Exploring the pathogenesis and treatment of IgA nephropathy based on epigenetics

被引:1
|
作者
Zhang, Yunfan [1 ,2 ]
Yang, Huanhuan [1 ,2 ]
Jiang, Ming [1 ,2 ]
Nie, Xiaojing [1 ,2 ,3 ]
机构
[1] Fujian Med Univ, Fuzong Clin Med Coll, Fuzhou 350025, Peoples R China
[2] 900th Hosp Joint Logist Support Force, Dept Gynecol & Obstet, PLA, Fuzhou 350025, Fujian, Peoples R China
[3] Xiamen Univ, Affiliated Dongfang Hosp, Dept Pediat, Fuzhou 350025, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
epigenetic; histone modifications; IgA nephropathy; methylation; miRNAs; pathogenesis; treatment; DNA METHYLATION; T-CELLS; EXPRESSION; MIR-148B;
D O I
10.2217/epi-2023-0318
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
IgA nephropathy is the most common primary glomerulonephritis worldwide. However, its exact cause remains unclear, with known genetic factors explaining only 11% of the variation. Recently, researchers have turned their attention to epigenetic abnormalities in immune-related diseases, recognizing their significance in IgA nephropathy's development and progression. This emerging field has revolutionized our understanding of epigenetics in IgA nephropathy research. Though in its early stages, studying IgA nephropathy's epigenetics holds promise for unraveling its pathogenesis and identifying new biomarkers and therapies. This review aims to comprehensively analyze epigenetics' role in IgA nephropathy's development and suggest avenues for potential therapeutic interventions. In the future, assessing and modulating epigenetics may become integral in diagnosing, tailoring treatments and assessing prognoses for IgA nephropathy. Epigenetics is involved in the occurrence and development of IgA nephropathy.
引用
收藏
页码:1017 / 1026
页数:10
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