{"title":"Urine Metabolomics Reveals Overlapping Metabolic Associations Between Preeclampsia and Gestational Diabetes.","authors":"Nupur Rani Agarwal, Garima Kachhawa, Bolaji Fatai Oyeyemi, Neel Sarovar Bhavesh","doi":"10.1007/s12291-022-01103-2","DOIUrl":null,"url":null,"abstract":"<p><p>Pregnancy is associated with numerous metabolic adaptations to meet the demands of the growing foetus. These adaptations could be perturbed during pregnancy due to preeclampsia (PE) and gestational diabetes (GDM). As these two obstetric aliments show some overlapping pathophysiology and similar biochemical dysregulation, the present study was undertaken to compare urine metabolome of PE and GDM with normal pregnancy (NT) in all trimesters of gestation using nuclear magnetic resonance spectroscopy-based metabolomics analysis to ascertain and compare metabolome in the study groups. We observed overlapping metabolic perturbations in PE and GDM. Though a study with a small sample size, this is the first report which confirms significantly differential metabolites in urine of both PE and GDM. Dimethylglycine and oxoglutaric acid were decreased while benzoic acid was increased in both the cases in all trimesters. Alanine, aspartate and glutamate metabolism, aminoacyl-tRNA biosynthesis, citrate and butanoate metabolism were the most perturbed pathways in both PE and GDM across pregnancy. These pathways have an association with energy metabolism, glucose homeostasis, insulin sensitivity and oxidative stress which play an important role in the development and progression of PE and GDM. In conclusion, our study showed that urine metabolome could reflect metabolic associations between PE and GDM and also in the identification of biomolecules that could be used as potential biomarker(s) for early detection of the metabolic diseases in pregnancy.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s12291-022-01103-2.</p>","PeriodicalId":89742,"journal":{"name":"Asia-Pacific biotech news","volume":"10 1","pages":"356-364"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11239642/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asia-Pacific biotech news","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s12291-022-01103-2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/12/6 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Pregnancy is associated with numerous metabolic adaptations to meet the demands of the growing foetus. These adaptations could be perturbed during pregnancy due to preeclampsia (PE) and gestational diabetes (GDM). As these two obstetric aliments show some overlapping pathophysiology and similar biochemical dysregulation, the present study was undertaken to compare urine metabolome of PE and GDM with normal pregnancy (NT) in all trimesters of gestation using nuclear magnetic resonance spectroscopy-based metabolomics analysis to ascertain and compare metabolome in the study groups. We observed overlapping metabolic perturbations in PE and GDM. Though a study with a small sample size, this is the first report which confirms significantly differential metabolites in urine of both PE and GDM. Dimethylglycine and oxoglutaric acid were decreased while benzoic acid was increased in both the cases in all trimesters. Alanine, aspartate and glutamate metabolism, aminoacyl-tRNA biosynthesis, citrate and butanoate metabolism were the most perturbed pathways in both PE and GDM across pregnancy. These pathways have an association with energy metabolism, glucose homeostasis, insulin sensitivity and oxidative stress which play an important role in the development and progression of PE and GDM. In conclusion, our study showed that urine metabolome could reflect metabolic associations between PE and GDM and also in the identification of biomolecules that could be used as potential biomarker(s) for early detection of the metabolic diseases in pregnancy.
Supplementary information: The online version contains supplementary material available at 10.1007/s12291-022-01103-2.
妊娠与许多新陈代谢适应相关,以满足胎儿成长的需求。在怀孕期间,子痫前期(PE)和妊娠糖尿病(GDM)可能会扰乱这些适应性。由于这两种产科疾病表现出一些重叠的病理生理学和类似的生化失调,本研究采用基于核磁共振波谱的代谢组学分析,对 PE 和 GDM 与正常妊娠(NT)在妊娠期所有三个月的尿液代谢组进行比较,以确定和比较研究组的代谢组。我们在 PE 和 GDM 中观察到了重叠的代谢紊乱。虽然这项研究的样本量较小,但这是第一份证实 PE 和 GDM 尿液中代谢物存在显著差异的报告。在两个病例中,二甲基甘氨酸和氧戊二酸在所有孕期都有所减少,而苯甲酸则有所增加。丙氨酸、天门冬氨酸和谷氨酸代谢、氨基酰-tRNA 生物合成、柠檬酸盐和丁酸盐代谢是 PE 和 GDM 在整个孕期受干扰最大的途径。这些途径与能量代谢、糖稳态、胰岛素敏感性和氧化应激有关,在 PE 和 GDM 的发生和发展中起着重要作用。总之,我们的研究表明,尿液代谢组能反映 PE 和 GDM 之间的代谢关联,还能鉴定出可用作早期检测妊娠期代谢性疾病的潜在生物标记物的生物大分子:在线版本包含补充材料,可在 10.1007/s12291-022-01103-2上查阅。