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活化蛋白C抵抗和凝血因子V莱顿突变可能与孕早期和孕中期复发性流产有关。

Activated protein C resistance and factor V Leiden mutation can be associated with first-as well as second-trimester recurrent pregnancy loss.

作者信息

Younis J S, Brenner B, Ohel G, Tal J, Lanir N, Ben-Ami M

机构信息

Department of Obstetrics and Gynecology, Poriya Hospital, Tiberias, Israel.

出版信息

Am J Reprod Immunol. 2000 Jan;43(1):31-5. doi: 10.1111/j.8755-8920.2000.430106.x.

Abstract

PROBLEM

To examine whether the occurrence of activated protein C resistance (APCR) and factor V Leiden mutation differs in women with first- compared to women with second-trimester unexplained recurrent pregnancy loss.

METHOD OF STUDY

Seventy eight consecutive women with two or more unexplained post-embryonic recurrent pregnancy losses and 139 fertile women with at least one successful pregnancy and no abortions were prospectively investigated for APCR and the factor V Leiden mutation. No women were pregnant at the time of investigation. APCR was defined as APC sensitivity ratio (APC SR) of < or = 2.0. All patients with an APC SR < or = 2.4 were investigated for the factor V Leiden mutation. Women in this study were divided into three groups. Group A included only women with a history of recurrent first-trimester embryonic loss (37 women) and Group B included women with second-trimester abortions with or without additional first-trimester abortions (41 women). Group C included the controls (139 women).

RESULTS

APCR and factor V Leiden mutations were significantly more prevalent in all recurrent pregnancy loss patients in this study as compared to controls. 38%(30/78) and 19%(15/78) in contrast to 8% (11/139) and 6% (8/139), respectively. All three groups in the study were comparable regarding age, parity, and number of living children, whereas Groups A and B were also comparable regarding gravidity. Mean APC SRs were significantly higher in Group C as compared to Groups A and B. The incidence of APCR was significantly higher in Groups A and B, as compared to controls, 27 and 49% in contrast to 8%, respectively. Moreover, the incidence of the factor V Leiden mutation was significantly higher in Groups A and B as compared to Group C, 16 and 22% as distinct from 6%, respectively. The incidence of APCR was higher in Group B as compared to Group A, 49% in contrast to 27%, with borderline significance: however, the factor V Leiden mutation did not significantly differ between the two groups.

CONCLUSIONS

APCR and factor V Leiden are associated with unexplained recurrent pregnancy loss. The occurrence of APCR and factor V Leiden seems to be linked to post-embryonic first-trimester as well as second-trimester recurrent pregnancy loss. The significance of acquired, non-heritable APCR in recurrent fetal loss patients, especially in the second-trimester aborters, is still to be determined.

摘要

问题

比较孕早期不明原因复发性流产女性与孕中期不明原因复发性流产女性中活化蛋白C抵抗(APCR)及凝血因子V莱顿突变的发生率是否存在差异。

研究方法

前瞻性调查了78例有两次或更多次胚胎期后不明原因复发性流产的女性以及139例至少有一次成功妊娠且无流产史的可育女性的APCR及凝血因子V莱顿突变情况。调查时所有女性均未怀孕。APCR定义为活化蛋白C敏感率(APC SR)≤2.0。所有APC SR≤2.4的患者均进行凝血因子V莱顿突变检测。本研究中的女性分为三组。A组仅包括有孕早期胚胎复发性流产史的女性(37例),B组包括有孕中期流产史且有或无孕早期流产史的女性(41例)。C组为对照组(139例)。

结果

与对照组相比,本研究中所有复发性流产患者的APCR及凝血因子V莱顿突变发生率显著更高。分别为38%(30/78)和19%(15/78),而对照组分别为8%(11/139)和6%(8/139)。研究中的三组在年龄、产次和存活子女数方面具有可比性,而A组和B组在妊娠次数方面也具有可比性。C组的平均APC SR显著高于A组和B组。与对照组相比,A组和B组的APCR发生率显著更高,分别为27%和49%,而对照组为8%。此外,与C组相比,A组和B组的凝血因子V莱顿突变发生率显著更高,分别为16%和22%,而C组为6%。B组的APCR发生率高于A组,分别为49%和27%,具有临界显著性;然而,两组之间的凝血因子V莱顿突变无显著差异。

结论

APCR及凝血因子V莱顿突变与不明原因复发性流产有关。APCR及凝血因子V莱顿突变的发生似乎与胚胎期后孕早期及孕中期复发性流产有关。获得性、非遗传性APCR在复发性流产患者尤其是孕中期流产患者中的意义仍有待确定。

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