The role of 39 psoriasis risk variants on age of psoriasis onset.

ISRN Dermatology Pub Date : 2013-09-23 eCollection Date: 2013-01-01 DOI:10.1155/2013/203941
Yingchang Lu, Sinae Kane, Haoyan Chen, Argentina Leon, Ethan Levin, Tien Nguyen, Maya Debbaneh, Jillian W Millsop, Rishu Gupta, Monica Huynh, Daniel Butler, Kelly Cordoro, Wilson Liao
{"title":"The role of 39 psoriasis risk variants on age of psoriasis onset.","authors":"Yingchang Lu,&nbsp;Sinae Kane,&nbsp;Haoyan Chen,&nbsp;Argentina Leon,&nbsp;Ethan Levin,&nbsp;Tien Nguyen,&nbsp;Maya Debbaneh,&nbsp;Jillian W Millsop,&nbsp;Rishu Gupta,&nbsp;Monica Huynh,&nbsp;Daniel Butler,&nbsp;Kelly Cordoro,&nbsp;Wilson Liao","doi":"10.1155/2013/203941","DOIUrl":null,"url":null,"abstract":"<p><p>Recent genome-wide association studies (GWAS) have identified multiple genetic risk factors for psoriasis, but data on their association with age of onset have been marginally explored. The goal of this study was to evaluate known risk alleles of psoriasis for association with age of psoriasis onset in three well-defined case-only cohorts totaling 1,498 psoriasis patients. We selected 39 genetic variants from psoriasis GWAS and tested these variants for association with age of psoriasis onset in a meta-analysis. We found that rs10484554 and rs12191877 near HLA-C and rs17716942 near IFIH1 were associated with age of psoriasis onset with false discovery rate < 0.05. The association between rs17716942 and age of onset was not replicated in a fourth independent cohort of 489 patients (P = 0.94). The imputed HLA-C∗06:02 allele demonstrated a much stronger association with age of psoriasis onset than rs10484554 and rs12191877. We conclude that despite the discovery of numerous psoriasis risk alleles, HLA-C∗06:02 still plays the most important role in determining the age of onset of psoriasis. Larger studies are needed to evaluate the contribution of other risk alleles, including IFIH1, to age of psoriasis onset. </p>","PeriodicalId":14682,"journal":{"name":"ISRN Dermatology","volume":" ","pages":"203941"},"PeriodicalIF":0.0000,"publicationDate":"2013-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2013/203941","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ISRN Dermatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2013/203941","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

Abstract

Recent genome-wide association studies (GWAS) have identified multiple genetic risk factors for psoriasis, but data on their association with age of onset have been marginally explored. The goal of this study was to evaluate known risk alleles of psoriasis for association with age of psoriasis onset in three well-defined case-only cohorts totaling 1,498 psoriasis patients. We selected 39 genetic variants from psoriasis GWAS and tested these variants for association with age of psoriasis onset in a meta-analysis. We found that rs10484554 and rs12191877 near HLA-C and rs17716942 near IFIH1 were associated with age of psoriasis onset with false discovery rate < 0.05. The association between rs17716942 and age of onset was not replicated in a fourth independent cohort of 489 patients (P = 0.94). The imputed HLA-C∗06:02 allele demonstrated a much stronger association with age of psoriasis onset than rs10484554 and rs12191877. We conclude that despite the discovery of numerous psoriasis risk alleles, HLA-C∗06:02 still plays the most important role in determining the age of onset of psoriasis. Larger studies are needed to evaluate the contribution of other risk alleles, including IFIH1, to age of psoriasis onset.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
39种牛皮癣风险变异对牛皮癣发病年龄的影响。
最近的全基因组关联研究(GWAS)已经确定了银屑病的多种遗传风险因素,但它们与发病年龄的关联数据尚未得到充分探讨。本研究的目的是在三个明确的病例队列中评估已知的牛皮癣风险等位基因与牛皮癣发病年龄的关系,共1498例牛皮癣患者。我们从银屑病GWAS中选择了39个遗传变异,并在荟萃分析中测试了这些变异与银屑病发病年龄的关系。我们发现靠近HLA-C的rs10484554和rs12191877以及靠近IFIH1的rs17716942与牛皮癣发病年龄相关,假发现率< 0.05。在489例患者的第四个独立队列中,rs17716942与发病年龄之间的关联未被复制(P = 0.94)。与rs10484554和rs12191877相比,HLA-C∗06:02等位基因与牛皮癣发病年龄的相关性更强。我们的结论是,尽管发现了许多牛皮癣风险等位基因,HLA-C∗06:02仍然在决定牛皮癣发病年龄方面起着最重要的作用。需要更大规模的研究来评估其他风险等位基因,包括IFIH1,对牛皮癣发病年龄的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Nanotechnology-based cosmeceuticals. Hypertrichosis Is Not so Prevalent in Becker's Nevus: Analysis of 47 Cases. Correlation of Vitamin D Levels with Pigmentation in Vitiligo Patients Treated with NBUVB Therapy. Histological comparison of two cryopeeling methods for photodamaged skin. Prevalence of psychological disorders in patients with alopecia areata in comparison with normal subjects.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1