Bibiloni Pere, Martin Jean-Charles, Cobo Pilar, Jiménez-Cabanillas María Victoria, DeLucas María, Tardivel Catherine, Picó Catalina, Serra Francisca, Sánchez Juana
Laboratory of Molecular Biology, Nutrition and Biotechnology (Nutrigenomics, Biomarkers and Risk Evaluation), Edifici Mateu Orfila, University of the Balearic Islands, Carretera de Valldemossa Km 7.5, 07122 Palma, Spain.
Health Research Institute of the Balearic Islands, IdISBa, 07010 Palma, Spain.
Int J Mol Sci. 2025 Sep 14;26(18):8953. doi: 10.3390/ijms26188953.
Prematurity is associated with a higher risk of developing short- and long-term metabolic complications. However, the concrete mechanisms are not yet fully understood. The purpose of this study was to characterize early urinary metabolic adaptations linked to preterm birth. Urine samples collected at one month of age were compared between extremely and very preterm neonates (<32 weeks gestation) ( = 45) and term newborns ( = 96). Liquid chromatography coupled to mass spectrometry (LC-MS) and nuclear magnetic resonance (NMR) techniques were both applied and analyzed independently. Univariate analysis and multivariate analyses were utilized to assess the impact of preterm birth on the metabolites identified. Multiblock analysis was further used to evaluate the effect of prematurity on biological functions. A profound impact of prematurity was observed. Both experimental groups differed in the concentrations of 240 metabolites from the LC-MS dataset and 52 from the NMR one. Multivariate analyses confirmed a significant and important separation between groups. Finally, multiblock analysis identified six major biological outcomes affected by preterm birth: nitrogen metabolism, growth, neurochemical metabolism, microbiota metabolism, cell defense, and metabolic alterations. Most of the observed variations exhibited biological plausibility and were consistent with reported health complications associated with preterm birth. In conclusion, preterm birth is linked to a specific fingerprint in the urinary metabolome, reflecting metabolic adaptations in multiple systems occurring at one month of age.
早产与发生短期和长期代谢并发症的较高风险相关。然而,具体机制尚未完全明确。本研究的目的是描述与早产相关的早期尿液代谢适应性变化。比较了极早产儿和超早产儿(孕周<32周)(n = 45)与足月儿(n = 96)在1月龄时采集的尿液样本。液相色谱-质谱联用(LC-MS)和核磁共振(NMR)技术均被应用并独立分析。采用单变量分析和多变量分析来评估早产对所鉴定代谢物的影响。进一步使用多组块分析来评估早产对生物学功能的影响。观察到早产有深远影响。两个实验组在LC-MS数据集中的240种代谢物浓度以及NMR数据集中的52种代谢物浓度上存在差异。多变量分析证实了两组之间存在显著且重要的区分。最后,多组块分析确定了受早产影响的六个主要生物学结果:氮代谢、生长、神经化学代谢、微生物群代谢、细胞防御和代谢改变。观察到的大多数变化具有生物学合理性,并且与报道的与早产相关的健康并发症一致。总之,早产与尿液代谢组中的特定指纹相关,反映了1月龄时多个系统发生的代谢适应性变化。