4.3 Article

length The role of LNPEP and ANPEP gene polymorphisms in the pathogenesis of pre-eclampsia

Publisher

ELSEVIER
DOI: 10.1016/j.ejogrb.2020.06.037

Keywords

Pre-eclampsia; LNPEP; ANPEP; Renin angiotensin system

Funding

  1. Ministry of Education, Science and Culture of Japan [22590909, 25461245, 17K09726]
  2. National Research Foundation/Japan Science and Technology Agency (NRF/JST) [J110000349]
  3. Strategic International Research Cooperative Program (SICP)
  4. College of Health Sciences (CHS)
  5. University of KwaZulu-Natal
  6. Grants-in-Aid for Scientific Research [22590909, 25461245, 17K09726] Funding Source: KAKEN

Ask authors/readers for more resources

Objective: The exact role of renin angiotensin system (RAS) in the pathogenesis of pre-eclampsia has not been established. Gene polymorphisms, however, have been implicated in the pathophysiology. Therefore, the aim of this study was to investigate the association of the Angiotensin IV receptor and aminopeptidase-N in the pathogenesis of pre-eclampsia. Study design: Stored blood samples of 637 South African women of African ancestry were utilized. The study population was divided into controls (n = 280) and pre-eclampsia (n = 357). Pre-eclampsia was subdivided into early (n = 187) and late (n = 170) onset subtypes. DNA was extracted from whole blood and genotyped. Odds ratio and 95 % confidence intervals were used to assess the association. Results: The allele and genotype frequencies of the angiotensin receptor IV and aminopeptidase-N showed no significant difference between the control versus the pre-eclampsia groups. Similarly, allele and genotype distributions of the control group versus the subtypes of pre-eclampsia (early onset and late onset pre-eclampsia) showed no significant differences. Conclusion: The single nucleotide polymorphisms of angiotensin IV receptor (rs18059) and aminopeptidase-N (rs6496603) are not associated with the pathogenesis of pre-eclampsia in women of African ancestry. (C) 2020 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available