Association of HLA Alleles and HLA Haplotypes with Psoriasis, Psoriatic Arthritis and Disease Severity in a Miscegenated Population

被引:9
作者
Cassia, Flavia de Freire [1 ]
Cardoso, Juliana Fernandes [2 ]
Porto, Luiz Cristovao [3 ]
Ramos-e-Silva, Marcia [1 ]
Carneiro, Sueli [4 ]
机构
[1] Fed Univ Rio Janeiro, Univ Hosp & Sch Med, Sect Dermatol, Postgrad Course Dermatol, Rua Jardim Bot,700-416, BR-22461000 Rio De Janeiro, Brazil
[2] Albert Einstein Israelite Hosp HIAE, Histocompatibil Sect, Special Tech Lab, Sao Paulo, Brazil
[3] Univ Estado Rio De Janeiro, Histocompatibil & Cryopreservat Lab, Rio De Janeiro, Brazil
[4] Univ Estado Rio De Janeiro, Univ Hosp & Sch Med Sci, Sect Dermatol, Rio De Janeiro, Brazil
关键词
psoriasis; psoriatic arthritis; HLA; population study; MAJOR HISTOCOMPATIBILITY COMPLEX; HUMAN-LEUKOCYTE ANTIGEN; A-ANTIGENS; CLASS-I; TURKISH POPULATION; VULGARIS; ONSET; RISK; SYSTEM; MHC;
D O I
10.2147/PTT.S258050
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: The study of HLA classes I and II in Brazilian psoriasis patients may contribute to a better understanding of their association with the disease. Objective: To describe HLA classes I and II of Brazilian patients with psoriasis, with or without arthritis, compare them to controls and correlate HLA markers with epidemiological and evolutional aspects of psoriasis. Methods: A total of 55 patients with more than 5 years of psoriasis, with or without arthritis, answered a questionnaire on ethnic background and disease severity. A total of 134 bone marrow donors were controls. HLA class I and II genotyping was determined by PCR-SSP. Results: Mean age was 42.4 years; 23 women and 32 men. HLA-B*57 was present in 23.6% patients and in 7.5% controls (p=0.00200, OR= 3.8381), and HLA-C*06 in 29.1% patients and in 16.4% controls (p= 0.04832, OR=2.0886). HLA-B*57 and HLA-C*18 were significantly present in patients with arthritis (p=0.00104, OR=6.6769 and p=0.00269, OR=16.50, respectively). HLA-B*57 was significantly present in patients with history of erythroderma (p=0.00548, OR= 5.1059), as was HLA-C*06 (p=0.02158, OR=3.0545). HLA-B*57 was also frequent in patients with history of hospital internment due to psoriasis (p= 0.00094, OR=7.8909) and in the ones with history of systemic treatment for psoriasis (p= 0.00011, OR= 5.3733). Haplotype HLA-A*02 B*57 C*06 DRB1*07DQB1*03 was the most common among the patients (p= 0.00069, OR= 3.528). Conclusion: HLA-B*57 and HLA-C*06 were significantly increased in the patients indicating risk for psoriasis. HLA-B*57 remained high in patients with history of erythroderma, hospital internment, systemic treatment, and psoriatic arthritis, showing association with disease severity. HLA-C*18 was significantly high only in patients with psoriatic arthritis. HLA-B*57 and HLA-C*06 and haplotype HLA-A*02B*57Cw*06DRB1*07 DQB1*03 seen in this study were already described before, associated with psoriasis. HLA-Cw*18 was not described in other populations in association with psoriasis.
引用
收藏
页码:41 / 51
页数:11
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