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基孔肯雅热严重程度和慢性化的生物标志物:系统评价和荟萃分析。

Biomarkers of severity and chronification in chikungunya fever: a systematic review and meta-analysis.

机构信息

Universidade Federal de São João Del-Rei, Campus Centro-Oeste Dona Lindu, Divinópolis, Minas Gerais, Brazil.

Universidade de Itaúna, Itaúna, Minas Gerais, Brazil.

出版信息

Rev Inst Med Trop Sao Paulo. 2021 Mar 1;63:e16. doi: 10.1590/S1678-9946202163016. eCollection 2021.

Abstract

Currently, there are no biomarkers for Chikungunya fever (CHIK) in clinical practice that can accurately predict the severity or chronification of the disease. The aim of this study is to evaluate the existing literature on biomarkers related to the severity and chronification of CHIK. In this sense, a systematic review was conducted based on the PRISMA Statement guideline. Articles that described the association of biomarkers with the evolution of the disease (severity or chronification), published until August 20th 2019 were considered eligible. The search was carried out in the PubMed, Scopus, Virtual Health Library (VHL) and Science Direct databases. After searching the databases, 17 articles were added to the review, and after analyzing the articles, several biomarkers were associated with severity, such as increased levels of IL-6, IP-10, IL-1b, MIG, MCP-1, and reduced levels of RANTES and IL-8 or chronification, such as increased levels of IL-6, TNF-α, MCP-1, IL-12, INF-α, IL-13, INF-γ, GM-CSF, CRP, IL-1a, IL-15, Factor VII, IP-10, IL-10, IL-4, IL-1RA, IL-8, MIP-1α, MIP-1β, ferritin, MIG, ESR, NO, malondialdehyde, and reduced levels of RANTES, ferritin, eotaxin, HGF, IL-27, IL-17A, IL-29, TGF-β, IL-10, and thiols. IL-6, CRP and TNF-α were included in the meta-analysis to assess the relationship with chronification, although they did not reach statistical significance. It was concluded that several biomarkers showed a relationship with severity and chronification of CHIK; the search for these biomarkers can reveal prognostic factors and important therapeutic targets for the treatment of the disease.

摘要

目前,临床实践中尚无可准确预测基孔肯雅热(CHIK)严重程度或慢性化的生物标志物。本研究旨在评估与 CHIK 严重程度和慢性化相关的现有生物标志物文献。为此,按照 PRISMA 声明指南进行了系统评价。符合条件的文章为描述生物标志物与疾病进展(严重程度或慢性化)之间关联的文章,发表时间截至 2019 年 8 月 20 日。检索数据库包括 PubMed、Scopus、Virtual Health Library(VHL)和 Science Direct。检索数据库后,有 17 篇文章被纳入综述,分析这些文章后,发现一些生物标志物与严重程度相关,如 IL-6、IP-10、IL-1b、MIG、MCP-1 水平升高,RANTES 和 IL-8 水平降低;与慢性化相关的生物标志物包括 IL-6、TNF-α、MCP-1、IL-12、INF-α、IL-13、INF-γ、GM-CSF、CRP、IL-1a、IL-15、Factor VII、IP-10、IL-10、IL-4、IL-1RA、IL-8、MIP-1α、MIP-1β、铁蛋白、MIG、ESR、NO、丙二醛水平升高,RANTES、铁蛋白、嗜酸性粒细胞趋化因子、HGF、IL-27、IL-17A、IL-29、TGF-β、IL-10、硫醇水平降低。对 IL-6、CRP 和 TNF-α 进行了荟萃分析,以评估其与慢性化的关系,但未达到统计学意义。结论是,一些生物标志物与 CHIK 的严重程度和慢性化有关;寻找这些生物标志物可以揭示疾病治疗的预后因素和重要治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa0c/7924982/42d432f7508f/1678-9946-rimtsp-63-S1678-9946202163016-gf01.jpg

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