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中国临床研究英文版:2022,35(10):1449-1453
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复发性流产与遗传性易栓症的研究进展
(1. 山西医科大学第一临床医学院,山西 太原 030000;2. 山西医科大学第一医院,山西 太原 030000;3. 山西省妇幼保健院,山西 太原 030000)
Research progress of recurrent abortion and hereditary thrombophilia
摘要
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Received:February 17, 2022   Published Online:October 20, 2022
中文摘要: 复发性流产(RSA)是指3次或3次以上于妊娠28周之前的胎儿丢失,目前认为连续发生2次流产即应重视并予评估。RSA发病机制较为复杂,目前已知的病因包括流行病学因素、子宫结构异常、血栓前状态、遗传因素、内分泌因素、感染因素、免疫因素、其他因素(如不良环境因素、压力因素等),但仍有50%~60%的病例无法解释。近年来RSA与血栓前状态的关系成为国内外的研究热点,遗传性易栓症包括蛋白C、蛋白S和抗凝血酶Ⅲ缺乏、FⅤL基因突变、HHcy、MTHFR基因突变、凝血酶原基因突变、凝血因子异常等。尽管遗传性易栓症与RSA的相关性备受争议,但有专家建议进行遗传性易栓症的筛查,并进行抗凝治疗,可在一定程度上改善其妊娠结局。本文对RSA与遗传性易栓症关系的研究进展作一综述。
Abstract:Recurrent spontaneous abortion(RSA) refers to 3 or more fetal loss before 28 weeks of gestation. Currently, it is considered that the occurrence of 2 consecutive abortions should be valued and evaluated.The pathogenesis of RSA is relatively complex. Currently known etiology includes epidemiological factors, abnormal uterine structure, prethrombotic state(also known as embolism), genetic factors, endocrine factors, infectious factors, immune factors, and other factors(such as adverse environmental factors, stress factors, etc.), but 50%-60% of cases cannot be explained.In recent years, the relationship between RSA and prethrombotic state has become a research hotspot at home and abroad. Hereditary thrombotic syndrome includes deficiency of protein C, protein S and antithrombin Ⅲ、the coagulation factor V gene mutation, HHcy, MTFHR gene mutation, prothrombin gene mutation, abnormal coagulation factor, etc.The association between inherited thrombophilias and RSA is controversial. Some experts suggest that screening for hereditary embolism and anticoagulant therapy can improve pregnancy outcomes to some extent. This article reviews the research progress on the relationship between RSA and hereditary thrombophilia.
文章编号:     中图分类号:R714.21    文献标志码:A
基金项目:国家自然科学基金项目(82000722)
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