Agarwal Nupur Rani, Kachhawa Garima, Oyeyemi Bolaji Fatai, Bhavesh Neel Sarovar
Transcription Regulation Group, International Centre for Genetic Engineering and Biotechnology (ICGEB), Aruna Asaf Ali Marg, New Delhi, 110067 India.
Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences (AIIMS), Ansari Nagar, New Delhi, 110029 India.
Indian J Clin Biochem. 2024 Jul;39(3):356-364. doi: 10.1007/s12291-022-01103-2. Epub 2022 Dec 6.
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.
The online version contains supplementary material available at 10.1007/s12291-022-01103-2.
妊娠伴随着许多代谢适应性变化以满足胎儿生长的需求。由于子痫前期(PE)和妊娠期糖尿病(GDM),这些适应性变化在孕期可能会受到干扰。由于这两种产科疾病表现出一些重叠的病理生理学和相似的生化失调,本研究采用基于核磁共振波谱的代谢组学分析方法,对妊娠各期的PE、GDM和正常妊娠(NT)的尿液代谢组进行比较,以确定和比较研究组中的代谢组。我们观察到PE和GDM存在重叠的代谢紊乱。尽管本研究样本量较小,但这是第一份证实PE和GDM尿液中存在显著差异代谢物的报告。在所有孕期,两种情况下二甲基甘氨酸和氧代戊二酸均降低,而苯甲酸均升高。丙氨酸、天冬氨酸和谷氨酸代谢、氨酰-tRNA生物合成、柠檬酸和丁酸代谢是整个孕期PE和GDM中受干扰最严重的途径。这些途径与能量代谢、葡萄糖稳态、胰岛素敏感性和氧化应激相关,在PE和GDM的发生和发展中起重要作用。总之,我们的研究表明,尿液代谢组可以反映PE和GDM之间的代谢关联,也有助于识别可作为孕期代谢疾病早期检测潜在生物标志物的生物分子。
在线版本包含可在10.1007/s12291-022-01103-2获取的补充材料。