Dabravolski Siarhei A, Churov Alexey V, Starodubtseva Irina A, Beloyartsev Dmitry F, Kovyanova Tatiana I, Sukhorukov Vasily N, Orekhov Nikolay A
Department of Biotechnology Engineering, Braude Academic College of Engineering, Snunit 51, Karmiel 2161002, Israel.
Institute of General Pathology and Pathophysiology, 8 Baltiyskaya Street, 125315 Moscow, Russia.
Diagnostics (Basel). 2024 Sep 13;14(18):2035. doi: 10.3390/diagnostics14182035.
Sjögren's syndrome (SS) is a chronic autoimmune disorder characterised by lymphocytic infiltration of the exocrine glands, which leads to dryness of the eyes and mouth; systemic manifestations such as arthritis, vasculitis, and interstitial lung disease; and increased risks of lymphoma and cardiovascular diseases. SS predominantly affects women, with a strong genetic component linked to sex chromosomes. Genome-wide association studies (GWASs) have identified numerous single-nucleotide polymorphisms (SNPs) associated with primary SS (pSS), revealing insights into its pathogenesis. The adaptive and innate immune systems are crucial to SS's development, with viral infections implicated as environmental triggers that exacerbate autoimmune responses in genetically susceptible individuals. Moreover, recent research has highlighted the role of vitamin D in modulating immune responses in pSS patients, suggesting its potential therapeutic implications. In this review, we focus on the recently identified SNPs in genes like OAS1, NUDT15, LINC00243, TNXB, and THBS1, which have been associated with increased risks of developing more severe symptoms and other diseases such as fatigue, lymphoma, neuromyelitis optica spectrum disorder (NMOSD), dry eye syndrome (DES), and adverse drug reactions. Future studies should focus on larger, multi-ethnic cohorts with standardised protocols to validate findings and identify new associations. Integrating genetic testing into clinical practise holds promise for improving SS management and treatment strategies, enabling personalised interventions based on comprehensive genetic profiles. By focusing on specific SNPs, vitamin D, and their implications, future research can lead to more effective and personalised approaches for managing pSS and its complications.
干燥综合征(SS)是一种慢性自身免疫性疾病,其特征是外分泌腺淋巴细胞浸润,导致眼干和口干;还会出现关节炎、血管炎和间质性肺病等全身表现;以及淋巴瘤和心血管疾病风险增加。SS主要影响女性,有一个与性染色体相关的强大遗传成分。全基因组关联研究(GWAS)已经确定了许多与原发性干燥综合征(pSS)相关的单核苷酸多态性(SNP),揭示了其发病机制。适应性免疫系统和先天性免疫系统对SS的发展至关重要,病毒感染被认为是环境触发因素,会加剧遗传易感个体的自身免疫反应。此外,最近的研究强调了维生素D在调节pSS患者免疫反应中的作用,表明了其潜在的治疗意义。在这篇综述中,我们重点关注最近在OAS1、NUDT15、LINC00243、TNXB和THBS1等基因中发现的SNP,这些SNP与出现更严重症状以及疲劳、淋巴瘤、视神经脊髓炎谱系障碍(NMOSD)、干眼症综合征(DES)和药物不良反应等其他疾病的风险增加有关。未来的研究应集中在更大规模、多民族的队列上,采用标准化方案来验证研究结果并确定新的关联。将基因检测纳入临床实践有望改善SS的管理和治疗策略,实现基于全面基因图谱的个性化干预。通过关注特定的SNP、维生素D及其影响,未来的研究可以为管理pSS及其并发症带来更有效和个性化的方法。