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dc.contributor.author
Rabaglino, Maria Belen
dc.contributor.author
Post Uiterweer, Emiel D.
dc.contributor.author
Jeyabalan, Arun
dc.contributor.author
Hogge, William A.
dc.contributor.author
Conrad, Kirk P.
dc.date.available
2018-01-30T18:13:13Z
dc.date.issued
2014-11
dc.identifier.citation
Rabaglino, Maria Belen; Post Uiterweer, Emiel D.; Jeyabalan, Arun; Hogge, William A.; Conrad, Kirk P.; Bioinformatics Approach Reveals Evidence for Impaired Endometrial Maturation Before and During Early Pregnancy in Women Who Developed Preeclampsia; Lippincott Williams; Hypertension; 65; 2; 11-2014; 421-429
dc.identifier.issn
0194-911X
dc.identifier.uri
http://hdl.handle.net/11336/35039
dc.description.abstract
Impaired uterine invasion by extravillous trophoblast in early gestation is implicated in the genesis of preeclampsia, a potentially lethal malady of human pregnancy. However, reasons for extravillous trophoblast dysfunction remain unclear because of virtual inaccessibility of early placental and uterine tissues from women who develop preeclampsia, and the absence of animal models in which the disease spontaneously occurs. Consequently, the possibility that deficient or defective maturation of the endometrium (decidualization) may compromise extravillous trophoblast invasion in preeclampsia remains unexplored. Using a bioinformatics approach, we tested this hypothesis identifying 396 differentially expressed genes (DEG) in chorionic villous samples from women at ≈11.5 gestational weeks who developed severe preeclampsia symptoms 6 months later compared with chorionic villous samples from normal pregnancies. A large number, 154 or 40%, overlapped with DEG associated with various stages of normal endometrial maturation before and after implantation as identified by other microarray data sets (P=4.7×10−14). One-hundred and sixteen of the 154 DEG or 75% overlapped with DEG associated with normal decidualization in the absence of extravillous trophoblast, ie, late-secretory endometrium (LSE) and endometrium from tubal ectopic pregnancy (EP; P=4.2×10−9). Finally, 112 of these 154 DEG or 73% changed in the opposite direction in microarray data sets related to normal endometrial maturation (P=0.01), including 16 DEG upregulated in decidual (relative to peripheral blood) natural killer cells that were downregulated in chorionic villous samples from women who developed preeclampsia (P<0.0001). Taken together, these results suggest that insufficient or defective maturation of endometrium and decidual natural killer cells during the secretory phase and early pregnancy preceded the development of preeclampsia.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Lippincott Williams
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Decidualization
dc.subject
Endometrial Cycle
dc.subject
Natural Killer Cell
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Pregnancy
dc.subject
Trophoblast
dc.subject.classification
Salud Ocupacional
dc.subject.classification
Ciencias de la Salud
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD
dc.title
Bioinformatics Approach Reveals Evidence for Impaired Endometrial Maturation Before and During Early Pregnancy in Women Who Developed Preeclampsia
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2018-01-29T19:44:44Z
dc.journal.volume
65
dc.journal.number
2
dc.journal.pagination
421-429
dc.journal.pais
Estados Unidos
dc.description.fil
Fil: Rabaglino, Maria Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto; Argentina
dc.description.fil
Fil: Post Uiterweer, Emiel D.. University of Utrecht; Países Bajos
dc.description.fil
Fil: Jeyabalan, Arun. Magee Womens Hospital; Estados Unidos
dc.description.fil
Fil: Hogge, William A.. Magee Womens Hospital; Estados Unidos
dc.description.fil
Fil: Conrad, Kirk P.. University of Florida; Estados Unidos
dc.journal.title
Hypertension
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://hyper.ahajournals.org/content/65/2/421.long
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1161/HYPERTENSIONAHA.114.04481
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