Effectiveness of metagenomic next-generation sequencing in the diagnosis of infectious diseases: A systematic review and meta-analysis
•Largest sample size meta-analysis of mNGS in diagnosing infections was performed.•mNGS exhibits a highest diagnostic value in central system infection.•The diagnostic accuracy of mNGS varies among different infectious types.•mNGS has a great potential to exclude infection in immunocompromised patie...
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Veröffentlicht in: | International journal of infectious diseases 2024-05, Vol.142, p.106996, Article 106996 |
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Sprache: | eng |
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Zusammenfassung: | •Largest sample size meta-analysis of mNGS in diagnosing infections was performed.•mNGS exhibits a highest diagnostic value in central system infection.•The diagnostic accuracy of mNGS varies among different infectious types.•mNGS has a great potential to exclude infection in immunocompromised patients.
Early diagnosis of infectious diseases remains a challenge. This study assessed the diagnostic value of mNGS in infections and explored the effect of various factors on the accuracy of mNGS.
An electronic article search of PubMed, Cochrane Library, and Embase was performed. A total of 85 papers were eligible for inclusion and analysis. Stata 12.0 was used for statistical calculation to evaluate the efficacy of mNGS for the diagnosis of infectious diseases.
The AUC of 85 studies was 0.88 (95%CI, 0.85-0.90). The AUC of the clinical comprehensive diagnosis and conventional test groups was 0.92 (95%CI, 0.89-0.94) and 0.82 (95%CI, 0.78-0.85), respectively. The results of subgroup analysis indicated that the PLR and NLR were 12.67 (95%CI, 6.01-26.70) and 0.05 (95%CI, 0.03-0.10), respectively, in arthrosis infections. The PLR was 24.41 (95%CI, 5.70-104.58) in central system infections and the NLR of immunocompromised patients was 0.08 (95%CI, 0.01-0.62).
mNGS demonstrated satisfactory diagnostic performance for infections, especially for bone and joint infections and central system infections. Moreover, mNGS also has a high value in the exclusion of infection in immunocompromised patients.
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ISSN: | 1201-9712 1878-3511 1878-3511 |
DOI: | 10.1016/j.ijid.2024.106996 |