Evidence map›Paper›PMID 36189292›Full record

ArticleFrontiers in immunology2022

Reduction of blood C-reactive protein concentration complements the resolution of sputum bacillary load in patients on anti-tuberculosis therapy.

Khalide Azam, Celso Khosa, Sofia Viegas, Isabel Massango, Nilesh Bhatt, Ilesh Jani, Norbert Heinrich, Michael Hoelscher, Stephen H Gillespie, Andrea Rachow and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Observational
  7. Review
  8. Article
  9. Article
  10. Frontiers in microbiology · 2024
    Review
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

11 authors.

Khalide AzamDirecção de Laboratórios de Saúde Pública, Instituto Nacional de Saúde (INS), Vila de Marracuene, Moçambique.
Celso KhosaCenter for International Health - CIHLMU, Munich, Germany.
Sofia ViegasDirecção de Laboratórios de Saúde Pública, Instituto Nacional de Saúde (INS), Vila de Marracuene, Moçambique.
Isabel MassangoCentro de Investigação e Treino em Saúde da Polana Caniço, Instituto Nacional de Saúde (INS), Cidade de Maputo, Moçambique.
Nilesh BhattCentro de Investigação e Treino em Saúde da Polana Caniço, Instituto Nacional de Saúde (INS), Cidade de Maputo, Moçambique.
Ilesh JaniDirecção de Laboratórios de Saúde Pública, Instituto Nacional de Saúde (INS), Vila de Marracuene, Moçambique.
Norbert HeinrichCenter for International Health - CIHLMU, Munich, Germany.
Michael HoelscherCenter for International Health - CIHLMU, Munich, Germany.
Stephen H GillespieDivision of Infection and Global Health, School of Medicine, University of St Andrews, St Andrews, United Kingdom.
Andrea RachowCenter for International Health - CIHLMU, Munich, Germany.
Wilber SabiitiDivision of Infection and Global Health, School of Medicine, University of St Andrews, St Andrews, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tuberculosis (TB) is a difficult-to-treat disease requiring the combination of four antibiotics for a minimum of 6 months. Rapid and quantitative biomarkers to monitor treatment response are urgently needed for individual patient management and clinical trials. C-reactive protein (CRP) is often used clinically as a rapid marker of inflammation caused by infection. We assessed the relationship of TB bacillary load and CRP as biomarkers of treatment response. Methods: Xpert MTB/RIF-confirmed pulmonary TB cases were enrolled for treatment response assessment in Mozambique. Treatment response was measured using the Tuberculosis Molecular Bacterial Load Assay (TB-MBLA) in comparison with standard-of-care Mycobacterium Growth Indicator Tube (MGIT) culture at baseline and at weeks 1, 2, 4, 8, 12, 17, and 26 of treatment. Blood CRP concentration was measured at baseline, week 8, and week 26. Treatment response was defined as increase in MGIT culture time to positivity (TTP), and reduction in TB-MBLA-measured bacillary load and blood CRP concentration. Results: Out of the 81 screened presumptive TB cases, 69 were enrolled for 6-month treatment follow-up resulting in 94% treatment completion rate. Four participants did not complete TB treatment and 22 participants had missing CRP or TB-MBLA results and were excluded from TB-MBLA-CRP analysis. The remaining 43 participants-median age, 31 years old [interquartile range (IQR): 18-56]; 70% (30/43) male; and 70% (30/43) infected with HIV-were considered for analysis. Culture TTP and bacillary load were inversely correlated, Spearman's Conclusion: TB-MBLA-measured bacillary load and blood CRP complement each other in response to anti-TB therapy. Slow CRP reduction probably reflects residual TB bacilli in the lung not expectorated in sputum. Combining both measures can improve the accuracy of these biomarkers for monitoring TB treatment response and shorten turnaround time since the results of both assays could be available in 24 h.

Indexed as

HIV InfectionsLacticaseibacillus caseiMycobacterium tuberculosisTuberculosisAdultAntitubercular AgentsBiomarkersC-Reactive ProteinHumansMaleSputumAntitubercular AgentsBiomarkersC-Reactive Proteinbacillary loadC-reactive proteintreatment responsetuberculosistuberculosis molecular bacterial load assay

Identifiers

PMID36189292
PMCPMC9523539

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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.