A Pilot Genome-Wide Association Study Identifies Novel Markers of Metabolic Syndrome in Patients with Psoriasis.

IF 1.5 4区 医学 Q3 DERMATOLOGY Annals of Dermatology Pub Date : 2023-08-01 DOI:10.5021/ad.22.196
Seung-Min Oh, Su-Kang Kim, Hye-Jin Ahn, Ki-Heon Jeong
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引用次数: 1

Abstract

Background: Recent studies have reported that psoriasis is associated with the development of metabolic syndrome. Genome-wide association studies have been used to discover gene variant markers that occur frequently in case group in relation to specific diseases.

Objective: The aim of the present study was to investigate the variants of specific genes involved in metabolic syndrome associated with psoriasis.

Methods: A total of 95 psoriasis patients were recruited and divided into two groups: one with metabolic syndrome (38 patients) and the other without (57 patients). After genotyping, imputation, and quality checking, the association between the several single nucleotide polymorphisms and metabolic syndrome in psoriasis was tested, followed by gene set enrichment analysis.

Results: We found 76 gene polymorphisms that conferred an increased risk for metabolic syndrome in patients with psoriasis. Four single nucleotide polymorphisms (rs17154774 of FRMD4A, rs77498336 of GPR116, rs75949580 and rs187682251 of MAPK4) showed the strongest association between metabolic syndrome and psoriasis. The epidermal growth factor receptor protein was located at the center of the protein interactions for the gene polymorphisms.

Conclusion: This study identified several previously unknown polymorphisms associated with metabolic syndrome in psoriasis. These results highlight the potential for future genetic studies to elucidate the development, and ultimately prevent the onset, of metabolic syndrome in patients with psoriasis.

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一项试点全基因组关联研究确定了银屑病患者代谢综合征的新标志物。
背景:最近的研究报道牛皮癣与代谢综合征的发展有关。全基因组关联研究已被用于发现与特定疾病相关的病例组中经常发生的基因变异标记。目的:本研究的目的是研究与牛皮癣相关的代谢综合征相关的特定基因变异。方法:招募95例银屑病患者,将其分为两组:有代谢综合征组(38例)和无代谢综合征组(57例)。经过基因分型、代入和质量检查,检测了几种单核苷酸多态性与银屑病代谢综合征之间的关系,然后进行基因集富集分析。结果:我们发现76个基因多态性与牛皮癣患者代谢综合征的风险增加有关。4个单核苷酸多态性(FRMD4A的rs17154774、GPR116的rs77498336、MAPK4的rs75949580和rs187682251)显示代谢综合征与银屑病的相关性最强。表皮生长因子受体蛋白位于基因多态性蛋白相互作用的中心。结论:本研究发现了一些以前未知的与银屑病代谢综合征相关的多态性。这些结果强调了未来遗传学研究的潜力,以阐明牛皮癣患者代谢综合征的发展,并最终预防发病。
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来源期刊
Annals of Dermatology
Annals of Dermatology 医学-皮肤病学
CiteScore
1.60
自引率
6.20%
发文量
77
审稿时长
6-12 weeks
期刊介绍: Annals of Dermatology (Ann Dermatol) is the official peer-reviewed publication of the Korean Dermatological Association and the Korean Society for Investigative Dermatology. Since 1989, Ann Dermatol has contributed as a platform for communicating the latest research outcome and recent trend of dermatology in Korea and all over the world. Ann Dermatol seeks for ameliorated understanding of skin and skin-related disease for clinicians and researchers. Ann Dermatol deals with diverse skin-related topics from laboratory investigations to clinical outcomes and invites review articles, original articles, case reports, brief reports and items of correspondence. Ann Dermatol is interested in contributions from all countries in which good and advanced research is carried out. Ann Dermatol willingly recruits well-organized and significant manuscripts with proper scope throughout the world.
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