Evidence map›Paper›PMID 25984723›Full record

ArticlePloS one2015

The Association between Mycobacterium Tuberculosis Genotype and Drug Resistance in Peru.

Louis Grandjean, Tomotada Iwamoto, Anna Lithgow, Robert H Gilman, Kentaro Arikawa, Noriko Nakanishi, Laura Martin, Edith Castillo, Valentina Alarcon, Jorge Coronel and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

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  11. Circulation ofPathogens and global health · 2019
    Review
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  20. 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

18 authors at 8 institutions in 4 countries.

Louis GrandjeanWellcome Centre for Clinical Tropical Medicine, Imperial College London, St Mary's Campus, Norfolk Place, London, United Kingdom; London School of Hygiene and Tropical Medicine, TB Centre and Department of Clinical Research, Keppel St., London, United Kingdom; Laboratorio de Investigacion y Desarrollo, Universidad Peruana Cayetano Heredia, San Martin de Porres, Lima, Peru.
Tomotada IwamotoDepartment of Infectious Diseases, Kobe Institute of Health, Chuo-ku, Kobe, Japan.
Anna LithgowLondon School of Hygiene and Tropical Medicine, TB Centre and Department of Clinical Research, Keppel St., London, United Kingdom.
Robert H GilmanLaboratorio de Investigacion y Desarrollo, Universidad Peruana Cayetano Heredia, San Martin de Porres, Lima, Peru; Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Kentaro ArikawaDepartment of Infectious Diseases, Kobe Institute of Health, Chuo-ku, Kobe, Japan.
Noriko NakanishiDepartment of Infectious Diseases, Kobe Institute of Health, Chuo-ku, Kobe, Japan.
Laura MartinWellcome Centre for Clinical Tropical Medicine, Imperial College London, St Mary's Campus, Norfolk Place, London, United Kingdom; Laboratorio de Investigacion y Desarrollo, Universidad Peruana Cayetano Heredia, San Martin de Porres, Lima, Peru.
Edith CastilloDIRESA de Callao, Bellavista, Callao, Peru.
Valentina AlarconUnidad Tecnica TB-MDR, Lima, Peru.
Jorge CoronelLaboratorio de Investigacion y Desarrollo, Universidad Peruana Cayetano Heredia, San Martin de Porres, Lima, Peru.
Walter SolanoLaboratorio de Investigacion y Desarrollo, Universidad Peruana Cayetano Heredia, San Martin de Porres, Lima, Peru.
Minoo AminianTB-Insight Research Group, Rensselaer Polytechnic Institute, Troy, New York, United States of America.
Claudia GuezalaNaval Medical Research Unit 6-Bellavista, Callao, Peru.
Nalin RastogiWHO Supranational TB Reference Laboratory, Institut Pasteur de la Guadeloupe, Abymes, Guadeloupe, France.
David CouvinWHO Supranational TB Reference Laboratory, Institut Pasteur de la Guadeloupe, Abymes, Guadeloupe, France.
Patricia SheenLaboratorio de Investigacion y Desarrollo, Universidad Peruana Cayetano Heredia, San Martin de Porres, Lima, Peru.
Mirko ZimicLaboratorio de Investigacion y Desarrollo, Universidad Peruana Cayetano Heredia, San Martin de Porres, Lima, Peru.
David A J MooreLondon School of Hygiene and Tropical Medicine, TB Centre and Department of Clinical Research, Keppel St., London, United Kingdom; Laboratorio de Investigacion y Desarrollo, Universidad Peruana Cayetano Heredia, San Martin de Porres, Lima, Peru.
Universidad Peruana Cayetano Heredia · PEImperial College London · GBInstitut Pasteur de la Guadeloupe · GPJohns Hopkins University · USNational University of Callao · PENaval Medical Research Unit Six · PERensselaer Polytechnic Institute · USUniversity of London · GB

Funding

Medical Research Council MR/K007467/1Wellcome TrustWellcome Trust 078067/Z/05/ZWellcome Trust WT088559MA
6 · The paper itself

Abstract

backgroundThe comparison of Mycobacterium tuberculosis bacterial genotypes with phenotypic, demographic, geospatial and clinical data improves our understanding of how strain lineage influences the development of drug-resistance and the spread of tuberculosis.

methodsTo investigate the association of Mycobacterium tuberculosis bacterial genotype with drug-resistance. Drug susceptibility testing together with genotyping using both 15-loci MIRU-typing and spoligotyping, was performed on 2,139 culture positive isolates, each from a different patient in Lima, Peru. Demographic, geospatial and socio-economic data were collected using questionnaires, global positioning equipment and the latest national census.

resultsThe Latin American Mediterranean (LAM) clade (OR 2.4, p<0.001) was significantly associated with drug-resistance and alone accounted for more than half of all drug resistance in the region. Previously treated patients, prisoners and genetically clustered cases were also significantly associated with drug-resistance (OR's 2.5, 2.4 and 1.8, p<0.001, p<0.05, p<0.001 respectively).

conclusionsTuberculosis disease caused by the LAM clade was more likely to be drug resistant independent of important clinical, genetic and socio-economic confounding factors. Explanations for this include; the preferential co-evolution of LAM strains in a Latin American population, a LAM strain bacterial genetic background that favors drug-resistance or the "founder effect" from pre-existing LAM strains disproportionately exposed to drugs.

Indexed as

GenotypeAdultDrug Resistance, BacterialFemaleHumansMaleMiddle AgedMycobacterium tuberculosisPeruTuberculosis, Multidrug-Resistant

Identifiers

PMID25984723
PMCPMC4435908
OpenAlexW2142146687

What OpenQuestion holds

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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.