López-Hernández Yamilé, Lima-Rogel Victoria, Mandal Rupasri, Zheng Jiamin, Zhang Lun, Oler Eponine, García-López David Alejandro, Torres-Calzada Claudia, Mejía-Elizondo Ana Ruth, Poelsner Jenna, López Jesús Adrián, Zubkowski Ashley, Wishart David S
Academic Unit of Biological Sciences, Metabolomics and Proteomics Laboratory, CONAHCyT-Autonomous University of Zacatecas, Zacatecas 98000, Mexico.
Hospital Central "Dr. Ignacio Morones Prieto", San Luis Potosi 78290, Mexico.
Metabolites. 2024 Jan 10;14(1):41. doi: 10.3390/metabo14010041.
Maternal pathological conditions such as infections and chronic diseases, along with unexpected events during labor, can lead to life-threatening perinatal outcomes. These outcomes can have irreversible consequences throughout an individual's entire life. Urinary metabolomics can provide valuable insights into early physiological adaptations in healthy newborns, as well as metabolic disturbances in premature infants or infants with birth complications. In the present study, we measured 180 metabolites and metabolite ratios in the urine of 13 healthy (hospital-discharged) and 38 critically ill newborns (admitted to the neonatal intensive care unit (NICU)). We used an in-house-developed targeted tandem mass spectrometry (MS/MS)-based metabolomic assay (TMIC Mega) combining liquid chromatography (LC-MS/MS) and flow injection analysis (FIA-MS/MS) to quantitatively analyze up to 26 classes of compounds. Average urinary concentrations (and ranges) for 167 different metabolites from 38 critically ill NICU newborns during their first 24 h of life were determined. Similar sets of urinary values were determined for the 13 healthy newborns. These reference data have been uploaded to the Human Metabolome Database. Urinary concentrations and ranges of 37 metabolites are reported for the first time for newborns. Significant differences were found in the urinary levels of 44 metabolites between healthy newborns and those admitted at the NICU. Metabolites such as acylcarnitines, amino acids and derivatives, biogenic amines, sugars, and organic acids are dysregulated in newborns with bronchopulmonary dysplasia (BPD), asphyxia, or newborns exposed to SARS-CoV-2 during the intrauterine period. Urine can serve as a valuable source of information for understanding metabolic alterations associated with life-threatening perinatal outcomes.
感染和慢性病等母体病理状况,以及分娩期间的意外事件,可能导致危及生命的围产期结局。这些结局可能会在个体的一生中产生不可逆转的后果。尿液代谢组学可以为健康新生儿的早期生理适应以及早产儿或有出生并发症的婴儿的代谢紊乱提供有价值的见解。在本研究中,我们测量了13名健康(已出院)新生儿和38名危重新生儿(入住新生儿重症监护病房(NICU))尿液中的180种代谢物和代谢物比率。我们使用了一种内部开发的基于靶向串联质谱(MS/MS)的代谢组学检测方法(TMIC Mega),该方法结合了液相色谱(LC-MS/MS)和流动注射分析(FIA-MS/MS),以定量分析多达26类化合物。测定了38名危重新生儿在出生后24小时内167种不同代谢物的平均尿液浓度(及范围)。为13名健康新生儿测定了类似的尿液值集。这些参考数据已上传至人类代谢组数据库。首次报告了新生儿37种代谢物的尿液浓度和范围。健康新生儿与入住NICU的新生儿之间,在44种代谢物的尿液水平上发现了显著差异。在患有支气管肺发育不良(BPD)、窒息的新生儿或宫内接触SARS-CoV-2的新生儿中,酰基肉碱、氨基酸及其衍生物、生物胺、糖类和有机酸等代谢物失调。尿液可以作为了解与危及生命的围产期结局相关的代谢改变的宝贵信息来源。