伊朗患者系统性红斑狼疮的遗传和分子生物学概述。

Q1 Medicine Auto-Immunity Highlights Pub Date : 2021-01-30 DOI:10.1186/s13317-020-00144-y
Meisam Gachpazan, Iman Akhlaghipour, Hamid Reza Rahimi, Ehsan Saburi, Majid Mojarrad, Mohammad Reza Abbaszadegan, Meysam Moghbeli
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摘要

背景:系统性红斑狼疮(SLE系统性红斑狼疮(SLE)是一种影响不同器官和组织的临床病理异质性慢性自身免疫性疾病。据报道,系统性红斑狼疮在伊朗人口中的发病率越来越高。此外,与其他国家相比,伊朗系统性红斑狼疮患者的临床表现更为严重。因此,需要引入新的方法来早期检测这一人群中的系统性红斑狼疮。系统性红斑狼疮的进展与各种环境和遗传因素有关:在本综述中,我们总结了所有已报道的与伊朗患者系统性红斑狼疮临床病理特征相关的基因:结论:除了已报道的细胞因子和趋化因子外,有趣的是,与细胞凋亡相关的基因和非编码 RNA 是已报道的与伊朗系统性红斑狼疮进展相关的最多的基因异常。这篇综述阐明了伊朗病例中系统性红斑狼疮进展的遗传学和分子生物学。此外,这篇综述还为在伊朗人群中引入高效的遗传标记小组,以便早期检测和更好地管理系统性红斑狼疮铺平了道路。
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Genetic and molecular biology of systemic lupus erythematosus among Iranian patients: an overview.

Background: Systemic lupus erythematosus (SLE) is a clinicopathologically heterogeneous chronic autoimmune disorder affecting different organs and tissues. It has been reported that there is an increasing rate of SLE incidence among Iranian population. Moreover, the Iranian SLE patients have more severe clinical manifestations compared with other countries. Therefore, it is required to introduce novel methods for the early detection of SLE in this population. Various environmental and genetic factors are involved in SLE progression.

Main body: In present review we have summarized all of the reported genes which have been associated with clinicopathological features of SLE among Iranian patients.

Conclusions: Apart from the reported cytokines and chemokines, it was interestingly observed that the apoptosis related genes and non-coding RNAs were the most reported genetic abnormalities associated with SLE progression among Iranians. This review clarifies the genetics and molecular biology of SLE progression among Iranian cases. Moreover, this review paves the way of introducing an efficient panel of genetic markers for the early detection and better management of SLE in this population.

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