Evidence map›Paper›PMID 36259791›Full record

ArticleMemorias do Instituto Oswaldo Cruz2022

Heterogeneous persistence of Mycobacterium leprae in oral and nasal mucosa of multibacillary patients during multidrug therapy.

Arthur da Silva Neumann, Amanda Nogueira Brum Fontes, Márcia Quinhones Pires Lopes, Philip Noel Suffys, Milton Ozório Moraes, Flávio Alves Lara

Open access · diamondAbstract read
In one paragraph

Article in Memorias do Instituto Oswaldo Cruz, 2022. 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 35% 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, 6 citations in OpenAlex.

  1. Human Skin as an Ex Vivo Model for MaintainingTropical medicine and infectious disease · 2024
    Article
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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 3 institutions in 2 countries.

Arthur da Silva NeumannFundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Microbiologia Celular, Rio de Janeiro, RJ, Brasil.
Amanda Nogueira Brum FontesMinistério da Saúde, Secretaria de Ciência, Tecnologia e Insumos Estratégicos, Departamento de Ciência e Tecnologia, Brasília, DF, Brasil.
Márcia Quinhones Pires LopesFundação Oswaldo Cruz-Fiocruz, Laboratório de Biologia Molecular Aplicada à Micobactérias, Rio de Janeiro, RJ, Brasil.
Philip Noel SuffysFundação Oswaldo Cruz-Fiocruz, Laboratório de Biologia Molecular Aplicada à Micobactérias, Rio de Janeiro, RJ, Brasil.
Milton Ozório MoraesFundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Hanseníase, Rio de Janeiro, RJ, Brasil.
Flávio Alves LaraFundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Microbiologia Celular, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0002-2717-6597
Fundação Oswaldo Cruz · BRMinistério da Saúde · STUniversidade Federal do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeprosy is curable by multidrug therapy (MDT) treatment regimen ranging from six to 12 months. The variable levels of tolerance and adherence among patients can, however, result in treatment failure and the emergence of drug-resistant strains.

objectivesDescribe the impact of MDT over Mycobacterium leprae viability in patient's oral and nasal mucosa along treatment.

methodsMycobacterium leprae viability was monitored by quantitative polymerase chain reaction (qPCR) quantification of 16S rRNA in lateral and contralateral scrapings of oral and nasal mucosa of 10 multibacillary patients along the initial five months of treatment.

findingsThe results demonstrated high heterogenicity of M. leprae viability among patients and between nasal and oral samples. Of six patients who presented good adherence and tolerance to the treatment, only four displayed absence of M. leprae viability in both samples three months after the first MDT dose, while for the other two, the absence of M. leprae viability in the oral and nasal cavities was only detected five months after the first dose. MAIN

conclusionsWe concluded that qPCR of 16S rRNA for the determination of M. leprae viability in nasal and oral scraping samples could represent an interesting approach to monitor treatment efficacy.

Indexed as

Leprostatic AgentsMycobacterium lepraeDNA, BacterialDrug Therapy, CombinationHumansNasal MucosaRNA, Ribosomal, 16SDNA, BacterialLeprostatic AgentsRNA, Ribosomal, 16S

Identifiers

PMID36259791
PMCPMC9575966
OpenAlexW4306833060

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.