Department of Epidemiology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Department of Preventive Medicine, Keck School of Medicine at the University of Southern California, Los Angeles, CA, USA.
Epigenetics. 2022 Mar;17(3):269-285. doi: 10.1080/15592294.2021.1899887. Epub 2021 Mar 18.
Circulating miRNA may contribute to the development of adverse birth outcomes. However, few studies have investigated extracellular vesicle (EV) miRNA, which play important roles in intercellular communication, or compared miRNA at multiple time points in pregnancy. In the current study, 800 miRNA were profiled for EVs from maternal plasma collected in early (median: 12.5 weeks) and late (median: 31.8 weeks) pregnancy from 156 participants in the MADRES Study, a health disparity pregnancy cohort. Associations between miRNA and birth weight, birth weight for gestational age (GA), and GA at birth were examined using covariate-adjusted robust linear regression. Differences by infant sex and maternal BMI were also investigated. Late pregnancy measures of 13 miRNA were associated with GA at birth (P<0.050). Negative associations were observed for eight miRNA (miR-4454+ miR-7975, miR-4516, let-7b-5p, miR-126-3p, miR-29b-3p, miR-15a-5p, miR-15b-5p, miR-19b-3p) and positive associations for five miRNA (miR-212-3p, miR-584-5p, miR-608, miR-210-3p, miR-188-5p). Predicted target genes were enriched (P<0.050) in pathways involved in organogenesis and placental development. An additional miRNA (miR-107), measured in late pregnancy, was positively associated with GA at birth in infants born to obese women (P for BMI interaction = 0.011). In primary analyses, the associations between early pregnancy miRNA and birth outcomes were not statistically significant (P≥0.05). However, sex-specific associations were observed for early pregnancy measures of 37 miRNA and GA at birth (P for interactions<0.050). None of the miRNA were associated with fetal growth measures (P≥0.050). Our findings suggest that EV miRNA in both early and late pregnancy may influence gestational duration.
循环 miRNA 可能有助于不良出生结局的发展。然而,很少有研究调查细胞外囊泡 (EV) miRNA,其在细胞间通讯中发挥重要作用,或比较妊娠多个时间点的 miRNA。在当前的研究中,从 MADRES 研究中 156 名参与者的母血浆中收集的 EV 中对 800 个 miRNA 进行了分析,MADRES 研究是一个健康差异妊娠队列。使用协变量调整的稳健线性回归检验 miRNA 与出生体重、胎龄体重和出生时胎龄的相关性。还研究了婴儿性别和母亲 BMI 的差异。13 个 miRNA 的晚期妊娠指标与出生时胎龄相关(P<0.050)。观察到 8 个 miRNA(miR-4454+miR-7975、miR-4516、let-7b-5p、miR-126-3p、miR-29b-3p、miR-15a-5p、miR-15b-5p、miR-19b-3p)呈负相关,而 5 个 miRNA(miR-212-3p、miR-584-5p、miR-608、miR-210-3p、miR-188-5p)呈正相关。预测的靶基因在参与器官发生和胎盘发育的途径中富集(P<0.050)。在肥胖女性所生婴儿的晚期妊娠中测量的另一个 miRNA(miR-107)与出生时胎龄呈正相关(BMI 交互作用的 P 值为 0.011)。在初步分析中,早期妊娠 miRNA 与出生结局之间的相关性没有统计学意义(P≥0.05)。然而,早期妊娠测量的 37 个 miRNA 与出生时胎龄的性别特异性关联(交互作用的 P 值<0.050)。没有一个 miRNA 与胎儿生长指标相关(P≥0.050)。我们的研究结果表明,妊娠早期和晚期的 EV miRNA 可能会影响妊娠期。