Comparison of Normal and Pre-Eclamptic Placental Gene Expression: A Systematic Review with Meta-Analysis

被引:58
作者
Brew, O. [1 ]
Sullivan, M. H. F. [2 ]
Woodman, A. [3 ]
机构
[1] Univ West London, Brentford, Middx, England
[2] Imperial Coll London, Inst Reprod & Dev Biol, Hammersmith Hosp Campus, London, England
[3] Univ West London, London, England
来源
PLOS ONE | 2016年 / 11卷 / 08期
关键词
ENDOTHELIAL GROWTH-FACTOR; NEUTROPHIL ACTIVATION; MICROARRAY DATA; PRECEDES COMMITMENT; MATERNAL DEATH; DNA MICROARRAY; PREGNANCY; ECLAMPSIA; HYPERTENSION; FAMILY;
D O I
10.1371/journal.pone.0161504
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pre-eclampsia (PE) is a serious multi-factorial disorder of human pregnancy. It is associated with changes in the expression of placental genes. Recent transcription profiling of placental genes withmicroarray analyses have offered better opportunities to define the molecular pathology of this disorder. However, the extent to which placental gene expression changes in PE is not fully understood. We conducted a systematic review of published PE and normal pregnancy (NP) control placental RNA microarrays to describe the similarities and differences between NP and PE placental gene expression, and examined how these differences could contribute to themolecular pathology of the disease. A total of 167 microarray samples were available for meta-analysis. We found the expression pattern of one group of genes was the same in PE and NP. The review also identified a set of genes (PE unique genes) including a subset, that were significantly (p < 0.05) down-regulated in pre-eclamptic placentae only. Using class prediction analysis, we further identified the expression of 88 genes that were highly associated with PE (p < 0.05), 10 of which (LEP, HTRA4, SPAG4, LHB, TREM1, FSTL3, CGB, INHA, PROCR, and LTF) were significant at p < 0.001. Our review also suggested that about 30% of genes currently being investigated as possibly of importance in PE placenta were not consistently and significantly affected in the PE placentae. We recommend further work to confirm the roles of the PE unique and associated genes, currently not being investigated in themolecular pathology of the disease.
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页数:20
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