Evidence map›Paper›PMID 38094744›Full record

ArticleFrontiers in cellular and infection microbiology2023

Clinical application of amplification-based versus amplification-free metagenomic next-generation sequencing test in infectious diseases.

Zhe-Ying Wang, Lu-Lu Li, Xue-Lei Cao, Ping Li, Jian Du, Ming-Jin Zou, Li-Li Wang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Zhe-Ying WangDepartment of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Lu-Lu LiDepartment of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Xue-Lei CaoDepartment of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Ping LiDepartment of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Jian DuDepartment of Urology, The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong, China.
Ming-Jin ZouDepartment of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Li-Li WangDepartment of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Qilu Hospital of Shandong University · CNShandong First Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Recently, metagenomic next-generation sequencing (mNGS) has been used in the diagnosis of infectious diseases (IDs) as an emerging and powerful tool. However, whether the complicated methodological variation in mNGS detections makes a difference in their clinical performance is still unknown. Here we conducted a method study on the clinical application of mNGS tests in the DNA detection of IDs. Methods: We analyzed the effect of several potential factors in the whole process of mNGS for DNA detection on microorganism identification in 98 samples of suspected ID patients by amplification-based mNGS. The amplification-based and amplification-free mNGS tests were successfully performed in 41 samples. Then we compared the clinical application of the two mNGS methods in the DNA detection of IDs. Results: We found that a higher concentration of extracted nucleic acid was more conducive to detecting microorganisms. Other potential factors, such as read depth and proportion of human reads, might not be attributed to microorganism identification. The concordance rate of amplification-based and amplification-free mNGS results was 80.5% (33/41) in the patients with suspected IDs. Amplification-based mNGS showed approximately 16.7% higher sensitivity than amplification-free mNGS. However, 4 cases with causative pathogens only detected by amplification-based mNGS were finally proved false-positive. In addition, empirical antibiotic treatments were adjusted in 18 patients following mNGS testing with unexpected pathogens. Conclusions: Amplification-based and amplification-free mNGS tests showed their specific advantages and disadvantages in the diagnosis of IDs. The clinical application of mNGS still needs more exploration from a methodological perspective. With advanced technology and standardized procedure, mNGS will play a promising role in the diagnosis of IDs and help guide the use of antibiotics.

Indexed as

Communicable DiseasesAnti-Bacterial AgentsDNAHigh-Throughput Nucleotide SequencingHumansMetagenomeMetagenomicsSensitivity and SpecificityAnti-Bacterial AgentsDNAamplification-free methodinfectious diseasesmetagenomic next-generation sequencingmethodologyPCR bias

Identifiers

PMID38094744
PMCPMC10716234
OpenAlexW4389151086

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.