Molecular Analysis of HLA-G in Women with High-Risk Pregnancy and Their Partners with Regard to Possible Complications
Olimpia Sipak,
Aleksandra Rył,
Anna Grzywacz,
Maria Laszczyńska,
Sławomir Szymański,
Beata Karakiewicz,
Iwona Rotter and
Cezary Cybulski
Additional contact information
Olimpia Sipak: Department of Obstetrics and Pathology of Pregnancy, Pomeranian Medical University in Szczecin, 71-210 Szczecin, ul. Żołnierska 48, Poland
Aleksandra Rył: Department of Medical Rehabilitation and Clinical Physiotherapy, Pomeranian Medical University in Szczecin, 71-210 Szczecin, ul. Żołnierska 48, Poland
Anna Grzywacz: Independent Laboratory of Health Promotion, Pomeranian Medical University in Szczecin, 70-103 Szczecin, ul. Gen. Dezyderego Chłapowskiego 1, Poland
Maria Laszczyńska: Department of Histology and Developmental Biology, Pomeranian Medical University in Szczecin, 71-210 Szczecin, ul. Żołnierska 48, Poland
Sławomir Szymański: Department of Obstetrics and Pathology of Pregnancy, Pomeranian Medical University in Szczecin, 71-210 Szczecin, ul. Żołnierska 48, Poland
Beata Karakiewicz: Department of Public Health, Pomeranian Medical University in Szczecin; 71-210 Szczecin, ul. Żołnierska 48, Poland
Iwona Rotter: Department of Medical Rehabilitation and Clinical Physiotherapy, Pomeranian Medical University in Szczecin, 71-210 Szczecin, ul. Żołnierska 48, Poland
Cezary Cybulski: Department of Genetics and Pathology, Pomeranian Medical University in Szczecin, 71-252 Szczecin, ul. Unii Lubelskiej 1, Poland
IJERPH, 2019, vol. 16, issue 6, 1-13
Abstract:
The understanding of the molecular and biochemical characteristics of the human leukocyte antigen-G ( HLA-G ) is important because of the diverse influence of this antigen’s polymorphisms on the course of a pregnancy. The aim of our study was to assess how the variation of the HLA-G allele and the HLA-G 14-bp ins/del polymorphism influence predisposition to a complicated pregnancy. The clinical material consisted of parental pairs with complicated pregnancies (210 women; 190 men). The control group included parental pairs without complications during pregnancy (89 women; 86 men). The study involved isolation of genome DNA from peripheral blood leukocytes, sequencing, and analysis of the 14-bp ins/del polymorphism in the 3?-untranslated region (3?-UTR) of the HLA-G gene based on polymerase chain reaction (PCR). The most common HLA-G allele in the group of women with complicated pregnancies was the HLA-G 10101 allele. There were no statistically significant differences in the frequencies of the 14-bp ins/del polymorphism in the 3?UTR of the HLA-G gene between the groups. Our results suggest that the risk of complications in pregnancy is influenced by the HLA-G 10101 , HLA-G 10108 , and HLA-G 10106 alleles and is not influenced by the 14-bp ins/del polymorphism in the 3?UTR of the HLA-G gene.
Keywords: HLA-G; allele; haplotype; pregnancy (search for similar items in EconPapers)
JEL-codes: I I1 I3 Q Q5 (search for similar items in EconPapers)
Date: 2019
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Persistent link: https://EconPapers.repec.org/RePEc:gam:jijerp:v:16:y:2019:i:6:p:982-:d:215119
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