Abstract
Purpose
To compare plasminogen activator inhibitor type1 (PAI-1) mutation rates in different groups of patients with the record of recurrent miscarriage (RM) or implantation failure (IF) with special emphasis on the number of missed pregnancies and/or implantation failures (RM ≥ 2, IF ≥ 2, RM + IF ≥ 2, RM ≥ 3, IF ≥ 3 and RM + IF ≥ 3).
Method
Case-control study from PCR products and RFLP data of DNA from blood of patients who referred to the infertility clinic including 595 patients (421 RM ≥ 2, 119 IF ≥ 2 and 55 RM + IF ≥ 2) as the case groups and 100 healthy women as the control group.
Results
All six different subgroups of patients showed increased frequencies of the mutant allele (4G) in comparison to the control group (p < 0.001) suggesting a role for PAI-1 mutation in RM and IF.
Conclusions
The different patient subgroups suffer similar rates of risk in developing RM and IF when compared to controls.
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Acknowledgments
The authors are grateful to the women who kindly accepted to enter this study. We also appreciate the staff of Avicenna Infertility Clinic for their assistance in sample collection and performing the experiments.
Funding
This work was supported by a grant (89-05) from Avicenna Research Institute, Tehran, Iran.
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Capsule The mutant (4G) allele of plasminogen activator inhibitor type 1 (PAI-1) is significantly increased in women with recurrent miscarriage (RM) and those with implantation failure (IF) compared to control women, suggesting a role for PAI-1 mutation in RM and IF.
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Khosravi, F., Zarei, S., Ahmadvand, N. et al. Association between plasminogen activator inhibitor 1 gene mutation and different subgroups of recurrent miscarriage and implantation failure. J Assist Reprod Genet 31, 121–124 (2014). https://doi.org/10.1007/s10815-013-0125-8
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DOI: https://doi.org/10.1007/s10815-013-0125-8