Activated Protein C Resistance and Factor V Leiden Mutation can be Associated with First- as well as Second-Trimester Recurrent Pregnancy Loss1
Autor: | Ben-Ami M, N. Lanir, Tal J, Benjamin Brenner, Gonen Ohel, Younis Js |
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Rok vydání: | 2000 |
Předmět: |
Gynecology
Pregnancy medicine.medical_specialty biology business.industry Incidence (epidemiology) Immunology C-reactive protein Obstetrics and Gynecology medicine.disease Thrombophilia Group A Group B Reproductive Medicine biology.protein Factor V Leiden Immunology and Allergy Medicine Activated protein C resistance business |
Zdroj: | American Journal of Reproductive Immunology. 43:31-35 |
ISSN: | 1046-7408 |
DOI: | 10.1111/j.8755-8920.2000.430106.x |
Popis: | PROBLEM: To examine whether the occurrence of activated protein C resistance (APCR) and factor V Leiden mutation differs in women ith 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 ≤ 2.0. All patients with an APC SR ≤ 2.4 ere 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. |
Databáze: | OpenAIRE |
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