Loading…

HLA alleles in Brazilian patients with fissured tongue

Background  Fissured tongue (FT) is a clinical condition manifested by numerous little furrows on the tongue’s surface. Previously, the authors observed an association with HLA‐C×06 in psoriasis (PS) and benign migratory glossitis (BMG); however, HLA‐C was not surveyed in FT. Objective  This study i...

Full description

Saved in:
Bibliographic Details
Published in:Journal of the European Academy of Dermatology and Venereology 2013-02, Vol.27 (2), p.e166-e170
Main Authors: Gonzaga, H.F.S., Marcos, E.V.C., Santana, F.C.S., Jorge, M.A., Tomimori, J.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Background  Fissured tongue (FT) is a clinical condition manifested by numerous little furrows on the tongue’s surface. Previously, the authors observed an association with HLA‐C×06 in psoriasis (PS) and benign migratory glossitis (BMG); however, HLA‐C was not surveyed in FT. Objective  This study investigated the association between HLA alleles and FT. Methods  Thirty‐three FT bearers were studied, after evaluation of criteria for inclusion. These patients did not present PS, BMG or any other conditions associated with FT. The control group (CG) was composed of 561 individuals with HLA‐A, 560 individuals with HLA‐B, 168 individuals with HLA‐C, 564 individuals with HLA‐DRB1 and 390 individuals with HLA‐DQB1. Samples from these individuals were processed to extract DNA. The HLA classes I and II were determined using the reverse line blot technique. The frequencies of HLA antigens found in patients were compared with the CG using Fisher’s exact test. Results  The comparison of the frequencies of HLA antigens found in the patient groups and in CG revealed no association with any of the alleles studied, except for HLA‐A*01, which exhibited a decreased frequency in patient groups. HLA‐C*06 was detected in 7.57% of FT patients and 10.42% of the CG (not significant). Conclusion  The lack of association of FT with HLA‐C*06 reinforces the proposal that this disease does not have a common genetic factor in the triad of BMG, FT and PS.
ISSN:0926-9959
1468-3083
DOI:10.1111/j.1468-3083.2012.04537.x