Evidence map›Paper›PMID 39731145›Full record

ArticleBMC infectious diseases2024

Potential of nanopore sequencing for tuberculosis diagnosis and drug resistance detection.

Fei Ren, JinBao Ma, LiYun Dang, AiFang Li, GuoLian Zhao, Yun Qi, You Xu, Han Yang, JianYing Li

Abstract read
In one paragraph

Article in BMC infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Drug resistance mechanisms inFrontiers in pharmacology · 2026
    Review
  5. 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

9 authors.

Fei Ren *Department of Drug-Resistance Tuberculosis, Xi'an Chest Hospital, Xi'an, China.
JinBao Ma *Department of Drug-Resistance Tuberculosis, Xi'an Chest Hospital, Xi'an, China.
LiYun DangDepartment of Drug-Resistance Tuberculosis, Xi'an Chest Hospital, Xi'an, China.
AiFang LiDepartment of Clinical Laboratory, Xi'an Chest Hospital, Xi'an, Shaanxi Province, China.
GuoLian ZhaoDepartment of Clinical Laboratory, Xi'an Chest Hospital, Xi'an, Shaanxi Province, China.
Yun QiDepartment of Gynecology and Pediatric Tuberculosis, Xi'an Chest Hospital, Xi'an, Shaanxi Province, China.
You XuDepartment of Drug-Resistance Tuberculosis, Xi'an Chest Hospital, Xi'an, China.
Han YangMedical Transformation Centre, Xi'an Chest Hospital, Yanta District, Xi'an, Shaanxi Province, China. xajhyanghan@163.com.
JianYing LiXi'an Chest Hospital, Xi'an, Shaanxi Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study evaluates the effectiveness of nanopore sequencing for accurate detection of Mycobacterium tuberculosis pathogens and drug resistance mutations in clinical specimens.

methodsA retrospective analysis of 2,421 specimens from suspected tuberculosis patients admitted to Xi'an Chest Hospital from 2022 to 2023 was conducted, with 131 specimens undergoing via real-time, fluorescence-based quantitative Polymerase Chain Reaction (qPCR), simultaneous amplification and testing RNA (RNA), Mycobacterium culture, Mycobacterium smear, and nanopore sequencing. Employing clinical tuberculosis diagnoses as the gold standard, sensitivity, specificity, positive predictive value, negative predictive value, concordance rate, and Kappa coefficient were measured for the five detection techniques. We compared nanopore sequencing with the Melting Curve method to detect drug-resistant gene mutations.

resultsNanopore sequencing has a significantly higher sensitivity (0.786) for tuberculosis diagnosis compared to qPCR (0.411), RNA (0.411), Mycobacterium culture (0.402), and Mycobacterium smear (0.241), against the gold-standard clinical diagnosis. It also exhibited a greater concordance rate (0.809) and Kappa coefficient (0.488), and outperformed the other methods in terms of the area under the ROC curve. Nanopore sequencing surpassed the Melting Curve method in identifying drug-resistant mutations.

conclusionNanopore sequencing significantly enhances the detection of tuberculosis pathogens and drug-resistant genes.

Indexed as

Mycobacterium tuberculosisNanopore SequencingSensitivity and SpecificityTuberculosisAdultDrug Resistance, BacterialFemaleHumansMaleMutationRetrospective StudiesComparative studyDrug-resistance genesMycobacteriumNanopore sequencingTBTuberculosis

Identifiers

PMID39731145
PMCPMC11681766

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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.