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Recurrent IVF failure and hereditary thrombophilia
Background: The largest percentage of failed invitro fertilization (IVF (cycles, are due to lack of implantation. As hereditary thrombophilia can cause in placentation failure, it may have a role in recurrent IVF failure. Objective: Aim of this case-control study was to determine whether hereditary...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research and Clinical Center for Infertility
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4126250/ https://www.ncbi.nlm.nih.gov/pubmed/25114668 |
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author | Safdarian, Leila Najmi, Zahra Aleyasin, Ashraf Aghahosseini, Marzieh Rashidi, Mandana Asadollah, Sara |
author_facet | Safdarian, Leila Najmi, Zahra Aleyasin, Ashraf Aghahosseini, Marzieh Rashidi, Mandana Asadollah, Sara |
author_sort | Safdarian, Leila |
collection | PubMed |
description | Background: The largest percentage of failed invitro fertilization (IVF (cycles, are due to lack of implantation. As hereditary thrombophilia can cause in placentation failure, it may have a role in recurrent IVF failure. Objective: Aim of this case-control study was to determine whether hereditary thrombophilia is more prevalent in women with recurrent IVF failures. Materials and Methods: Case group comprised 96 infertile women, with a history of recurrent IVF failure. Control group was comprised of 95 healthy women with proven fertility who had conceived spontaneously. All participants were assessed for the presence of inherited thrombophilias including: factor V Leiden, methilen tetrahydrofolate reductase (MTHFR) mutation, prothrombin mutation, homocystein level, protein S and C deficiency, antithrombin III (AT-III) deficiency and plasminogen activator inhibitor-1 (PAI-1) mutation. Presence of thrombophilia was compared between groups. Results: Having at least one thrombophilia known as a risk factor for recurrent IVF failure (95% CI=1.74-5.70, OR=3.15, p=0.00). Mutation of factor V Leiden (95% CI=1.26-10.27, OR=3.06, P=0.01) and homozygote form of MTHFR mutation (95% CI=1.55-97.86, OR=12.33, p=0.05) were also risk factors for recurrent IVF failure. However, we could not find significant difference in other inherited thrombophilia’s. Conclusion: Inherited thrombophilia is more prevalent in women with recurrent IVF failure compared with healthy women. Having at least one thrombophilia, mutation of factor V Leiden and homozygote form of MTHFR mutation were risk factors for recurrent IVF failure. |
format | Online Article Text |
id | pubmed-4126250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Research and Clinical Center for Infertility |
record_format | MEDLINE/PubMed |
spelling | pubmed-41262502014-08-11 Recurrent IVF failure and hereditary thrombophilia Safdarian, Leila Najmi, Zahra Aleyasin, Ashraf Aghahosseini, Marzieh Rashidi, Mandana Asadollah, Sara Iran J Reprod Med Original Article Background: The largest percentage of failed invitro fertilization (IVF (cycles, are due to lack of implantation. As hereditary thrombophilia can cause in placentation failure, it may have a role in recurrent IVF failure. Objective: Aim of this case-control study was to determine whether hereditary thrombophilia is more prevalent in women with recurrent IVF failures. Materials and Methods: Case group comprised 96 infertile women, with a history of recurrent IVF failure. Control group was comprised of 95 healthy women with proven fertility who had conceived spontaneously. All participants were assessed for the presence of inherited thrombophilias including: factor V Leiden, methilen tetrahydrofolate reductase (MTHFR) mutation, prothrombin mutation, homocystein level, protein S and C deficiency, antithrombin III (AT-III) deficiency and plasminogen activator inhibitor-1 (PAI-1) mutation. Presence of thrombophilia was compared between groups. Results: Having at least one thrombophilia known as a risk factor for recurrent IVF failure (95% CI=1.74-5.70, OR=3.15, p=0.00). Mutation of factor V Leiden (95% CI=1.26-10.27, OR=3.06, P=0.01) and homozygote form of MTHFR mutation (95% CI=1.55-97.86, OR=12.33, p=0.05) were also risk factors for recurrent IVF failure. However, we could not find significant difference in other inherited thrombophilia’s. Conclusion: Inherited thrombophilia is more prevalent in women with recurrent IVF failure compared with healthy women. Having at least one thrombophilia, mutation of factor V Leiden and homozygote form of MTHFR mutation were risk factors for recurrent IVF failure. Research and Clinical Center for Infertility 2014-07 /pmc/articles/PMC4126250/ /pubmed/25114668 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Safdarian, Leila Najmi, Zahra Aleyasin, Ashraf Aghahosseini, Marzieh Rashidi, Mandana Asadollah, Sara Recurrent IVF failure and hereditary thrombophilia |
title | Recurrent IVF failure and hereditary thrombophilia |
title_full | Recurrent IVF failure and hereditary thrombophilia |
title_fullStr | Recurrent IVF failure and hereditary thrombophilia |
title_full_unstemmed | Recurrent IVF failure and hereditary thrombophilia |
title_short | Recurrent IVF failure and hereditary thrombophilia |
title_sort | recurrent ivf failure and hereditary thrombophilia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4126250/ https://www.ncbi.nlm.nih.gov/pubmed/25114668 |
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