11-12 岁儿童端粒长度与妊娠并发症无关

DNA Pub Date : 2024-06-11 DOI:10.3390/dna4020011
T. Bianco-Miotto, Sadia Hossain, Nahal Habibi, Dandara G. Haag, J. Grieger
{"title":"11-12 岁儿童端粒长度与妊娠并发症无关","authors":"T. Bianco-Miotto, Sadia Hossain, Nahal Habibi, Dandara G. Haag, J. Grieger","doi":"10.3390/dna4020011","DOIUrl":null,"url":null,"abstract":"Children born from pregnancy complications are at higher risk of chronic diseases in adulthood. Identifying which children born from a complicated pregnancy are likely to suffer from later chronic disease is important in order to intervene to prevent or delay the onset of disease. This study examined the associations between the major pregnancy complications (gestational diabetes, high blood pressure, small- and large for gestational age, and preterm birth) and child telomere length, a biomarker of chronic disease risk. This was a population-based longitudinal analysis using data from the Longitudinal Study of Australian Children. The primary outcome is telomere length, measured in 11–12-year-old children. Multivariable linear regression was used to estimate the association between pregnancy complications and child telomere length, adjusting for a range of a priori confounders. Data from 841 families were used. One in four pregnancies (27.1%) featured a pregnancy complication. In the adjusted analysis, there was no association between pregnancy complications and child telomere length (high blood pressure: mean difference (95% CI): 0.00 (−0.12, 0.12); gestational diabetes (0.05 (−0.10, 0.19)); small for gestational age (0.07 (−0.04, 0.19)); large for gestational age (−0.06 (−0.15, 0.03)); and preterm birth (−0.10 (−0.21, 0.01)). Our results do not support the notion that telomere length is shorter in children born to mothers after a pregnancy complication. Methodological considerations should be rigorous to improve the reproducibility of findings.","PeriodicalId":72835,"journal":{"name":"DNA","volume":"3 10","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Child Telomere Length at 11–12 Years of Age Is Not Associated with Pregnancy Complications\",\"authors\":\"T. Bianco-Miotto, Sadia Hossain, Nahal Habibi, Dandara G. Haag, J. Grieger\",\"doi\":\"10.3390/dna4020011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Children born from pregnancy complications are at higher risk of chronic diseases in adulthood. Identifying which children born from a complicated pregnancy are likely to suffer from later chronic disease is important in order to intervene to prevent or delay the onset of disease. This study examined the associations between the major pregnancy complications (gestational diabetes, high blood pressure, small- and large for gestational age, and preterm birth) and child telomere length, a biomarker of chronic disease risk. This was a population-based longitudinal analysis using data from the Longitudinal Study of Australian Children. The primary outcome is telomere length, measured in 11–12-year-old children. Multivariable linear regression was used to estimate the association between pregnancy complications and child telomere length, adjusting for a range of a priori confounders. Data from 841 families were used. One in four pregnancies (27.1%) featured a pregnancy complication. In the adjusted analysis, there was no association between pregnancy complications and child telomere length (high blood pressure: mean difference (95% CI): 0.00 (−0.12, 0.12); gestational diabetes (0.05 (−0.10, 0.19)); small for gestational age (0.07 (−0.04, 0.19)); large for gestational age (−0.06 (−0.15, 0.03)); and preterm birth (−0.10 (−0.21, 0.01)). Our results do not support the notion that telomere length is shorter in children born to mothers after a pregnancy complication. Methodological considerations should be rigorous to improve the reproducibility of findings.\",\"PeriodicalId\":72835,\"journal\":{\"name\":\"DNA\",\"volume\":\"3 10\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"DNA\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/dna4020011\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"DNA","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/dna4020011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

因妊娠并发症而出生的儿童成年后患慢性病的风险较高。确定哪些妊娠并发症患儿日后可能罹患慢性疾病,对于采取干预措施预防或推迟疾病的发生非常重要。这项研究考察了主要妊娠并发症(妊娠糖尿病、高血压、胎龄小和胎龄大以及早产)与儿童端粒长度(一种慢性病风险生物标志物)之间的关系。这是一项基于人群的纵向分析,使用的数据来自澳大利亚儿童纵向研究。主要结果是端粒长度,测量对象是11-12岁的儿童。多变量线性回归用于估计妊娠并发症与儿童端粒长度之间的关系,并对一系列先验混杂因素进行了调整。研究使用了来自 841 个家庭的数据。每四个孕妇中就有一个(27.1%)出现妊娠并发症。在调整后的分析中,妊娠并发症与儿童端粒长度之间没有关联(高血压:平均差(95% CI):0.00 (-0.12, 0.12);妊娠糖尿病(0.05 (-0.10, 0.19));胎龄小(0.07 (-0.04, 0.19));胎龄大(-0.06 (-0.15, 0.03));早产(-0.10 (-0.21, 0.01))。我们的结果并不支持妊娠并发症后母亲所生子女端粒长度较短的观点。为了提高研究结果的可重复性,我们应该对研究方法进行严格的审查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Child Telomere Length at 11–12 Years of Age Is Not Associated with Pregnancy Complications
Children born from pregnancy complications are at higher risk of chronic diseases in adulthood. Identifying which children born from a complicated pregnancy are likely to suffer from later chronic disease is important in order to intervene to prevent or delay the onset of disease. This study examined the associations between the major pregnancy complications (gestational diabetes, high blood pressure, small- and large for gestational age, and preterm birth) and child telomere length, a biomarker of chronic disease risk. This was a population-based longitudinal analysis using data from the Longitudinal Study of Australian Children. The primary outcome is telomere length, measured in 11–12-year-old children. Multivariable linear regression was used to estimate the association between pregnancy complications and child telomere length, adjusting for a range of a priori confounders. Data from 841 families were used. One in four pregnancies (27.1%) featured a pregnancy complication. In the adjusted analysis, there was no association between pregnancy complications and child telomere length (high blood pressure: mean difference (95% CI): 0.00 (−0.12, 0.12); gestational diabetes (0.05 (−0.10, 0.19)); small for gestational age (0.07 (−0.04, 0.19)); large for gestational age (−0.06 (−0.15, 0.03)); and preterm birth (−0.10 (−0.21, 0.01)). Our results do not support the notion that telomere length is shorter in children born to mothers after a pregnancy complication. Methodological considerations should be rigorous to improve the reproducibility of findings.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
DNA
DNA
自引率
0.00%
发文量
0
期刊最新文献
8-OxodG: A Potential Biomarker for Chronic Oxidative Stress Induced by High-LET Radiation. Origin of Type II tRNA Variable Loops, Aminoacyl-tRNA Synthetase Allostery from Distal Determinants, and Diversification of Life Comparative Analysis of Five Forensic PCR Kits in Duplets Efficient Elimination of mtDNA from Mammalian Cells with 2′,3′-Dideoxycytidine Child Telomere Length at 11–12 Years of Age Is Not Associated with Pregnancy Complications
×
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:481959085
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