# Analysis of serum calprotectin levels in ménière’s patients and investigation of its effect on disease severity

**Authors:** Hüseyin Işık, Deniz Baklaci, Tuba Candar, Duygu Erdem, Ergin Bilgin

PMC · DOI: 10.1371/journal.pone.0340121 · 2026-01-29

## TL;DR

This study found that Ménière’s Disease patients have higher calprotectin levels during acute attacks, which drop after treatment and correlate with symptom duration.

## Contribution

The study identifies calprotectin as a potential inflammatory biomarker for Ménière’s Disease severity and treatment response.

## Key findings

- MD patients had significantly higher serum calprotectin levels during acute attacks compared to controls.
- Calprotectin levels in MD patients correlated strongly with symptom duration.
- Calprotectin levels decreased significantly after treatment in MD patients.

## Abstract

This prospective observational study aimed to evaluate serum calprotectin levels in patients with definite Ménière’s Disease (MD) and to investigate their association with symptom duration and disease severity.

Thirty-nine patients (16 males, 23 females; mean age 37.2 ± 11.9 years) diagnosed with definite MD according to the AAO–HNS criteria and 28 age- and sex-matched healthy controls (14 males, 14 females; mean age 39.2 ± 13.3 years) without vestibular or auditory complaints were included. Individuals with active infection, autoimmune or chronic inflammatory disease, recent antibiotic or steroid use, or other otologic pathologies were excluded. Serum calprotectin levels were measured during an acute vertigo attack in the MD group and once in controls. Between-group differences and correlations with clinical variables were analyzed using appropriate parametric and non-parametric tests.

Mean serum calprotectin levels during acute attack were significantly higher in the MD group than in controls (1031 ± 364 vs. 611 ± 231 ng/mL, p < 0.001). Within the MD group, calprotectin levels showed a strong positive correlation with symptom duration (Spearman’s ρ = 0.914, p < 0.001). In patients with MD, calprotectin levels decreased significantly after treatment, from 1031 ± 364 to 582 ± 339 ng/mL (mean difference 449 ng/mL, 95% CI 353–545; t(38) = 9.46, p < 0.001; Cohen’s d = 1.51), indicating a large effect size.

Patients with Ménière’s Disease exhibit elevated serum calprotectin levels during acute attacks, which correlate strongly with symptom duration and decrease significantly after treatment. These findings suggest that calprotectin may be a potential inflammatory biomarker associated with disease burden and treatment response in MD; however, longitudinal studies with larger cohorts are needed to determine its diagnostic and prognostic utility.

## Linked entities

- **Diseases:** autoimmune disease (MONDO:0007179)

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, OTOL1 (otolin 1) [NCBI Gene 131149] {aka C1QTNF15, C1QTNF16}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CETN1 (centrin 1) [NCBI Gene 1068] {aka CEN1, CETN}
- **Diseases:** MD (MESH:D008575), tinnitus (MESH:D014012), infection (MESH:D007239), vestibular neuritis (MESH:D020338), autoimmune (MESH:D001327), ISSHL (MESH:D006319), hearing loss (MESH:D034381), inflammatory bowel disease (MESH:D015212), malignant (MESH:D009369), Infectious (MESH:D003141), Rheumatoid Arthritis (MESH:D001172), endolymphatic hydrops (MESH:D018159), AOSD (MESH:D016706), food allergies (MESH:D005512), trauma (MESH:D014947), benign paroxysmal positional vertigo (MESH:D065635), vestibular or auditory complaints (MESH:D015837), dizziness (MESH:D004244), inner ear disorder (MESH:D007759), rheumatic diseases (MESH:D012216), inflammation (MESH:D007249), Sjogren's Syndrome (MESH:D012859), nasal obstruction (MESH:D015508), vertigo (MESH:D014717), autoimmune or chronic inflammatory disease (MESH:D019693), allergy (MESH:D004342)
- **Chemicals:** methylprednisolone (MESH:D008775), acetazolamide (MESH:D000086), steroid (MESH:D013256), alcohol (MESH:D000438), LPS (MESH:D008070)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12854440/full.md

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Source: https://tomesphere.com/paper/PMC12854440