Mousa Hanaa, Elrayess Mohamed A, Diboun Ilhame, Jackson Simon K, Zughaier Susu M
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.
Metabolites. 2022 Aug 22;12(8):771. doi: 10.3390/metabo12080771.
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.
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。