妊娠期体重指数不影响新生儿过氧化物酶体增殖体激活受体γ启动子区(-359至-260)甲基化。

Vre Casamadrid, C A Amaya, Z H Mendieta
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引用次数: 2

摘要

背景:妊娠期肥胖可导致表观遗传改变。目的:评估孕期体重指数(BMI)是否与母体和新生儿白细胞过氧化物酶体增殖物激活受体γ (PPAR)启动子区(-359至- 260)甲基化变化相关。对象和方法:在这项匹配的队列研究中,41名孕妇被分为两组:(a)体重正常(n = 21)和(b)超重(n = 20)。使用MagNA Pure LC DNA分离试剂盒1(德国罗氏公司)从母体和新生儿白细胞(4000- 10000个细胞)中提取DNA。用亚硫酸氢钠(EZ DNA methyl- direct™Kit)处理DNA (2 μg);Zymo研究)。采用SYBR(®)Advantage(®)qPCR预混试剂盒(Clontech),在LightCycler 2.0 (Roche)中进行实时定量聚合酶链反应(qPCR)。PPARG γ共激活剂(PPARG) M3的引物为5′- aagacggtttggtcgatc-3′(正向)和5′- cgaaaaaatccgaaattaa -3′(反向),未甲基化的PPARG的引物为5′- gggaagatggtttttggttgatt -3′(正向)和5′- ttccaaaaaaaaatccaaaattaa -3′(反向)。组间差异采用Mann-Whitney u检验,组内差异采用Wilcoxon检验(IBM SPSS Statistics for Windows, Version 19.0)。纽约州阿蒙克市:IBM Corp.)。结果:两组之间的BMI、孕前体重和产后体重均有显著差异,但PPARγ启动子区域的甲基化状态无显著差异(-359至- 260)。结论:妊娠期外周白细胞PPARγ启动子区(-359 ~ - 260)不太可能发生肥胖诱导的甲基化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Body Mass Index in Pregnancy Does Not Affect Peroxisome Proliferator-activated Receptor Gamma Promoter Region (-359 to -260) Methylation in the Neonate.

Body Mass Index in Pregnancy Does Not Affect Peroxisome Proliferator-activated Receptor Gamma Promoter Region (-359 to -260) Methylation in the Neonate.

Body Mass Index in Pregnancy Does Not Affect Peroxisome Proliferator-activated Receptor Gamma Promoter Region (-359 to -260) Methylation in the Neonate.

Body Mass Index in Pregnancy Does Not Affect Peroxisome Proliferator-activated Receptor Gamma Promoter Region (-359 to -260) Methylation in the Neonate.

Background: Obesity in pregnancy can contribute to epigenetic changes.

Aim: To assess whether body mass index (BMI) in pregnancy is associated with changes in the methylation of the peroxisome proliferator-activated receptor γ (PPAR) promoter region (-359 to - 260) in maternal and neonatal leukocytes.

Subjects and methods: In this matched, cohort study 41 pregnant women were allocated into two groups: (a) Normal weight (n = 21) and (b) overweight (n = 20). DNA was extracted from maternal and neonatal leukocytes (4000-10,000 cells) in MagNA Pure (Roche) using MagNA Pure LC DNA Isolation Kit 1 (Roche, Germany). Treatment of DNA (2 μg) was performed with sodium bisulfite (EZ DNA Methylation-Direct™ Kit; Zymo Research). Real-time quantitative polymerase chain reaction (qPCR) was performed in a LightCycler 2.0 (Roche) using the SYBR(®) Advantage(®) qPCR Premix Kit (Clontech). The primers used for PPARγ coactivator (PPARG) M3 were 5'- aagacggtttggtcgatc-3' (forward), and5'- cgaaaaaaaatccgaaatttaa-3' (reverse) and those for PPARG unmethylated were: 5'-gggaagatggtttggttgatt-3' (forward) and 5'- ttccaaaaaaaaatccaaaatttaa-3' (reverse). Intergroup differences were calculated using the Mann-Whitney U-test, and intragroup differences, with the Wilcoxon test (IBM SPSS Statistics for Windows, Version 19.0. Armonk, NY: IBM Corp.).

Results: Significant differences were found in BMI, pregestational weight, and postdelivery weight between groups but not in the methylation status of the PPARγ promoter region (-359 to - 260).

Conclusion: The PPARγ promoter region (-359 to - 260) in peripheral leukocytes is unlikely to get an obesity-induced methylation in pregnancy.

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来源期刊
Annals of Medical and Health Sciences Research
Annals of Medical and Health Sciences Research HEALTH CARE SCIENCES & SERVICES-
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