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miRNA 和代谢物在肺癌诊断中的表现:一项荟萃分析。

The diagnostic performance of micro-RNA and metabolites in lung cancer: A meta-analysis.

机构信息

Department of Pathology, Center of Traumatology and Major Burns, Ben Arous, Tunis, Tunisia.

University Tunis El Manar, Faculty of Medicine of Tunis, Tunisia.

出版信息

Asian Cardiovasc Thorac Ann. 2024 Jan;32(1):45-65. doi: 10.1177/02184923231215538. Epub 2023 Nov 27.

Abstract

BACKGROUND

The diagnosis of lung cancer is based on the microscopic exam of tissue or liquid. During the recent decade, many biomarkers have been pointed to have a potential diagnostic role. These biomarkers may be assessed in blood, pleural effusion or sputum and they could avoid biopsies or other risky procedures. The authors aimed to assess the diagnostic performances of biomarkers focusing on micro-RNA and metabolites.

METHODS

This meta-analysis was conducted under the PRISMA guidelines during a nine-year-period (2013-2022). the Meta-Disc software 5.4 (free version) was used. Q test and statistics were carried out to explore the heterogeneity among studies. Meta-regression was performed in case of significant heterogeneity. Publication bias was assessed using the funnel plot test and the Egger's test (free version JASP).

RESULTS

According to our inclusion criteria, 165 studies from 79 articles were included. The pooled SEN, SPE and dOR accounted, respectively, for 0.76, 0.79 and 13.927. The AUC was estimated to 0.859 suggesting a good diagnostic accuracy. The heterogeneity in the pooled SEN and SPE was statistically significant. The meta-regression analysis focusing on the technique used, the sample, the number of biomarkers, the biomarker subtype, the tumor stage and the ethnicity revealed the biomarker number (  =  0.009) and the tumor stage (  =  0.0241) as potential sources of heterogeneity.

CONCLUSION

Even if this meta-analysis highlighted the potential diagnostic utility of biomarkers, more prospective studies should be performed, especially to assess the biomarkers' diagnostic potential in early-stage lung cancers.

摘要

背景

肺癌的诊断基于组织或液体的显微镜检查。在最近十年中,许多生物标志物被指出具有潜在的诊断作用。这些生物标志物可以在血液、胸腔积液或痰液中进行评估,并且可以避免活检或其他有风险的程序。作者旨在评估重点为 micro-RNA 和代谢物的生物标志物的诊断性能。

方法

本荟萃分析是在 9 年期间(2013-2022 年)根据 PRISMA 指南进行的。使用 Meta-Disc 软件 5.4(免费版本)进行 Q 检验和 统计分析以探索研究之间的异质性。如果存在显著异质性,则进行元回归分析。使用漏斗图测试和 Egger 检验(免费版本 JASP)评估发表偏倚。

结果

根据我们的纳入标准,从 79 篇文章中纳入了 165 项研究。汇总的 SEN、SPE 和 dOR 分别为 0.76、0.79 和 13.927。AUC 估计为 0.859,表明诊断准确性良好。汇总的 SEN 和 SPE 的异质性具有统计学意义。针对所使用的技术、样本、生物标志物数量、生物标志物亚型、肿瘤分期和种族进行的元回归分析表明,生物标志物数量( = 0.009)和肿瘤分期( = 0.0241)是异质性的潜在来源。

结论

尽管这项荟萃分析强调了生物标志物的潜在诊断效用,但应进行更多的前瞻性研究,特别是评估生物标志物在早期肺癌中的诊断潜力。

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