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Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51
BACKGROUND/AIMS: The clinical manifestations of Behcet disease (BD) have been reported to differ according to country, region, and race. Gender, onset age, and human leukocyte antigen (HLA)-B51 have also been known as the factors that influence the clinical features of BD. The aim of this study is t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Internal Medicine
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129630/ https://www.ncbi.nlm.nih.gov/pubmed/28073242 http://dx.doi.org/10.3904/kjim.2016.202 |
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author | Ryu, Hee Jung Seo, Mi Ryoung Choi, Hyo Jin Baek, Han Joo |
author_facet | Ryu, Hee Jung Seo, Mi Ryoung Choi, Hyo Jin Baek, Han Joo |
author_sort | Ryu, Hee Jung |
collection | PubMed |
description | BACKGROUND/AIMS: The clinical manifestations of Behcet disease (BD) have been reported to differ according to country, region, and race. Gender, onset age, and human leukocyte antigen (HLA)-B51 have also been known as the factors that influence the clinical features of BD. The aim of this study is to investigate the clinical phenotypes of Korean patients who visited the rheumatology clinic with BD with respect to gender, onset age, and HLA-B51. METHODS: Total 193 Korean patients (129 females and 64 males) fulfilling the international criteria for BD were retrospectively assessed. RESULTS: The mean age at disease onset and disease duration of the BD patients were 32.2 ± 11.1 and 14.2 ± 9.3 years, retrospectively. Females suffered more frequently from genital ulcers (90.7% vs. 75.0%, p < 0.01), peripheral arthritis (67.4% vs. 43.8%, p < 0.01), and inf lammatory low back pain (38.8% vs. 23.4%, p = 0.03) than males, while skin involvement was more frequent in males than in females (90.6% vs. 75.2%, p = 0.01). The patients with late onset of BD (> 40 years) suffered from neurologic involvement (15.9% vs. 4.2%, p = 0.007) more frequently than those with early onset of BD. The patients with HLA-B51 showed earlier onset of disease than without HLA-B51 (28.3 ± 11.4 years vs. 33.8±11.6 years, p = 0.02) and the neurologic and gastrointestinal involvements were more frequent in the patients without HLA-B51 than with HLA-B51 (17.2% vs. 2.5%, p = 0.02 and 20.7% vs. 2.5%, p = 0.01, respectively). CONCLUSIONS: The clinical phenotypes in Korean patients with BD may be influenced by gender, onset age and HLA-B51. |
format | Online Article Text |
id | pubmed-6129630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Association of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-61296302018-09-11 Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51 Ryu, Hee Jung Seo, Mi Ryoung Choi, Hyo Jin Baek, Han Joo Korean J Intern Med Original Article BACKGROUND/AIMS: The clinical manifestations of Behcet disease (BD) have been reported to differ according to country, region, and race. Gender, onset age, and human leukocyte antigen (HLA)-B51 have also been known as the factors that influence the clinical features of BD. The aim of this study is to investigate the clinical phenotypes of Korean patients who visited the rheumatology clinic with BD with respect to gender, onset age, and HLA-B51. METHODS: Total 193 Korean patients (129 females and 64 males) fulfilling the international criteria for BD were retrospectively assessed. RESULTS: The mean age at disease onset and disease duration of the BD patients were 32.2 ± 11.1 and 14.2 ± 9.3 years, retrospectively. Females suffered more frequently from genital ulcers (90.7% vs. 75.0%, p < 0.01), peripheral arthritis (67.4% vs. 43.8%, p < 0.01), and inf lammatory low back pain (38.8% vs. 23.4%, p = 0.03) than males, while skin involvement was more frequent in males than in females (90.6% vs. 75.2%, p = 0.01). The patients with late onset of BD (> 40 years) suffered from neurologic involvement (15.9% vs. 4.2%, p = 0.007) more frequently than those with early onset of BD. The patients with HLA-B51 showed earlier onset of disease than without HLA-B51 (28.3 ± 11.4 years vs. 33.8±11.6 years, p = 0.02) and the neurologic and gastrointestinal involvements were more frequent in the patients without HLA-B51 than with HLA-B51 (17.2% vs. 2.5%, p = 0.02 and 20.7% vs. 2.5%, p = 0.01, respectively). CONCLUSIONS: The clinical phenotypes in Korean patients with BD may be influenced by gender, onset age and HLA-B51. The Korean Association of Internal Medicine 2018-09 2017-01-12 /pmc/articles/PMC6129630/ /pubmed/28073242 http://dx.doi.org/10.3904/kjim.2016.202 Text en Copyright © 2017 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ryu, Hee Jung Seo, Mi Ryoung Choi, Hyo Jin Baek, Han Joo Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51 |
title | Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51 |
title_full | Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51 |
title_fullStr | Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51 |
title_full_unstemmed | Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51 |
title_short | Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51 |
title_sort | clinical phenotypes of korean patients with behcet disease according to gender, age at onset, and hla-b51 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129630/ https://www.ncbi.nlm.nih.gov/pubmed/28073242 http://dx.doi.org/10.3904/kjim.2016.202 |
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