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斑块状银屑病和点滴状银屑病中的三种视黄酸X受体基因多态性

Three retinoid X receptor gene polymorphisms in plaque psoriasis and psoriasis guttata.

作者信息

Vasků Vladimír, Bienertová Vasků Julie, Pávková Goldbergová Monika, Vasků Anna

机构信息

1st Department of Dermatology, St. Ann's Faculty Hospital, Masaryk University, Brno, Czech Republic.

出版信息

Dermatology. 2007;214(2):118-24. doi: 10.1159/000098569.

DOI:10.1159/000098569
PMID:17341859
Abstract

AIM

Polymorphisms in retinoid X receptors (RXRs) are very interesting from the point of view of a possible association of their variability with psoriasis.

METHODS

A total of 293 patients with plaque psoriasis, 82 patients with psoriasis guttata and 202 control subjects were enrolled in this study focused on 3 polymorphisms in RXRA and RXRB gene associations.

RESULTS

A marginally significant increase in AA allelic frequency of the RXRA A39526AA polymorphism in plaque psoriatic men compared to healthy men was proved. In women with psoriasis guttata, the higher risk for genotypes AA and TT in the RXRB 3'+140A/T polymorphism compared to healthy women was identified (p(corr) = 0.01). The genotypes A/A and AA/AA are more frequent in plaque psoriasis patients with a positive family history of psoriasis compared to the patients with a negative family history of psoriasis (p(corr) = 0.02). The A/A genotype is more frequent in patients with plaque psoriasis and repeated tonsillitis/tonsillectomy (p = 0.02). In the RXRB polymorphism, no genotype TT is observed in patients with psoriasis guttata with a positive personal history of repeated tonsillitis (p(corr) = 0.001).

CONCLUSION

Individual gene characteristics of patients with psoriasis improve the possibilities of pharmacotherapy using pharmacogenomic approaches which could be further stratified in future according to the subtypes of psoriasis.

摘要

目的

从类视黄醇X受体(RXRs)变异性与银屑病可能存在关联的角度来看,其多态性非常有趣。

方法

本研究纳入了293例斑块状银屑病患者、82例点滴状银屑病患者和202例对照受试者,重点关注RXRA和RXRB基因关联中的3种多态性。

结果

与健康男性相比,斑块状银屑病男性中RXRA A39526AA多态性的AA等位基因频率有边缘性显著增加。在点滴状银屑病女性中,与健康女性相比,RXRB 3'+140A/T多态性中AA和TT基因型的风险更高(校正p值 = 0.01)。与无银屑病家族史的斑块状银屑病患者相比,有银屑病家族史的斑块状银屑病患者中A/A和AA/AA基因型更为常见(校正p值 = 0.02)。A/A基因型在有斑块状银屑病且反复发生扁桃体炎/扁桃体切除术的患者中更为常见(p = 0.02)。在RXRB多态性中,有反复扁桃体炎个人史的点滴状银屑病患者未观察到TT基因型(校正p值 = 0.001)。

结论

银屑病患者的个体基因特征提高了使用药物基因组学方法进行药物治疗的可能性,未来可根据银屑病亚型进一步分层。

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