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Asporin levels in patients with temporomandibular joint disorders
Author(s) -
Ege Bilal,
Erdogmus Zozan,
Bozgeyik Esra,
Koparal Mahmut,
Kurt Muhammed Yusuf,
Gulsun Belgin
Publication year - 2021
Publication title -
journal of oral rehabilitation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.991
H-Index - 93
eISSN - 1365-2842
pISSN - 0305-182X
DOI - 10.1111/joor.13234
Subject(s) - temporomandibular joint , medicine , pathogenesis , homogeneous , biomarker , gastroenterology , pathology , biology , biochemistry , physics , thermodynamics
Abstract Background Understanding the pathogenesis of temporomandibular joint disorder (TMD) is important for diagnosis and treatment planning. Thus, biochemical analysis is usually used for the detection of tissue damage. Objective In this study, we aimed to investigate the serum asporin levels in patients with TMD. Methods Our study was planned to be performed on 43 healthy individuals (control group) without any joint problems and 43 patients with temporomandibular joint internal derangement (TMJ‐ID; patients group) according to the Wilkes classification (stages 3, 4 and 5). Serum asporin levels were determined by the enzyme‐linked immunosorbent assay (ELISA) method and compared between groups. Asporin levels were analysed according to the demographic and clinical characteristics of the patients, and the differences between them were demonstrated. Results Asporin levels were found to be significantly increased in the patients group compared to control group ( p = .0303). The age and gender distributions of the samples in the control and patients groups were homogeneous, and there was no statistically significant difference between the groups. In addition, while there was no significant change in asporin levels in females in the patients group compared with the control group, the asporin levels were significantly increased in males in the patients group ( p = .0403). Conclusions Consequently, asporin seems to be an important biomarker in the pathobiology of TMJ‐ID as it is significantly upregulated in these patients.