Evidence map›Paper›PMID 26206685›Full record

ArticleAnnals of laboratory medicine2015

Phenotypic and genotypic analysis of anti-tuberculosis drug resistance in Mycobacterium tuberculosis isolates in Myanmar.

Wah Wah Aung, Phyu Win Ei, Wint Wint Nyunt, Thyn Lei Swe, Thandar Lwin, Mi Mi Htwe, Kyung Jun Kim, Jong Seok Lee, Chang Ki Kim, Sang Nae Cho and 2 more

Abstract read
In one paragraph

Article in Annals of laboratory medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Prevalence ofJournal of clinical tuberculosis and other mycobacterial diseases · 2023
    Article
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  6. Review
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  12. Spoligotyping and drug sensitivity ofNew microbes and new infections · 2020
    Article
  13. Article
  14. Article
  15. Molecular screening of multidrug-resistance tuberculosis by a designated public health laboratory in Taiwan.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2017
    Article
  16. Article
  17. Molecular characterisation of rifampicin-resistantAfrican journal of laboratory medicine · 2017
    Article
  18. Article
  19. 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

12 authors.

Wah Wah AungAdvanced Molecular Research Centre, Department of Medical Research, Yangon, Myanmar. drwahwahaung@gmail.com.
Phyu Win EiAdvanced Molecular Research Centre, Department of Medical Research, Yangon, Myanmar.
Wint Wint NyuntNational Tuberculosis Program, Nay Pyi Taw, Myanmar.
Thyn Lei SweNational Tuberculosis Program, Nay Pyi Taw, Myanmar.
Thandar LwinNational Tuberculosis Program, Nay Pyi Taw, Myanmar.
Mi Mi HtweAdvanced Molecular Research Centre, Department of Medical Research, Yangon, Myanmar.
Kyung Jun KimDepartment of Laboratory Medicine, Pusan National University Yangsan Hospital, Yangsan, Korea.
Jong Seok LeeInternational Tuberculosis Research Center, Changwon, Korea.
Chang Ki KimKorean Institute of Tuberculosis, Osong, Korea.
Sang Nae ChoYonsei University College of Medicine, Seoul, Korea.
Sun Dae SongInternational Tuberculosis Research Center, Changwon, Korea.
Chulhun L ChangDepartment of Laboratory Medicine, Pusan National University Yangsan Hospital, Yangsan, Korea. cchl@pusan.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTuberculosis (TB) is one of the most serious health problems in Myanmar. Because TB drug resistance is associated with genetic mutation(s) relevant to responses to each drug, genotypic methods for detecting these mutations have been proposed to overcome the limitations of classic phenotypic drug susceptibility testing (DST). We explored the current estimates of drug-resistant TB and evaluated the usefulness of genotypic DST in Myanmar.

methodsWe determined the drug susceptibility of Mycobacterium tuberculosis isolated from sputum smear-positive patients with newly diagnosed pulmonary TB at two main TB centers in Myanmar during 2013 by using conventional phenotypic DST and the GenoType MTBDRplus assay (Hain Lifescience, Germany). Discrepant results were confirmed by sequencing the genes relevant to each type of resistance (rpoB for rifampicin; katG and inhA for isoniazid).

resultsOf 191 isolates, phenotypic DST showed that 27.7% (n=53) were resistant to at least one first-line drug and 20.9% (n=40) were resistant to two or more, including 18.3% (n=35) multidrug-resistant TB (MDR-TB) strains. Monoresistant strains accounted for 6.8% (n=13) of the samples. Genotypic assay of 189 isolates showed 17.5% (n=33) MDR-TB and 5.3% (n=10) isoniazid-monoresistant strains. Genotypic susceptibility results were 99.5% (n=188) concordant and agreed almost perfectly with phenotypic DST (kappa=0.99; 95% confidence interval 0.96-1.01).

conclusionsThe results highlight the burden of TB drug resistance and prove the usefulness of the genotypic DST in Myanmar.

Indexed as

AdultAntitubercular AgentsDNA, BacterialDrug Resistance, Multiple, BacterialFemaleGenotypeHumansMaleMicrobial Sensitivity TestsMiddle AgedMyanmarMycobacterium tuberculosisPhenotypePolymerase Chain ReactionSputumTuberculosisAntitubercular AgentsDNA, BacterialDrugGenotypeMyanmarMycobacterium tuberculosisResistance

Identifiers

PMID26206685
PMCPMC4510501

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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.