Gai Wanxia, Yu Stephanie C Y, Chan W T Charlotte, Peng Wenlei, Lau So Ling, Leung Tak Y, Jiang Peiyong, Chan K C Allen, Lo Y M Dennis
Centre for Novostics, Hong Kong Science Park, Pak Shek Kok, New Territories, Hong Kong SAR, China.
Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Prenat Diagn. 2023 Oct;43(11):1385-1393. doi: 10.1002/pd.6432. Epub 2023 Sep 1.
Long cell-free DNA (cfDNA) can be found in the plasma of pregnant women and cancer patients. We investigated if droplet digital PCR (ddPCR) can analyze such molecules for diagnostic purposes using preeclampsia as a model.
Plasma samples from ten preeclamptic and sixteen normal pregnancies were analyzed. Two ddPCR assays targeting a single-copy gene, VCP, and one ddPCR assay targeting LINE-1 repetitive regions were used to measure the percentages of long cfDNA >533, 1001, and 170 bp, respectively. The LINE-1 assay was developed as guided by in silico PCR analyses to better differentiate preeclamptic and normal pregnancies.
Preeclamptic patients had a significantly lower median percentage of long cfDNA than healthy pregnant controls, as determined by the LINE-1 170 bp assay (28.9% vs. 35.1%, p < 0.0001) and the VCP 533 bp assay (6.6% vs. 8.7%, p = 0.014). The LINE-1 assay provided a better differentiation than the VCP 533 bp assay (area under ROC curves, 0.94 vs. 0.79).
ddPCR is a cost-effective approach for unlocking diagnostic information carried by long cfDNA in plasma and may have applications for the detection of preeclampsia. Further longitudinal studies with larger cohorts are required to assess the clinical utility of this test.
在孕妇和癌症患者的血浆中可检测到长链游离DNA(cfDNA)。我们以子痫前期为模型,研究了液滴数字PCR(ddPCR)能否分析此类分子用于诊断目的。
分析了来自10例子痫前期患者和16例正常妊娠孕妇的血浆样本。使用两种针对单拷贝基因VCP的ddPCR检测方法以及一种针对LINE-1重复区域的ddPCR检测方法,分别测量长链cfDNA>533、1001和170 bp的百分比。LINE-1检测方法是在计算机模拟PCR分析的指导下开发的,以更好地区分子痫前期和正常妊娠。
通过LINE-1 170 bp检测方法(28.9%对35.1%,p<0.0001)和VCP 533 bp检测方法(6.6%对8.7%,p = 0.014)确定,子痫前期患者长链cfDNA的中位百分比显著低于健康孕妇对照组。LINE-1检测方法比VCP 533 bp检测方法具有更好的区分度(ROC曲线下面积,0.94对0.79)。
ddPCR是一种经济有效的方法,可用于解读血浆中长链cfDNA携带的诊断信息,可能在子痫前期检测中具有应用价值。需要进一步开展更大样本量的纵向研究来评估该检测方法的临床实用性。