• 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

关于表面活性蛋白-B(SFTPB)多态性与新生儿呼吸窘迫综合征易感性关系的综合数据汇编。

A Comprehensive Compilation of Data on the Relationship Between Surfactant Protein-B (SFTPB) Polymorphisms and Susceptibility to Neonatal Respiratory Distress Syndrome.

机构信息

Department of Pediatrics, Islamic Azad University of Yazd, Yazd, Iran.

Neonatal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Fetal Pediatr Pathol. 2024 Sep-Oct;43(5):399-418. doi: 10.1080/15513815.2024.2390932. Epub 2024 Aug 19.

DOI:10.1080/15513815.2024.2390932
PMID:39159013
Abstract

BACKGROUND

This study aims to explore the association between variations in the Surfactant Protein-B (SFTPB) gene and the risk of neonatal respiratory distress syndrome (NRDS).

METHODS

A comprehensive literature search was conducted across PubMed, Scopus, EMBASE, and CNKI databases up to February 10, 2024, to identify pertinent studies.

RESULTS

A total of seventeen studies examining the +1580 C/T polymorphism (2,058 cases and 2,596 controls) and five studies investigating the -18 A/C polymorphism (680 cases and 739 controls) were included in the analysis. The pooled data indicated that the +1580 C/T polymorphism confers a protective effect against NRDS in various populations and ethnic groups. Conversely, the -18 A/C polymorphism did not demonstrate a significant association either globally or among Asian neonates.

CONCLUSIONS

The +1580 C/T variant appears to be protective against NRDS, whereas the -18 A/C polymorphism shows minimal impact on the disease's progression.

摘要

背景

本研究旨在探讨表面活性蛋白-B(SFTPB)基因变异与新生儿呼吸窘迫综合征(NRDS)风险之间的关联。

方法

对 PubMed、Scopus、EMBASE 和中国知网(CNKI)数据库进行全面文献检索,检索时间截至 2024 年 2 月 10 日,以确定相关研究。

结果

共纳入 17 项研究,分析了 +1580C/T 多态性(2058 例病例和 2596 例对照),纳入 5 项研究,分析了-18A/C 多态性(680 例病例和 739 例对照)。汇总数据表明,+1580C/T 多态性在不同人群和种族中均对 NRDS 具有保护作用。相反,-18A/C 多态性在全球或亚洲新生儿中均与 NRDS 无显著关联。

结论

+1580C/T 变异似乎对 NRDS 具有保护作用,而-18A/C 多态性对疾病的进展影响较小。

相似文献

1
A Comprehensive Compilation of Data on the Relationship Between Surfactant Protein-B (SFTPB) Polymorphisms and Susceptibility to Neonatal Respiratory Distress Syndrome.关于表面活性蛋白-B(SFTPB)多态性与新生儿呼吸窘迫综合征易感性关系的综合数据汇编。
Fetal Pediatr Pathol. 2024 Sep-Oct;43(5):399-418. doi: 10.1080/15513815.2024.2390932. Epub 2024 Aug 19.
2
[Relationship between reduced expression of surfactant protein B and neonatal respiratory distress syndrome in twenty Han ethnic group neonates in China].[中国20例汉族新生儿表面活性物质蛋白B表达降低与新生儿呼吸窘迫综合征的关系]
Zhonghua Er Ke Za Zhi. 2008 Jan;46(1):9-12.
3
Comprehensive genetic variant discovery in the surfactant protein B gene.表面活性蛋白B基因的全面遗传变异发现
Pediatr Res. 2007 Aug;62(2):170-5. doi: 10.1203/PDR.0b013e3180a03232.
4
Surfactant protein B deficiency and gene mutations for neonatal respiratory distress syndrome in China Han ethnic population.中国汉族人群中新生儿呼吸窘迫综合征的表面活性物质蛋白B缺乏与基因突变
Int J Clin Exp Pathol. 2013;6(2):267-72. Epub 2013 Jan 15.
5
[Genetic markers of predisposition to infectious complications in neonatal infants with respiratory distress syndrome].[新生儿呼吸窘迫综合征感染性并发症易感性的遗传标志物]
Anesteziol Reanimatol. 2009 Jan-Feb(1):46-8.
6
[Relationship between pulmonary surfactant-associated protein B polymorphisms and the susceptibility to neonatal respiratory distress syndrome].肺表面活性物质相关蛋白B基因多态性与新生儿呼吸窘迫综合征易感性的关系
Zhongguo Dang Dai Er Ke Za Zhi. 2012 Jan;14(1):24-7.
7
Human Surfactant Proteins A2 (SP-A2) and B (SP-B) Genes as Determinants of Respiratory Distress Syndrome.人类表面活性物质蛋白A2(SP-A2)和B(SP-B)基因作为呼吸窘迫综合征的决定因素
Indian Pediatr. 2015 May;52(5):391-4. doi: 10.1007/s13312-015-0643-9.
8
A Comprehensive Consolidation of Data on the Relationship Between Surfactant Protein-B (SFTPB) Polymorphisms and Susceptibility to Bronchopulmonary Dysplasia.全面整理关于表面活性蛋白-B(SFTPB)多态性与支气管肺发育不良易感性之间关系的数据。
Fetal Pediatr Pathol. 2024 Nov-Dec;43(6):436-454. doi: 10.1080/15513815.2024.2400145. Epub 2024 Sep 8.
9
Genetic Polymorphisms of SP-A, SP-B, and SP-D and Risk of Respiratory Distress Syndrome in Preterm Neonates.表面活性蛋白A、表面活性蛋白B和表面活性蛋白D的基因多态性与早产儿呼吸窘迫综合征的风险
Med Sci Monit. 2016 Dec 24;22:5091-5100. doi: 10.12659/msm.898553.
10
Association of SP-B gene 9306 A/G polymorphism (rs7316) and risk of RDS.表面活性蛋白B基因9306 A/G多态性(rs7316)与呼吸窘迫综合征风险的关联。
J Matern Fetal Neonatal Med. 2018 Nov;31(22):2965-2970. doi: 10.1080/14767058.2017.1359829. Epub 2017 Aug 7.

引用本文的文献

1
Advancements in biomarkers and machine learning for predicting of bronchopulmonary dysplasia and neonatal respiratory distress syndrome in preterm infants.生物标志物和机器学习在预测早产儿支气管肺发育不良和新生儿呼吸窘迫综合征方面的进展。
Front Pediatr. 2025 Apr 25;13:1521668. doi: 10.3389/fped.2025.1521668. eCollection 2025.
2
Decoding bronchopulmonary dysplasia in premature infants through an epigenetic lens.从表观遗传学角度解读早产儿支气管肺发育不良
Front Med (Lausanne). 2025 Apr 3;12:1531169. doi: 10.3389/fmed.2025.1531169. eCollection 2025.
3
Association of TNF-α genetic variants with neonatal bronchopulmonary dysplasia: consolidated results.
肿瘤坏死因子-α基因变异与新生儿支气管肺发育不良的关联:综合结果
Front Pediatr. 2024 Dec 19;12:1511355. doi: 10.3389/fped.2024.1511355. eCollection 2024.