Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss
Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the F...
Ausführliche Beschreibung
Autor*in: |
Asaad MA. Babker [verfasserIn] Huda Ahamed Fadlalmula [verfasserIn] Amanda Gamal G. Elggourish [verfasserIn] Hanan Khalid Fadul Ahmed [verfasserIn] Shima Yousri Masoud Awad [verfasserIn] Salaheldein G Elzaki [verfasserIn] Rania Saad Suliman [verfasserIn] Abdulkarim S. Bin Shaya [verfasserIn] Abdulaziz Alfahed [verfasserIn] Nahed S. Alharthi [verfasserIn] Ahmed M Hjazi [verfasserIn] Nora Y. Hakami [verfasserIn] Mohammed Ageeli Hakami [verfasserIn] Alhomidi Almotiri [verfasserIn] Hisham Ali Waggiallah [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2024 |
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Übergeordnetes Werk: |
In: BMC Research Notes - BMC, 2008, 17(2024), 1, Seite 7 |
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Übergeordnetes Werk: |
volume:17 ; year:2024 ; number:1 ; pages:7 |
Links: |
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DOI / URN: |
10.1186/s13104-024-06715-w |
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Katalog-ID: |
DOAJ092193641 |
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520 | |a Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). Conclusion Our results indicate a link between Human Platelet Antigen-1 (HPA-1), Human Platelet Antigen-3 (HPA-3) and Factor XIII gene polymorphism with RPL. | ||
650 | 4 | |a Recurrent pregnancy loss | |
650 | 4 | |a Human platelets antigen (HPA) | |
650 | 4 | |a HPA-1 | |
650 | 4 | |a HPA-3 | |
650 | 4 | |a Factor XIII | |
653 | 0 | |a Medicine | |
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653 | 0 | |a Biology (General) | |
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700 | 0 | |a Huda Ahamed Fadlalmula |e verfasserin |4 aut | |
700 | 0 | |a Amanda Gamal G. Elggourish |e verfasserin |4 aut | |
700 | 0 | |a Hanan Khalid Fadul Ahmed |e verfasserin |4 aut | |
700 | 0 | |a Shima Yousri Masoud Awad |e verfasserin |4 aut | |
700 | 0 | |a Salaheldein G Elzaki |e verfasserin |4 aut | |
700 | 0 | |a Rania Saad Suliman |e verfasserin |4 aut | |
700 | 0 | |a Abdulkarim S. Bin Shaya |e verfasserin |4 aut | |
700 | 0 | |a Abdulaziz Alfahed |e verfasserin |4 aut | |
700 | 0 | |a Nahed S. Alharthi |e verfasserin |4 aut | |
700 | 0 | |a Ahmed M Hjazi |e verfasserin |4 aut | |
700 | 0 | |a Nora Y. Hakami |e verfasserin |4 aut | |
700 | 0 | |a Mohammed Ageeli Hakami |e verfasserin |4 aut | |
700 | 0 | |a Alhomidi Almotiri |e verfasserin |4 aut | |
700 | 0 | |a Hisham Ali Waggiallah |e verfasserin |4 aut | |
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10.1186/s13104-024-06715-w doi (DE-627)DOAJ092193641 (DE-599)DOAJ36633c64b7974addad504f14d736c906 DE-627 ger DE-627 rakwb eng QH301-705.5 Q1-390 Asaad MA. Babker verfasserin aut Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). Conclusion Our results indicate a link between Human Platelet Antigen-1 (HPA-1), Human Platelet Antigen-3 (HPA-3) and Factor XIII gene polymorphism with RPL. Recurrent pregnancy loss Human platelets antigen (HPA) HPA-1 HPA-3 Factor XIII Medicine R Biology (General) Science (General) Huda Ahamed Fadlalmula verfasserin aut Amanda Gamal G. Elggourish verfasserin aut Hanan Khalid Fadul Ahmed verfasserin aut Shima Yousri Masoud Awad verfasserin aut Salaheldein G Elzaki verfasserin aut Rania Saad Suliman verfasserin aut Abdulkarim S. Bin Shaya verfasserin aut Abdulaziz Alfahed verfasserin aut Nahed S. Alharthi verfasserin aut Ahmed M Hjazi verfasserin aut Nora Y. Hakami verfasserin aut Mohammed Ageeli Hakami verfasserin aut Alhomidi Almotiri verfasserin aut Hisham Ali Waggiallah verfasserin aut In BMC Research Notes BMC, 2008 17(2024), 1, Seite 7 (DE-627)559431805 (DE-600)2413336-X 17560500 nnns volume:17 year:2024 number:1 pages:7 https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/article/36633c64b7974addad504f14d736c906 kostenfrei https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/toc/1756-0500 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024 1 7 |
