Literature DB >> 25207021

Investigation of Monnose-Binding Lectin gene Polymorphism in Patients with Erythema Multiforme, Stevens-Johnson Syndrome and Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Overlap Syndrome.

Mutlu Karkucak1, Emel Başkan Bülbül2, Hakan Turan3, Tahsin Yakut1, Sevil Toka2, Hayriye Sarıcaoğlu2.   

Abstract

OBJECTIVE: Monnose-Binding lectin (MBL) appears to play an important role in the immune system. The genetic polymorphisms in the MBL2 gene can result in a reduction of serum levels, leading to a predisposition to recurrent infection. The aim of this study is to investigate the influence of a polymorphism in codon 54 of the MBL2 gene on the susceptibility to Erythema Multiforme, Stevens-Johnson Syndrome and Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Overlap Syndrome (EM, SJS and SJS/TEN overlap syndrome).
MATERIAL AND METHODS: Our study included 64 patients who were clinically and/or histopathologically diagnosed with EM, SJS, and SJS/TEN overlap syndrome and 66 healthy control subjects who were genotyped for the MBL2 gene codon 54 polymorphism using the PCR-RFLP method. For all statistical analyses, the level of significance was set at p<0.05.
RESULTS: The prevalence of the B allele was 18% in the EM, SJS and SJS/TEN patient groups and 13% in the control group. No significant differences in allele frequencies of any polymorphism were observed between the patient and control groups, although the B allele was more frequent in the patient groups (p=0.328).
CONCLUSION: Our results provide no evidence of a relationship between MBL2 gene codon 54 polymorphism and the susceptibility to EM, SJS and SJS/ TEN overlap syndrome. However, these findings should be confirmed in studies with a larger sample size.

Entities:  

Keywords:  Erythema multiforme; MBL2 gene; Polymorphism; Stevens-Johnson syndrome; Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome

Year:  2012        PMID: 25207021      PMCID: PMC4115830          DOI: 10.5152/balkanmedj.2012.018

Source DB:  PubMed          Journal:  Balkan Med J        ISSN: 2146-3123            Impact factor:   2.021


  28 in total

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5.  Erythema multiforme, Stevens-Johnson syndrome and toxic epidermal necrolysis in children: a review of 10 years' experience.

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8.  Distinct physicochemical characteristics of human mannose binding protein expressed by individuals of differing genotype.

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10.  Interplay between promoter and structural gene variants control basal serum level of mannan-binding protein.

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