Gene polymorphisms and serum levels of mannose‐binding lectin in Czech patients with recurrent aphthous stomatitis: A case–control study

Background Recurrent aphthous stomatitis is one of the most prevalent oral mucosal immunological diseases. A recent case–control study in the Egyptian population suggested that single nucleotide polymorphism Gly54Asp (rs1800450) of the mannose‐binding lectin 2 gene might affect the mannose‐binding l...

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Published inJournal of oral pathology & medicine Vol. 52; no. 1; pp. 81 - 90
Main Authors Izakovicova, Pavla, Slezakova, Simona, Jiraskova Zakostelska, Zuzana, Sistkova, Jana, Mlcuchova, Natalie, Bartova, Jirina, Petanova, Jitka, Kuklinek, Pavel, Fassmann, Antonin, Dusek, Ladislav, Izakovicova Holla, Lydie, Borilova Linhartova, Petra
Format Journal Article
LanguageEnglish
Published Denmark Wiley Subscription Services, Inc 01.01.2023
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ISSN0904-2512
1600-0714
1600-0714
DOI10.1111/jop.13385

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Summary:Background Recurrent aphthous stomatitis is one of the most prevalent oral mucosal immunological diseases. A recent case–control study in the Egyptian population suggested that single nucleotide polymorphism Gly54Asp (rs1800450) of the mannose‐binding lectin 2 gene might affect the mannose‐binding lectin serum level and recurrent aphthous stomatitis development. The aim of this study was to determine the distribution of six functional mannose‐binding lectin 2 gene polymorphisms and analyse their role in recurrent aphthous stomatitis susceptibility in the Czech population. Methods The study included 227 subjects; 137 healthy people and 90 patients with recurrent aphthous stomatitis. Six mannose‐binding lectin 2 gene polymorphisms (rs11003125, rs7096206, rs7095891, rs5030737, rs1800450, rs1800451) were analysed by the SNaPshot assay method, mannose‐binding lectin serum levels were determined by enzyme‐linked immunosorbent assay (ELISA) method in a subgroup of subjects (N = 87). Results No significant differences in mean of mannose‐binding lectin serum levels between healthy controls and patients with recurrent aphthous stomatitis were observed (383 ng/ml ± 249 standard deviation (SD) vs. 316 ng/ml ± 177 SD in remission phase vs. 343 ng/ml ± 254 SD in active phase; p > 0.05), also the allele and genotype frequencies of the studied mannose‐binding lectin 2 polymorphisms did not differ significantly between the two groups (p > 0.05, odds ratio (OR): 0.75–1.23). Moreover, the distribution of mannose‐binding lectin 2 haplotypes and haplogenotypes was similar in the healthy subjects and patients with recurrent aphthous stomatitis (p > 0.05, OR: 0.75–1.23). Conclusions This study did not confirm the previously reported association of the mannose‐binding lectin 2 Gly54Asp gene variant and low mannose‐binding lectin serum level as the risk factors for susceptibility to recurrent aphthous stomatitis. In addition, no significant relationships between mannose‐binding lectin 2 functional haplotypes or haplogenotypes and recurrent aphthous stomatitis were observed.
Bibliography:Lydie Izakovicova Holla and Petra Borilova Linhartova should be considered joint senior author.
Funding information
The Ministry of Health of the Czech Republic, Grant/Award Number: AZV15‐29336A; CETOCOEN EXCELLENCE, Grant/Award Number: CZ.02.1.01/0.0/0.0/17_043/0009632; European Union´s Horizon 2020 Research and Innovation Programme: CETOCOEN Excellence Teaming Phase II, Grant/Award Number: 857560; Masaryk University, Grant/Award Number: MUNI/A/1445/2021; RECETOX RI, Grant/Award Number: LM2018121; Czech Ministry of Education, Youth and Sports
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ISSN:0904-2512
1600-0714
1600-0714
DOI:10.1111/jop.13385