Evidence map›Paper›PMID 41287483›Full record

ArticleJournal of Korean medical science2025

Performance of Allplex™ MG & AziR Assay for Detecting Macrolide-Resistant

Gilho Lee, Yumi Seo, Donghoon Lim, Seung-Ju Lee

Abstract read
In one paragraph

Article in Journal of Korean medical science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Gilho LeeDepartment of Urology, Dankook University College of Medicine, Cheonan, Korea. multiorigins@yahoo.com.ORCID https://orcid.org/0000-0002-9253-6245
Yumi SeoDepartment of Urology, Dankook University College of Medicine, Cheonan, Korea.ORCID https://orcid.org/0000-0001-8027-7170
Donghoon LimDepartment of Urology, Chosun University Hospital, Gwangju, Korea.ORCID https://orcid.org/0000-0002-4932-3754
Seung-Ju LeeDepartment of Urology, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0003-0072-8010

Funding

Seegene
6 · The paper itself

Abstract

background

methodsUsing 279

resultsThe AziR assay targeting positions 2058 and 2059 in the 23S rRNA gene revealed that 133 and 146 cases, respectively, carried the wild and mutant types of adenosine, while sequencing detected the wild and mutant types in 134 and 145 cases, respectively. The AziR assay demonstrated a sensitivity of 100% (95% confidence interval [CI], 0.968-1) and specificity of 99.254% (95% CI, 0.953-1) in distinguishing wild type from mutant variants. Of the 279 samples, only six showed genetic discrepancies between the two tests: one wild type by sequencing was found to have A2059G by the AziR assay, two A2059Gs were discordant as A2058Ts, one A2059G was discordant as A2058G, and two A2058Gs by sequencing were reported as A2059Gs by the AziR assay.

conclusionOur results show that the AziR assay can identify specific mutants in a single reaction and demonstrates high sensitivity and specificity for detecting macrolide resistant

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialMacrolidesMycoplasma genitaliumAzithromycinDNA, BacterialFemaleHumansMaleMicrobial Sensitivity TestsMutationMycoplasma InfectionsRNA, Ribosomal, 23SSensitivity and SpecificitySequence Analysis, DNAAnti-Bacterial AgentsAzithromycinDNA, BacterialMacrolidesRNA, Ribosomal, 23SAssayDrug ResistanceMacrolide

Identifiers

PMID41287483
PMCPMC12643956

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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.