A comparative lipidomic study of the human placenta from women with or without gestational diabetes mellitus

妊娠期糖尿病 脂类学 血脂 胎盘 血脂谱 脂质代谢 内科学 内分泌学 糖尿病 甘油磷脂 生物 医学 怀孕 磷脂 生物化学 胎儿 妊娠期 胆固醇 遗传学
作者
Dongmei Jiang,Jin He,Siyu Hua,Jiahua Zhang,Lan Liu,Chunjian Shan,Xianwei Cui,Chenbo Ji
出处
期刊:Molecular omics [The Royal Society of Chemistry]
卷期号:18 (6): 545-554 被引量:3
标识
DOI:10.1039/d2mo00083k
摘要

Gestational diabetes mellitus (GDM) is always accompanied by lipid disorders. The placenta serves as a center for lipid synthesis and transport and plays a critical role in establishing GDM. Thus, the changes in the type and content of lipids in the placenta may contribute to the development of GDM. Here, we performed an untargeted lipidomic analysis to profile the alterations of lipids in the placenta induced by GDM. Principal component analysis (PCA) was used to reduce the dimensionality of lipid data, and orthogonal projections to latent structures-discriminate analysis (OPLS-DA) was launched to show the differences in the lipid profile between the GDM group and normal controls. Additional multivariate data processing was carried out, including classification, pathway analysis and correlation analysis between dysregulated lipids and maternal blood glucose levels. We finally identified 1202 lipids in positive mode and 924 lipids in negative mode, of which 63 lipids were strongly associated with GDM. Notably, most dysregulated lipids were clustered in two major subtypes: glycerophospholipids and glycerolipids. Consistently, a significant down-regulation of glycerophospholipid metabolism was observed from pathway analysis. In addition, we found that SHexCer(d50:1), TAG(15:0/20:6/20:6) and PE(18:1e/21:2) were positively correlated with blood glucose levels, while PC(12:0/22:3), PC(22:4e/18:5) and PE(18:1e/26:4) showed negative correlations. Combining these lipids with fasting blood glucose showed high accuracy in the discrimination of women with GDM. In general, we explored the placental lipidomic abnormalities induced by GDM, and these findings may help us understand the pathological mechanisms of GDM.
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