Polymorphism in killer cell immunoglobulin-like receptors and human leukocyte antigen-c and predisposition to preeclampsia in Ethiopian pregnant women population.
Adolescent
Adult
Case-Control Studies
Ethiopia
/ epidemiology
Female
Fetus
/ immunology
Gene Frequency
Genetic Predisposition to Disease
HLA-C Antigens
/ genetics
Humans
Immune Tolerance
/ genetics
Killer Cells, Natural
/ immunology
Polymorphism, Single Nucleotide
Pre-Eclampsia
/ blood
Pregnancy
Protective Factors
Receptors, KIR
/ genetics
Young Adult
HLA
KIR
Natural killer cell
Preeclampsia
Trophoblast cell
Journal
Journal of reproductive immunology
ISSN: 1872-7603
Titre abrégé: J Reprod Immunol
Pays: Ireland
ID NLM: 8001906
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
received:
21
03
2020
revised:
29
05
2020
accepted:
15
06
2020
pubmed:
1
7
2020
medline:
21
9
2021
entrez:
1
7
2020
Statut:
ppublish
Résumé
Preeclampsia (PE) is a human specific pregnancy-related syndrome of unknown etiology that affects 2-8 % of pregnancies. Polymorphism in maternal Killer Cell Immunoglobulin-like Receptors (KIRs) and the ligand fetal Human Leukocyte Antigen-C (HLA-C) may predispose pregnant mothers for PE due to defective trophoblast invasion into the maternal decidua. Our study aimed to investigate the association between maternal KIR and fetal HLA-C polymorphism and PE in Ethiopian pregnant women. We included a total of 288 (157 controls and 131 PE cases) in a case-controls study at Adama Regional Referral Hospital, Ethiopia. The KIR and HLA-C genotyping was done using traditional polymerase chain reaction on genomic DNA extracted form maternal venous and cord blood followed by 2% agarose gel electrophoresis. The statistical associations between variables were evaluated using Pearson's Chi-square test. P < 0.05, with 95 % confidence interval was considered statistically significant. A significant association was observed between the KIR2DS1 and PE, with a higher frequency (60.5 %) of the gene in the control group. Similarly, a significant association was observed between KIR AA genotype and PE, with a higher frequency (38.2 %) of this genotype in the PE group. Ethiopians share the same risk genotype for PE as seen in previous African and European studies, namely homozygosity of a maternal KIR AA genotype. However, Ethiopians differ from other East African populations by sharing the same protective KIR2DS1 gene as Europeans.
Identifiants
pubmed: 32603992
pii: S0165-0378(20)30090-5
doi: 10.1016/j.jri.2020.103169
pii:
doi:
Substances chimiques
HLA-C Antigens
0
KIR2DS1 protein, human
0
Receptors, KIR
0
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
103169Informations de copyright
Copyright © 2020 The Author(s). Published by Elsevier B.V. All rights reserved.