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妊娠代谢综合征及其与儿童端粒长度的关系。

The metabolic syndrome in pregnancy and its association with child telomere length.

机构信息

Robinson Research Institute, University of Adelaide, North Adelaide, SA, 5005, Australia.

Adelaide Medical School, University of Adelaide, Adelaide, Australia.

出版信息

Diabetologia. 2020 Oct;63(10):2140-2149. doi: 10.1007/s00125-020-05242-0. Epub 2020 Jul 29.

Abstract

AIMS/HYPOTHESIS: The aim of this study was to determine whether presence of the metabolic syndrome in pregnancy associates with child telomere length or child anthropometry (weight, BMI) and BP, measured at 10 years of age.

METHODS

The Screening for Pregnancy Endpoints study (SCOPE) was a multicentre, international prospective cohort of nulliparous pregnant women recruited from Australia, New Zealand, Ireland and the UK (N = 5628). The current analysis is a 10 year follow-up of SCOPE pregnant women and their children, from the Australian cohort. Clinical data collected at 14-16 weeks' gestation during the SCOPE study were used to diagnose the metabolic syndrome using IDF criteria. Telomere length, a biomarker of ageing, was assessed by quantitative PCR from children's saliva collected at 10 years of age.

RESULTS

In women who completed follow-up (n = 255), 20% had the metabolic syndrome in pregnancy. After adjusting for a range of confounders, children of mothers who had the metabolic syndrome in pregnancy had 14% shorter telomeres than children of mothers without the metabolic syndrome in pregnancy (mean difference -0.36 [95% CI -0.74, 0.01]). Height- and weight-for-age, and BMI z scores were similar in children of mothers who did and did not have the metabolic syndrome during pregnancy.

CONCLUSIONS/INTERPRETATION: Children of mothers who had the metabolic syndrome in pregnancy have shorter telomeres, a biomarker of accelerated ageing. These findings warrant further studies in larger cohorts of children, as well as investigations into whether telomere length measured in cord blood associates with telomere length in childhood.

摘要

目的/假设:本研究旨在确定妊娠期间代谢综合征的存在是否与儿童端粒长度或儿童体格(体重、BMI)和血压有关,这些指标在 10 岁时测量。

方法

筛查妊娠终点研究(SCOPE)是一项多中心、国际前瞻性队列研究,纳入了来自澳大利亚、新西兰、爱尔兰和英国的初产妇(n=5628)。目前的分析是 SCOPE 孕妇及其儿童的 10 年随访,来自澳大利亚队列。在 SCOPE 研究期间,在 14-16 周妊娠期间收集的临床数据用于使用 IDF 标准诊断代谢综合征。端粒长度是衰老的生物标志物,通过定量 PCR 从 10 岁儿童的唾液中评估。

结果

在完成随访的女性中(n=255),20%在妊娠期间患有代谢综合征。在调整了一系列混杂因素后,母亲在妊娠期间患有代谢综合征的儿童的端粒比母亲在妊娠期间没有代谢综合征的儿童短 14%(平均差异-0.36 [95%CI-0.74, 0.01])。母亲在妊娠期间患有和不患有代谢综合征的儿童的身高-年龄、体重-年龄和 BMI z 评分相似。

结论/解释:母亲在妊娠期间患有代谢综合征的儿童的端粒较短,这是加速衰老的生物标志物。这些发现需要在更大的儿童队列中进一步研究,以及调查脐带血中测量的端粒长度是否与儿童期的端粒长度相关。

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