(5):L441-8. doi: 10.1152/ajplung.00137.2015. Epub 2015 Jul 2.
7
Associations between maternal and infant morbidities and sRAGE within the first week of life in extremely preterm infants.极早产儿生后第一周母儿并发症与 sRAGE 的相关性研究。
PLoS One. 2013 Dec 6;8(12):e82537. doi: 10.1371/journal.pone.0082537. eCollection 2013.
8
Cyclooxygenase-2 in newborn hyperoxic lung injury.环氧化酶-2与新生儿高氧肺损伤
Free Radic Biol Med. 2013 Aug;61:502-11. doi: 10.1016/j.freeradbiomed.2013.04.012. Epub 2013 Apr 25.

本文引用的文献

1
Lung function and respiratory symptoms at 11 years in children born extremely preterm: the EPICure study.极早产儿 11 岁时的肺功能和呼吸症状:EPICure 研究。
Am J Respir Crit Care Med. 2010 Jul 15;182(2):237-45. doi: 10.1164/rccm.200912-1806OC. Epub 2010 Apr 8.
2
Is COPD in adulthood really so far removed from early development?成年期的慢性阻塞性肺疾病(COPD)真的与早期发育如此脱节吗?
Eur Respir J. 2010 Jan;35(1):12-3. doi: 10.1183/09031936.00145809.
3
Targeted chiral lipidomics analysis of bioactive eicosanoid lipids in cellular systems.细胞系统中生物活性类二十烷酸脂质的靶向手性脂质组学分析。
BMB Rep. 2009 Jul 31;42(7):401-10. doi: 10.5483/bmbrep.2009.42.7.401.
4
Soluble vascular endothelial growth factor receptor 1 in tracheal aspirate fluid of preterm neonates at birth may be predictive of bronchopulmonary dysplasia/chronic lung disease.出生时早产儿气管吸出液中的可溶性血管内皮生长因子受体1可能是支气管肺发育不良/慢性肺病的预测指标。
Pediatrics. 2009 Jun;123(6):1541-7. doi: 10.1542/peds.2008-1670.
5
Pulmonary Biomarkers of Bronchopulmonary Dysplasia.支气管肺发育不良的肺部生物标志物
Biomark Insights. 2008 Jul 2;3:361-373. doi: 10.4137/bmi.s834.
6
New aspects of the role of hydroxyeicosatetraenoic acids in cell growth and cancer development.羟基二十碳四烯酸在细胞生长和癌症发展中的作用的新方面。
Biochem Pharmacol. 2009 Jan 1;77(1):1-10. doi: 10.1016/j.bcp.2008.07.033. Epub 2008 Aug 5.
7
Chorioamnionitis and ontogeny of circulating prostaglandin and thromboxane in preterm infants.早产婴儿绒毛膜羊膜炎与循环前列腺素和血栓素的个体发生
Am J Perinatol. 2008 Sep;25(8):491-7. doi: 10.1055/s-0028-1085068. Epub 2008 Aug 22.
8
Bronchopulmonary dysplasia and inflammatory biomarkers in the premature neonate.早产儿支气管肺发育不良与炎症生物标志物
Arch Dis Child Fetal Neonatal Ed. 2008 Nov;93(6):F455-61. doi: 10.1136/adc.2007.121327. Epub 2008 Aug 1.
9
Cardiopulmonary outcomes of extreme prematurity.极早早产儿的心肺结局
Semin Perinatol. 2008 Feb;32(1):28-34. doi: 10.1053/j.semperi.2007.12.005.
10
Lung development and adult lung diseases.肺发育与成人肺部疾病
Chest. 2007 Aug;132(2):651-6. doi: 10.1378/chest.06-2663.