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斑秃埃及患者的脂联素血清水平和 ADIPOQ(rs2241766) 多态性。

Adiponectin serum levels and ADIPOQ (rs2241766) polymorphism in alopecia areata Egyptian patients.

机构信息

Dermatology, Andrology and STDs Department, Faculty of Medicine, Menoufia University, Shebin El-Kom, Menoufia, Egypt.

Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Menoufia University, Shebin El-Kom, Menoufia, Egypt.

出版信息

An Bras Dermatol. 2024 Mar-Apr;99(2):181-188. doi: 10.1016/j.abd.2023.05.003. Epub 2023 Nov 18.

Abstract

BACKGROUND

Alopecia Areata (AA) is an acquired autoimmune form of non-scarring hair loss. Adiponectin and its gene polymorphism were related to many autoimmune disorders.

OBJECTIVE

Assessment of adiponectin serum levels and adiponectin gene (ADIPOQ) (rs2241766) Single Nucleoid Polymorphism (SNP) in AA patients and correlating the results with the disease severity in those patients.

METHODS

This study included 75 AA patients and 75 age and gender-matched healthy subjects (controls). The severity of Alopecia Tool (SALT) score assessment to evaluate AA severity was done. Adiponectin serum levels by ELISA and ADIPOQ (rs2241766) SNP using PCR were performed.

RESULTS

Adiponectin serum levels were significantly lower in AA patients than controls (p = 0.001). ADIPOQ (rs2241766) TG genotype and G allele were significantly predominant in AA patients increasing its risk by 5 and 4 folds (OR = 5.17, p = 0.001), (OR = 3.82, p = 0.001) respectively. Serum adiponectin levels were negatively correlated with SALT score (r = -0.435, p = 0.001) and associated with alopecia totalis (p = 0.016). ADIPOQ (rs2241766) TG genotype was significantly associated with low serum adiponectin levels and higher SALT score (p = 0.001).

STUDY LIMITATIONS

The small sample size.

CONCLUSIONS

ADIPOQ (rs2241766) gene polymorphism (TG genotype and G allele) may modulate AA risk and contribute to the development of AA in Egyptian populations. Decreased circulating adiponectin levels may have a dynamic role in AA etiopathogenesis. Adiponectin serum concentration can be considered a severity marker of hair loss in AA.

摘要

背景

斑秃(AA)是一种获得性自身免疫性非瘢痕性脱发。脂联素及其基因多态性与许多自身免疫性疾病有关。

目的

评估斑秃患者血清脂联素水平和脂联素基因(ADIPOQ)(rs2241766)单核苷酸多态性(SNP),并将结果与患者疾病严重程度相关联。

方法

本研究纳入 75 例斑秃患者和 75 名年龄和性别匹配的健康对照者(对照组)。采用脱发严重程度评估工具(SALT)评分评估 AA 严重程度。采用 ELISA 法检测血清脂联素水平,采用 PCR 法检测 ADIPOQ(rs2241766)SNP。

结果

与对照组相比,斑秃患者血清脂联素水平显著降低(p=0.001)。ADIPOQ(rs2241766)TG 基因型和 G 等位基因在斑秃患者中明显占优势,其风险分别增加 5 倍和 4 倍(OR=5.17,p=0.001),(OR=3.82,p=0.001)。血清脂联素水平与 SALT 评分呈负相关(r=-0.435,p=0.001),与全秃相关(p=0.016)。ADIPOQ(rs2241766)TG 基因型与低血清脂联素水平和高 SALT 评分显著相关(p=0.001)。

研究局限性

样本量小。

结论

ADIPOQ(rs2241766)基因多态性(TG 基因型和 G 等位基因)可能调节 AA 风险,并有助于埃及人群中 AA 的发生。循环脂联素水平降低可能在 AA 的发病机制中起动态作用。血清脂联素浓度可作为 AA 脱发严重程度的标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b1/10943264/fafa07d92445/gr1.jpg

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