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住院治疗对新冠肺炎患者血清代谢组的影响。

The Effects of Hospitalisation on the Serum Metabolome in COVID-19 Patients.

作者信息

Hensen Tim, Fässler Daniel, O'Mahony Liam, Albrich Werner C, Barda Beatrice, Garzoni Christian, Kleger Gian-Reto, Pietsch Urs, Suh Noémie, Hertel Johannes, Thiele Ines

机构信息

School of Medicine, University of Galway, H91 TK33 Galway, Ireland.

School of Microbiology, University of Galway, H91 TK33 Galway, Ireland.

出版信息

Metabolites. 2023 Aug 16;13(8):951. doi: 10.3390/metabo13080951.

Abstract

COVID-19, a systemic multi-organ disease resulting from infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is known to result in a wide array of disease outcomes, ranging from asymptomatic to fatal. Despite persistent progress, there is a continued need for more accurate determinants of disease outcomes, including post-acute symptoms after COVID-19. In this study, we characterised the serum metabolomic changes due to hospitalisation and COVID-19 disease progression by mapping the serum metabolomic trajectories of 71 newly hospitalised moderate and severe patients in their first week after hospitalisation. These 71 patients were spread out over three hospitals in Switzerland, enabling us to meta-analyse the metabolomic trajectories and filter consistently changing metabolites. Additionally, we investigated differential metabolite-metabolite trajectories between fatal, severe, and moderate disease outcomes to find prognostic markers of disease severity. We found drastic changes in serum metabolite concentrations for 448 out of the 901 metabolites. These results included markers of hospitalisation, such as environmental exposures, dietary changes, and altered drug administration, but also possible markers of physiological functioning, including carboxyethyl-GABA and fibrinopeptides, which might be prognostic for worsening lung injury. Possible markers of disease progression included altered urea cycle metabolites and metabolites of the tricarboxylic acid (TCA) cycle, indicating a SARS-CoV-2-induced reprogramming of the host metabolism. Glycerophosphorylcholine was identified as a potential marker of disease severity. Taken together, this study describes the metabolome-wide changes due to hospitalisation and COVID-19 disease progression. Moreover, we propose a wide range of novel potential biomarkers for monitoring COVID-19 disease course, both dependent and independent of the severity.

摘要

新型冠状病毒肺炎(COVID-19)是由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染引起的一种全身性多器官疾病,已知会导致从无症状到致命的一系列疾病结局。尽管取得了持续进展,但仍持续需要更准确的疾病结局决定因素,包括COVID-19后的急性后遗症。在本研究中,我们通过绘制71名新入院的中重度患者入院后第一周的血清代谢组学轨迹,对因住院和COVID-19疾病进展导致的血清代谢组学变化进行了特征分析。这71名患者分布在瑞士的三家医院,使我们能够对代谢组学轨迹进行荟萃分析,并筛选出持续变化的代谢物。此外,我们研究了致命、重度和中度疾病结局之间代谢物-代谢物轨迹的差异,以寻找疾病严重程度的预后标志物。我们发现901种代谢物中有448种血清代谢物浓度发生了剧烈变化。这些结果包括住院的标志物,如环境暴露、饮食变化和药物管理改变,也包括生理功能的可能标志物,如羧乙基-GABA和纤维蛋白肽,它们可能对肺损伤恶化具有预后价值。疾病进展的可能标志物包括尿素循环代谢物和三羧酸(TCA)循环代谢物的改变,表明SARS-CoV-2诱导了宿主代谢的重编程。甘油磷酰胆碱被确定为疾病严重程度的潜在标志物。综上所述,本研究描述了因住院和COVID-19疾病进展导致的全代谢组变化。此外,我们提出了一系列新型潜在生物标志物,用于监测COVID-19疾病进程,无论其严重程度如何。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/095e/10456321/fd98d56f9f1c/metabolites-13-00951-g001.jpg

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