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Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study

BACKGROUND: A large proportion of cases of recurrent pregnancy loss (RPL) are associated with immunological factors. OBJECTIVE: This study investigated the association between single nucleotide polymorphisms of cytotoxic T-lymphocyte-associated protein (CTLA)-4 gene in women with a history of RPL co...

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Autores principales: Vaziri Nezamdoust, Fereshteh, Hadinedoushan, Hossein, Ghasemi, Nasrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982320/
https://www.ncbi.nlm.nih.gov/pubmed/36875506
http://dx.doi.org/10.18502/ijrm.v21i1.12664
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author Vaziri Nezamdoust, Fereshteh
Hadinedoushan, Hossein
Ghasemi, Nasrin
author_facet Vaziri Nezamdoust, Fereshteh
Hadinedoushan, Hossein
Ghasemi, Nasrin
author_sort Vaziri Nezamdoust, Fereshteh
collection PubMed
description BACKGROUND: A large proportion of cases of recurrent pregnancy loss (RPL) are associated with immunological factors. OBJECTIVE: This study investigated the association between single nucleotide polymorphisms of cytotoxic T-lymphocyte-associated protein (CTLA)-4 gene in women with a history of RPL compared to healthy women. MATERIALS AND METHODS: A case-control study was performed on 2 groups consisting of 120 healthy women with no history of abortion and at least one delivery (control) and 120 women with a history of 2 or more primary RPLs (case). In addition, 5 mL of peripheral blood sample was taken from all subjects. The frequencies of CTLA-4 rs3087243 and rs231775 polymorphisms were assayed by restriction fragment length polymorphism polymerase chain reaction and rs5742909 using the high-resolution melting real-time polymerase chain reaction method. RESULTS: The mean age of the women in the control and RPL groups were 30.03 [Formula: see text] 4.23 (range 21-37), and 28.64 [Formula: see text] 3.61 yr (range 20-35), respectively. Pregnancy loss numbers ranged between 2-6 in women with a history of RPL, and between 1 and 4 in the successful pregnancy group. Statistical analysis showed a significant difference between the genotypes of GG and AG in the 2 groups in rs3087243 polymorphism (OR 1.00 for GG genotype and OR 2.87 for AG genotype, p = 0.0043). No significant difference was observed in the genotype frequencies of rs231775 and rs5742909 polymorphisms, of the 2 groups (p = 0.37, and p = 0.095), respectively. CONCLUSION: Our findings indicated that CTLA-4 polymorphism, rs3087243, might be associated with a risk of RPL in Iranian women.
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spelling pubmed-99823202023-03-04 Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study Vaziri Nezamdoust, Fereshteh Hadinedoushan, Hossein Ghasemi, Nasrin Int J Reprod Biomed Original Article BACKGROUND: A large proportion of cases of recurrent pregnancy loss (RPL) are associated with immunological factors. OBJECTIVE: This study investigated the association between single nucleotide polymorphisms of cytotoxic T-lymphocyte-associated protein (CTLA)-4 gene in women with a history of RPL compared to healthy women. MATERIALS AND METHODS: A case-control study was performed on 2 groups consisting of 120 healthy women with no history of abortion and at least one delivery (control) and 120 women with a history of 2 or more primary RPLs (case). In addition, 5 mL of peripheral blood sample was taken from all subjects. The frequencies of CTLA-4 rs3087243 and rs231775 polymorphisms were assayed by restriction fragment length polymorphism polymerase chain reaction and rs5742909 using the high-resolution melting real-time polymerase chain reaction method. RESULTS: The mean age of the women in the control and RPL groups were 30.03 [Formula: see text] 4.23 (range 21-37), and 28.64 [Formula: see text] 3.61 yr (range 20-35), respectively. Pregnancy loss numbers ranged between 2-6 in women with a history of RPL, and between 1 and 4 in the successful pregnancy group. Statistical analysis showed a significant difference between the genotypes of GG and AG in the 2 groups in rs3087243 polymorphism (OR 1.00 for GG genotype and OR 2.87 for AG genotype, p = 0.0043). No significant difference was observed in the genotype frequencies of rs231775 and rs5742909 polymorphisms, of the 2 groups (p = 0.37, and p = 0.095), respectively. CONCLUSION: Our findings indicated that CTLA-4 polymorphism, rs3087243, might be associated with a risk of RPL in Iranian women. Knowledge E 2023-02-08 /pmc/articles/PMC9982320/ /pubmed/36875506 http://dx.doi.org/10.18502/ijrm.v21i1.12664 Text en Copyright © 2023 Vaziri Nezamdoust et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Vaziri Nezamdoust, Fereshteh
Hadinedoushan, Hossein
Ghasemi, Nasrin
Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study
title Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study
title_full Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study
title_fullStr Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study
title_full_unstemmed Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study
title_short Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study
title_sort association of cytotoxic t-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: a case-control study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982320/
https://www.ncbi.nlm.nih.gov/pubmed/36875506
http://dx.doi.org/10.18502/ijrm.v21i1.12664
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