Evidence map›Paper›PMID 31142816›Full record

ArticleScientific reports2019

Molecular degree of perturbation of plasma inflammatory markers associated with tuberculosis reveals distinct disease profiles between Indian and Chinese populations.

Deivide Oliveira-de-Souza, Caian L Vinhaes, Maria B Arriaga, Nathella Pavan Kumar, Juan M Cubillos-Angulo, Ruiru Shi, Wang Wei, Xing Yuan, Guolong Zhang, Ying Cai and 8 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 32 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

18 authors at 6 institutions in 3 countries.

Deivide Oliveira-de-SouzaInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, 40296-710, Brazil.
Caian L VinhaesInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, 40296-710, Brazil.
Maria B ArriagaInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, 40296-710, Brazil.
Nathella Pavan KumarNational Institutes of Health- National Institute for Research in Tuberculosis, International Center for Excellence in Research, Chennai, 600031, India.
Juan M Cubillos-AnguloInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, 40296-710, Brazil.
Ruiru ShiHenan Chest Hospital, Zhengzhou, 450000, China.
Wang WeiHenan Chest Hospital, Zhengzhou, 450000, China.
Xing YuanHenan Chest Hospital, Zhengzhou, 450000, China.
Guolong ZhangSino-US International Research Center for Tuberculosis, and Henan Public Health Center, Zhengzhou, 450000, China.
Ying CaiLaboratory of Clinical Immunology and Microbiology, NIAID, NIH, Bethesda, 20892, USA.
Clifton E BarryLaboratory of Clinical Immunology and Microbiology, NIAID, NIH, Bethesda, 20892, USA.
Laura E ViaLaboratory of Clinical Immunology and Microbiology, NIAID, NIH, Bethesda, 20892, USA.
Alan SherLaboratory of Parasitic Diseases, NIAID, NIH, Bethesda, 20892, USA.
Subash BabuNational Institutes of Health- National Institute for Research in Tuberculosis, International Center for Excellence in Research, Chennai, 600031, India.
Katrin D Mayer-BarberLaboratory of Clinical Immunology and Microbiology, NIAID, NIH, Bethesda, 20892, USA.ORCID http://orcid.org/0000-0002-0311-3233
Helder I NakayaDepartment of Pathophysiology and Toxicology, School of Pharmaceutical Sciences, University of São Paulo, São Paulo, 05508, Brazil.ORCID http://orcid.org/0000-0001-5297-9108
Kiyoshi F FukutaniInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, 40296-710, Brazil.ORCID http://orcid.org/0000-0003-2223-0918
Bruno B AndradeInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, 40296-710, Brazil. bruno.andrade@fiocruz.br.ORCID http://orcid.org/0000-0001-6833-3811
National Institutes of Health · USFaculdade de Tecnologia e Ciências · BRHenan Provincial Chest Hospital · CNFundação Oswaldo Cruz · BRUniversidade de São Paulo · BRVanderbilt University · US

Funding

CCASAnet: Caribbean, Central and South America NetworkU01AI069923 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Pedro Enrique Cahn, Jessica L Castilho · 2006 to 2026
$41.6M
India International Center for Excellence in ResearchZIAAI001065 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI NUTMAN, THOMAS · 2009 to 2025
$19.0M
Innate inflammatory responses during pulmonary infectionsZIAAI001207 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MAYER-BARBER, KATRIN · 2015 to 2025
$13.6M
International Tuberculosis Research in ChinaZIAAI001081 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BARRY, CLIFTON · 2010 to 2025
$12.2M
Regulation Of Immunopathology In Bacterial And Parasitic DiseaseZIAAI000843 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SHER, ALAN · 2009 to 2022
$11.1M
Innate Determinants of Microbial ImmunityZIAAI001044 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SHER, ALAN · 2009 to 2022
$8.8M
Inflammatory determinants of disease severity and treatment outcome in TB patientsU01AI115940 · NIAID · UNIVERSITY OF CAPE TOWN · PI SHER, ALAN, WILKINSON, ROBERT JOHN · 2015 to 2019
$1.1M
NIAID NIH HHS U01 AI069923NIAID NIH HHS U01 AI115940
6 · The paper itself

Abstract

Tuberculosis (TB) is a chronic inflammatory disease caused by Mycobacterium tuberculosis infection which causes tremendous morbidity and mortality worldwide. Clinical presentation of TB patients is very diverse and disease heterogeneity is associated with changes in biomarker signatures. Here, we compared at the molecular level the extent of individual inflammatory perturbation of plasma protein and lipid mediators associated with TB in patients in China versus India. We performed a cross-sectional study analyzing the overall degree of inflammatory perturbation in treatment-naïve pulmonary TB patients and uninfected individuals from India (TB: n = 97, healthy: n = 20) and China (TB: n = 100, healthy: n = 11). We employed the molecular degree of perturbation (MDP) adapted to plasma biomarkers to examine the overall changes in inflammation between these countries. M. tuberculosis infection caused a significant degree of molecular perturbation in patients from both countries, with higher perturbation detected in India. Interestingly, there were differences in biomarker perturbation patterns and the overall degree of inflammation. Patients with severe TB exhibited increased MDP values and Indian patients with this condition exhibited even higher degree of perturbation compared to Chinese patients. Network analyses identified IFN-α, IFN-β, IL-1RI and TNF-α as combined biomarkers that account for the overall molecular perturbation in the entire study population. Our results delineate the magnitude of the systemic inflammatory perturbation in pulmonary TB and reveal qualitative changes in inflammatory profiles between two countries with high disease prevalence.

Indexed as

AdultBiomarkersBlood ProteinsChinaCytokinesFemaleHumansIndiaInflammationInterferon-gammaLatent TuberculosisLipidsMaleMycobacterium tuberculosisTuberculosis, PulmonaryTumor Necrosis Factor-alphaBiomarkersBlood ProteinsCytokinesInterferon-gammaLipidsTumor Necrosis Factor-alpha

Identifiers

PMID31142816
PMCPMC6541651
OpenAlexW2947871685

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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.