COVID-19急性期和恢复期住院患者干扰素介导的代谢途径

IF 2.7 Q3 NEUROSCIENCES
Mario Gietl, Francesco Burkert, Stefanie Seiwald, Anna Böhm, Stefanie Hofer, Johanna M Gostner, Talia Piater, Simon Geisler, Guenter Weiss, Judith Loeffler-Ragg, Thomas Sonnweber, Ivan Tancevski, Alex Pizzini, Sabina Sahanic, Dietmar Fuchs, Rosa Bellmann-Weiler, Katharina Kurz
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引用次数: 1

摘要

背景:在COVID-19期间和之后,疲劳、睡眠障碍和神经系统症状很常见,可能与炎症引起的色氨酸(Trp)和苯丙氨酸(Phe)代谢的变化有关。目的:本中试研究干扰素γ诱导的新冠肺炎急性期及恢复期生化途径(即色氨酸分解代谢、新蝶呤、酪氨酸[Tyr]和亚硝酸盐形成)。患者和方法:对2020年初(3 - 5月)在因斯布鲁克大学医院收治的31例中重度新冠肺炎患者进行随访。在急性感染期间和感染后60天随访(FU)分析神经递质前体色氨酸(Trp)、苯丙氨酸(Phe)、酪氨酸(Tyr)以及犬尿氨酸(Kyn)、新蝶呤(neopterin)、亚硝酸盐(亚硝酸盐)和常规实验室参数。记录患者的临床症状(神经系统症状、疲劳、睡眠障碍),并调查与实验室参数浓度的关系。结果与结论:近一半的患者在急性COVID-19期间出现神经系统症状(48.4%),大多数患者出现睡眠困难(56.7%)。几乎所有病人都有疲劳症状。急性COVID-19期间,c反应蛋白(CRP)、白细胞介素-6 (IL-6)、新蝶呤、Kyn、Phe浓度显著升高,色氨酸水平降低。急性疾病期间伴有睡眠障碍和神经系统症状的患者CRP和IL-6浓度升高,睡眠障碍患者色氨酸水平较低。一般来说,炎症标志物在康复期间下降。高比例的患者在FU时有持续症状(神经系统症状:17.2%,疲劳:51.7%,睡眠障碍:34.5%),并且CRP浓度较高。睡眠困难患者的亚硝酸盐和Phe水平在FU时较低,神经症状患者的Kyn/Trp比率作为IDO活性的指标在FU时明显低于无神经症状患者。综上所述,炎症诱导的氨基酸代谢改变可能与COVID-19的急性和持续性症状有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19.

Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19.

Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19.

Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19.

Background: Fatigue, sleep disturbance, and neurological symptoms during and after COVID-19 are common and might be associated with inflammation-induced changes in tryptophan (Trp) and phenylalanine (Phe) metabolism.

Aim: This pilot study investigated interferon gamma inducible biochemical pathways (namely Trp catabolism, neopterin, tyrosine [Tyr], and nitrite formation) during acute COVID-19 and reconvalescence.

Patients and methods: Thirty one patients with moderate to severe COVID-19 admitted to the University Hospital of Innsbruck in early 2020 (March-May) were followed up. Neurotransmitter precursors Trp, Phe, Tyr as well as kynurenine (Kyn), neopterin, nitrite, and routine laboratory parameters were analyzed during acute infection and at a follow-up (FU) 60 days thereafter. Clinical symptoms of patients (neurological symptoms, fatigue, sleep disturbance) were recorded and associations with concentrations of laboratory parameters investigated.

Results and conclusion: Almost half of the patients suffered from neurological symptoms (48.4%), the majority of patients experienced sleep difficulties (56.7%) during acute COVID-19. Fatigue was present in nearly all patients. C-reactive protein (CRP), interleukin-6 (IL-6), neopterin, Kyn, Phe concentrations were significantly increased, and Trp levels depleted during acute COVID-19. Patients with sleep impairment and neurological symptoms during acute illness presented with increased CRP and IL-6 concentrations, Trp levels were lower in patients with sleep disturbance. In general, inflammatory markers declined during reconvalescence. A high percentage of patients suffered from persistent symptoms at FU (neurological symptoms: 17.2%, fatigue: 51.7%, sleeping disturbance: 34.5%) and had higher CRP concentrations. Nitrite and Phe levels were lower in patients with sleeping difficulties at FU and Kyn/Trp ratio, as indicator of IDO activity, was significantly lower in patients with neurological symptoms compared to patients without them at FU. In summary, inflammation induced alterations of amino acid metabolism might be related to acute and persisting symptoms of COVID-19.

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CiteScore
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