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游离DNA检测中的胎儿分数能否预测胎儿生长受限的发生?

Can fetal fractions in the cell-free DNA test predict the onset of fetal growth restriction?

作者信息

Adiyaman Duygu, Konuralp Atakul Bahar, Kuyucu Melda, Toklu Gizem, Golbasi Hakan, Koc Altug, Kaya Ozge Ozer, Ozdemir Taha Resid, Ekin Atalay

机构信息

Tepecik Training and Research Hospital, Department of Obstetrics and Gynecology, Division of Perinatology, Izmir, Turkey.

present address: Güney Mah., 1140/1. Sk. No: 1, 35180 Yenişehir, Konak, Izmir, Turkey.

出版信息

J Perinat Med. 2020 Apr 2. doi: 10.1515/jpm-2020-0010.

Abstract

Objective To investigate the possible predictive value of fetal fraction in the cell-free DNA (cfDNA) test in pregnancies with early- and late-onset fetal growth restriction (FGR). Methods This retrospective study comprised 247 women who were screened using the cfDNA test for aneuploidies during the first or second trimester and had deliveries at our institution from January 2016 to December 2019. The fetal fractions of women with early- (n = 14) and late-onset (n = 83) FGR and those with uncomplicated pregnancies (n = 150) were compared. Results The median fetal fractions for the early-onset FGR, late-onset FGR, and control groups were 5.7 [interquartile range (IQR) 2.65], 7 (IQR 5), and 7.35 (IQR 3.65), respectively. The fetal fractions were significantly lower in the early-onset FGR group than in the late-onset FGR and control groups (P = 0.047 and P = 0.037, respectively). There was no difference in fetal fractions between the late-onset FGR and control groups (P = 1.00). Conclusion As a placenta-related disease, early-onset FGR had lower fetal fractions in the cfDNA test than uncomplicated pregnancies. For clinical use, lower fetal fractions can contribute as a biomarker for screening asymptomatic women for possible placenta-related diseases, such as early-onset FGR. However, more studies are needed to define the "lower" limit.

摘要

目的 探讨游离DNA(cfDNA)检测中胎儿游离DNA比例在早发型和晚发型胎儿生长受限(FGR)妊娠中的可能预测价值。方法 这项回顾性研究纳入了247名妇女,她们在2016年1月至2019年12月期间于我院进行了孕早期或孕中期的cfDNA非整倍体筛查并分娩。比较了早发型FGR(n = 14)、晚发型FGR(n = 83)以及正常妊娠(n = 150)妇女的胎儿游离DNA比例。结果 早发型FGR组、晚发型FGR组和对照组的胎儿游离DNA比例中位数分别为5.7[四分位数间距(IQR)2.65]、7(IQR 5)和7.35(IQR 3.65)。早发型FGR组的胎儿游离DNA比例显著低于晚发型FGR组和对照组(分别为P = 0.047和P = 0.037)。晚发型FGR组和对照组之间的胎儿游离DNA比例无差异(P = 1.00)。结论 作为一种与胎盘相关的疾病,早发型FGR在cfDNA检测中的胎儿游离DNA比例低于正常妊娠。在临床应用中,较低的胎儿游离DNA比例可作为一种生物标志物,用于筛查可能患有胎盘相关疾病(如早发型FGR)的无症状妇女。然而,需要更多研究来确定“较低”的界限。

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