Medical University Clinic, Division of Endocrinology, Diabetes & Metabolism, Kantonsspital Aarau, Aarau, Switzerland.
Functional Genomics Center Zurich, ETH and University of Zurich, Zurich, Switzerland.
Clin Nutr. 2021 Sep;40(9):5062-5070. doi: 10.1016/j.clnu.2021.07.029. Epub 2021 Jul 31.
BACKGROUND & AIMS: The EFFORT trial reported a substantial risk reduction for adverse events and mortality in medical in-patients receiving a nutritional support intervention. With the use of an untargeted metabolomics approach, we investigated the prognostic and therapeutic potential of metabolomic markers to understand, whether there are distinct metabolic patterns associated with malnutrition risk as assessed by the Nutritional Risk screening (NRS 2002) score, the risk of 30-day mortality and the response to nutritional support, respectively.
Out of the 2088 samples we randomly selected 120 blood samples drawn on day 1 after hospital admission and before treatment initiation. Samples were stratified by NRS 2002, treatment allocation (intervention vs. control), and mortality at 30 days, but not on the type of medical illness. We performed untargeted analysis by liquid chromatography mass spectrometry (LC-MS/MS).
We measured 1389 metabolites in 120 patients of which 81 (67.5%) survived until day 30. After filtering, 371 metabolites remained, and 200 were matched to one or more Human Metabolome Data Base (HMDB) entries. Between group analysis showed a slight distinction between the treatment groups for patients with a NRS 3, but not for those with NRS 4 and ≥ 5. C-statistic between those who died and survived at day 30 ranged from 0.49 (95% confidence interval 0.35-0.68) for a combination of 5 metabolites/predictors to 0.66 (95% confidence interval 0.53-0.79) for a combination of 100 metabolites. Pathway analysis found significant enrichment in the pathways for nitrogen, vitamin B3 (nicotinate and nicotinamide), leukotriene, and arachidonic acid metabolisms in nutritional support responders compared to non-responders.
In our heterogenous population of medical inpatients with different illnesses and comorbidities, metabolomic markers showed little prognostic and therapeutic potential for better phenotyping malnutrition and response to nutritional therapy. Future studies should focus on more selected patient populations to understand whether a metabolomic approach can advance the nutritional care of patients.
EFFORT 试验报道,在接受营养支持干预的住院患者中,不良事件和死亡率的风险显著降低。本研究采用非靶向代谢组学方法,探究代谢组学标志物的预后和治疗潜力,以了解是否存在与营养不良风险(通过营养风险筛查 2002 评分(NRS 2002)评估)、30 天死亡率以及对营养支持的反应相关的不同代谢模式。
在 2088 个样本中,我们随机选择了 120 个入院后第 1 天、治疗开始前采集的血样。根据 NRS 2002、治疗分配(干预组与对照组)和 30 天死亡率对样本进行分层,但未根据医疗疾病的类型分层。我们通过液相色谱-质谱联用技术(LC-MS/MS)进行非靶向分析。
我们在 120 名患者中测量了 1389 种代谢物,其中 81 名(67.5%)患者存活至第 30 天。经过过滤,剩余 371 种代谢物,其中 200 种代谢物与一个或多个人类代谢组数据库(HMDB)条目匹配。在 NRS 3 的患者中,治疗组之间存在轻微差异,但在 NRS 4 和≥5 的患者中不存在差异。在第 30 天死亡和存活的患者之间,C 统计量的范围从 5 种代谢物/预测因子组合的 0.49(95%置信区间 0.35-0.68)到 100 种代谢物组合的 0.66(95%置信区间 0.53-0.79)。途径分析发现,与非应答者相比,营养支持应答者的氮代谢、维生素 B3(烟酸和烟酰胺)、白三烯和花生四烯酸代谢途径明显富集。
在我们患有不同疾病和合并症的异质住院患者人群中,代谢组学标志物对更好地表型营养不良和对营养治疗的反应的预后和治疗潜力很小。未来的研究应集中在更具选择性的患者人群上,以了解代谢组学方法是否可以改善患者的营养护理。