Abstract

Objectives: The present study aimed to assess the expression of caspase-1 and caspase-1-dependent processing of cytokines, such as interleukin (IL)-1β and IL-18, in the middle ear effusion of children with otitis media with effusion (OME) in order to identify the potential role of inflammasomes in OME.Methods: This study included 29 children scheduled for myringotomy with the insertion of tympanostomy tubes due to OME. Middle ear effusion (MEE) was collected during the surgery. Caspase-1, IL-1β, and IL-18 were assayed using enzyme-linked immunosorbent assay kits. The levels were compared between those with mucoid and serous MEE and those with and without a history of ventilation tube insertion.Results: Caspase-1, IL-1β, and IL-18 were detected in all samples. The caspase-1, IL-1β, and IL-18 levels did not significantly differ between mucoid samples and serous samples. No statistical significances were discovered in caspase-1, IL-1β, and IL-18 levels between with and without a history of ventilation tube groups. There was a significant negative correlation between IL-1β and IL-18 and the duration of OME (p < 0.05). However, no significant correlation was found between caspase-1 and disease duration.Conclusions: Inflammasomes may participate in the inflammatory process of OME. IL-1β and IL-18 levels in the MEE decreased over time.

Highlights

  • Otitis media with effusion (OME), a common disease in children, is characterized by the collection of fluid in the middle ear without acute inflammatory manifestations [1, 2]

  • IL-1β is produced as an immature form that needs to be cleaved into a mature active form, which is mediated by an inflammasome [9]

  • Caspase-1, IL-1β, and IL-18 were detected in all middle ear effusion (MEE) samples (100%), and the levels of caspase1, IL-1β, and IL-18 were 1520.81 (22.84–53669.4) pg/mg TP, 5.64 (0.01–443.57)pg/mg TP and 578.09 (0.38–2300.79) pg/mg TP, respectively

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Summary

Introduction

Otitis media with effusion (OME), a common disease in children, is characterized by the collection of fluid in the middle ear without acute inflammatory manifestations [1, 2]. This disease is a chronic, low-grade inflammatory condition of the middle ear, and current medication cannot effectively resolve the inflammation. Many studies have shown that IL-1β plays a crucial role in this inflammatory process [6–8]. IL-1β is produced as an immature form that needs to be cleaved into a mature active form, which is mediated by an inflammasome [9]. A study reported linkage between chronic OME and/or recurrent otitis media and chromosome 19q containing several genes involved in the inflammasome protein complex [10]. Inflammasomes are suspected to be a key regulator in the pathogenesis of OME

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