Medical Genetics Unit, Histology & Cell Biology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Faculty of Medicine, Center of Excellence in Molecular and Cellular Medicine, Suez Canal University, Ismailia, Egypt.
Mol Diagn Ther. 2023 May;27(3):405-423. doi: 10.1007/s40291-023-00646-1. Epub 2023 Apr 4.
Psoriasis and vitiligo are both chronic, skin-specific diseases classified as autoimmune diseases due to the involvement of several biochemical pathways in their pathogenesis, similar to those altered in other autoimmune diseases. The role of miRNAs in regulating skin autoimmune function has yet to be fully characterized.
The aim of this study was to assess the expression profile of a panel of 11 circulating immune-related miRNAs in patients with autoimmune skin diseases, specifically psoriasis and vitiligo, and correlate their expression signature with the clinicopathological features of the diseases.
Relative gene expression quantification for 11 immune-related circulating miRNAs in plasma was done for 300 subjects-100 patients with psoriasis, 100 patients with vitiligo and 100 normal healthy volunteers-followed by different modalities of bioinformatics analysis for the results.
The expression levels of all the studied immune-related miRNAs were elevated in both autoimmune skin disorders, with much higher levels of expression in psoriasis than in vitiligo patients. There was a significant correlation between most of the studied miRNAs, suggesting shared target genes and/or pathways. Moreover, all the studied miRNAs showed significant results as biomarkers for autoimmune skin disease, with miRNA-145 being the best candidate. Regarding the clinicopathological data, miRNA-7, miRNA-9, miRNA-145, miRNA-148a, and miRNA-148b were positively correlated with age. All the miRNAs were inversely correlated with obesity and disease duration.
This study highlights the critical role of miRNAs in skin-specific autoimmune diseases that proved to be potential biomarkers for autoimmune skin disorders, warranting their exploration as therapeutic targets.
银屑病和白癜风都是慢性、特定于皮肤的疾病,由于其发病机制涉及到几个生化途径,因此被归类为自身免疫性疾病,与其他自身免疫性疾病改变的途径相似。miRNAs 在调节皮肤自身免疫功能中的作用尚未得到充分描述。
本研究旨在评估一组 11 种循环免疫相关 miRNAs 在自身免疫性皮肤病患者(特别是银屑病和白癜风患者)中的表达谱,并将其表达特征与疾病的临床病理特征相关联。
对 300 名受试者(100 名银屑病患者、100 名白癜风患者和 100 名健康志愿者)的血浆中 11 种免疫相关循环 miRNAs 的相对基因表达进行定量,然后对结果进行不同模式的生物信息学分析。
所有研究的免疫相关 miRNAs 在两种自身免疫性皮肤病中均升高,银屑病患者的表达水平明显高于白癜风患者。大多数研究的 miRNAs 之间存在显著相关性,表明存在共同的靶基因和/或途径。此外,所有研究的 miRNAs 均作为自身免疫性皮肤病的生物标志物显示出显著结果,miRNA-145 是最佳候选者。关于临床病理数据,miRNA-7、miRNA-9、miRNA-145、miRNA-148a 和 miRNA-148b 与年龄呈正相关。所有 miRNA 与肥胖和疾病持续时间呈负相关。
本研究强调了 miRNAs 在皮肤特异性自身免疫性疾病中的关键作用,证明它们是自身免疫性皮肤病的潜在生物标志物,值得进一步探索作为治疗靶点。