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Lack of association between alopecia areata and HLA class I and II in a southeastern Brazilian population
Barbosa, Ângela Marques; Prestes-Carneiro, Luiz Euribel; Sobral, Aldri Roberta Sodoschi; Sakiyama, Marcelo Jun; Lemos, Bruna Cerávolo; Abreu, Marilda Aparecida Milanez Morgado de; Martos, Luciana Leite Crivelin; Moliterno, Ricardo Alberto.
  • Barbosa, Ângela Marques; Universidade do Oeste Paulista. Presidente Prudente. BR
  • Prestes-Carneiro, Luiz Euribel; Universidade do Oeste Paulista. Presidente Prudente. BR
  • Sobral, Aldri Roberta Sodoschi; Universidade do Oeste Paulista. Presidente Prudente. BR
  • Sakiyama, Marcelo Jun; Universidade do Oeste Paulista. Presidente Prudente. BR
  • Lemos, Bruna Cerávolo; Universidade do Oeste Paulista. Presidente Prudente. BR
  • Abreu, Marilda Aparecida Milanez Morgado de; Universidade do Oeste Paulista. Presidente Prudente. BR
  • Martos, Luciana Leite Crivelin; Universidade do Oeste Paulista. Presidente Prudente. BR
  • Moliterno, Ricardo Alberto; Universidade do Oeste Paulista. Presidente Prudente. BR
An. bras. dermatol ; 91(3): 284-289, tab
Article in English | LILACS | ID: lil-787286
ABSTRACT
Abstract

Background:

Alopecia areata (AA) is a common disorder of unknown etiology that affects approximately 0.7% to 3.8% of patients among the general population. Currently, genetic and autoimmune factors are emphasized as etiopathogenic. Studies linking Human Leukocyte Antigens (HLA) to AA have suggested that immunogenetic factors may play a role in the disease's onset/development.

Objectives:

To investigate an association between AA and HLA class I/II in white Brazilians.

Methods:

Patients and control groups comprised 33 and 112 individuals, respectively. DNA extraction was performed by column method with BioPur kit. Allele's classification was undertaken using the PCR-SSO technique. HLA frequencies were obtained through direct counting and subjected to comparison by means of the chi-square test.

Results:

Most patients were aged over 16, with no familial history, and developed partial AA, with no recurrent episodes. Patients showed a higher frequency of HLA-B*40, HLA-B*45, HLA-B*53 and HLA-C*04 compared with controls, although P was not significant after Bonferroni correction. Regarding HLA class II, only HLA-DRB1*07 revealed statistical significance; nevertheless, it featured more prominently in controls than patients (P=0.04; Pc=0.52; OR=0.29; 95%; CI=0.07 to 1.25). P was not significant after Bonferroni correction.

Conclusions:

The development of AA does not seem to be associated with HLA in white Brazilians, nor with susceptibility or resistance. The studies were carried out in populations with little or no miscegenation, unlike the Brazilian population in general, which could explain the inconsistency found.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Histocompatibility Antigens Class I / Histocompatibility Antigens Class II Type of study: Observational study / Prevalence study / Risk factors Limits: Adolescent / Adult / Female / Humans / Male Country/Region as subject: South America / Brazil Language: English Journal: An. bras. dermatol Journal subject: Dermatology Year: 2016 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade do Oeste Paulista/BR

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Full text: Available Index: LILACS (Americas) Main subject: Histocompatibility Antigens Class I / Histocompatibility Antigens Class II Type of study: Observational study / Prevalence study / Risk factors Limits: Adolescent / Adult / Female / Humans / Male Country/Region as subject: South America / Brazil Language: English Journal: An. bras. dermatol Journal subject: Dermatology Year: 2016 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade do Oeste Paulista/BR