Evidence mapPaperPMID 39267759Full record

ArticleFrontiers in immunology2024

Cytokine and chemokine profiles in pulmonary tuberculosis with pre-diabetes.

Anuradha Rajamanickam, Sanaadhan P Kothandaraman, Nathella Pavan Kumar, Vijay Viswanathan, Sivakumar Shanmugam, Syed Hissar, Sujatha Nott, Hardy Kornfeld, Subash Babu

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Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
field-weighted citation impact
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

3 citing papers in PubMed.

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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.

Anuradha RajamanickamInternational Center for Excellence in Research, National Institute of Allergy and Infectious Diseases (NIAID), Chennai, India.
Sanaadhan P KothandaramanStanley Medical College, Chennai, India.
Nathella Pavan KumarDepartment of Immunology, Indian Council of Medical Research (ICMR)-National Institute for Research in Tuberculosis, Chennai, India.
Vijay ViswanathanProf. M. Viswanathan Diabetes Research Center, Chennai, India.
Sivakumar ShanmugamDepartment of Bacteriology, Indian Council of Medical Research (ICMR)-National Institute for Research in Tuberculosis, Chennai, India.
Syed HissarDepartment of Clinical Research, Indian Council of Medical Research (ICMR)-National Institute for Research in Tuberculosis, Chennai, India.
Sujatha NottInfectious Diseases, Dignity Health, Chandler, AZ, United States.
Hardy KornfeldDepartment of Medicine, University of Massachusetts Medical School (UMass) Chan Medical School, Worcester, MA, United States.
Subash BabuInternational Center for Excellence in Research, National Institute of Allergy and Infectious Diseases (NIAID), Chennai, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Tuberculosis (TB) remains a significant health concern in India, and its complexity is exacerbated by the rising occurrence of non-communicable diseases such as diabetes mellitus (DM). Recognizing that DM is a risk factor for active TB, the emerging comorbidity of TB and PDM (TB-PDM) presents a particular challenge. Our study focused on the impact of PDM on cytokine and chemokine profiles in patients with pulmonary tuberculosis TB) who also have PDM. Materials and methods: We measured and compared the cytokine (GM-CSF, IFN-γ, IL-1α/IL-1F1, IL-1β/IL-1F2, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12p70, IL-13, IL-17/IL-17A, IL-18/IL-1F4, TNF-α) and chemokine (CCL1, CCL2, CCL3, CCL4, CCL11, CXCL1, CXCL2, CXCL9, CXCL10, and CXCL11) levels in plasma samples of TB-PDM, only TB or only PDM using multiplex assay. Results: We observed that PDM was linked to higher mycobacterial loads in TB. Patients with coexisting TB and PDM showed elevated levels of various cytokines (including IFNγ, TNFα, IL-2, IL-17, IL-1α, IL-1β, IL-6, IL-12, IL-18, and GM-CSF) and chemokines (such as CCL1, CCL2, CCL3, CCL4, CCL11, CXCL1, CXCL9, CXCL10, and CXCL11). Additionally, cytokines such as IL-18 and GM-CSF, along with the chemokine CCL11, were closely linked to levels of glycated hemoglobin (HbA1c), hinting at an interaction between glycemic control and immune response in TB patients with PDM. Conclusion: Our results highlight the complex interplay between metabolic disturbances, immune responses, and TB pathology in the context of PDM, particularly highlighting the impact of changes in HbA1c levels. This emphasizes the need for specialized approaches to manage and treat TB-PDM comorbidity.

Indexed as

CytokinesPrediabetic StateTuberculosis, PulmonaryAdultBiomarkersChemokinesFemaleHumansIndiaMaleMiddle AgedMycobacterium tuberculosisBiomarkersChemokinesCytokineschemokinescytokinesimmunitymetabolismpre-diabetestuberculosis

Identifiers

PMID39267759
PMCPMC11390597

What Socratic holds

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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 Socratic graph.