Evidence map›Paper›PMID 42756990›Full record

ArticleBMJ neurology open2026

Inflammatory biomarkers as predictors of paradoxical reaction in tubercular meningitis: a prospective observational study.

Satinder Deswal, Abdul Qavi, Ajai Kumar Singh, Pradeep Kumar Maurya, Dinkar Kulshreshtha, Arshi Ansari

Abstract read
In one paragraph

Article in BMJ neurology open, 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

What it found

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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

6 authors.

Satinder DeswalNeurology, Dr Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.
Abdul QaviNeurology, Dr Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.ORCID https://orcid.org/0000-0002-4223-5540
Ajai Kumar SinghNeurology, Dr Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.
Pradeep Kumar MauryaNeurology, Dr Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.
Dinkar KulshreshthaNeurology, Dr Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.
Arshi AnsariCommunity Medicine and Public Health, Dr Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Tubercular meningitis (TBM) is associated with high morbidity and mortality due to intense inflammatory responses causing basal exudates, vasculitic infarcts, hydrocephalus and cranial nerve palsies. Paradoxical reaction (PR) occurs in nearly 30% of patients and contributes to clinical deterioration during treatment. Dysregulated inflammatory mediators in serum and cerebrospinal fluid (CSF) have been implicated in PR and adverse outcomes in TBM. Objective: This study evaluated baseline serum and CSF inflammatory biomarkers for predicting PR and vasculitic infarcts in newly diagnosed TBM patients. Methods: In this prospective observational study, 151 treatment-naïve TBM patients fulfilling Marais consensus criteria were enrolled. Baseline clinical, radiological, serum and CSF inflammatory markers were assessed and repeated during PR/stroke. Serum markers included high-sensitivity C reactive protein (hsCRP), erythrocyte sedimentation rate (ESR), lactate dehydrogenase (LDH), ferritin, albumin, D-dimer, neutrophil-lymphocyte ratio (NLR) and systemic immune-inflammation index. CSF analysis included adenosine deaminase, NLR, protein, glucose and leucocyte count. Results: Among 151 patients (mean age 32.7±14.5 years), 43 (28.4%) developed PR, most commonly within 1-2 months of antitubercular therapy initiation. Altered sensorium (58.1%) and progression of hydrocephalus (60.5%) were common manifestations. Higher baseline ESR, hsCRP, LDH, ferritin, D-dimer and lower serum albumin were significantly associated with PR. Serum ferritin showed the best predictive accuracy (area under the curve 0.910; cut-off ≥451 µg/L; sensitivity 88.4%, specificity 88.9%). On multivariable analysis, serum ferritin (OR 1.004; p=0.001) and ESR (OR 1.020; p=0.033) remained independent predictors. Conclusions: Serum inflammatory markers, particularly ferritin and ESR, may serve as useful predictors of PR in TBM. These findings support an immune-mediated mechanism underlying paradoxical worsening and may help identify high-risk patients who could benefit from early anti-inflammatory or immune-modulatory therapy.

Indexed as

CSFINFLAMMATIONNEUROIMMUNOLOGYSTROKETUBERCULOSIS

Identifiers

PMID42756990
PMCPMC13583852

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