{"title":"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。","authors":"Vre Casamadrid, C A Amaya, Z H Mendieta","doi":"10.4103/2141-9248.180272","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Obesity in pregnancy can contribute to epigenetic changes.</p><p><strong>Aim: </strong>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.</p><p><strong>Subjects and methods: </strong>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.).</p><p><strong>Results: </strong>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).</p><p><strong>Conclusion: </strong>The PPARγ promoter region (-359 to - 260) in peripheral leukocytes is unlikely to get an obesity-induced methylation in pregnancy.</p>","PeriodicalId":8186,"journal":{"name":"Annals of Medical and Health Sciences Research","volume":"6 1","pages":"38-43"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/82/07/AMHSR-6-38.PMC4849114.pdf","citationCount":"2","resultStr":"{\"title\":\"Body Mass Index in Pregnancy Does Not Affect Peroxisome Proliferator-activated Receptor Gamma Promoter Region (-359 to -260) Methylation in the Neonate.\",\"authors\":\"Vre Casamadrid, C A Amaya, Z H Mendieta\",\"doi\":\"10.4103/2141-9248.180272\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Obesity in pregnancy can contribute to epigenetic changes.</p><p><strong>Aim: </strong>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.</p><p><strong>Subjects and methods: </strong>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.).</p><p><strong>Results: </strong>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).</p><p><strong>Conclusion: </strong>The PPARγ promoter region (-359 to - 260) in peripheral leukocytes is unlikely to get an obesity-induced methylation in pregnancy.</p>\",\"PeriodicalId\":8186,\"journal\":{\"name\":\"Annals of Medical and Health Sciences Research\",\"volume\":\"6 1\",\"pages\":\"38-43\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/82/07/AMHSR-6-38.PMC4849114.pdf\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Medical and Health Sciences Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/2141-9248.180272\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Medical and Health Sciences Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/2141-9248.180272","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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。
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.