Suppr超能文献

与血脂异常相关的维生素D状态的代谢组学分析

Metabolomics Profiling of Vitamin D Status in Relation to Dyslipidemia.

作者信息

Mousa Hanaa, Elrayess Mohamed A, Diboun Ilhame, Jackson Simon K, Zughaier Susu M

机构信息

College of Medicine, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.

Biomedical Research Center (BRC), QU Health, Qatar University, Doha P.O. Box 2731, Qatar.

出版信息

Metabolites. 2022 Aug 22;12(8):771. doi: 10.3390/metabo12080771.

Abstract

Vitamin D deficiency is a global disorder associated with several chronic illnesses including dyslipidemia and metabolic syndrome. The impact of this association with both dyslipidemia and vitamin D deficiency on metabolomics profile is not yet fully understood. This study analyses the metabolomics and lipidomic signatures in relation to vitamin D status and dyslipidemia. Metabolomics data were collected from Qatar Biobank database and categorized into four groups based on vitamin D and dyslipidemia status. Metabolomics multivariate analysis was performed using the orthogonal partial least square discriminate analysis (OPLS-DA) whilst linear models were used to assess the per-metabolite association with each of the four dyslipidemia/vitamin D combination groups. Our results indicate a high prevalence of vitamin D deficiency among the younger age group, while dyslipidemia was more prominent in the older group. A significant alteration of metabolomics profile was observed among the dyslipidemic and vitamin D deficient individuals in comparison with control groups. These modifications reflected changes in some key pathways including ceramides, diacylglycerols, hemosylceramides, lysophospholipids, phosphatidylcholines, phosphatidylethanol amines, and sphingomyelins. Vitamin D deficiency and dyslipidemia have a deep impact on sphingomyelins profile. The modifications were noted at the level of ceramides and are likely to propagate through downstream pathways.

摘要

维生素D缺乏是一种全球性疾病,与包括血脂异常和代谢综合征在内的多种慢性疾病相关。这种与血脂异常和维生素D缺乏的关联对代谢组学特征的影响尚未完全了解。本研究分析了与维生素D状态和血脂异常相关的代谢组学和脂质组学特征。代谢组学数据从卡塔尔生物样本库数据库收集,并根据维生素D和血脂异常状态分为四组。使用正交偏最小二乘判别分析(OPLS-DA)进行代谢组学多变量分析,同时使用线性模型评估每种代谢物与四个血脂异常/维生素D组合组中每组的关联。我们的结果表明,维生素D缺乏在较年轻年龄组中患病率较高,而血脂异常在较年长组中更为突出。与对照组相比,在血脂异常和维生素D缺乏的个体中观察到代谢组学特征的显著改变。这些改变反映了一些关键途径的变化,包括神经酰胺、二酰基甘油、血苷神经酰胺、溶血磷脂、磷脂酰胆碱、磷脂酰乙醇胺和鞘磷脂。维生素D缺乏和血脂异常对鞘磷脂特征有深远影响。这些改变在神经酰胺水平上被注意到,并且可能通过下游途径传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9334/9416284/e5a857f903ce/metabolites-12-00771-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验