Evidence map›Paper›PMID 24777100›Full record

ArticleAntimicrobial agents and chemotherapy2014

The T2 Mycobacterium tuberculosis genotype, predominant in Kampala, Uganda, shows negative correlation with antituberculosis drug resistance.

Deus Lukoye, Fred A Katabazi, Kenneth Musisi, David P Kateete, Benon B Asiimwe, Moses Okee, Moses L Joloba, Frank G J Cobelens

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

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

  1. Pooled it
  2. Trial
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  6. Exploring the usefulness of molecular epidemiology of tuberculosis in Africa: a systematic review.International journal of molecular epidemiology and genetics · 2020
    Review
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  8. Resistance ofHeliyon · 2019
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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

8 authors.

Deus LukoyeNational Tuberculosis and Leprosy Program, Kampala, Uganda.
Fred A KatabaziDepartment of Medical Microbiology, Makerere University College of Health Sciences, Kampala, Uganda.
Kenneth MusisiNational Tuberculosis Reference Laboratory, Kampala, Uganda.
David P KateeteDepartment of Medical Microbiology, Makerere University College of Health Sciences, Kampala, Uganda.
Benon B AsiimweDepartment of Medical Microbiology, Makerere University College of Health Sciences, Kampala, Uganda.
Moses OkeeDepartment of Medical Microbiology, Makerere University College of Health Sciences, Kampala, Uganda.
Moses L JolobaDepartment of Medical Microbiology, Makerere University College of Health Sciences, Kampala, Uganda National Tuberculosis Reference Laboratory, Kampala, Uganda.
Frank G J CobelensDepartment of Global Health and Amsterdam Institute for Global Health and Development, Academic Medical Center, Amsterdam, The Netherlands KNCV Tuberculosis Foundation, The Hague, The Netherlands f.cobelens@aighd.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Surveillance of the circulating Mycobacterium tuberculosis complex (MTC) strains in a given locality is important for understanding tuberculosis (TB) epidemiology. We performed molecular epidemiological studies on sputum smear-positive isolates that were collected for anti-TB drug resistance surveillance to establish the variability of MTC lineages with anti-TB drug resistance and HIV infection. Spoligotyping was performed to determine MTC phylogenetic lineages. We compared patients' MTC lineages with drug susceptibility testing (DST) patterns and HIV serostatus. Out of the 533 isolates, 497 (93.2%) had complete DST, PCR, and spoligotyping results while 484 (90.1%) participants had results for HIV testing. Overall, the frequency of any resistance was 75/497 (15.1%), highest among the LAM (34.4%; 95% confidence interval [CI], 18.5 to 53.2) and lowest among the T2 (11.5%; 95% CI, 7.6 to 16.3) family members. By multivariate analysis, LAM (adjusted odds ratio [OR(adj)], 5.0; 95% CI, 2.0 to 11.9; P < 0.001) and CAS (OR(adj), 2.9; 95% CI, 1.4.0 to 6.3; P = 0.006) families were more likely to show any resistance than was T2. All other MTC lineages combined were more likely to be resistant to any of the anti-TB drugs than were the T2 strains (OR(adj), 1.7; 95% CI, 1.0 to 2.9; P = 0.040). There were no significant associations between multidrug resistance and MTC lineages, but numbers of multidrug-resistant TB strains were small. No association was established between MTC lineages and HIV status. In conclusion, the T2 MTC lineage negatively correlates with anti-TB drug resistance, which might partly explain the reported low levels of anti-TB drug resistance in Kampala, Uganda. Patients' HIV status plays no role with respect to the MTC lineage distribution.

Indexed as

AdolescentAdultAIDS SerodiagnosisAntitubercular AgentsDrug Resistance, BacterialDrug Resistance, Multiple, BacterialFemaleHIV InfectionsHumansMaleMicrobial Sensitivity TestsMiddle AgedMolecular EpidemiologyMycobacterium tuberculosisPublic Health SurveillanceTuberculosis, Multidrug-ResistantAntitubercular Agents

Identifiers

PMID24777100
PMCPMC4068514

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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.