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10.1186/s13104-024-06715-w doi (DE-627)DOAJ092193641 (DE-599)DOAJ36633c64b7974addad504f14d736c906 DE-627 ger DE-627 rakwb eng QH301-705.5 Q1-390 Asaad MA. Babker verfasserin aut Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). Conclusion Our results indicate a link between Human Platelet Antigen-1 (HPA-1), Human Platelet Antigen-3 (HPA-3) and Factor XIII gene polymorphism with RPL. Recurrent pregnancy loss Human platelets antigen (HPA) HPA-1 HPA-3 Factor XIII Medicine R Biology (General) Science (General) Huda Ahamed Fadlalmula verfasserin aut Amanda Gamal G. Elggourish verfasserin aut Hanan Khalid Fadul Ahmed verfasserin aut Shima Yousri Masoud Awad verfasserin aut Salaheldein G Elzaki verfasserin aut Rania Saad Suliman verfasserin aut Abdulkarim S. Bin Shaya verfasserin aut Abdulaziz Alfahed verfasserin aut Nahed S. Alharthi verfasserin aut Ahmed M Hjazi verfasserin aut Nora Y. Hakami verfasserin aut Mohammed Ageeli Hakami verfasserin aut Alhomidi Almotiri verfasserin aut Hisham Ali Waggiallah verfasserin aut In BMC Research Notes BMC, 2008 17(2024), 1, Seite 7 (DE-627)559431805 (DE-600)2413336-X 17560500 nnns volume:17 year:2024 number:1 pages:7 https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/article/36633c64b7974addad504f14d736c906 kostenfrei https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/toc/1756-0500 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024 1 7 |
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10.1186/s13104-024-06715-w doi (DE-627)DOAJ092193641 (DE-599)DOAJ36633c64b7974addad504f14d736c906 DE-627 ger DE-627 rakwb eng QH301-705.5 Q1-390 Asaad MA. Babker verfasserin aut Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). Conclusion Our results indicate a link between Human Platelet Antigen-1 (HPA-1), Human Platelet Antigen-3 (HPA-3) and Factor XIII gene polymorphism with RPL. Recurrent pregnancy loss Human platelets antigen (HPA) HPA-1 HPA-3 Factor XIII Medicine R Biology (General) Science (General) Huda Ahamed Fadlalmula verfasserin aut Amanda Gamal G. Elggourish verfasserin aut Hanan Khalid Fadul Ahmed verfasserin aut Shima Yousri Masoud Awad verfasserin aut Salaheldein G Elzaki verfasserin aut Rania Saad Suliman verfasserin aut Abdulkarim S. Bin Shaya verfasserin aut Abdulaziz Alfahed verfasserin aut Nahed S. Alharthi verfasserin aut Ahmed M Hjazi verfasserin aut Nora Y. Hakami verfasserin aut Mohammed Ageeli Hakami verfasserin aut Alhomidi Almotiri verfasserin aut Hisham Ali Waggiallah verfasserin aut In BMC Research Notes BMC, 2008 17(2024), 1, Seite 7 (DE-627)559431805 (DE-600)2413336-X 17560500 nnns volume:17 year:2024 number:1 pages:7 https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/article/36633c64b7974addad504f14d736c906 kostenfrei https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/toc/1756-0500 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024 1 7 |
