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子痫前期与胎盘16三体嵌合体之间的关联。

The association between preeclampsia and placental trisomy 16 mosaicism.

作者信息

Yong Paul J, Langlois Sylvie, von Dadelszen Peter, Robinson Wendy

机构信息

Department of Medical Genetics, Vancouver, BC, Canada.

出版信息

Prenat Diagn. 2006 Oct;26(10):956-61. doi: 10.1002/pd.1534.

Abstract

BACKGROUND

Prenatally diagnosed trisomy 16 mosaicism is associated with the increased risk of poor pregnancy outcome including intrauterine growth restriction, intrauterine death and fetal malformation. While maternal preeclampsia has also been reported in some cases, this has not been systematically evaluated.

METHODS

To better define the risk of preeclampsia and the clinical course of preeclampsia in these pregnancies and to identify associated clinical variables, we reviewed 25 cases of prenatally diagnosed trisomy 16 mosaicism for which molecular studies were undertaken and sufficient obstetrical data were present to include/exclude the diagnosis of preeclampsia.

RESULTS

Six of 25 (24%) mosaic trisomy 16 cases exhibited preeclampsia as compared to 3 of 44 (7%) matched controls. There were no differences between those mosaic trisomy 16 cases presenting with preeclampsia and those that did not, in terms of the presence/absence of UPD, IUGR, malformation, or trisomy on amniocentesis. Four of the 6 (67%) preeclampsia-associated fetuses were male, compared with only 4 of 19 (21%) (p = 0.06) nonpreeclampsia case fetuses, and three of these also had hypospadias. The levels of trisomy tended to be high in placentas associated with preeclampsia; however very high levels of placental trisomy were also often seen in the absence of preeclampsia.

CONCLUSION

As it is impossible to predict which subset of cases is at highest risk, all women receiving a prenatal diagnosis of trisomy 16 mosaicism should be closely monitored for signs of preeclampsia.

摘要

背景

产前诊断的16三体嵌合体与不良妊娠结局风险增加相关,包括宫内生长受限、宫内死亡和胎儿畸形。虽然在某些病例中也报告了母体先兆子痫,但尚未进行系统评估。

方法

为了更好地确定这些妊娠中先兆子痫的风险和先兆子痫的临床过程,并确定相关的临床变量,我们回顾了25例产前诊断为16三体嵌合体的病例,这些病例进行了分子研究,并有足够的产科数据来纳入/排除先兆子痫的诊断。

结果

25例(24%)16三体嵌合体病例中有6例出现先兆子痫,而44例匹配对照中有3例(7%)出现先兆子痫。在出现或未出现单亲二倍体(UPD)、宫内生长受限(IUGR)、畸形或羊膜穿刺术时的三体性方面,出现先兆子痫的16三体嵌合体病例与未出现先兆子痫的病例之间没有差异。6例与先兆子痫相关的胎儿中有4例(67%)为男性,相比之下,19例(21%)非先兆子痫病例的胎儿中只有4例(p = 0.06),其中3例还患有尿道下裂。与先兆子痫相关的胎盘三体水平往往较高;然而,在没有先兆子痫的情况下也经常出现非常高的胎盘三体水平。

结论

由于无法预测哪些病例子集风险最高,所有接受产前诊断为16三体嵌合体的女性都应密切监测先兆子痫的迹象。

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