摘要
特发性血小板减少性紫癜是一种异质性自身免疫性疾病,是儿童最常见的出血性疾病,尤其慢性患儿的健康相关生活质量受到严重影响,但其病因及发病机制目前仍不清楚。研究发现,遗传因素可能参与该病的发生及预后。该文从其危险因素、基因多态性和表达水平与其易患性及病情严重情况的关系、表观遗传的作用、慢性难治性特发性血小板减少性紫癜相关研究等方面作一综述。
Idiopathic thrombocytopenic purpura (ITP),as a heterogeneous autoimmune disease,is the most common bleeding disorder,of which etiology and pathogenesis are still unclear. Health related quality of life are severely affected,especally in chronic patients . Studys on chronic idiopathic thrombocytopenic purpura pathogenesis ,both in China and abroad,have found that genetic factors may be involved in the occurrence and prognosis of the disease. The paper gives a review from the follow aspects,such as its risk factors,relationship between genetic polymorphisms or expression levels and chronic ITP susceptibility and seriousness,the role of epigenetic,researchs about chronic and refractory ITP,et al.
出处
《国际儿科学杂志》
2014年第5期534-537,共4页
International Journal of Pediatrics
基金
上海市科委重大课题子项目(12411952406)