Evidence map›Paper›PMID 27287260›Full record

ArticleBMC infectious diseases2016

Variation in C - reactive protein response according to host and mycobacterial characteristics in active tuberculosis.

James Brown, Kristina Clark, Colette Smith, Jennifer Hopwood, Oliver Lynard, Michael Toolan, Dean Creer, Jack Barker, Ronan Breen, Tim Brown and 2 more

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 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 47 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

12 authors at 4 institutions in 2 countries.

James BrownDepartment of Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK. james.brown13@nhs.net.ORCID 0000-0001-5962-0253
Kristina ClarkDepartment of Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.
Colette SmithDepartment of Infection and Population Health, University College London, London, UK.
Jennifer HopwoodDepartment of Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.
Oliver LynardDepartment of Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.
Michael ToolanDepartment of Respiratory Medicine, Guys and St Thomas' NHS Foundation Trust, London, UK.
Dean CreerDepartment of Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.
Jack BarkerDepartment of Respiratory Medicine, King's College Hospital NHS Foundation Trust, London, UK.
Ronan BreenDepartment of Respiratory Medicine, Guys and St Thomas' NHS Foundation Trust, London, UK.
Tim BrownNational Mycobacterial Reference Laboratory, London, UK.
Ian CropleyDepartment of Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.
Marc LipmanDepartment of Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.
Royal Free London NHS Foundation Trust · GBGuy's and St Thomas' NHS Foundation Trust · GBKing's College Hospital NHS Foundation Trust · GBUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe C - reactive protein (CRP) response is often measured in patients with active tuberculosis (TB) yet little is known about its relationship to clinical features in TB, or whether responses differ between ethnic groups or with different Mycobacterium tuberculosis (M.tb) strain types. We report the relationship between baseline serum CRP prior to treatment and disease characteristics in a metropolitan population with TB resident in a low TB incidence region.

methodsPeople treated for TB at four London, UK sites between 2003 and 2014 were assessed and data collected on the following characteristics: baseline CRP level; demographics (ethnicity, gender and age); HIV status; site of TB disease; sputum smear (in pulmonary cases) and culture results. The effect of TB strain-type was also assessed in culture-positive pulmonary cases using VNTR typing data.

resultsThree thousands two hundred twenty-two patients were included in the analysis of which 72 % had a baseline CRP at or within 4 weeks prior to starting TB treatment. CRP results were significantly higher in culture positive cases compared to culture negative cases: median 49 mg/L (16-103 mg/L) vs 19 mg/L (IQR 5-72 mg/L), p = <0.001. In those with pulmonary disease, smear positive cases had a higher CRP than smear negative cases: 67 mg/L (31-122 mg/L) vs 24 mg/L (7-72 mg/L), p < 0.001. HIV positive cases had higher baseline CRPs than HIV negative cases: 75 mg/L (26-136 mg/L) vs 37 mg/L (10-88 mg/L), p <0.001. Differing sites of disease were associated with differences in baseline CRP: locations that might be expected to have a high mycobacterial load (e.g. pulmonary disease and disseminated disease) had a significantly higher CRP than those such as skin, lymph node or CNS disease, where the mycobacterial load is typically low in HIV negative subjects. In a multivariable log-scale linear regression model adjusting for host characteristics and M.tb strain type, infection with the East African Indian strain was associated with significantly lower baseline-CRP (fold-change in CRP 0.51 (0.34-0.77), p < 0.01).

conclusionsHost and mycobacterial factors are strongly associated with baseline CRP response in tuberculosis. This analysis suggests that there are important differences in innate immune response according to ethnicity, Mtb strain type and site of disease. This may reflect differing mycobacterial loads or host immune responses.

Indexed as

AdolescentAdultAsian PeopleBlack PeopleCohort StudiesCoinfectionC-Reactive ProteinFemaleHIV InfectionsHumansLinear ModelsLondonMaleMiddle AgedMultivariate AnalysisMycobacterium tuberculosisC-Reactive ProteinAcute phase responseC-reactive proteinInnate immune responseTuberculosis

Identifiers

PMID27287260
PMCPMC4901496
OpenAlexW2411597242

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.