# Inflammatory biomarker panels in peripheral blood: association with myasthenia gravis onset and severity

**Authors:** Hong Jin, Yuxin Cui, Yunya Ren, Xinmiao Ma, Yishi Wang, Qi Fan, Yulan Cao, Chun-feng Liu, Jing Chen

PMC · DOI: 10.3389/fneur.2026.1673022 · 2026-02-03

## TL;DR

The study finds that certain blood-based inflammatory markers are linked to the onset and severity of myasthenia gravis, a neuromuscular disorder.

## Contribution

The study identifies specific inflammatory biomarkers (PLR and NLR) as potential indicators for MG onset and severity, including myasthenic crisis.

## Key findings

- PLR is independently associated with MG onset, while NLR and thymoma are linked to myasthenic crisis.
- NLR, PLR, and SII are significantly higher in generalized and severe MG cases compared to milder forms.
- Inflammatory biomarkers may help in risk stratification and clinical decision-making for MG patients.

## Abstract

To investigate the association between peripheral blood inflammatory biomarkers and the clinical phenotypes, severity, and prognosis of myasthenia gravis (MG).

This retrospective study analyzed 134 MG patients (including 23 with myasthenic crisis [MC]) and 58 age- and sex-matched healthy controls hospitalized at the Second Affiliated Hospital of Soochow University (August 2016–March 2024). Peripheral blood inflammatory markers were compared across subgroups. Infection was strictly excluded based on clinical and laboratory criteria. Multivariate logistic regression and receiver operating characteristic (ROC) curve analyses were performed to identify risk factors and diagnostic value.

Compared to controls, MG patients exhibited significantly elevated neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), and systemic inflammation response index (SIRI) (all p < 0.05). Patients with MC were characterized by a higher prevalence of generalized MG (GMG) and thymoma, as well as elevated leukocyte counts, NLR, and SIRI compared to non-MC patients. Multivariate analysis identified elevated PLR [OR: 1.01, 95% CI: 1.00–1.02] as independent risk factors associated with MG onset, while elevated NLR [OR: 1.20, 95% CI: 1.05–1.41] and the presence of thymoma [OR: 13.44, 95% CI: 4.42–48.54] were independently associated with MC. Furthermore, inflammatory indices (NLR, PLR, and SII) were significantly higher in GMG and moderate-to-severe cases (MGFA III–V) compared to ocular and mild cases.

Systemic inflammatory biomarkers, particularly PLR and NLR, are significantly elevated in MG and correlate with disease severity and clinical subtypes. While PLR is associated with MG onset, NLR and thymoma are potential indicators for myasthenic crisis. These readily available markers may facilitate risk stratification in clinical practice.

## Linked entities

- **Diseases:** myasthenia gravis (MONDO:0009688)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, MPO (myeloperoxidase) [NCBI Gene 4353]
- **Diseases:** autoimmune (MESH:D001327), NETs (MESH:C536657), respiratory failure (MESH:D012131), fever (MESH:D005334), blockade of neuromuscular transmission (MESH:D020511), NLR (MESH:D015467), hepatic/renal dysfunction (MESH:D008107), Chronic inflammation (MESH:D007249), MC (MESH:D020294), muscle (MESH:D019042), Malignancy (MESH:D009369), muscle weakness (MESH:D018908), autoimmune or neuroinflammatory disorders (MESH:D000090862), Thymoma (MESH:D013945), neuromuscular involvement (MESH:D009468), MGFA III-V (MESH:D015419), GMG (MESH:D009157), T-cell dysregulation (MESH:D016399), immune (MESH:D007154), Infection (MESH:D007239), cytotoxic (MESH:D064420)
- **Chemicals:** neostigmine (MESH:D009388), MC (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12909240/full.md

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Source: https://tomesphere.com/paper/PMC12909240