中国人群中COX2功能多态性与白癜风风险的关联。

Association of COX2 functional polymorphisms and the risk of vitiligo in Chinese populations.

作者信息

Li Miao, Gao Ying, Li Chunying, Liu Ling, Li Kai, Gao Lin, Wang Gang, Zhang Zhengdong, Gao Tianwen

机构信息

Department of Dermatology of Xijing Hospital, Fourth Military Medical University, Xi'an, China.

出版信息

J Dermatol Sci. 2009 Mar;53(3):176-81. doi: 10.1016/j.jdermsci.2008.09.010. Epub 2008 Nov 12.

Abstract

BACKGROUND

Cyclooxygenase-2 (COX2) plays an important role in the production of prostaglandin E2 (PGE2), which is made by epidermal keratinocytes in response to ultraviolet radiation (UVR). PGE2 is important for the proliferation and melanogenesis of epidermal melanocytes, the loss of which leads to vitiligo. COX2-1195A>G, -765G>C, and -8473T>C polymorphisms may influence the mRNA levels of COX2 and affect the production of PGE2 subsequently. Therefore, we supposed that these polymorphisms may be associated with vitiligo.

OBJECTIVE

The aim of the study was to elucidate the association between three functional COX2 polymorphisms and the risk of vitiligo.

METHODS

This was a hospital-based, case-control study of 755 vitiligo patients and 774 vitiligo-free controls who were frequency matched by age and sex. We genotyped COX2-1195A>G, -765G>C, and -8473T>C polymorphisms by using PCR-restriction fragment length polymorphism (RFLP) method and assessed their respective associations with the risk of vitiligo in Han Chinese populations.

RESULTS

We found a statistically significant increased risk of vitiligo to be associated with the COX2-1195 G variant allele (p=0.004). Significantly higher vitiligo risks were found among subgroups with these characteristics: age >20 years, male, active, nonsegmental vitiligo, and onset age >20 years. In addition, the interaction between COX2-1195 and COX2-8473 was statistically significant (p=0.004).

CONCLUSION

For the first time, we provide evidence that functional polymorphisms in the COX2 gene may influence the risk of vitiligo in Han Chinese populations, suggesting new clues that help to clarify the pathogenesis of vitiligo. Larger studies are needed to verify these findings.

摘要

背景

环氧合酶-2(COX2)在前列腺素E2(PGE2)的产生中起重要作用,PGE2由表皮角质形成细胞响应紫外线辐射(UVR)产生。PGE2对表皮黑素细胞的增殖和黑素生成很重要,其缺失会导致白癜风。COX2 -1195A>G、-765G>C和-8473T>C多态性可能影响COX2的mRNA水平,进而影响PGE2的产生。因此,我们推测这些多态性可能与白癜风有关。

目的

本研究旨在阐明COX2三个功能性多态性与白癜风风险之间的关联。

方法

这是一项基于医院的病例对照研究,纳入755例白癜风患者和774例无白癜风的对照,按年龄和性别进行频率匹配。我们采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对COX2 -1195A>G、-765G>C和-8473T>C多态性进行基因分型,并评估它们与汉族人群白癜风风险的各自关联。

结果

我们发现携带COX2 -1195 G变异等位基因与白癜风风险显著增加相关(p = 0.004)。在具有以下特征的亚组中发现白癜风风险显著更高:年龄>20岁、男性、进展期、非节段性白癜风以及发病年龄>20岁。此外,COX2 -1195与COX2 -8473之间的相互作用具有统计学意义(p = 0.004)。

结论

我们首次提供证据表明,COX2基因中的功能性多态性可能影响汉族人群患白癜风的风险,为阐明白癜风的发病机制提供了新线索。需要更大规模的研究来验证这些发现。

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