Placental Network Differences Among Obstetric Syndromes Identified With An Integrated Multiomics Approach

Samantha N Piekos, Oren Barak, Andrew Baumgartner, Tianjiao Chu, W Tony Parks, Jennifer Hadlock, Leroy Hood, Nathan Price, Yoel Sadovsky
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Abstract

The placenta is essential for a healthy pregnancy, and placental pathology can endanger both maternal and fetal health. Placental function is affected by dynamic, complex, and interconnected molecular, cellular, and environmental events; therefore, we need a systems biology approach to study disease in normal physiological placenta function. We use placental multiomics (short and bulk transcriptomics, untargeted metabolomics, and targeted proteomics) paired with clinical data and placental histopathology reports from 321 placentas across multiple obstetric conditions: fetal growth restriction (FGR), FGR with pregnancy-related hypertension (FGR+HDP), preeclampsia (PE), and spontaneous preterm delivery (PTD). We first performed cellular deconvolution to estimate cell type numbers from bulk transcriptomes: FGR+HDP placentas were the most different from control placentas driven by a higher estimated number of extravillous trophoblast (p<0.0001). Next, we evaluated the impact of fetal sex and gestational age on analyte levels, adjusting for these confounders. We then generated obstetric condition-specific correlation networks and identified communities of related analytes associated with physiology and disease. We demonstrated how network connectivity and its disruption in disease can be used to identify signatures unique to a clinical outcome. We examined a community defined in control placentas for which the most connected node was miR-365a-3p in contrast to the corresponding community in FGR+HDP placentas for which the most connected node was hypoxia-induced miR-210-3p. From this community, we identified a signature containing mRNA transcripts implicated in placental dysfunction (e.g. FLT1, FSTL3, HTRA4, LEP, and PHYHIP). This signature distinguishes between FGR+HDP placentas and placentas of differing clinical outcomes in high-dimensional space. These findings illustrate the power of systems biology-driven interomics network analysis in a single tissue type, laying the groundwork for future multi-tissue studies.
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用综合多组学方法识别产科综合征的胎盘网络差异
胎盘对健康妊娠至关重要,而胎盘病变会危及母体和胎儿的健康。胎盘功能受到动态、复杂和相互关联的分子、细胞和环境事件的影响;因此,我们需要一种系统生物学方法来研究正常生理胎盘功能中的疾病。我们利用胎盘多组学(短和大容量转录组学、非靶向代谢组学和靶向蛋白质组学)与临床数据和胎盘组织病理学报告配对,研究了321个胎盘的多种产科情况:胎儿生长受限(FGR)、FGR合并妊娠相关高血压(FGR+HDP)、子痫前期(PE)和自发性早产(PTD)。我们首先进行了细胞去卷积,以便从大量转录组中估计细胞类型的数量:FGR+HDP胎盘与对照胎盘的差异最大,原因是滋养层外滋养细胞的估计数量更高(p<0.0001)。接下来,我们评估了胎儿性别和胎龄对分析物水平的影响,并对这些混杂因素进行了调整。然后,我们生成了产科条件特异性相关网络,并确定了与生理和疾病相关的分析物群落。我们展示了如何利用网络连通性及其在疾病中的中断来识别临床结果的独特特征。我们研究了对照胎盘中定义的一个群落,其中连接最多的节点是 miR-365a-3p,而 FGR+HDP 胎盘中的相应群落中连接最多的节点是缺氧诱导的 miR-210-3p。从这个群落中,我们发现了一个包含与胎盘功能障碍有关的 mRNA 转录本(如 FLT1、FSTL3、HTRA4、LEP 和 PHYHIP)的特征。这一特征可在高维空间中区分 FGR+HDP 胎盘和不同临床结果的胎盘。这些发现说明了在单一组织类型中系统生物学驱动的组间网络分析的威力,为未来的多组织研究奠定了基础。
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