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首页> 外文期刊>Prenatal Diagnosis >Testing normality of fetal DNA concentration in maternal plasma at 10-12 completed weeks' gestation: a preliminary approach to a new marker for genetic screening.
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Testing normality of fetal DNA concentration in maternal plasma at 10-12 completed weeks' gestation: a preliminary approach to a new marker for genetic screening.

机译:在妊娠10-12周时检测母体血浆中胎儿DNA浓度的正常性:这是遗传筛选新标记的初步方法。

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OBJECTIVES: To test the distribution of fetal DNA in maternal plasma expressed as gen/eq in a population of normal pregnancies. METHODS: Peripheral blood samples were obtained from 63 women (85% > or =35 years of age at delivery) bearing a euploid male fetus. Each patient underwent chorionic villus sampling (CVS) for karyotype analysis and/or beta thalassemia screening. Ultrasound scanning was used to determine gestational age. At 10-12 weeks' gestation, a peripheral blood sample was collected followed by CVS. To detect the Y chromosome specific sequences (SRY) quantitative polymerase chain reaction (PCR) analysis was used. Normal distribution of the data was tested by means of the Kolmogorov-Smirnov (KS) test. A Symmetry test (reliability p>0.05) was used to evaluate the reliability of the median. RESULTS: Only after natural logarithmic transformation did the data display a normal distribution. The median value of fetal DNA was 23.3 gen/eq (range 2.08-195), interquartile range 18.57-45.4. A Pearson test showed a significant correlation between gestational age and fetal DNA concentration (r=0.25, p=0.045). CONCLUSION: The present finding is a preliminary step towards a possible integration of fetal DNA with other variables (biochemical and/or ultrasound). It may serve to improve the discrimination of the screening for genetic diseases in the first trimester. Because of the relatively high dispersion, adjustments for possible covariates would appear to be necessary in further studies. Copyright 2002 John Wiley & Sons, Ltd.
机译:目的:测试在正常妊娠人群中以gen / eq表示的母体血浆中胎儿DNA的分布。方法:从63名具有整倍体男性胎儿的妇女(85%≥35岁的分娩年龄)获得外周血样本。每位患者均接受绒毛膜绒毛取样(CVS)进行核型分析和/或β地中海贫血筛查。超声扫描用于确定胎龄。妊娠10-12周时,收集外周血样本,然后进行CVS。为了检测Y染色体特异性序列(SRY),使用了定量聚合酶链反应(PCR)分析。数据的正态分布通过Kolmogorov-Smirnov(KS)检验进行了检验。使用对称性检验(可靠性p> 0.05)评估中位数的可靠性。结果:仅在自然对数转换后,数据才显示正态分布。胎儿DNA的中位数值为23.3 gen / eq(范围2.08-195),四分位数范围为18.57-45.4。皮尔逊检验显示胎龄与胎儿DNA浓度之间存在显着相关性(r = 0.25,p = 0.045)。结论:目前的发现是胎儿DNA与其他变量(生化和/或超声)可能整合的第一步。它可能有助于改善对孕早期遗传疾病的筛查。由于相对较高的离散度,在进一步的研究中似乎有必要对可能的协变量进行调整。版权所有2002 John Wiley&Sons,Ltd.

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