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血清白细胞介素-1β水平升高作为疟疾感染和重症疟疾的潜在指标:一项荟萃分析

Elevation of serum interleukin-1β levels as a potential indicator for malarial infection and severe malaria: a meta-analysis.

作者信息

Mahittikorn Aongart, Kwankaew Pattamaporn, Rattaprasert Pongruj, Kotepui Kwuntida Uthaisar, Masangkay Frederick Ramirez, Kotepui Manas

机构信息

Department of Protozoology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

Medical Technology, School of Allied Health Sciences, Walailak University, Tha Sala, Nakhon Si Thammarat, Thailand.

出版信息

Malar J. 2022 Oct 29;21(1):308. doi: 10.1186/s12936-022-04325-0.

Abstract

BACKGROUND

Interleukin (IL)-1β is a proinflammatory cytokine that has a role in disease-related inflammation, including malaria. However, reports on the effect of IL-1β on malaria severity are inconsistent. Therefore, meta-analyses to compare differences in IL-1β levels between patients with severe malaria, patients with uncomplicated malaria and healthy controls were performed.

METHODS

The PRISMA standards were used to perform a systematic review and meta-analysis. A search of PubMed, Scopus, EMBASE and reference lists was conducted for articles providing data on IL-1β levels between patients with severe malaria, patients with uncomplicated malaria and healthy controls between January 1988 and March 2022, using a combination of search terms. The quality of all studies included in this review was determined using the Strengthening the Reporting of Observational Studies in Epidemiology statement: guidelines for reporting observational studies. The evidence was synthesized quantitatively and qualitatively. The differences in IL-1 levels across participant groups were recounted narratively for qualitative synthesis. For quantitative synthesis, the mean difference in IL-1β levels across groups of participants was calculated using a random effects meta-analysis. The publication bias was assessed using funnel plots, Egger's test and a contour-enhanced funnel plot.

RESULTS

A total of 1281 articles were discovered, and the 17 that satisfied the inclusion criteria were included for syntheses. The meta-analysis results using data from 555 cases of severe malaria and 1059 cases of uncomplicated malaria showed that severe malaria had a higher mean of IL-1β levels than uncomplicated malaria (P < 0.01, pooled mean difference: 1.92 pg/mL, 95% confidence interval: 0.60-3.25 pg/mL, I: 90.41%, 6 studies). The meta-analysis results using data from 542 cases of uncomplicated malaria and 455 healthy controls showed no difference in mean IL-1β levels between the two groups (P = 0.07, pooled mean difference: 1.42 pg/mL, 95% confidence interval: - 0.1-2.94 pg/mL, I: 98.93%, 6 studies).

CONCLUSION

The results from the meta-analysis revealed that IL-1β levels were higher in patients with severe malaria than in patients with uncomplicated malaria; however, IL-1β levels were similar in patients with uncomplicated malaria and healthy controls. Based on the limitations of the number of studies included in the meta-analysis and high levels of heterogeneity, further studies are needed to conclude that differences in IL-1β levels can be useful for monitoring the malaria severity.

摘要

背景

白细胞介素(IL)-1β是一种促炎细胞因子,在包括疟疾在内的疾病相关炎症中起作用。然而,关于IL-1β对疟疾严重程度影响的报道并不一致。因此,进行了荟萃分析以比较重症疟疾患者、非重症疟疾患者和健康对照者之间IL-1β水平的差异。

方法

采用PRISMA标准进行系统评价和荟萃分析。使用检索词组合在PubMed、Scopus、EMBASE及参考文献列表中检索1988年1月至2022年3月间提供重症疟疾患者、非重症疟疾患者和健康对照者IL-1β水平数据的文章。使用《加强流行病学观察性研究报告声明:观察性研究报告指南》确定本综述纳入的所有研究的质量。对证据进行定量和定性综合。对各参与者组间IL-1水平的差异进行叙述性复述以进行定性综合。对于定量综合,使用随机效应荟萃分析计算各参与者组间IL-1β水平的平均差异。使用漏斗图、Egger检验和等高线增强漏斗图评估发表偏倚。

结果

共检索到1281篇文章,17篇符合纳入标准的文章被纳入综合分析。对555例重症疟疾患者和1059例非重症疟疾患者的数据进行的荟萃分析结果显示,重症疟疾患者的IL-1β水平均值高于非重症疟疾患者(P<0.01,合并平均差异:1.92 pg/mL,95%置信区间:0.60 - 3.25 pg/mL,I²:90.41%,6项研究)。对542例非重症疟疾患者和455例健康对照者的数据进行的荟萃分析结果显示,两组间IL-1β水平均值无差异(P = 0.07,合并平均差异:1.42 pg/mL,95%置信区间:-0.1 - 2.94 pg/mL,I²:98.93%,6项研究)。

结论

荟萃分析结果显示,重症疟疾患者的IL-1β水平高于非重症疟疾患者;然而,非重症疟疾患者和健康对照者的IL-1β水平相似。基于荟萃分析纳入研究数量的局限性和高度异质性,需要进一步研究以得出IL-1β水平差异可用于监测疟疾严重程度的结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/9617441/5ed74dc7c78b/12936_2022_4325_Fig1_HTML.jpg

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