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10.1186/s13104-024-06715-w doi (DE-627)DOAJ092193641 (DE-599)DOAJ36633c64b7974addad504f14d736c906 DE-627 ger DE-627 rakwb eng QH301-705.5 Q1-390 Asaad MA. Babker verfasserin aut Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). Conclusion Our results indicate a link between Human Platelet Antigen-1 (HPA-1), Human Platelet Antigen-3 (HPA-3) and Factor XIII gene polymorphism with RPL. Recurrent pregnancy loss Human platelets antigen (HPA) HPA-1 HPA-3 Factor XIII Medicine R Biology (General) Science (General) Huda Ahamed Fadlalmula verfasserin aut Amanda Gamal G. Elggourish verfasserin aut Hanan Khalid Fadul Ahmed verfasserin aut Shima Yousri Masoud Awad verfasserin aut Salaheldein G Elzaki verfasserin aut Rania Saad Suliman verfasserin aut Abdulkarim S. Bin Shaya verfasserin aut Abdulaziz Alfahed verfasserin aut Nahed S. Alharthi verfasserin aut Ahmed M Hjazi verfasserin aut Nora Y. Hakami verfasserin aut Mohammed Ageeli Hakami verfasserin aut Alhomidi Almotiri verfasserin aut Hisham Ali Waggiallah verfasserin aut In BMC Research Notes BMC, 2008 17(2024), 1, Seite 7 (DE-627)559431805 (DE-600)2413336-X 17560500 nnns volume:17 year:2024 number:1 pages:7 https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/article/36633c64b7974addad504f14d736c906 kostenfrei https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/toc/1756-0500 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024 1 7 |
allfieldsSound |
10.1186/s13104-024-06715-w doi (DE-627)DOAJ092193641 (DE-599)DOAJ36633c64b7974addad504f14d736c906 DE-627 ger DE-627 rakwb eng QH301-705.5 Q1-390 Asaad MA. Babker verfasserin aut Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). Conclusion Our results indicate a link between Human Platelet Antigen-1 (HPA-1), Human Platelet Antigen-3 (HPA-3) and Factor XIII gene polymorphism with RPL. Recurrent pregnancy loss Human platelets antigen (HPA) HPA-1 HPA-3 Factor XIII Medicine R Biology (General) Science (General) Huda Ahamed Fadlalmula verfasserin aut Amanda Gamal G. Elggourish verfasserin aut Hanan Khalid Fadul Ahmed verfasserin aut Shima Yousri Masoud Awad verfasserin aut Salaheldein G Elzaki verfasserin aut Rania Saad Suliman verfasserin aut Abdulkarim S. Bin Shaya verfasserin aut Abdulaziz Alfahed verfasserin aut Nahed S. Alharthi verfasserin aut Ahmed M Hjazi verfasserin aut Nora Y. Hakami verfasserin aut Mohammed Ageeli Hakami verfasserin aut Alhomidi Almotiri verfasserin aut Hisham Ali Waggiallah verfasserin aut In BMC Research Notes BMC, 2008 17(2024), 1, Seite 7 (DE-627)559431805 (DE-600)2413336-X 17560500 nnns volume:17 year:2024 number:1 pages:7 https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/article/36633c64b7974addad504f14d736c906 kostenfrei https://doi.org/10.1186/s13104-024-06715-w kostenfrei https://doaj.org/toc/1756-0500 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024 1 7 |
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Asaad MA. Babker @@aut@@ Huda Ahamed Fadlalmula @@aut@@ Amanda Gamal G. Elggourish @@aut@@ Hanan Khalid Fadul Ahmed @@aut@@ Shima Yousri Masoud Awad @@aut@@ Salaheldein G Elzaki @@aut@@ Rania Saad Suliman @@aut@@ Abdulkarim S. Bin Shaya @@aut@@ Abdulaziz Alfahed @@aut@@ Nahed S. Alharthi @@aut@@ Ahmed M Hjazi @@aut@@ Nora Y. Hakami @@aut@@ Mohammed Ageeli Hakami @@aut@@ Alhomidi Almotiri @@aut@@ Hisham Ali Waggiallah @@aut@@ |
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Babker</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2024</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). 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Asaad MA. Babker misc QH301-705.5 misc Q1-390 misc Recurrent pregnancy loss misc Human platelets antigen (HPA) misc HPA-1 misc HPA-3 misc Factor XIII misc Medicine misc R misc Biology (General) misc Science (General) Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss |
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QH301-705.5 Q1-390 Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss Recurrent pregnancy loss Human platelets antigen (HPA) HPA-1 HPA-3 Factor XIII |
