在墨西哥人群中血栓形成和复发性妊娠丢失的风险

V. Manuel, Luján Irastorza Jesús Estuardo, D. Carlos, K. Alejandro, H. Roberto, Ávila Pérez Felipe de Jesús, G. Juan, Á. Daniela, P. Maruxa, Paredes Núñez María Angélica
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Material and method: Retrospective, observational and cross-sectional study, which includes 277 pregnancies of 95 women and three groups were formed: 1) Control: deliveries of patients without pregnancy loss, without problems during the development of pregnancy and with a study of hereditary thrombophilias, 2) idiopathic fetal death : Deliveries of patients with idiopathic gestational loss (=1) and with study of thrombophilias, and 3) recurrent pregnancy loss. Deliveries of patients with idiopathic recurrent pregnancy loss and with study of hereditary thrombophilias; patient data was collected; age, weight and height, newborn data, weeks of gestation, weight and height, which are reported with mean ± standard error and analyzed with the student's t test, and thrombophilias, cesarean sections, deliveries and spontaneous abortions are reported in percentages and analyzed with chi2, in both cases the SPSS version 25 statistical package was used. 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引用次数: 1

摘要

背景:ESHRE将复发性妊娠丢失(RPL)定义为连续两次或两次以上妊娠丢失。本研究目的是评价纤溶酶原激活物抑制剂-1 (4G/5G) (PAI-1, 4G/5G)与V - Leiden因子(FVL, G1691A)、凝血酶原G20210A (PRT, G20210A)、亚甲基四氢叶酸还原酶G677A (MTHFR C677AT)的关系;与墨西哥妇女的复发性妊娠丢失和围产期数据。材料和方法:回顾性、观察性和横断面研究,包括95名妇女的277例妊娠,分为三组:1)对照组:没有妊娠丢失、妊娠发展过程中没有问题并有遗传性血栓形成研究的患者分娩;2)特发性胎儿死亡:特发性妊娠丢失(=1)并有血栓形成研究的患者分娩;3)复发性妊娠丢失。特发性复发性妊娠丢失患者的分娩和遗传性血栓病的研究收集患者资料;年龄、体重、身高、新生儿资料、妊娠周数、体重、身高报告均采用均数±标准误差,采用学生t检验进行分析;血栓形成、剖宫产、分娩、自然流产以百分比报告,采用chi2进行分析,均采用SPSS 25版统计软件包。结果:纳入的95名女性中,各组的年龄、体重、身高在不同比例上无显著差异;FVL-G1691A是在不同人群中被评估的一种血栓性疾病,观察到FVL-G1691A仅发生在复发性妊娠丢失(15.4%);纯合子和杂合子的翻译,观察到FVL-G1691A仅出现在复发性妊娠丢失中,围产期数据显示,复发性妊娠丢失母亲的新生儿妊娠周数减少,体重和体型下降。结论:母体遗传性血栓性疾病的存在增加了复发性流产、早产和出生时体重和身高下降的风险。
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Thrombofilias and the risk of recurring pregnancy loss in a Mexican population
Background: Recurrent gestational loss (RPL) is defined by the ESHRE as the loss of 2 or more consecutive pregnancies. The objective of this study is to evaluate the relationship of Factor V Leiden (FVL, G1691A), prothrombin G20210A (PRT, G20210A), methylenetetrahydrofolate reductase G677A (MTHFR C677AT) and plasminogen activator inhibitor-1 (4G/5G) (PAI-1, 4G/5G); with recurrent gestational loss and perinatal data of Mexican women. Material and method: Retrospective, observational and cross-sectional study, which includes 277 pregnancies of 95 women and three groups were formed: 1) Control: deliveries of patients without pregnancy loss, without problems during the development of pregnancy and with a study of hereditary thrombophilias, 2) idiopathic fetal death : Deliveries of patients with idiopathic gestational loss (=1) and with study of thrombophilias, and 3) recurrent pregnancy loss. Deliveries of patients with idiopathic recurrent pregnancy loss and with study of hereditary thrombophilias; patient data was collected; age, weight and height, newborn data, weeks of gestation, weight and height, which are reported with mean ± standard error and analyzed with the student's t test, and thrombophilias, cesarean sections, deliveries and spontaneous abortions are reported in percentages and analyzed with chi2, in both cases the SPSS version 25 statistical package was used. Results: Of the 95 women included there were no significant differences in age, weight and height in the different rates of each group; one of the thrombophilias to be evaluated in the different populations, it was observed that FVL-G1691A only occurs in recurrent pregnancy loss (15.4%); the translation of homozygous and heterozygous, it was observed that FVL-G1691A only appeared in recurrent pregnancy loss, perinatal data showed a decrease in the weeks of gestation in newborns of mothers with recurrent pregnancy loss, with a decrease in weight and size. Conclusions: the presence of inherited maternal thrombophilias increases the risk of recurrent pregnancy loss, premature birth, and decreased weight and height at birth.
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