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Gene expression in chorionic villous samples at 11 weeks of gestation in women who develop pre‐eclampsia later in pregnancy: implications for screening
Author(s) -
Farina Antonio,
Zucchini Cinzia,
De Sanctis Paola,
Morano Danila,
Sekizawa Akihiko,
Purwosunu Yuditiya,
Okai Takashi,
Rizzo Nicola
Publication year - 2011
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.2675
Subject(s) - andrology , biology , pregnancy , in utero , chorionic villi , gestation , placenta , gynecology , medicine , genetics , fetus
Abstract Objectives To determine the gene expression profile in chorionic villous samples (CVSs) of women destined to develop pre‐eclampsia (PE). Method Case‐control study encompassing five women destined to develop PE [cases matched for gestational age with 30 controls]. We quantified mRNA expression on tissue samples from CVS of normal and PE patients. We then assessed mRNA expressions of cathepsin (CTSD), angiopoietin 2 (ANGPT2), interleukin 8, chemokine (C‐X‐C motif) ligand 10, neurokinin B (NKB), matrix metallopeptidase 9, major histocompatibility complex, class I, C (HLA‐C)and human leukocyte antigen‐G (HLA‐G). Data were analyzed by nonparametric rank analysis. Results For all the mRNA species considered in this study, except CTSD and ANGPT2, all the mean observed ranks in the PE group were significantly altered compared with the rank expectation among controls. mRNA for NKB and HLA‐C were the markers with the highest degree of aberration in PE, compared with those in controls. Conclusion Our study has directly showed that gene expressions relating to trophoblastic cell invasion or utero‐placental hemodynamic adaptation are altered in the first trimester trophoblasts that go on to develop PE later. These results posit the use of residual CVS as a possible screening method for PE. Copyright © 2011 John Wiley & Sons, Ltd.