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Combination of TNF-RII, CYP1A1 and GSTM1 polymorphisms and the risk of Japanese SLE: findings from the KYSS study.

https://repo.qst.go.jp/records/46141
https://repo.qst.go.jp/records/46141
e0af93f7-fa63-4836-bb7d-2fb657b1b6ea
Item type 学術雑誌論文 / Journal Article(1)
公開日 2011-07-14
タイトル
タイトル Combination of TNF-RII, CYP1A1 and GSTM1 polymorphisms and the risk of Japanese SLE: findings from the KYSS study.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Horiuchi, Takahiko

× Horiuchi, Takahiko

WEKO 459382

Horiuchi, Takahiko

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Washio, Masakazu

× Washio, Masakazu

WEKO 459383

Washio, Masakazu

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Kiyohara, Chikako

× Kiyohara, Chikako

WEKO 459384

Kiyohara, Chikako

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Asami, Toyoko

× Asami, Toyoko

WEKO 459385

Asami, Toyoko

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Kobashi, Gen

× Kobashi, Gen

WEKO 459386

Kobashi, Gen

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et.al

× et.al

WEKO 459387

et.al

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小橋 元

× 小橋 元

WEKO 459388

en 小橋 元

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抄録
内容記述タイプ Abstract
内容記述 OBJECTIVES: Association of the polymorphisms of the genes, TNF receptor type II gene (TNF-RII), cytochrome P4501A1 gene (CYP1A1) and glutathione S-transferase M1 gene (GSTM1), with SLE was investigated. TNF-RII mediates inflammatory and immune response, whereas CYP1A1 and GSTM1 are involved in the metabolism of xenobiotics. These three genes are involved in the generation of reactive oxygen species (ROS), which play a critical role for autoimmune diseases.
\nMETHODS: A total of 152 SLE patients and 427 healthy individuals in a female Japanese population were enrolled in the study. Case-control studies were performed for the polymorphisms of these three genes.
\nRESULTS: The carriers of TNF-RII 196R were at a significantly increased risk for SLE with odds ratio (OR) of 1.59 (95% CI = 1.01, 2.52). CYP1A1 3801C homozygotes had a significantly increased risk of SLE (OR = 2.47, 95% CI = 1.28, 4.78). On the other hand, GSTM1 null genotype was not associated with SLE risk. As for combination action of two loci, CYP1A1 3801C/GSTM1 null combination was more strongly associated with an increased risk of SLE (OR = 4.35; 95% CI = 1.76, 10.73). Moreover, TNF-RII 196M/CYP1A1 3801C/GSTM1 null genotype combination was most significantly associated with SLE (OR = 5.83; 95% CI = 2, 17.04).
\nCONCLUSIONS: The individuals carrying two or more 'at-risk' genotypes of TNF-RII, CYP1A1 and GSTM1 had a significantly more increased risk for SLE compared with those having each 'at-risk' genotype. Combination of the risk genotypes will be important to more clearly identify the population at risk for SLE.
書誌情報 Rheumatology

巻 48, 号 9, p. 1045-1049, 発行日 2009-09
ISSN
収録物識別子タイプ ISSN
収録物識別子 1462-0324
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