Clinical and Translational Neuroscience Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Brain Aging and Behavior Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Int J Mol Sci. 2020 Feb 16;21(4):1324. doi: 10.3390/ijms21041324.
Metabolic syndrome (MetS) affects an increasing number of older adults worldwide. Cross-cultural comparisons can provide insight into how factors, including genetic, environmental, and lifestyle, may influence MetS prevalence. Metabolomics, which measures the biochemical products of cell processes, can be used to enhance a mechanistic understanding of how biological factors influence metabolic outcomes. In this study we examined associations between serum metabolite concentrations, representing a range of biochemical pathways and metabolic syndrome in two older adult cohorts: The Tsuruoka Metabolomics Cohort Study (TMCS) from Japan ( = 104) and the Baltimore Longitudinal Study of Aging (BLSA) from the United States ( = 146). We used logistic regression to model associations between MetS and metabolite concentrations. We found that metabolites from the phosphatidylcholines-acyl-alkyl, sphingomyelin, and hexose classes were significantly associated with MetS and risk factor outcomes in both cohorts. In BLSA, metabolites across all classes were uniquely associated with all outcomes. In TMCS, metabolites from the amino acid, biogenic amines, and free fatty acid classes were uniquely associated with MetS, and metabolites from the sphingomyelin class were uniquely associated with elevated triglycerides. The metabolites and metabolite classes we identified may be relevant for future studies exploring disease mechanisms and identifying novel precision therapy targets for individualized medicine.
代谢综合征(MetS)在全球范围内影响着越来越多的老年人。跨文化比较可以深入了解遗传、环境和生活方式等因素如何影响 MetS 的患病率。代谢组学可以测量细胞过程的生化产物,可用于增强对生物因素如何影响代谢结果的机制理解。在这项研究中,我们研究了来自日本的鹤冈代谢组学队列研究(TMCS)(n=104)和来自美国的巴尔的摩纵向衰老研究(BLSA)(n=146)中两个老年队列的血清代谢物浓度与代谢综合征之间的关联。我们使用逻辑回归来模拟 MetS 与代谢物浓度之间的关联。我们发现,磷脂酰胆碱-酰基-烷基、神经鞘磷脂和己糖类中的代谢物与两个队列中的 MetS 和危险因素结局显著相关。在 BLSA 中,所有类别中的代谢物都与所有结局独特相关。在 TMCS 中,来自氨基酸、生物胺和游离脂肪酸类别的代谢物与 MetS 独特相关,来自神经鞘磷脂类别的代谢物与甘油三酯升高独特相关。我们鉴定的代谢物和代谢物类别可能与未来探索疾病机制和确定个体化医学新型精准治疗靶点的研究有关。