a Laboratory of Environmental Epigenetics, Exposure, Epidemiology and Risk Program ; Department of Environmental Health, Harvard T.H. Chan School of Public Health , Boston , MA , USA.
b Department of Neonatology , Beth Israel Deaconess Medical Center and Division of Newborn Medicine, Boston Children's Hospital and Harvard Medical School , Boston , MA , USA.
Epigenetics. 2017 Sep;12(9):804-810. doi: 10.1080/15592294.2017.1358345. Epub 2017 Sep 26.
Healthy feto-maternal communication is critical during pregnancy and is orchestrated by the placenta. Dysfunction of the placenta leads to fetal growth complications; however, the underlying biological mechanisms have yet to be fully elucidated. Circulating extracellular microRNAs (exmiRNAs) in the blood have been implicated in cell-to-cell communication. Therefore, exmiRNAs may provide useful biological information about communication between the mother, the fetus, and the placenta during pregnancy. We used logistic regression to determine the association of exmiRNAs with abnormal fetal growth by comparing mothers of infants classified as small-for-gestational age (SGA) (n = 36) and large-for-gestational age (LGA) (n = 13) to appropriate-for-gestational age (AGA), matched by gestational age at delivery and infant sex. In addition, we used linear regression to determine associations between exmiRNAs and birth weight-for-gestational age (BWGA) z-score (n = 100), adjusting for maternal age, body mass index, and parity. We found that higher levels of miR-20b-5p, miR-942-5p, miR-324-3p, miR-223-5p, and miR-127-3p in maternal serum were associated with lower odds for having a SGA vs. AGA infant, and higher levels of miR-661, miR-212-3p, and miR-197-3p were associated with higher odds for having a LGA vs. AGA infant. We also found associations between miR-483-5p, miR-10a-5p, miR-204-5p, miR-202-3p, miR-345-5p, miR-885-5p, miR-127-3p, miR-148b-3p, miR-324-3p, miR-1290, miR-597-5p, miR-139-5p, miR-215-5p, and miR-99b-5p and BWGA z-score. We also found sex-specific associations with exmiRNAs and fetal growth. Our findings suggest that exmiRNAs circulating in maternal blood at second trimester are associated with fetal growth. Validation of our findings may lead to the development of minimally-invasive biomarkers of fetal growth during pregnancy.
健康的胎母通讯在妊娠期间至关重要,由胎盘协调。胎盘功能障碍会导致胎儿生长并发症;然而,其潜在的生物学机制尚未完全阐明。血液中的循环细胞外 microRNAs(exmiRNAs)已被牵连到细胞间通讯中。因此,exmiRNAs 可能为妊娠期间母亲、胎儿和胎盘之间的通讯提供有用的生物学信息。我们使用逻辑回归通过比较小胎龄儿(SGA)(n = 36)和大胎龄儿(LGA)(n = 13)与适当胎龄儿(AGA)的母亲来确定 exmiRNA 与异常胎儿生长的关联,通过分娩时的胎龄和婴儿性别匹配。此外,我们使用线性回归来确定 exmiRNAs 与出生体重与胎龄(BWGA)z 评分(n = 100)之间的关联,调整了母亲的年龄、体重指数和产次。我们发现,母体血清中 miR-20b-5p、miR-942-5p、miR-324-3p、miR-223-5p 和 miR-127-3p 水平升高与 SGA 婴儿的可能性降低相关,而 miR-661、miR-212-3p 和 miR-197-3p 水平升高与 LGA 婴儿的可能性升高相关。我们还发现 miR-483-5p、miR-10a-5p、miR-204-5p、miR-202-3p、miR-345-5p、miR-885-5p、miR-127-3p、miR-148b-3p、miR-324-3p、miR-1290、miR-597-5p、miR-139-5p、miR-215-5p 和 miR-99b-5p 与 BWGA z 评分之间存在关联。我们还发现 exmiRNAs 与胎儿生长的性别特异性关联。我们的研究结果表明,妊娠中期母体血液中循环的 exmiRNAs 与胎儿生长有关。如果我们的研究结果得到验证,可能会开发出妊娠期间胎儿生长的微创生物标志物。