首页> 外文期刊>Medical principles and practice: international journal of the Kuwait University, Health Science Centre >Polymerase-chain-reaction-based detection of fetal rhesus D and Y-chromosome-specific DNA in the whole blood of pregnant women during different trimesters of pregnancy.
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Polymerase-chain-reaction-based detection of fetal rhesus D and Y-chromosome-specific DNA in the whole blood of pregnant women during different trimesters of pregnancy.

机译:基于聚合酶链反应的孕妇不同孕期全血中胎儿恒河猴D和Y染色体特异性DNA的检测。

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OBJECTIVE: The aim of this study was to determine whether or not a noninvasive procedure utilizing maternal peripheral blood as the source of DNA and polymerase chain reaction (PCR) could be used to detect fetal rhesus D (RhD) status as well as fetal gender during different gestational stages of pregnancy. MATERIALS AND METHODS: Maternal blood samples were obtained from 54 RhD-negative pregnant women during the first trimester (6-13 weeks, n = 14), second trimester (14-26 weeks, n 26) and third trimester (27-40 weeks, n the whole blood and analyzed by seminested and nested PCR for detection of DNA sequences corresponding to RhD (n = 54) and Y chromosome (n = 48) using RhD and Y-chromosome-specific oligonucleotide primers, respectively. The seminestedested PCR results were compared with the RhD status and gender of the babies after delivery. RESULTS: The sensitivity and specificity of seminested PCR for detection of fetal RhD positivity in whole blood of pregnant women were 81 and 100%, respectively, while the sensitivity and specificity of nested PCR for detection of male fetuses, using Y-chromosome-specific DNA as a marker, were 96 and 91%, respectively. There were no significant differences in the PCR results with samples obtained from women at different gestational stages of pregnancy. CONCLUSION: Seminested and nested PCRs for detection of fetal RhD and gender status, respectively, by using the blood of pregnant women during different gestational stages of pregnancy, are reliable noninvasive procedures with high sensitivity and specificity.
机译:目的:本研究的目的是确定是否可以使用以母亲外周血为DNA来源和聚合酶链反应(PCR)的非侵入性程序来检测胎儿恒河猴D(RhD)的状态以及胎儿性别。怀孕的不同妊娠阶段。材料与方法:孕妇的血液样本是在妊娠中期(6-13周,n = 14),妊娠中期(14-26周,n 26)和妊娠晚期(27-40周)期间从54例RhD阴性孕妇中获得的。 ,在全血中,通过半巢式和巢式PCR分析,分别使用RhD和Y染色体特异性寡核苷酸引物检测对应于RhD(n = 54)和Y染色体(n = 48)的DNA序列。结果:半巢式PCR检测孕妇全血中胎儿RhD阳性的敏感性和特异性分别为81%和100%,而敏感性和特异性分别为81%和100%。以Y染色体特异性DNA为标记的巢式PCR检测男性胎儿的比例分别为96%和91%,从妊娠不同孕期妇女获得的PCR结果之间无显着差异cy。结论:半巢式和巢式PCR分别通过在妊娠不同妊娠阶段使用孕妇的血液检测胎儿RhD和性别状态,是可靠,无创,高灵敏度和特异性的方法。

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