Analysis of Factors Affecting Fetal Fraction in Cell-Free DNA Test

Behdad Amirgholami, Sara Masihi, Reza Samie, Hamid Galehdari, Gholam Reza Shariati
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Abstract

Background: Noninvasive prenatal testing (NIPT) serves as a screening method to assess the risk of chromosomal abnormalities in the fetus, including trisomy 18, 21, and 13. The reliability and success of this test are influenced by the proportion of circulating cell-free DNA obtained from the feto-placental unit, known as the fetal fraction (FF). Objectives: Our study aims to investigate the fetal and maternal factors affecting FF. Methods: Our research involved 1 150 patients referred for NIPT due to various reasons such as maternal age over 35, high-risk screening tests in the first or second trimester, history of trisomy in previous pregnancies, or patient request. Patients completed a questionnaire providing variables including maternal and fetal age, body mass index (BMI), smoking status, multiple pregnancies, and medication use such as Heparin or enoxaparin. Noninvasive prenatal testing was conducted on blood samples using Ion proton technology by Premaitha of the UK. The results, including fetal sex, trisomy risk, fetal fraction, and abnormal sex chromosomes, were analyzed using IBM SPSS 27 to assess the relationship between FF percentage and other variables. Results: The study included 1150 NIPT cases, with maternal ages ranging from 13 to 48 years, BMI from 15 to 70, and gestational age from 10 to 27 weeks. Among these, 96.4% were singleton pregnancies and 3.6% were twin pregnancies. Spontaneous pregnancies accounted for 88.9%, while 9.2% were IVF and 1.2% were IUI. Fetal sex distribution was 45.9% female and 54.1% male. FF ranged from 4% to 20.7%, with a mean FF of 11.07. No significant correlation was found between maternal age, fetal age, maternal BMI, trisomies, and FF. Conclusions: We can see that maternal age has no significant correlation with the fetal fraction. Although fetal age increases, the fetal fraction does too, but this increase was not significant. Body mass index, the route of pregnancy, and the sex of the fetus had no effect on FF. Despite NIPS being safer and yielding better results, other factors can still influence the outcomes of NIPS. Therefore, this test remains a screening tool, and clinical counseling should be conducted both before and after the test.
影响无细胞 DNA 检测中胎儿比例的因素分析
背景:无创产前检测(NIPT)是一种评估胎儿染色体异常(包括 18、21 和 13 三体综合征)风险的筛查方法。该检测的可靠性和成功率受从胎儿-胎盘单位(称为胎儿组分(FF))中获得的循环无细胞 DNA 比例的影响。研究目的我们的研究旨在调查影响 FF 的胎儿和母体因素。研究方法我们的研究涉及 1 150 名因各种原因转诊进行 NIPT 的患者,如产妇年龄超过 35 岁、在第一或第二孕期进行高风险筛查试验、既往妊娠三体综合征病史或患者要求。患者填写了一份问卷,提供的变量包括孕产妇和胎儿的年龄、体重指数(BMI)、吸烟状况、多胎妊娠以及肝素或依诺肝素等药物的使用情况。英国 Premaitha 公司利用离子质子技术对血液样本进行了无创产前检测。检测结果包括胎儿性别、三体症风险、胎儿比例和性染色体异常,并使用 IBM SPSS 27 进行分析,以评估胎儿比例与其他变量之间的关系。结果研究共纳入 1150 例 NIPT 病例,孕妇年龄介于 13 至 48 岁之间,体重指数介于 15 至 70 之间,孕周介于 10 至 27 周之间。其中,96.4%为单胎妊娠,3.6%为双胎妊娠。自然妊娠占 88.9%,体外受精占 9.2%,人工授精占 1.2%。胎儿性别分布为女性占 45.9%,男性占 54.1%。FF从4%到20.7%不等,平均FF为11.07。产妇年龄、胎儿年龄、产妇体重指数、三体症和FF之间没有发现明显的相关性。结论我们可以看出,产妇年龄与胎儿分数无明显相关性。虽然胎儿年龄增加,胎儿分数也会增加,但这种增加并不明显。体重指数、妊娠途径和胎儿性别对胎儿分数没有影响。尽管NIPS更安全且结果更好,但其他因素仍会影响NIPS的结果。因此,该检查仍是一种筛查工具,在检查前后都应进行临床咨询。
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