Evidence map›Paper›PMID 27494953›Full record

ArticleBMC infectious diseases2016

Associations between systemic inflammation, mycobacterial loads in sputum and radiological improvement after treatment initiation in pulmonary TB patients from Brazil: a prospective cohort study.

Eliene D D Mesquita, Leonardo Gil-Santana, Daniela Ramalho, Elise Tonomura, Elisangela C Silva, Martha M Oliveira, Bruno B Andrade, Afrânio Kritski, Rede-TB Study group

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Insulin Resistance and Inflammation.International journal of molecular sciences · 2026
    Review
  4. Article
  5. Article
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  13. The cause-effect relation of tuberculosis on incidence of diabetes mellitus.Frontiers in cellular and infection microbiology · 2023
    Review
  14. Review
  15. Article
  16. Observational
  17. Article
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  19. Article
  20. Observational
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

9 authors at 3 institutions in 1 country.

Eliene D D MesquitaAry Parreira Institute, State Secretary of Health of Rio de Janeiro, Rio de Janeiro, Brazil.
Leonardo Gil-SantanaUnidade de Medicina Investigativa, Laboratório Integrado de Microbiologia e Imunorregulação (LIMI), Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Daniela RamalhoTuberculosis Academic Program, School of Medicine, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Elise TonomuraRadiology Department, School of Medicine, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Elisangela C SilvaTuberculosis Academic Program, School of Medicine, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Martha M OliveiraDevelopment Center for Technology on Health, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Bruno B AndradeUnidade de Medicina Investigativa, Laboratório Integrado de Microbiologia e Imunorregulação (LIMI), Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil. bruno.andrade@bahia.fiocruz.br.
Afrânio KritskiTuberculosis Academic Program, School of Medicine, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil. kritskia@gmail.com.
Rede-TB Study group
Universidade Federal do Rio de Janeiro · BRFaculdade de Tecnologia e Ciências · BRFundação Oswaldo Cruz · BR

Funding

CCASAnet: Caribbean, Central and South America NetworkU01AI069923 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Pedro Enrique Cahn, Jessica L Castilho · 2006 to 2026
$41.6M
NIAID NIH HHS U01 AI069923
6 · The paper itself

Abstract

backgroundMycobacterium tuberculosis infection is known to cause inflammation and lung tissue damage in high-risk populations. Nevertheless, direct associations between mycobacterial loads, systemic inflammation and pulmonary lesions upon treatment initiation have not been fully characterized. In the present exploratory study, we prospectively depict the immune profile, microbial clearance and evolution of radiographic lesions in a pulmonary tuberculosis (PTB) patient cohort before and 60 days after anti-tuberculous treatment (ATT) initiation.

methodsCirculating levels of cytokines (IL-2, IL-4, IL-6, IL-10, IFN-γ, TNF-α) and C-reactive protein (CRP), as well as values of erythrocyte sedimentation rate (ESR) were measured in cryopreserved serum samples obtained from 73 PTB patients at pre-ATT and day 60 of treatment. Changes of the immune profile over time were compared with mycobacterial loads in sputum and culture conversion at day 60 of ATT. Additional analyses tested associations between improvement of chest radiographic lesions at day 60 and pre-treatment status of inflammation and mycobacterial loads.

resultsWithin the inflammatory parameters evaluated, values of CRP, IL-2, IL-4, TNF-α and ESR significantly decreased upon treatment initiation. On the converse, IL-10 levels substantially increased at day 60 of ATT, whereas concentrations of IL-6 and IFN-γ remained unchanged. Multidimensional analyses revealed that ESR, IL-2, IL-4 and CRP were the parameters with the highest power to discriminate individuals before and after treatment initiation. We further demonstrated that higher bacterial loads in sputum at pre-ATT were associated with increased systemic inflammation and higher risk for positive M. tuberculosis sputum cultures at day 60 of treatment. Furthermore, we found that pre-ATT mycobacterial loads in sputum and systemic inflammation synergistically associated with the status of radiographic lesions during treatment (Relative risk for chest X-ray improvement: 10.0, 95 % confidence interval: 2.4-40.0, P = 0.002).

conclusionsM. tuberculosis loads in sputum are directly associated to the status of systemic inflammation and potentially impact the immune profile, culture conversion and evolution of lung lesions upon ATT initiation.

Indexed as

Bacterial LoadAdultBrazilCase-Control StudiesCohort StudiesC-Reactive ProteinCytokinesFemaleHumansInflammationLongitudinal StudiesMaleMiddle AgedMycobacterium tuberculosisRadiography, ThoracicSputumC-Reactive ProteinCytokinesTumor Necrosis Factor-alphaAcid-fast bacilliAnti-tuberculous treatmentBiomarkerC-reactive proteinErythrocyte sedimentation rateInflammationRadiographic evaluationTuberculosis

Identifiers

PMID27494953
PMCPMC4974760
OpenAlexW2499731113

What OpenQuestion holds

Textmetadata
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.