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幼儿血浆25-羟基维生素D浓度与多不饱和脂肪酸代谢产物相关:维生素D预防产前哮喘试验的结果

Plasma 25-Hydroxyvitamin D Concentrations are Associated with Polyunsaturated Fatty Acid Metabolites in Young Children: Results from the Vitamin D Antenatal Asthma Reduction Trial.

作者信息

Huang Mengna, Kelly Rachel S, Kachroo Priyadarshini, Chu Su H, Lee-Sarwar Kathleen, Chawes Bo L, Bisgaard Hans, Litonjua Augusto A, Weiss Scott T, Lasky-Su Jessica

机构信息

Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.

Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.

出版信息

Metabolites. 2020 Apr 14;10(4):151. doi: 10.3390/metabo10040151.

Abstract

Vitamin D deficiency contributes to a multitude of health conditions, but its biological mechanisms are not adequately understood. Untargeted metabolomics offers the opportunity to comprehensively examine the metabolic profile associated with variations in vitamin D concentrations. The objective of the current analysis was to identify metabolites and metabolic pathways associated with plasma 25-hydroxyvitamin D [25(OH)D] concentrations. The current study included children of pregnant women in the Vitamin D Antenatal Asthma Reduction Trial, who had 25(OH)D and global metabolomics data at age 1 and 3 years. We assessed the cross-sectional associations between individual metabolites and 25(OH)D using linear regression adjusting for confounding factors. Twelve metabolites were significantly associated with plasma 25(OH)D concentrations at both age 1 and 3 after correction for multiple comparisons, including three members of the n-6 polyunsaturated fatty acid (PUFA) metabolism pathway (linoleate, arachidonate, and docosapentaenoate) inversely associated with 25(OH)D. These PUFAs along with four other significant metabolites were replicated in the independent Childhood Asthma Management Program (CAMP) cohort. Both vitamin D and n-6 PUFAs are involved in inflammatory processes, and evidence from cell and animal studies demonstrate a plausible biological mechanism where the active form of 25(OH)D may influence n-6 PUFA metabolism. These relationships warrant further investigation in other populations.

摘要

维生素D缺乏会导致多种健康问题,但其生物学机制尚未得到充分了解。非靶向代谢组学为全面研究与维生素D浓度变化相关的代谢谱提供了机会。当前分析的目的是确定与血浆25-羟基维生素D [25(OH)D]浓度相关的代谢物和代谢途径。本研究纳入了维生素D产前哮喘减少试验中孕妇的子女,这些儿童在1岁和3岁时拥有25(OH)D和全代谢组学数据。我们使用线性回归并校正混杂因素来评估个体代谢物与25(OH)D之间的横断面关联。在进行多重比较校正后,12种代谢物在1岁和3岁时均与血浆25(OH)D浓度显著相关,其中包括n-6多不饱和脂肪酸(PUFA)代谢途径的三个成员(亚油酸、花生四烯酸和二十二碳五烯酸),它们与25(OH)D呈负相关。这些多不饱和脂肪酸以及其他四种显著的代谢物在独立的儿童哮喘管理项目(CAMP)队列中得到了重复验证。维生素D和n-6多不饱和脂肪酸都参与炎症过程,细胞和动物研究的证据表明了一种合理的生物学机制,即25(OH)D的活性形式可能影响n-6多不饱和脂肪酸的代谢。这些关系值得在其他人群中进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd4/7240965/6d53749a6408/metabolites-10-00151-g001.jpg

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