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通过基因扩增检测孕早期经宫颈拭子中的胎儿DNA:产前诊断的新途径?

Detection of fetal DNA in trans-cervical swabs from first trimester pregnancies by gene amplification: a new route to prenatal diagnosis?

作者信息

Griffith-Jones M D, Miller D, Lilford R J, Scott J, Bulmer J

机构信息

University Department of Obstetrics and Gynaecology, St. Jame's University Hospital, Leeds, W. Yorkshire, UK.

出版信息

Br J Obstet Gynaecol. 1992 Jun;99(6):508-11. doi: 10.1111/j.1471-0528.1992.tb13792.x.

Abstract

OBJECTIVE

To determine whether fetal sex can be predicted from fetal DNA retrieved transcervically from the lower part of the uterine cavity in the first trimester of pregnancy.

DESIGN

Prospective observational study.

SETTING

St James's University Hospital, Leeds.

SUBJECTS

33 women undergoing legal termination of pregnancy at 9 to 13 weeks gestational age.

INTERVENTIONS

Before termination of pregnancy samples for DNA analysis were obtained with cotton wool swabs from the vagina, cervix and transcervically in 26 women. In the other seven women samples were obtained using a transcervical cell retrieval (TraCeR) procedure involving flushing the lower uterine cavity with 5 ml saline.

MAIN OUTCOME MEASURES

Detection of Y-chromosome specific DNA sequences by the polymerase chain reaction (PCR) in cotton wool swabs taken from the lower uterus in the first trimester of pregnancy to predict fetal sex in comparison with standard cytogenetic analysis. Histological and immunohistochemical analysis of samples obtained by flushing of the lower uterine cavity (TraCeR) to confirm the presence of trophoblast.

RESULTS

Fetal sex was predicted accurately in 25 of the 26 pregnancies investigated. Immunohistochemical analysis identified syncytial trophoblast fragments in all seven pregnancies investigated by TraCeR.

CONCLUSION

Trophoblast may be retrieved from the lower uterus in the first trimester by swabs or TraCeR. When purification of these syncytial fragments can be achieved using immuno-magnetic technology, this test will enable prenatal diagnosis of single gene defects in the fetus by the polymerase chain reaction.

摘要

目的

确定能否通过在妊娠早期经宫颈从子宫腔下部获取的胎儿DNA来预测胎儿性别。

设计

前瞻性观察性研究。

地点

利兹市圣詹姆斯大学医院。

研究对象

33名妊娠9至13周接受合法终止妊娠的妇女。

干预措施

在26名妇女终止妊娠前,用棉拭子从阴道、宫颈及经宫颈获取用于DNA分析的样本。另外7名妇女采用经宫颈细胞采集(TraCeR)程序,即用5毫升生理盐水冲洗子宫腔下部获取样本。

主要观察指标

通过聚合酶链反应(PCR)检测妊娠早期从子宫下部获取的棉拭子中的Y染色体特异性DNA序列,以预测胎儿性别,并与标准细胞遗传学分析进行比较。对通过冲洗子宫腔下部(TraCeR)获得的样本进行组织学和免疫组织化学分析,以确认滋养层的存在。

结果

在26例受调查的妊娠中,有25例胎儿性别被准确预测。免疫组织化学分析在所有7例采用TraCeR程序调查的妊娠中均鉴定出合体滋养层碎片。

结论

在妊娠早期可通过拭子或TraCeR程序从子宫下部获取滋养层。当使用免疫磁技术能够实现这些合体碎片的纯化时,该检测将能够通过聚合酶链反应对胎儿单基因缺陷进行产前诊断。

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