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维生素D受体基因多态性rs1544410 T/T基因型作为寻常型银屑病患者维生素D阈值缺乏因素的预测指标——一项初步研究

The vitamin D receptor gene polymorphism rs1544410 T/T genotype as a predictor of factor vitamin D thresholds deficiency in patients with psoriasis vulgaris-A preliminary study.

作者信息

AbdElneam Ahmed Ibrahim, Al-Dhubaibi Mohammed Saleh, Bahaj Saleh Salem, Mohammed Ghada Farouk

机构信息

Department of Clinical Biochemistry and, Department of Basic Medical Sciences, College of Medicine, Shaqra University, Dawadmi, Saudi Arabia.

Molecular Genetics and Enzymology Department, Human Genetics and Genome Research Institute, National Research Center, Cairo, Egypt.

出版信息

J Cosmet Dermatol. 2023 May;22(5):1642-1646. doi: 10.1111/jocd.15625. Epub 2023 Jan 31.

Abstract

BACKGROUND

Many clinical features of psoriasis include a rash with itchy, scaly patches, most frequently on the knees, elbows, trunk, and scalp. By studying genes involved with psoriasis receptivity, the pathologic pathways of psoriasis become clearer and more understood.

AIM

To predict the participation of rs1544410 in serum vitamin D levels (SDL) in psoriasis, psoriasis susceptibility, and severity.

PATIENTS/METHODS: One hundred five patients with psoriasis were categorized by body surface area as mild, moderate, and severe. SDL and genetic analysis of rs1544410 were performed using polymerase chain reaction and standard Sanger methods.

RESULT

Our findings revealed that SDL were higher in healthy subjects than in patients. The rs1544410 genotype TT was more prevalent in patients, while CT was more prevalent in controls. Our findings revealed that the T alleles were frequently more in the patient group than in the controls. (p ≤ 0.001). While in healthy normal individuals, the C alleles were frequently more (p ≤ 0.001). SDL are lower in patients with the TT genotype. Patients with moderate form of psoriasis have higher SDL than those with mild or severe form.

CONCLUSION

rs1544410 polymorphism has been linked to a higher probability of psoriasis and SDL deficiency. However, grander scale studies in a larger number of people are necessary.

摘要

背景

银屑病的许多临床特征包括出现伴有瘙痒、鳞屑斑块的皮疹,最常见于膝盖、肘部、躯干和头皮。通过研究与银屑病易感性相关的基因,银屑病的病理途径变得更加清晰且易于理解。

目的

预测rs1544410在银屑病患者血清维生素D水平(SDL)、银屑病易感性及严重程度中的作用。

患者/方法:105例银屑病患者按体表面积分为轻度、中度和重度。采用聚合酶链反应和标准桑格法进行SDL测定及rs1544410基因分析。

结果

我们的研究结果显示,健康受试者的SDL高于患者。rs1544410基因型TT在患者中更为常见,而CT在对照组中更为常见。我们的研究结果显示,患者组中的T等位基因频率通常高于对照组(p≤0.001)。而在健康正常个体中,C等位基因频率通常更高(p≤0.001)。TT基因型患者的SDL较低。中度银屑病患者的SDL高于轻度或重度患者。

结论

rs1544410多态性与银屑病发生概率较高及SDL缺乏有关。然而,需要在更多人群中进行更大规模的研究。

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