Evidence map›Paper›PMID 24722524›Full record

ArticlePLoS neglected tropical diseases2014

Combined inflammatory and metabolic defects reflected by reduced serum protein levels in patients with Buruli ulcer disease.

Richard O Phillips, Fred S Sarfo, Jordi Landier, Reid Oldenburg, Michael Frimpong, Mark Wansbrough-Jones, Kabiru Abass, William Thompson, Mark Forson, Arnaud Fontanet and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

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  10. ELISA in the multiplex era: potentials and pitfalls.Proteomics. Clinical applications · 2015
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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 9 institutions in 3 countries.

Richard O PhillipsKomfo Anokye Teaching Hospital, Kumasi, Ghana; Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Fred S SarfoKomfo Anokye Teaching Hospital, Kumasi, Ghana.
Jordi LandierInstitut Pasteur, Unité de Recherche et d'Expertise Epidémiologie des Maladies Emergentes, Paris, France.
Reid OldenburgInstitut Pasteur, Unité d'Immunobiologie de l'Infection, Paris, France; CNRS URA 1961, Paris, France.
Michael FrimpongKumasi Centre for Collaborative Research, Kumasi, Ghana.
Mark Wansbrough-JonesSt George's University of London, London, United Kingdom.
Kabiru AbassAgogo Presbyterian Hospital, Agogo, Ghana.
William ThompsonAgogo Presbyterian Hospital, Agogo, Ghana.
Mark ForsonTepa Government Hospital, Tepa, Ghana.
Arnaud FontanetInstitut Pasteur, Unité de Recherche et d'Expertise Epidémiologie des Maladies Emergentes, Paris, France; Conservatoire National des Arts et Métiers, Paris, France.
Fatoumata NiangInstitut Pasteur, Unité d'Immunobiologie de l'Infection, Paris, France; CNRS URA 1961, Paris, France.
Caroline DemangelInstitut Pasteur, Unité d'Immunobiologie de l'Infection, Paris, France; CNRS URA 1961, Paris, France.
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FRPresbyterian University, Ghana · GHConservatoire National des Arts et Métiers · FRGhana Education Service · GHKomfo Anokye Teaching Hospital · GHKumasi Centre for Collaborative Research in Tropical Medicine · GHKwame Nkrumah University of Science and Technology · GHSt George's, University of London · GB

Funding

Medical Research Council MR/J01477X/1
6 · The paper itself

Abstract

Buruli ulcer is a skin disease caused by Mycobacterium ulcerans that is spreading in tropical countries, with major public health and economic implications in West Africa. Multi-analyte profiling of serum proteins in patients and endemic controls revealed that Buruli ulcer disease down-regulates the circulating levels of a large array of inflammatory mediators, without impacting on the leukocyte composition of peripheral blood. Notably, several proteins contributing to acute phase reaction, lipid metabolism, coagulation and tissue remodelling were also impacted. Their down-regulation was selective and persisted after the elimination of bacteria with antibiotic therapy. It involved proteins with various functions and origins, suggesting that M. ulcerans infection causes global and chronic defects in the host's protein metabolism. Accordingly, patients had reduced levels of total serum proteins and blood urea, in the absence of signs of malnutrition, or functional failure of liver or kidney. Interestingly, slow healers had deeper metabolic and coagulation defects at the start of antibiotic therapy. In addition to providing novel insight into Buruli ulcer pathogenesis, our study therefore identifies a unique proteomic signature for this disease.

Indexed as

AdolescentAdultAfrica, WesternBlood ProteinsBuruli UlcerChildFemaleHumansMaleMiddle AgedSerumUreaYoung AdultBlood ProteinsUrea

Identifiers

PMID24722524
PMCPMC3983110
OpenAlexW2026650188

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.