了解复发性流产:其病因、临床诊断和治疗的最新进展。

Medical review (Berlin, Germany) Pub Date : 2022-12-19 eCollection Date: 2022-12-01 DOI:10.1515/mr-2022-0030
Chunwei Cao, Shiyu Bai, Jing Zhang, Xiaoyue Sun, Anming Meng, Hui Chen
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引用次数: 4

摘要

复发性流产(RPL)已成为世界范围内一个重要的生殖健康问题。RPL影响约2%-3%的育龄妇女,对妇女的身心健康构成严重威胁。然而,大约50%的RPL病例的病因仍然未知(原因不明的RPL),这对这些患者的临床管理构成了巨大挑战。RPL被广泛认为是一种复杂的疾病,其病因可归因于多种因素。迄今为止,已经确定了RPL的各种风险因素,如母亲年龄、遗传因素、解剖结构异常、内分泌功能障碍、血栓前状态、免疫因素和感染。更重要的是,下一代测序技术的发展和应用大大增加了发现RPL染色体畸变和单基因变异的机会,这为其致病机制提供了新的见解。此外,根据患者的诊断评估和病因诊断,制定了具体的治疗建议。这篇综述将重点介绍目前对RPL的理解和最新进展,特别关注免疫和遗传病因、临床诊断和治疗管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Understanding recurrent pregnancy loss: recent advances on its etiology, clinical diagnosis, and management.

Understanding recurrent pregnancy loss: recent advances on its etiology, clinical diagnosis, and management.

Understanding recurrent pregnancy loss: recent advances on its etiology, clinical diagnosis, and management.

Recurrent pregnancy loss (RPL) has become an important reproductive health issue worldwide. RPL affects about 2%-3% of reproductive-aged women, and makes serious threats to women's physical and mental health. However, the etiology of approximately 50% of RPL cases remains unknown (unexplained RPL), which poses a big challenge for clinical management of these patients. RPL has been widely regarded as a complex disease where its etiology has been attributed to numerous factors. Heretofore, various risk factors for RPL have been identified, such as maternal ages, genetic factors, anatomical structural abnormalities, endocrine dysfunction, prethrombotic state, immunological factors, and infection. More importantly, development and applications of next generation sequencing technology have significantly expanded opportunities to discover chromosomal aberrations and single gene variants responsible for RPL, which provides new insight into its pathogenic mechanisms. Furthermore, based upon patients' diagnostic evaluation and etiologic diagnosis, specific therapeutic recommendations have been established. This review will highlight current understanding and recent advances on RPL, with a special focus on the immunological and genetic etiologies, clinical diagnosis and therapeutic management.

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