Evidence map›Paper›PMID 26115421›Full record

ArticlePloS one2015

Cytokine Kinetics in the First Week of Tuberculosis Therapy as a Tool to Confirm a Clinical Diagnosis and Guide Therapy.

Alice L den Hertog, María Montero-Martín, Rachel L Saunders, Matthew Blakiston, Sandra Menting, Jeevan B Sherchand, Lovett Lawson, Olanrewaju Oladimeji, Saddiq T Abdurrahman, Luis E Cuevas and 1 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

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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

11 authors at 5 institutions in 4 countries.

Alice L den HertogRoyal Tropical Institute (KIT), KIT Biomedical Research, Amsterdam, The Netherlands.
María Montero-MartínLiverpool School of Tropical Medicine, Liverpool, United Kingdom.
Rachel L SaundersLiverpool School of Tropical Medicine, Liverpool, United Kingdom.
Matthew BlakistonLiverpool School of Tropical Medicine, Liverpool, United Kingdom.
Sandra MentingRoyal Tropical Institute (KIT), KIT Biomedical Research, Amsterdam, The Netherlands.
Jeevan B SherchandTribhuvan University Institute of Medicine, Kathmandu, Nepal.
Lovett LawsonZankli Medical Centre, Abuja, Nigeria.
Olanrewaju OladimejiZankli Medical Centre, Abuja, Nigeria.
Saddiq T AbdurrahmanAbuja Federal Capital Territory Tuberculosis Control Programme, Abuja, Nigeria.
Luis E CuevasLiverpool School of Tropical Medicine, Liverpool, United Kingdom.
Richard M AnthonyRoyal Tropical Institute (KIT), KIT Biomedical Research, Amsterdam, The Netherlands.
Liverpool School of Tropical Medicine · GBRoyal Tropical Institute · NLZankli Medical Centre · NGTribhuvan University · NPUniversity of Abuja · NG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany patients treated for tuberculosis (TB) in low and middle income countries are treated based on clinical suspicion without bacteriological confirmation. This is often due to lack of rapid simple accurate diagnostics and low healthcare provider confidence in the predictive value of current tests. We previously reported in an animal TB model that levels of host markers rapidly change in response to treatment initiation.

methodsWe assessed the potential of host biomarker kinetics of TB patients during the first two weeks of therapy to identify patients responding to treatment. Adult patients clinically diagnosed with and treated for TB, 29 in Nigeria and 24 in Nepal, were analyzed.

resultsChanges in concentrations of non-specific host biomarkers, particularly IP-10, in response to the first week of anti-TB therapy were strongly associated with bacteriological confirmation of TB. A decrease in IP-10 level of >300pg/ml between 0 and 7 days of treatment identified 75% of both smear-positive and smear-negative culture positive patients and correctly excluded TB in all nine culture negative patients.

conclusionsMonitoring of early IP-10 responses to treatment could form the basis of a simplified assay and could help identify patients who were erroneously clinically diagnosed with TB or those infected with drug resistant strains on inappropriate treatment. We believe this approach may be particularly appropriate for difficult to diagnose patients, e.g. smear-negative HIV-positive, or those with extra-pulmonary TB, often treated without bacterial confirmation.

Indexed as

AdolescentAdultAgedAntitubercular AgentsAutoantibodiesBiomarkersChemokine CXCL10CoinfectionCytokinesFemaleFollow-Up StudiesHIV SeropositivityHumansKineticsMaleMiddle AgedAntitubercular AgentsAutoantibodiesBiomarkersChemokine CXCL10Cytokines

Identifiers

PMID26115421
PMCPMC4482639
OpenAlexW1544268516

What OpenQuestion holds

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LicenceCC BY
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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.