Martino J, Sebert S, Segura M T, García-Valdés L, Florido J, Padilla M C, Marcos A, Rueda R, McArdle H J, Budge H, Symonds M E, Campoy C
Early Life Research Unit (J.M., S.S., H.B., M.E.S.), Division of Child Health and Obstetrics & Gynaecology, School of Medicine, University of Nottingham, Nottingham NG7 2UH, United Kingdom; EURISTIKOS Excellence Centre for Paediatric Research (J.M., M.T.S., L.G.-V., C.C.), University of Granada, 18016 Granada, Spain; Department of Obstetrics and Gynaecology (J.F., M.C.P.), University of Granada, Granada, Spain; Immunonutrition Research Group (A.M.), Department of Metabolism and Nutrition, Institute of Food Science and Technology and Nutrition, Spanish National Research Council, E-28040 Madrid, Spain; Abbott Nutrition (R.R.), 18004 Granada, Spain; The Rowett Institute of Nutrition and Health (H.J.M.), University of Bucksburn, Aberdeen, AB21 9SB,United Kingdom; Institute of Health Sciences and Biocenter Oulu (S.S.), University of Oulu, 90014 Oulu, Finland.
J Clin Endocrinol Metab. 2016 Jan;101(1):59-68. doi: 10.1210/jc.2015-2590. Epub 2015 Oct 29.
Maternal obesity and gestational diabetes mellitus (GDM) can both contribute to adverse neonatal outcomes. The extent to which this may be mediated by differences in placental metabolism and nutrient transport remains to be determined.
Our objective was to examine whether raised maternal body mass index (BMI) and/or GDM contributed to a resetting of the expression of genes within the placenta that are involved in energy sensing, oxidative stress, inflammation, and metabolic pathways.
Pregnant women from Spain were recruited as part of the "Study of Maternal Nutrition and Genetics on the Foetal Adiposity Programming" survey at the first antenatal visit (12-20 weeks of gestation) and stratified according to prepregnancy BMI and the incidence of GDM. At delivery, placenta and cord blood were sampled and newborn anthropometry measured.
Obese women with GDM had higher estimated fetal weight at 34 gestational weeks and a greater risk of preterm deliveries and cesarean section. Birth weight was unaffected by BMI or GDM; however, women who were obese with normal glucose tolerance had increased placental weight and higher plasma glucose and leptin at term. Gene expression for markers of placental energy sensing and oxidative stress, were primarily affected by maternal obesity as mTOR was reduced, whereas SIRT-1 and UCP2 were both upregulated. In placenta from obese women with GDM, gene expression for AMPK was also reduced, whereas the downstream regulator of mTOR, p70S6KB1 was raised.
Placental gene expression is sensitive to both maternal obesity and GDM which both impact on energy sensing and could modulate the effect of either raised maternal BMI or GDM on birth weight.
孕妇肥胖和妊娠期糖尿病(GDM)均可能导致不良新生儿结局。胎盘代谢和营养转运差异在其中的介导程度尚待确定。
我们的目的是研究孕妇体重指数(BMI)升高和/或GDM是否导致胎盘内参与能量感应、氧化应激、炎症和代谢途径的基因表达重置。
在首次产前检查(妊娠12 - 20周)时,招募来自西班牙的孕妇作为“胎儿肥胖编程母体营养与遗传学研究”调查的一部分,并根据孕前BMI和GDM发病率进行分层。分娩时,采集胎盘和脐带血样本并测量新生儿人体测量学指标。
患有GDM的肥胖女性在妊娠34周时估计胎儿体重较高,早产和剖宫产风险更大。出生体重不受BMI或GDM影响;然而,糖耐量正常的肥胖女性足月时胎盘重量增加,血浆葡萄糖和瘦素水平升高。胎盘能量感应和氧化应激标志物的基因表达主要受母体肥胖影响,mTOR降低,而SIRT - 1和UCP2均上调。在患有GDM的肥胖女性的胎盘中,AMPK的基因表达也降低,而mTOR的下游调节因子p70S6KB1升高。
胎盘基因表达对母体肥胖和GDM均敏感,这两者均影响能量感应,并可能调节母体BMI升高或GDM对出生体重的影响。