Differential Placental Gene Expression in Term Pregnancies Affected by Fetal Growth Restriction and Macrosomia

被引:23
作者
Sabri, Amin [1 ,2 ]
Lai, Donna [2 ]
D'Silva, Arlene [1 ]
Seeho, Sean [3 ]
Kaur, Jasjot [1 ]
Ng, Cecilia [1 ,4 ]
Hyett, Jon [1 ,4 ]
机构
[1] Univ Sydney, Queen Elizabeth Res Inst Mothers & Infants 2, Dept Obstet Gynaecol & Neonatol, Sydney, NSW 2006, Australia
[2] Univ Sydney, Bosch Inst, Mol Biol Facil, Sydney, NSW 2006, Australia
[3] Univ Sydney, Kolling Inst Med Res, Perinatal Res Grp, Sydney, NSW 2006, Australia
[4] Royal Prince Alfred Hosp, RPA Women & Babies, Sydney, NSW, Australia
关键词
Fetal growth restriction; Macrosomia; Development; Microarrays; Candidate genes; FOR-GESTATIONAL-AGE; BLOOD LEPTIN CONCENTRATIONS; CORD BLOOD; SEVERE PREECLAMPSIA; IMPRINTED GENES; MATERNAL SERUM; FACTOR-I; BIRTH; ADIPONECTIN; INSULIN;
D O I
10.1159/000360535
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Introduction: Extremes of fetal growth are associated with increased perinatal mortality and morbidity and a higher prevalence of cardiovascular disease, obesity and diabetes in later life. We aimed to identify changes in placental gene expression in pregnancies with evidence of growth dysfunction and candidate genes that may be used to identify abnormal patterns of growth prior to delivery. Methods: Growth-restricted (n = 4), macrosomic (n = 6) and normal term (n = 5) placentas were selected from a banked series (n = 200) collected immediately after caesarean section. RNA was extracted prior to microarray analysis using Affymetrix HG-U219 arrays to determine variation in gene expression. Genes of interest were confirmed using qRT-PCR. Results: 338 genes in the growth-restricted and 41 genes in the macrosomic group were identified to be significantly dysregulated (>2-fold change; p < 0.05). CPXM2 and CLDN1 were upregulated and TXNDC5 and LRP2 downregulated in fetal growth restriction. In macrosomia, PHLDB2 and CLDN1 were upregulated and LEP and GCH1 were downregulated. Discussion:Dysfunctional growth is associated with differential placental gene expression and affects genes with a whole spectrum of developmental and cellular functions. Better elucidation of these pathways may allow the development of biomarkers to identify growth abnormalities and effective prenatal intervention. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:173 / 180
页数:8
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