Evidence map›Paper›PMID 31818258›Full record

ArticleBMC infectious diseases2019

Systemic RAGE ligands are upregulated in tuberculosis individuals with diabetes co-morbidity and modulated by anti-tuberculosis treatment and metformin therapy.

Nathella Pavan Kumar, Kadar Moideen, Arul Nancy, Vijay Viswanathan, Basavaradhya S Shruthi, Shanmugam Sivakumar, Syed Hissar, Hardy Kornfeld, Subash Babu

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Article in BMC infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 16 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

9 authors at 4 institutions in 2 countries.

Nathella Pavan KumarNational Institutes of Health-NIRT- International Center for Excellence in Research, No. 1 Mayor Sathyamoothy Road, Chetpet, Chennai, India. pavankumarn@nirt.res.in.ORCID http://orcid.org/0000-0002-4901-1507
Kadar MoideenNational Institutes of Health-NIRT- International Center for Excellence in Research, No. 1 Mayor Sathyamoothy Road, Chetpet, Chennai, India.
Arul NancyNational Institutes of Health-NIRT- International Center for Excellence in Research, No. 1 Mayor Sathyamoothy Road, Chetpet, Chennai, India.
Vijay ViswanathanProf. M. Viswanathan Diabetes Research Center, Chennai, India.
Basavaradhya S ShruthiProf. M. Viswanathan Diabetes Research Center, Chennai, India.
Shanmugam SivakumarNational Institute for Research in Tuberculosis, Chennai, India.
Syed HissarNational Institute for Research in Tuberculosis, Chennai, India.
Hardy KornfeldUniversity of Massachusetts Medical School, Worcester, MA, USA.
Subash BabuNational Institutes of Health-NIRT- International Center for Excellence in Research, No. 1 Mayor Sathyamoothy Road, Chetpet, Chennai, India.
India Diabetes Research Foundation · INInternational Centers for Excellence in Research · INNational Institute of Research in Tuberculosis · INUniversity of Massachusetts Chan Medical School · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLigands of the receptor for advanced glycation end products (RAGE) are key signalling molecules in the innate immune system but their role in tuberculosis-diabetes comorbidity (TB-DM) has not been investigated.

methodsWe examined the systemic levels of soluble RAGE (sRAGE), advanced glycation end products (AGE), S100A12 and high mobility group box 1 (HMGB1) in participants with either TB-DM, TB, DM or healthy controls (HC).

resultsSystemic levels of AGE, sRAGE and S100A12 were significantly elevated in TB-DM and DM in comparison to TB and HC. During follow up, AGE, sRAGE and S100A12 remained significantly elevated in TB-DM compared to TB at 2nd month and 6th month of anti-TB treatment (ATT). RAGE ligands were increased in TB-DM individuals with bilateral and cavitary disease. sRAGE and S100A12 correlated with glycated hemoglobin levels. Within the TB-DM group, those with known diabetes (KDM) revealed significantly increased levels of AGE and sRAGE compared to newly diagnosed DM (NDM). KDM participants on metformin treatment exhibited significantly diminished levels of AGE and sRAGE in comparison to those on non-metformin regimens.

conclusionsOur data demonstrate that RAGE ligand levels reflect disease severity and extent in TB-DM, distinguish KDM from NDM and are modulated by metformin therapy.

Indexed as

AdultAgedAntigens, NeoplasmAntitubercular AgentsCase-Control StudiesComorbidityDiabetes MellitusFemaleGlycation End Products, AdvancedHMGB1 ProteinHumansHypoglycemic AgentsMaleMetforminMiddle AgedMitogen-Activated Protein KinasesAntigens, NeoplasmAntitubercular AgentsGlycation End Products, AdvancedHMGB1 ProteinHMGB1 protein, humanHypoglycemic AgentsMetforminMitogen-Activated Protein KinasesMOK protein, humanS100A12 ProteinS100A12 protein, humanDiabetes mellitusMycobacterium tuberculosisRAGE ligands

Identifiers

PMID31818258
PMCPMC6902343
OpenAlexW2996678019

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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.