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A Prospective study to evaluate the demographic variation of gender independent sequences in cell-free fetal DNA (cffDNA) concentration and to predict pregnancy outcomes by non-kit based economical method

机译:评估无细胞胎儿DNA(CFFDNA)浓度的性别独立序列的人口统计变异的前瞻性研究,并基于非套件的经济方法预测妊娠结果

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This gender-independent detection of cell-free fetal DNA in maternal plasma using RASSF1A/β-actin has curtained off a new dimension regarding its utility to predict the adverse pregnancy outcomes. Recent efforts have been directed at developing sequences from cell-free fetal DNA (cffDNA) as markers for pregnancy outcomes. The utility of cffDNA using the methylation-dependent DSCR3 and RASSF1A markers along with total cell-free DNA (cf-DNA) in maternal serum by HYP2 marker are useful in predicting adverse pregnancy outcomes. Increased amount (>95th percentile) of cffDNA fraction in the second trimester is associated with preterm birth. Indigenously developed low-cost method of the gender-independent sequence markers from cffDNA was investigated and evaluated with the standardized commercial kits as predictive markers for adverse pregnancy outcomes. Our results indicated that indigenously developed method for detection of geneder-independent cffDNA can be applicable for screening test of adverse pregnancy outcome.
机译:使用Rassf1a /β-actin的母体血浆中无细胞胎儿DNA的这种性别无关的胎儿DNA对其效用进行了新的尺寸,以预测不良妊娠结果。最近的努力已经涉及从无细胞胎儿DNA(CFFDNA)的序列作为妊娠结果的标志物。通过Hyp2标记使用甲基化依赖性DSCR3和RASSF1A标记的CFFDNA使用甲基化依赖性DSCR3和RASSF1a标记的纯细胞DNA(CF-DNA)可用于预测不良妊娠结果。第二三个月中的CFFDNA分数增加(> 95百分位数)与早产有关。对CFFDNA的性别无关的序列标记的本土开发的低成本方法被研究,并用标准化的商业套件评估为预测标志物,用于不良妊娠结果。我们的研究结果表明,本土开发的用于检测Geneder无关的CFFDNA的方法可用于筛查不良妊娠结果的试验。

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