Literature DB >> 1976809

Lack of gene deletion for complement C4A deficiency in Japanese patients with systemic lupus erythematosus.

H Yamada1, A Watanabe, A Mimori, K Nakano, F Takeuchi, K Matsuta, K Tanimoto, T Miyamoto, Y Yukiyama, K Tokunaga.   

Abstract

The frequency of C4A gene deletion was studied in Japanese patients with systemic lupus erythematosus (SLE) and was compared with healthy controls. DNA preparations were extracted from peripheral blood leukocytes from 59 patients with SLE and from 166 healthy persons, and digested by restriction enzymes. They were hybridized with C4 complementary DNA by the Southern blotting method and the deletion of C4A gene was judged from restriction fragment length polymorphism. At the same time phenotypic C4A deficiency (C4AQ0) was measured. Our results showed that the frequency of phenotypic C4A deficiency was 44.1% in Japanese patients with SLE and this value was comparable with that (43.2%) in Caucasian patients. On the other hand the deletion of C4A gene was not found in Japanese patients with SLE (0%), or in healthy controls (0.6%). Our results indicate that C4AQ0 may contribute to the pathogenesis of SLE beyond the ethnical differences but Japanese patients with SLE have a different genetic background from Caucasian patients with the C4A gene deleted.

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Year:  1990        PMID: 1976809

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  7 in total

1.  A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population.

Authors:  Tetsuya Oishi; Aritoshi Iida; Shigeru Otsubo; Yoichiro Kamatani; Masayuki Usami; Takashi Takei; Keiko Uchida; Ken Tsuchiya; Susumu Saito; Yozo Ohnisi; Katsushi Tokunaga; Kosaku Nitta; Yasushi Kawaguchi; Naoyuki Kamatani; Yuta Kochi; Kenichi Shimane; Kazuhiko Yamamoto; Yusuke Nakamura; Wako Yumura; Koichi Matsuda
Journal:  J Hum Genet       Date:  2008-01-25       Impact factor: 3.172

2.  Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4-deficient patients with systemic lupus erythematosus (SLE).

Authors:  M A Dragon-Durey; N Rougier; J P Clauvel; S Caillat-Zucman; P Remy; L Guillevin; F Liote; J Blouin; F Ariey; B U Lambert; M D Kazatchkine; L Weiss
Journal:  Clin Exp Immunol       Date:  2001-01       Impact factor: 4.330

3.  Confirmation of C4 gene copy number variation and the association with systemic lupus erythematosus in Chinese Han population.

Authors:  Yongmei Lv; Sumin He; Zheng Zhang; Yang Li; Dayan Hu; Kunju Zhu; Hui Cheng; Fusheng Zhou; Gang Chen; Xiaodong Zheng; Pan Li; Yunqing Ren; Xianyong Yin; Yong Cui; Liangdan Sun; Sen Yang; Xuejun Zhang
Journal:  Rheumatol Int       Date:  2011-09-09       Impact factor: 2.631

4.  DNase I hypersensitivity mapping and promoter polymorphism analysis of human C4.

Authors:  A K Vaishnaw; R Hargreaves; R D Campbell; B J Morley; M J Walport
Journal:  Immunogenetics       Date:  1995       Impact factor: 2.846

5.  Major histocompatibility complex haplotypes and complement C4 alleles in systemic lupus erythematosus. Results of a multicenter study.

Authors:  K Hartung; M P Baur; R Coldewey; M Fricke; J R Kalden; H J Lakomek; H H Peter; D Schendel; P M Schneider; S A Seuchter
Journal:  J Clin Invest       Date:  1992-10       Impact factor: 14.808

6.  Fc gamma RIIA alleles are heritable risk factors for lupus nephritis in African Americans.

Authors:  J E Salmon; S Millard; L A Schachter; F C Arnett; E M Ginzler; M F Gourley; R Ramsey-Goldman; M G Peterson; R P Kimberly
Journal:  J Clin Invest       Date:  1996-03-01       Impact factor: 14.808

7.  Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population.

Authors:  Yoichiro Kamatani; Koichi Matsuda; Tetsuya Ohishi; Shigeru Ohtsubo; Keiko Yamazaki; Aritoshi Iida; Naoya Hosono; Michiaki Kubo; Wako Yumura; Kosaku Nitta; Toyomasa Katagiri; Yasushi Kawaguchi; Naoyuki Kamatani; Yusuke Nakamura
Journal:  J Hum Genet       Date:  2007-12-06       Impact factor: 3.172

  7 in total

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