Evidence map›Paper›PMID 27539060›Full record

Observational studyScientific reports2016

S100A12 is up-regulated in pulmonary tuberculosis and predicts the extent of alveolar infiltration on chest radiography: an observational study.

Luis C Berrocal-Almanza, Surabhi Goyal, Abid Hussain, Tilman E Klassert, Dominik Driesch, Zarko Grozdanovic, Gadamm Sumanlatha, Niyaz Ahmed, Vijayalakshmi Valluri, Melanie L Conrad and 4 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 20 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

14 authors at 4 institutions in 2 countries.

Luis C Berrocal-AlmanzaInstitute for Microbiology and Hygiene, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Surabhi GoyalInstitute for Microbiology and Hygiene, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Abid HussainDepartment of Immunology, Bhagwan Mahavir Medical Research Centre, Hyderabad, India.
Tilman E KlassertSeptomics Research Center, Jena University Hospital, Jena, Germany.
Dominik DrieschBioControl Jena GmbH, Jena, Germany.
Zarko GrozdanovicDepartment of Radiology, Campus Benjamin Franklin, Charité - Universitätsmedizin Berlin, Germany.
Gadamm SumanlathaDepartment of Immunology, Bhagwan Mahavir Medical Research Centre, Hyderabad, India.
Niyaz AhmedPathogen Biology Laboratory, Department of Biotechnology and Bioinformatics, University of Hyderabad, Hyderabad, India.
Vijayalakshmi ValluriImmunology and Molecular Biology, LEPRA Society- Blue Peter Research Centre, Hyderabad, India.
Melanie L ConradInstitute for Microbiology and Hygiene, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Nickel DittrichInstitute for Microbiology and Hygiene, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Ralf R SchumannInstitute for Microbiology and Hygiene, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Birgit LalaDepartment of Paediatric Radiology, Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin, Germany.
Hortense SlevogtSeptomics Research Center, Jena University Hospital, Jena, Germany.
Charité - Universitätsmedizin Berlin · DEJena University Hospital · DELepra Society · INUniversity of Hyderabad · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary tuberculosis (PTB) results in lung functional impairment and there are no surrogate markers to monitor the extent of lung involvement. We investigated the clinical significance of S100A12 and soluble receptor for advanced glycation end-products (sRAGE) for predicting the extent of lung involvement. We performed an observational study in India with 119 newly diagnosed, treatment naïve, sputum smear positive, HIV-negative PTB patients and 163 healthy controls. All patients were followed-up for six months. Sociodemographic variables and the serum levels of S100A12, sRAGE, esRAGE, HMGB-1, TNF-α, IFN-γ and CRP were measured. Lung involvement in PTB patients was assessed by chest radiography. Compared with healthy controls, PTB patients had increased serum concentrations of S100A12 while sRAGE was decreased. S100A12 was an independent predictor of disease occurrence (OR 1.873, 95%CI 1.212-2.891, p = 0.004). Under DOTS therapy, S100A12 decreased significantly after 4 months whereas CRP significantly decreased after 2 months (p < 0.0001). Importantly, although CRP was also an independent predictor of disease occurrence, only S100A12 was a significant predictor of lung alveolar infiltration (OR 2.60, 95%CI 1.35-5.00, p = 0.004). These results suggest that S100A12 has the potential to assess the extent of alveolar infiltration in PTB.

Indexed as

Pulmonary AlveoliPulmonary EmbolismS100A12 ProteinTomography, X-Ray ComputedUp-RegulationAdultAntigens, NeoplasmCytokinesFemaleHMGB1 ProteinHumansMaleMitogen-Activated Protein KinasesAntigens, NeoplasmCytokinesHMGB1 ProteinHMGB1 protein, humanMitogen-Activated Protein KinasesMOK protein, humanS100A12 ProteinS100A12 protein, human

Identifiers

PMID27539060
PMCPMC4990910
OpenAlexW2507791577

What OpenQuestion holds

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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.