Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Washington, Seattle, WA (Drs Shree, Kolarova, Mackinnon, and Chandrasekaran).
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Washington, Seattle, WA (Drs Shree, Kolarova, Mackinnon, and Chandrasekaran).
Am J Obstet Gynecol MFM. 2022 Sep;4(5):100671. doi: 10.1016/j.ajogmf.2022.100671. Epub 2022 May 27.
Hypertensive disorders of pregnancy contribute to maternal and offspring morbidity and mortality. Studies suggest that a lower early pregnancy fetal fraction is associated with an increased risk of hypertensive disorders of pregnancy. However, maternal obesity significantly affects fetal fraction and is a risk factor for hypertensive disorders of pregnancy.
We determined the association between fetal fraction (using a standardized single-institution platform, including male and female fetuses) and hypertensive disorders of pregnancy, stratified by obesity status. Second, we evaluated differences in total cell-free DNA concentration and correlation of fetal fraction with clinical markers of hypertensive disorders of pregnancy severity.
This was a retrospective, single-institution study of a previously validated cell-free DNA-based noninvasive prenatal screening assay of 1058 samples. Maternal body mass index at the time of noninvasive prenatal screening was assessed, and hypertensive disorders of pregnancy were confirmed by a detailed medical record review. Differences in fetal fraction and total cell-free DNA concentration between the groups were assessed with univariate analyses. Multivariable regression was used to evaluate the association between fetal fraction and hypertensive disorders of pregnancy, adjusted for body mass index, maternal age, gestational age at noninvasive prenatal screening, and fetal sex. The association between fetal fraction and hypertensive disorders of pregnancy among individuals with obesity (body mass index, ≥30 kg/m) and individuals without obesity (body mass index, <30 kg/m) was investigated while controlling for the aforementioned covariates. Lastly, multivariable linear regression was used to evaluate the association between fetal fraction and clinical markers of hypertensive disorders of pregnancy severity.
We identified individuals with (n=117) and without (n=941) hypertensive disorders of pregnancy with noninvasive prenatal screening drawn before 20 weeks of gestation and with fetal fraction and body mass index data available. Those with hypertensive disorders of pregnancy had a lower fetal fraction (10.2%±4.2% vs 11.6%±4.7%; P<.01), without differences in total cell-free DNA concentration (P=.14). When groups were stratified by obesity status, this relationship was only valid for individuals without obesity (P=.02). Only when logistic regression analysis was restricted to individuals without obesity did the likelihood of hypertensive disorders of pregnancy rise with decreasing fetal fraction (odds ratio, 0.93; 95% confidence interval, 0.88-0.99; P=.02). In addition, fetal fraction was inversely associated with maximum systolic blood pressure at the time of hypertensive disorders of pregnancy only in the population without obesity (β, -0.08; 95% confidence interval, -0.147 to -0.01; P=.02).
Although a lower fetal fraction is associated with the development of hypertensive disorders of pregnancy, the use of this parameter for the prediction may be problematic in individuals with obesity, as obesity has such a profound effect on fetal fraction. However, we uniquely noted that among individuals without obesity, fetal fraction is lower for those that develop hypertensive disorders of pregnancy and lower fetal fraction increases the odds of hypertensive disorders of pregnancy development. Lastly, low fetal fraction in the population without obesity that developed hypertensive disorders of pregnancy was associated with higher systolic blood pressure at the time of hypertensive disorders of pregnancy, an important clinical marker of hypertensive disorders of pregnancy severity. As analytical approaches of cell-free DNA interrogation advance, the prediction of placental-mediated disorders with first-trimester sampling is likely to improve, although this may remain challenging in gravidas with obesity, a cohort at high risk of developing hypertensive disorders of pregnancy.
妊娠高血压疾病会导致母婴发病率和死亡率升高。研究表明,孕早期胎儿分数较低与妊娠高血压疾病的风险增加有关。然而,母体肥胖显著影响胎儿分数,是妊娠高血压疾病的一个危险因素。
我们确定了胎儿分数(使用包括男性和女性胎儿的标准化单机构平台)与妊娠高血压疾病之间的关联,并按肥胖状况进行分层。其次,我们评估了总游离 DNA 浓度的差异以及胎儿分数与妊娠高血压疾病严重程度的临床标志物的相关性。
这是一项回顾性的、单机构的研究,对之前经过验证的基于游离 DNA 的非侵入性产前筛查检测进行了 1058 个样本的检测。在进行非侵入性产前筛查时评估了母体的体重指数,并通过详细的病历回顾确认了妊娠高血压疾病。使用单变量分析评估了各组之间胎儿分数和总游离 DNA 浓度的差异。使用多变量回归来评估胎儿分数与妊娠高血压疾病之间的关联,调整了体重指数、母体年龄、非侵入性产前筛查时的孕龄和胎儿性别。在控制上述协变量的情况下,研究了肥胖者(体重指数≥30kg/m)和非肥胖者(体重指数<30kg/m)中胎儿分数与妊娠高血压疾病之间的关联。最后,使用多变量线性回归来评估胎儿分数与妊娠高血压疾病严重程度的临床标志物之间的关联。
我们确定了在 20 周妊娠前进行非侵入性产前筛查且具有胎儿分数和体重指数数据的患有(n=117)和未患有(n=941)妊娠高血压疾病的个体。患有妊娠高血压疾病的个体胎儿分数较低(10.2%±4.2%vs11.6%±4.7%;P<.01),总游离 DNA 浓度无差异(P=.14)。当按肥胖状况对组进行分层时,这种关系仅适用于非肥胖者(P=.02)。只有当逻辑回归分析仅限于非肥胖者时,胎儿分数的降低才与妊娠高血压疾病的发生几率增加相关(比值比,0.93;95%置信区间,0.88-0.99;P=.02)。此外,仅在非肥胖人群中,胎儿分数与妊娠高血压疾病时的最大收缩压呈负相关(β,-0.08;95%置信区间,-0.147 至-0.01;P=.02)。
虽然胎儿分数较低与妊娠高血压疾病的发生有关,但在肥胖者中使用该参数进行预测可能存在问题,因为肥胖对胎儿分数有如此深远的影响。然而,我们特别注意到,在非肥胖者中,发生妊娠高血压疾病的个体胎儿分数较低,而较低的胎儿分数增加了妊娠高血压疾病发生的几率。最后,在发生妊娠高血压疾病的非肥胖人群中,胎儿分数较低与妊娠高血压疾病时的收缩压升高有关,这是妊娠高血压疾病严重程度的一个重要临床标志物。随着游离 DNA 分析方法的进步,使用第一孕期采样来预测胎盘介导的疾病可能会得到改善,尽管在肥胖孕妇中这可能仍然具有挑战性,肥胖孕妇是发生妊娠高血压疾病的高风险人群。