Study of leptin gene polymorphism and leptin serum level in alopecia areata patients.

Q2 Health Professions
Heba Bazid, Mostafa Hammam, Mohammed Mostafa, Yasmine Gamal, Eman M Abd El Gayed
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引用次数: 0

Abstract

Leptin, produced by adipocytes, regulates metabolism, hunger, and immune response. The inflammatory role of leptin has been linked to autoimmune diseases. To assess leptin gene polymorphism and serum level in alopecia areata and their relation to metabolic syndrome (MS). This case-control study was conducted on 100 alopecia areata patients (50 with MS and 50 without MS) and 50 age- and gender-matched controls. Leptin gene polymorphism and serum level were assessed through the use of PCR and ELISA, respectively. GG genotype was the highest in AA with MS (54%), lower in AA without MS (42%), and the lowest in controls (20%). G allele was more expressed in cases, than in controls (P < .001). The serum leptin level was the highest in AA with MS, lower in AA without MS, and the lowest in controls (P value = 0.001). Leptin level was significantly higher in GG polymorphism than AG and AA. Leptin gene polymorphism (GG genotype) and serum level appear to play a significant role in AA. Absent difference regarding leptin gene polymorphism and MS might indicate a separate inflammatory role of leptin or the future risk of MS development in AA patients.

斑秃患者瘦素基因多态性及血清瘦素水平的研究。
瘦素由脂肪细胞产生,调节新陈代谢、饥饿感和免疫反应。瘦素的炎症作用与自身免疫性疾病有关。探讨斑秃患者瘦素基因多态性及血清水平与代谢综合征(MS)的关系。本病例对照研究对100名斑秃患者(50名多发性硬化症患者和50名非多发性硬化症患者)和50名年龄和性别匹配的对照组进行了研究。分别采用PCR和ELISA检测瘦素基因多态性和血清水平。GG基因型在AA合并多发性硬化症中最高(54%),在AA不合并多发性硬化症中最低(42%),在对照组中最低(20%)。G等位基因在病例中的表达高于对照组(P值= 0.001)。GG多态性中瘦素水平显著高于AG和AA。瘦素基因多态性(GG基因型)和血清水平在AA中起重要作用。瘦素基因多态性与多发性硬化症无差异,可能提示AA患者瘦素有单独的炎症作用或未来发生多发性硬化症的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
38
审稿时长
>12 weeks
期刊介绍: The Journal of Immunoassay & Immunochemistry is an international forum for rapid dissemination of research results and methodologies dealing with all aspects of immunoassay and immunochemistry, as well as selected aspects of immunology. They include receptor assay, enzyme-linked immunosorbent assay (ELISA) in all of its embodiments, ligand-based assays, biological markers of ligand-receptor interaction, in vivo and in vitro diagnostic reagents and techniques, diagnosis of AIDS, point-of-care testing, clinical immunology, antibody isolation and purification, and others.
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