Department of Intensive Care Medicine, The Second Affiliated Hospital of Nanjing Medical University, Nanjing 210000, People's Republic of China.
Department of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing 210000, People's Republic of China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2024 Apr 15;1237:124101. doi: 10.1016/j.jchromb.2024.124101. Epub 2024 Mar 26.
Vitamins are essential micronutrients that play key roles in many biological pathways associated with sepsis. The gut microbiome plays a pivotal role in the progression of sepsis and may contribute to the onset of multi-organ dysfunction syndrome (MODS). The aim of this study was to investigate the changes in serum vitamins, and their correlation with intestinal flora and metabolomic profiles in patients with sepsis.
The serum levels of vitamins were determined by Ultra Performance Liquid Chromatography (UPLC). 16S rRNA gene sequencing and Liquid Chromatography-tandem Mass Spectrometry (LC-MS/MS) targeted metabolomics were used for microbiome and metabolome analysis.
In the training cohort: After univariate, multivariate (OPLS-DA) and Spearman analyses, it was concluded that vitamin levels of 25 (OH) VD3 and (VD2 + VD3), as well as vitamins A and B9, differed significantly among healthy controls (HC), non-septic critical patients (NS), and sepsis patients (SS) (P < 0.05). The validation cohort confirmed the differential vitamin findings from the training cohort. Moreover, analyses of gut flora and metabolites in septic patients and healthy individuals revealed differential flora, metabolites, and metabolic pathways that were linked to alterations in serum vitamin levels. We found for the first time that vitamin B9 was negatively correlated with g_Sellimonas.
Sepsis patients exhibited significantly lower levels of 25 (OH) VD3 and (VD2 + VD3), vitamins A and B9, which hold potential as predictive markers for sepsis prognosis. The changes in these vitamins may be associated with inflammatory factors, oxidative stress, and changes in gut flora.
维生素是必需的微量营养素,在许多与脓毒症相关的生物途径中发挥关键作用。肠道微生物群在脓毒症的进展中起着关键作用,并可能导致多器官功能障碍综合征(MODS)的发生。本研究旨在探讨脓毒症患者血清维生素的变化及其与肠道菌群和代谢组学特征的相关性。
采用超高效液相色谱法(UPLC)测定血清维生素水平。采用 16S rRNA 基因测序和液质联用(LC-MS/MS)靶向代谢组学方法进行微生物组和代谢组分析。
在训练队列中:经过单变量、多变量(OPLS-DA)和 Spearman 分析,得出结论,25(OH)VD3 和(VD2+VD3)以及维生素 A 和 B9 的维生素水平在健康对照组(HC)、非脓毒症危重病患者(NS)和脓毒症患者(SS)之间存在显著差异(P<0.05)。验证队列证实了训练队列中差异维生素的发现。此外,对脓毒症患者和健康个体的肠道菌群和代谢物进行分析,揭示了与血清维生素水平变化相关的差异菌群、代谢物和代谢途径。我们首次发现维生素 B9 与 g_Sellimonas 呈负相关。
脓毒症患者的 25(OH)VD3 和(VD2+VD3)、维生素 A 和 B9 水平显著降低,这些维生素可能是脓毒症预后的预测标志物。这些维生素的变化可能与炎症因子、氧化应激和肠道菌群变化有关。