Evidence map›Paper›PMID 42745132›Full record

ArticleIndian journal of pediatrics2026

Evaluation of Systemic Inflammation in Pediatric Rheumatic Diseases Using a Composite Systemic Inflammation Score.

Debjani Bandhopadhyay, Biswabandhu Bankura, Avijit Hazra, Mihir Sarkar, Rakesh Kumar Mondal

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Article in Indian journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Debjani BandhopadhyayDepartment of Pediatrics, Medical College and Hospital, Kolkata, 700073, India.
Biswabandhu BankuraMultidisciplinary Research Unit, Medical College and Hospital, Kolkata, 700073, India.
Avijit HazraDepartment of Pharmacology, Institute of Postgraduate Medical Education & Research, Kolkata, 700020, India.
Mihir SarkarDepartment of Pediatrics, Medical College and Hospital, Kolkata, 700073, India.
Rakesh Kumar MondalDepartment of Pediatrics, Medical College and Hospital, Kolkata, 700073, India. ivanrakesh2001@gmail.com.ORCID http://orcid.org/0000-0002-2241-3514

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIsolated inflammatory markers have been proposed to assess systemic inflammation, but a comprehensive composite measure is still needed. The current study aimed to evaluate systemic inflammation in Pediatric Rheumatic Diseases by developing a biomarker-based composite systemic inflammation score (CSIS).

methodsThis prospective observational study enrolled 117 children with rheumatic diseases-systemic-onset juvenile idiopathic arthritis (SOJIA), systemic lupus erythematosus (SLE), IgA vasculitis (IgAV), and Kawasaki disease (KD), along with 50 age, gender and temporal matched healthy controls. Associations between disease groups and inflammatory biomarkers [neutrophil-to-lymphocyte ratio (NLR), platelet count, ESR, CRP, D-dimer, procalcitonin, ferritin, fibrinogen, and albumin] were evaluated. The CSIS was developed using eight validated, routinely available parameters, with a total score ranging from 0 to 16. Prediction accuracy was evaluated with the area under the receiver operating characteristic curve (AUC).

resultsComparative analysis demonstrated significantly higher levels of inflammatory markers in patients than in controls, including NLR, platelet count, erythrocyte ESR, CRP, D-dimer, ferritin, fibrinogen, and albumin (all p <0.001). These eight significantly associated biomarkers were incorporated into the scoring systems' development. The CSIS was stratified into four categories to reflect the degree of inflammatory burden: 0-2 (no inflammation), >2-7 (mild inflammation), >7-10 (moderate inflammation), and >10 (severe inflammation).

conclusionsThe CSIS can be readily applied to gauge inflammation severity in the clinical setting. Changes in inflammation scores over time can also reflect disease progression or remission, allowing for timely interventions and better outcomes.

Indexed as

Autoimmune diseasesInflammation scoreKawasaki diseaseSystemic lupus erythematosusSystemic-onset juvenile idiopathic arthritis

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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.