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TNFB Gene Polymorphism in Patients with Systemic Lupus Erythematosus in Korean
OBJECTIVES: To elucidate the gene frequency of TNFB Ncol polymorphism and its association with HLA class II antigen in patients with systemic lupus erythematosus (SLE) in Korea. METHODS: We investigated the gene frequency of the TNFB alleles using DNA obtained from peripheral mononuclear cells in 14...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association of Internal Medicine
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532044/ https://www.ncbi.nlm.nih.gov/pubmed/7495771 http://dx.doi.org/10.3904/kjim.1995.10.2.130 |
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author | Kim, Ho-Youn Lee, Sang-Heon Yang, Hyung-In Park, Sung-Hwan Cho, Chul-Soo Kim, Tai-Gyu Han, Hoon Kim, Dong-Jip |
author_facet | Kim, Ho-Youn Lee, Sang-Heon Yang, Hyung-In Park, Sung-Hwan Cho, Chul-Soo Kim, Tai-Gyu Han, Hoon Kim, Dong-Jip |
author_sort | Kim, Ho-Youn |
collection | PubMed |
description | OBJECTIVES: To elucidate the gene frequency of TNFB Ncol polymorphism and its association with HLA class II antigen in patients with systemic lupus erythematosus (SLE) in Korea. METHODS: We investigated the gene frequency of the TNFB alleles using DNA obtained from peripheral mononuclear cells in 141 healthy controls and in 58 patients with SLE. The polymorphisms of TNFB gene (735 bp) were studied by Ncol PCR-RELP. A portion of TNFB gene(735 bp) was amplified by PCR and its products were digested with Ncol restriction enzyme. The digested samples of amplified DNA were analyzed by agarose gel electrophoresis. TNFB(*)1 and TNFB(*)2 alleles were identified according to polymorphic fragments on Ncol restriction site in the first intron of the TNFB gene. The generic types of HLA-DRBI were also determined by PCR with sequence specific primers (SSP) using genomic DNA from the same subjects. RESULTS: The genotypic frequency of TNFB(*)2 homozygote was significantly increased in patients with SLE compared with controls (RR=2.36, P=0.011). The frequency of HLA-DRBI(*)15 was also significantly increased in patients (RR=2.27, P=0.029). However, the increased frequency of TNFB(*)2 homozygote was apparently increased in nephritis group (RR=2.79, P=0.035), whereas the significance of TNFB(*)2 homozygote was weakend in non-nephritis group. CONCLUSIONS: Our results suggest that genetic predisposition of TNFB(*)2 homozygote is another risk factor in Korean SLE, especially in DR2 negative patients. In addition, TNFB(*)2 homozygote could have a tendency for the development of nephritis in patients with SLE. |
format | Online Article Text |
id | pubmed-4532044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Korean Association of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-45320442015-10-02 TNFB Gene Polymorphism in Patients with Systemic Lupus Erythematosus in Korean Kim, Ho-Youn Lee, Sang-Heon Yang, Hyung-In Park, Sung-Hwan Cho, Chul-Soo Kim, Tai-Gyu Han, Hoon Kim, Dong-Jip Korean J Intern Med Original Article OBJECTIVES: To elucidate the gene frequency of TNFB Ncol polymorphism and its association with HLA class II antigen in patients with systemic lupus erythematosus (SLE) in Korea. METHODS: We investigated the gene frequency of the TNFB alleles using DNA obtained from peripheral mononuclear cells in 141 healthy controls and in 58 patients with SLE. The polymorphisms of TNFB gene (735 bp) were studied by Ncol PCR-RELP. A portion of TNFB gene(735 bp) was amplified by PCR and its products were digested with Ncol restriction enzyme. The digested samples of amplified DNA were analyzed by agarose gel electrophoresis. TNFB(*)1 and TNFB(*)2 alleles were identified according to polymorphic fragments on Ncol restriction site in the first intron of the TNFB gene. The generic types of HLA-DRBI were also determined by PCR with sequence specific primers (SSP) using genomic DNA from the same subjects. RESULTS: The genotypic frequency of TNFB(*)2 homozygote was significantly increased in patients with SLE compared with controls (RR=2.36, P=0.011). The frequency of HLA-DRBI(*)15 was also significantly increased in patients (RR=2.27, P=0.029). However, the increased frequency of TNFB(*)2 homozygote was apparently increased in nephritis group (RR=2.79, P=0.035), whereas the significance of TNFB(*)2 homozygote was weakend in non-nephritis group. CONCLUSIONS: Our results suggest that genetic predisposition of TNFB(*)2 homozygote is another risk factor in Korean SLE, especially in DR2 negative patients. In addition, TNFB(*)2 homozygote could have a tendency for the development of nephritis in patients with SLE. Korean Association of Internal Medicine 1995-07 /pmc/articles/PMC4532044/ /pubmed/7495771 http://dx.doi.org/10.3904/kjim.1995.10.2.130 Text en Copyright © 1995 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 Kim, Ho-Youn Lee, Sang-Heon Yang, Hyung-In Park, Sung-Hwan Cho, Chul-Soo Kim, Tai-Gyu Han, Hoon Kim, Dong-Jip TNFB Gene Polymorphism in Patients with Systemic Lupus Erythematosus in Korean |
title | TNFB Gene Polymorphism in Patients with Systemic Lupus Erythematosus in Korean |
title_full | TNFB Gene Polymorphism in Patients with Systemic Lupus Erythematosus in Korean |
title_fullStr | TNFB Gene Polymorphism in Patients with Systemic Lupus Erythematosus in Korean |
title_full_unstemmed | TNFB Gene Polymorphism in Patients with Systemic Lupus Erythematosus in Korean |
title_short | TNFB Gene Polymorphism in Patients with Systemic Lupus Erythematosus in Korean |
title_sort | tnfb gene polymorphism in patients with systemic lupus erythematosus in korean |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532044/ https://www.ncbi.nlm.nih.gov/pubmed/7495771 http://dx.doi.org/10.3904/kjim.1995.10.2.130 |
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