Sebina Ismail, Bidgood Charles, Stalley Felicity, Hartel Gunter, Stark Terra, Callaway Leonie, Amoako Akwasi, Lehner Christoph, Dekker Nitert Marloes, Phipps Simon
Infection and Inflammation Program, QIMR Berghofer Medical Research Institute, Herston, QLD, 4006, Australia.
Faculty of Medicine, The University of Queensland, Brisbane, QLD, 4072, Australia.
Sci Rep. 2024 Dec 3;14(1):30027. doi: 10.1038/s41598-024-81194-4.
Mechanisms linking pre-pregnancy obesity to increased preterm birth risk are unclear. Here, we examined the impact of pre-pregnancy obesity on metabolites, Fms-related tyrosine kinase 3 ligand (Flt3L), and proinflammatory cytokine profiles in preterm birth. We used cytokine bead array, ELISA and Gas Chromatography-Mass Spectrometry (GC-MS) to determine cytokine and metabolite profiles in maternal and cord blood samples from 124 pregnant women in Australia, who gave birth at term (n = 86) or preterm (n = 38). Besides the expected variations in birth weight and gestational age, all demographic characteristics, including pre-pregnancy body mass index, were similar between the term and preterm birth groups. Mothers in the preterm birth group had reduced Flt3L (P = 0.002) and elevated IL-6 (P = 0.002) compared with term birthing mothers. Among mothers who gave birth preterm, those with pre-pregnancy obesity had lower Flt3L levels (P = 0.02) compared with lean mothers. Flt3L and IL-6 were similar in cord blood across both groups, but TNFα levels (P = 0.02) were reduced in preterm newborns. Metabolomic analysis revealed significant shifts in essential metabolites in women with pre-pregnancy obesity, some of which were linked to preterm births. Our findings suggest that maternal pre-pregnancy obesity alters the metabolome and reduces Flt3L expression, potentially increasing risk of preterm birth.
孕前肥胖与早产风险增加之间的关联机制尚不清楚。在此,我们研究了孕前肥胖对早产时母体代谢物、Fms相关酪氨酸激酶3配体(Flt3L)和促炎细胞因子谱的影响。我们使用细胞因子微珠阵列、酶联免疫吸附测定(ELISA)和气相色谱-质谱联用仪(GC-MS)来测定澳大利亚124名孕妇的母血和脐血样本中的细胞因子和代谢物谱,这些孕妇足月分娩(n = 86)或早产(n = 38)。除了出生体重和孕周的预期差异外,足月分娩组和早产组之间的所有人口统计学特征,包括孕前体重指数,均相似。与足月分娩的母亲相比,早产组母亲的Flt3L水平降低(P = 0.002),白细胞介素-6(IL-6)水平升高(P = 0.002)。在早产的母亲中,孕前肥胖的母亲与体型偏瘦的母亲相比,Flt3L水平较低(P = 0.02)。两组脐血中的Flt3L和IL-6水平相似,但早产新生儿的肿瘤坏死因子α(TNFα)水平降低(P = 0.02)。代谢组学分析显示,孕前肥胖女性的必需代谢物有显著变化,其中一些与早产有关。我们的研究结果表明,孕前肥胖会改变代谢组并降低Flt3L表达,可能会增加早产风险。