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Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss |
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Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss |
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Asaad MA. Babker Huda Ahamed Fadlalmula Amanda Gamal G. Elggourish Hanan Khalid Fadul Ahmed Shima Yousri Masoud Awad Salaheldein G Elzaki Rania Saad Suliman Abdulkarim S. Bin Shaya Abdulaziz Alfahed Nahed S. Alharthi Ahmed M Hjazi Nora Y. Hakami Mohammed Ageeli Hakami Alhomidi Almotiri Hisham Ali Waggiallah |
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detection of human platelets antigen polymorphism (hpa-1 and hpa-3) and human factor xiii mutation in sudanese women with recurrent pregnancy loss |
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QH301-705.5 |
title_auth |
Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss |
abstract |
Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). Conclusion Our results indicate a link between Human Platelet Antigen-1 (HPA-1), Human Platelet Antigen-3 (HPA-3) and Factor XIII gene polymorphism with RPL. |
abstractGer |
Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). Conclusion Our results indicate a link between Human Platelet Antigen-1 (HPA-1), Human Platelet Antigen-3 (HPA-3) and Factor XIII gene polymorphism with RPL. |
abstract_unstemmed |
Abstract Background Recurrent pregnancy Loss (RPL) is common problem affecting many couples. A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. A significant difference was observed in overall allele frequency for B allele (97.0%) and expected frequency of A allele was (81.1%) using the Hardy-Weinberg distribution (p < 0.001). The genotype A/A was most common in these patients (90.3%) and controls (100%), while B/B genotype was only (9.7%) in patients regarding HPA-3. Furthermore, the frequency of Val/Val genotype was higher in cases (88.3%) as compared with controls (90.3%). The risk of RPL in patients was nearly the same in Val/Leu individuals and controls group but all these differences were not statistically significant (p < 0.05). Conclusion Our results indicate a link between Human Platelet Antigen-1 (HPA-1), Human Platelet Antigen-3 (HPA-3) and Factor XIII gene polymorphism with RPL. |
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Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss |
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Huda Ahamed Fadlalmula Amanda Gamal G. Elggourish Hanan Khalid Fadul Ahmed Shima Yousri Masoud Awad Salaheldein G Elzaki Rania Saad Suliman Abdulkarim S. Bin Shaya Abdulaziz Alfahed Nahed S. Alharthi Ahmed M Hjazi Nora Y. Hakami Mohammed Ageeli Hakami Alhomidi Almotiri Hisham Ali Waggiallah |
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A certain genetic variants link to increase the danger of this condition particularly HPA-1, HPA-3 and Human Factor XIII Val34Leu Mutation. The present study aims to find an association between RPL and the Factor XIII Val34Leu polymorphism, as well as HPA-1 and HPA-3 in Sudanese women with RPL. Methods This case-control study conducted between June 2022 and December 2022 included 216 women, with 103 cases having minimum three abortions in the past, and 113 healthy controls with at least two full-term births and no abortion history. DNA was isolated from whole blood and the status of three genetic polymorphisms (HPA-1, HPA-3, and factor XIII) was done using a polymerase chain reaction (PCR). Data was analysed using the SPSS version 24 software. Results The A/A genotype was found to be more prevalent in cases (79.6%) and controls (96.5%) regarding HPA-1. 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