Evidence map›Paper›PMID 30027701›Full record

ArticleAnnals of laboratory medicine2018

Detection of Rifampicin- and Isoniazid-Resistant Mycobacterium tuberculosis Using the Quantamatrix Multiplexed Assay Platform System.

Hye Young Wang, Young Uh, Seoyong Kim, Eunjin Cho, Jong Seok Lee, Hyeyoung Lee

Open access · diamondAbstract read
In one paragraph

Article in Annals of laboratory medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Identification and quantification ofJournal of clinical microbiology · 2025
    Article
  4. Article
  5. The Structural Basis ofMolecules (Basel, Switzerland) · 2022
    Article
  6. False detection of rifampicin resistance using XpertJAC-antimicrobial resistance · 2021
    Article
  7. Article
  8. 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

6 authors at 2 institutions in 1 country.

Hye Young WangOptipharm, Inc., Wonju Eco Environmental Technology Center, Wonju, Korea.
Young UhDepartment of Laboratory Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea. u931018@yonsei.ac.kr.ORCID https://orcid.org/0000-0002-2879-7870
Seoyong KimDepartment of Biomedical Laboratory Science, College of Health Sciences, Yonsei University, Wonju, Korea.
Eunjin ChoDepartment of Microbiology, International Tuberculosis Research Center, Changwon, Korea.
Jong Seok LeeDepartment of Microbiology, International Tuberculosis Research Center, Changwon, Korea.
Hyeyoung LeeDepartment of Biomedical Laboratory Science, College of Health Sciences, Yonsei University, Wonju, Korea. hyelee@yonsei.ac.kr.ORCID https://orcid.org/0000-0003-1572-5250
Yonsei University · KRInternational Tuberculosis Research Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe increasing prevalence of drug-resistant tuberculosis (TB) infection represents a global public health emergency. We evaluated the usefulness of a newly developed multiplexed, bead-based bioassay (Quantamatrix Multiplexed Assay Platform [QMAP], QuantaMatrix, Seoul, Korea) to rapidly identify the Mycobacterium tuberculosis complex (MTBC) and detect rifampicin (RIF) and isoniazid (INH) resistance-associated mutations.

methodsA total of 200 clinical isolates from respiratory samples were used. Phenotypic anti-TB drug susceptibility testing (DST) results were compared with those of the QMAP system, reverse blot hybridization (REBA) MTB-MDR assay, and gene sequencing analysis.

resultsCompared with the phenotypic DST results, the sensitivity and specificity of the QMAP system were 96.4% (106/110; 95% confidence interval [CI] 0.9072-0.9888) and 80.0% (72/90; 95% CI 0.7052-0.8705), respectively, for RIF resistance and 75.0% (108/144; 95% CI 0.6731-0.8139) and 96.4% (54/56; 95% CI 0.8718-0.9972), respectively, for INH resistance. The agreement rates between the QMAP system and REBA MTB-MDR assay for RIF and INH resistance detection were 97.6% (121/124; 95% CI 0.9282-0.9949) and 99.1% (109/110; 95% CI 0.9453-1.0000), respectively. Comparison between the QMAP system and gene sequencing analysis showed an overall agreement of 100% for RIF resistance (110/110; 95% CI 0.9711-1.0000) and INH resistance (124/124; 95% CI 0.9743-1.0000).

conclusionsThe QMAP system may serve as a useful screening method for identifying and accurately discriminating MTBC from non-tuberculous mycobacteria, as well as determining RIF- and INH-resistant MTB strains.

Indexed as

Multiplex Polymerase Chain ReactionAntitubercular AgentsDNA, BacterialDrug Resistance, BacterialHumansIsoniazidMycobacterium tuberculosisNontuberculous MycobacteriaRifampinSequence Analysis, DNATuberculosis, Multidrug-ResistantAntitubercular AgentsDNA, BacterialIsoniazidRifampinDrug susceptibility testingIsoniazidMycobacterium tuberculosis complexQuantamatrix Multiplexed Assay PlatformRifampicin

Identifiers

PMID30027701
PMCPMC6056394
OpenAlexW2884074804

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.