[covid -19后综合征患者临床特征及细胞因子基因表达]。

María Magdalena Valencia-Gutiérrez, Modesto Gómez-López, Nadia Mabel Pérez-Vielma, Paulina Lázaro-Aguilar, Víctor Ricardo Aguilera-Sosa
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引用次数: 0

摘要

背景:COVID-19后综合征发生在COVID-19感染后3个月,持续时间至少2个月。与免疫系统失调相关的基因信息不足。目的:探讨基因表达及其与covid -19后综合征的关系。材料和方法:对56例covid -19后综合征患者进行横断面、回顾性和分析性研究。记录临床特征,使用TRIzol®试剂和PCR-RT技术分析血清素IL-4、IL-1β、SOCS3、ILF13和IFNL4基因。结果:新冠肺炎后综合征患病率为82.1%,与症状严重程度及合并症无相关性。与该综合征存在相关的临床特征为女性,比值比(OR)为4.25(95%可信区间[95% CI] 1.02 ~ 17.69),与用药相关的比值比为8.25 (95% CI 0.97 ~ 70.50)。疲劳的保护因素是血清素表达,OR为0.238 (95% CI 0.060-0.949);对于注意力集中问题,使用SOCS3, OR为0.188 (95% CI 0.037-0.946);对于记忆障碍,使用IFNL4, OR为0.094 (95% CI 0.015-0.586)。结论:女性、药物使用、血清素、INFL4和SOCS3基因异常与covid -19后综合征相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinical characteristics and cytokine gene expression in patients with post-COVID-19 syndrome].

Background: Post-COVID-19 syndrome occurs 3 months after COVID-19 infection and lasts at least 2 months. There is insufficient information on the genes associated with immune system dysregulation.

Objective: To evaluate gene expression and its relationship with post-COVID-19 syndrome.

Material and methods: Cross-sectional, retrolective and analytical study which included 56 patients with post-COVID-19 syndrome. Clinical characteristics were recorded and serotonin IL-4, IL-1β, SOCS3, ILF13, and IFNL4 genes were analyzed with TRIzol® Reagent and PCR-RT techniques.

Results: The prevalence of post-COVID-19 syndrome was 82.1%, with no differences in relation to the severity of symptoms or comorbidities. The clinical characteristics related to the presence of the syndrome were female sex with an odds ratio (OR) of 4.25 (95% confidence interval [95% CI] 1.02-17.69), and drug consumption with an OR of 8.25 (95% CI 0.97-70.50). Protective factors for fatigue were serotonin expression with an OR of 0.238 (95% CI 0.060-0.949); for concentration problems, SOCS3 with an OR of 0.188 (95% CI 0.037-0.946), and for memory impairment the IFNL4 with an OR of 0.094 (95% CI 0.015-0.586).

Conclusions: The associated factors with post-COVID-19 syndrome were female sex, drug use, and gene dysregulation of serotonin, INFL4 and SOCS3.

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