Suppr超能文献

植入和胎盘形成缺陷:为妊娠并发症奠定蓝图。

Defective implantation and placentation: laying the blueprint for pregnancy complications.

作者信息

Norwitz Errol R

机构信息

Department of Obstetrics, Gynecology and Reproductive Sciences, Yale-New Haven Hospital, Yale University School of Medicine, 333 Cedar Street, LCI 800, New Haven, CT 06443, USA.

出版信息

Reprod Biomed Online. 2006 Oct;13(4):591-9. doi: 10.1016/s1472-6483(10)60649-9.

Abstract

Normal implantation and placentation is critical for pregnancy success. Many pregnancy-related complications that present late in gestation (such as pre-eclampsia and preterm labour) appear to have their origins early in pregnancy with abnormalities in implantation and placental development. Implantation is characterized by invasion of the maternal tissues of the uterus by fetal trophoblast, and the degree to which trophoblast invades these tissues appears to be a major determinant of pregnancy outcome. Excessive invasion can lead to abnormally firm attachment of the placenta to the myometrium (placenta accreta) with increased maternal and perinatal morbidity. Inadequate invasion, specifically restricted endovascular invasion, has been implicated in the pathophysiology of such conditions as pre-eclampsia (gestational proteinuric hypertension), preterm premature rupture of membranes, preterm labour, and intrauterine growth restriction. The molecular and cellular mechanisms responsible for implantation remain enigmatic. This review will include an overview of implantation followed by a discussion of a number of molecular mechanisms implicated in defective implantation and placentation including the role of decidual prostaglandins and haemorrhage in regulating trophoblast invasion. An improved understanding of the molecular mechanisms responsible for abnormal implantation and placentation will likely improve clinicians' abilities to treat disorders that occur along this continuum, including infertility, recurrent pregnancy loss, pre-eclampsia, and preterm birth.

摘要

正常的着床和胎盘形成对于妊娠成功至关重要。许多在妊娠晚期出现的与妊娠相关的并发症(如子痫前期和早产)似乎在妊娠早期就已出现,起因是着床和胎盘发育异常。着床的特征是胎儿滋养层侵入子宫的母体组织,滋养层侵入这些组织的程度似乎是妊娠结局的主要决定因素。过度侵入可导致胎盘与子宫肌层异常牢固附着(胎盘植入),增加母体和围产期发病率。侵入不足,特别是血管内侵入受限,与子痫前期(妊娠蛋白尿性高血压)、胎膜早破、早产和胎儿生长受限等疾病的病理生理有关。负责着床的分子和细胞机制仍然不明。本综述将包括着床的概述,随后讨论一些与着床和胎盘形成缺陷有关的分子机制,包括蜕膜前列腺素和出血在调节滋养层侵入中的作用。更好地理解导致异常着床和胎盘形成的分子机制可能会提高临床医生治疗这一系列疾病的能力,包括不孕症、复发性流产、子痫前期和早产。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验