Platelet characteristics in extremely preterm infants after fatty acid supplementation: a randomized controlled trial

IF 3.1 3区 医学 Q1 PEDIATRICS Pediatric Research Pub Date : 2024-12-19 DOI:10.1038/s41390-024-03775-3
Pia Lundgren, Aldina Pivodic, Anders K. Nilsson, Gunnel Hellgren, Hanna Danielsson, Dirk Wackernagel, Ingrid Hansen Pupp, David Ley, Karin Sävman, Mattias Uhlén, Lois E. H. Smith, Ann Hellström
{"title":"Platelet characteristics in extremely preterm infants after fatty acid supplementation: a randomized controlled trial","authors":"Pia Lundgren, Aldina Pivodic, Anders K. Nilsson, Gunnel Hellgren, Hanna Danielsson, Dirk Wackernagel, Ingrid Hansen Pupp, David Ley, Karin Sävman, Mattias Uhlén, Lois E. H. Smith, Ann Hellström","doi":"10.1038/s41390-024-03775-3","DOIUrl":null,"url":null,"abstract":"Two risk factors for severe retinopathy of prematurity (ROP) in extremely preterm infants are thrombocytopenia and low levels of arachidonic acid (AA) and docosahexaenoic acid (DHA). To date, these risk factors have not been linked. Infants born < 28 weeks gestational age (GA) from 2016 to 2019 were randomized to postnatal enteral AA/DHA supplementation or standard care (controls). Levels of AA and DHA, platelet counts ( < 100 × 109/L defined as thrombocytopenia) and platelet-related proteins in the infants’ first four weeks of life were evaluated for their association with severe ROP. The mean birthweight of 178 included infants was 806 ± 200 grams, and the mean GA was 25.6 ± 1.4 weeks. During the first four postnatal weeks, 20.2% of AA/DHA-supplemented infants had thrombocytopenia versus 27.7% of controls (p = 0.29). In infants with thrombocytopenia, fewer AA/DHA-supplemented infants developed severe ROP than non-supplemented controls, 29.4% (5/17) versus 65.4% (17/26) (p = 0.031). Thrombocytopenia and serum levels of AA and DHA correlated with several platelet-related proteins involved in angiogenesis and ROP, such as platelet-derived growth factor subunits A and B and vascular endothelial growth factor. AA and DHA supplementation is associated with less severe ROP in thrombocytopenic infants, possibly by modulating platelet activation and function.","PeriodicalId":19829,"journal":{"name":"Pediatric Research","volume":"98 2","pages":"680-689"},"PeriodicalIF":3.1000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.comhttps://www.nature.com/articles/s41390-024-03775-3.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Research","FirstCategoryId":"3","ListUrlMain":"https://www.nature.com/articles/s41390-024-03775-3","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Two risk factors for severe retinopathy of prematurity (ROP) in extremely preterm infants are thrombocytopenia and low levels of arachidonic acid (AA) and docosahexaenoic acid (DHA). To date, these risk factors have not been linked. Infants born < 28 weeks gestational age (GA) from 2016 to 2019 were randomized to postnatal enteral AA/DHA supplementation or standard care (controls). Levels of AA and DHA, platelet counts ( < 100 × 109/L defined as thrombocytopenia) and platelet-related proteins in the infants’ first four weeks of life were evaluated for their association with severe ROP. The mean birthweight of 178 included infants was 806 ± 200 grams, and the mean GA was 25.6 ± 1.4 weeks. During the first four postnatal weeks, 20.2% of AA/DHA-supplemented infants had thrombocytopenia versus 27.7% of controls (p = 0.29). In infants with thrombocytopenia, fewer AA/DHA-supplemented infants developed severe ROP than non-supplemented controls, 29.4% (5/17) versus 65.4% (17/26) (p = 0.031). Thrombocytopenia and serum levels of AA and DHA correlated with several platelet-related proteins involved in angiogenesis and ROP, such as platelet-derived growth factor subunits A and B and vascular endothelial growth factor. AA and DHA supplementation is associated with less severe ROP in thrombocytopenic infants, possibly by modulating platelet activation and function.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
补充脂肪酸后极度早产儿的血小板特征:随机对照试验。
背景:极早产儿严重早产儿视网膜病变(ROP)的两个危险因素是血小板减少症和低水平的花生四烯酸(AA)和二十二碳六烯酸(DHA)。到目前为止,这些风险因素还没有联系起来。方法:对出生时浓度为9/L(定义为血小板减少)的婴儿和出生后4周的血小板相关蛋白进行评估,以确定其与严重ROP的关系。结果:178例新生儿平均出生体重为806±200 g,平均出生总年龄为25.6±1.4周。在出生后的前四周,20.2%补充AA/ dha的婴儿有血小板减少症,而对照组为27.7% (p = 0.29)。在患有血小板减少症的婴儿中,补充AA/ dha的婴儿发生严重ROP的人数少于未补充AA/ dha的对照组,分别为29.4%(5/17)和65.4% (17/26)(p = 0.031)。血小板减少症和血清AA和DHA水平与几种参与血管生成和ROP的血小板相关蛋白相关,如血小板源性生长因子亚基A和B和血管内皮生长因子。结论:补充AA和DHA可能通过调节血小板激活和功能,与血小板减少婴儿较轻的ROP相关。影响:产后肠内补充花生四烯酸(AA)和二十二碳六烯酸(DHA)给极早产儿降低严重早产儿视网膜病变(ROP)的风险与血小板减少症的婴儿。AA和DHA的影响可能,至少部分是通过改变血小板活化介导的。我们发现AA和DHA可能通过调节参与血管生成的血小板相关蛋白来降低严重ROP的风险。我们的研究结果有力地支持了对极早产儿补充AA和DHA是至关重要的,可以显著影响他们的健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
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
期刊最新文献
Prognostic value of cystatin C for chronic kidney disease in pediatric urologic malformations. Hydrocortisone administration in preterm infants is not associated with adverse cardiovascular outcomes in childhood. General movement based therapy to support neurodevelopment of preterm infants: a randomized clinical trial. Commentary: Extracurricular physical activity as an early biological investment. Impact of shared storybook reading on child development: The Japan Environment and Children's Study.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1