Association of angiotensin-converting enzyme intron 16 insertion/deletion polymorphism with history of foetal loss
Introduction. The angiotensin-converting enzyme (ACE) intron 16 insertion/deletion (I/D) polymorphism is associated with ACE activity and has been discussed as a risk factor for pre-eclampsia. Disturbances of uteroplacental circulation are involved in the pathogenesis of pre-eclampsia. In this study...
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2009-12-01
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Series: | Journal of the Renin-Angiotensin-Aldosterone System |
Online Access: | https://doi.org/10.1177/1470320309343813 |
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doaj-9b34e23f775b4bab91cbfd1ae1afd8922021-05-02T19:14:48ZengHindawi - SAGE PublishingJournal of the Renin-Angiotensin-Aldosterone System1470-32032009-12-011010.1177/1470320309343813Association of angiotensin-converting enzyme intron 16 insertion/deletion polymorphism with history of foetal lossLarisa BukreevaAlexander GrigorovHolger KiesewetterBerthold HoppeIntroduction. The angiotensin-converting enzyme (ACE) intron 16 insertion/deletion (I/D) polymorphism is associated with ACE activity and has been discussed as a risk factor for pre-eclampsia. Disturbances of uteroplacental circulation are involved in the pathogenesis of pre-eclampsia. In this study, we tested whether the ACE I/D genotype is associated with history of foetal loss (FL) or uteroplacental dysfunction (UPD). Patients and methods. ACE I/D genotype was determined in 312 women presenting with a history of FL and 112 women admitted because of UPD. The association of the ACE I/D genotype with FL or UPD was assessed in a case-control study using 527 patients with diagnoses other than FL or UPD. To exclude potential biases due to associations of this genotype with other diagnoses, we additionally performed a case-control study using 553 healthy controls. Results. ACE I/D genotype was significantly associated with history of FL in both case-control studies (patient controls: odds ratio 1.52, p<0.02; healthy controls: odds ratio 1.48, p=0.02). There was no evidence for allele-dose dependency. No association of the ACE I/D genotype with UPD could be detected. Conclusions. The ACE I/D genotype exhibits a statistically significant association with a history of FL. These results corroborate an involvement of the renin-angiotensin system in pregnancy complications.https://doi.org/10.1177/1470320309343813 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Larisa Bukreeva Alexander Grigorov Holger Kiesewetter Berthold Hoppe |
spellingShingle |
Larisa Bukreeva Alexander Grigorov Holger Kiesewetter Berthold Hoppe Association of angiotensin-converting enzyme intron 16 insertion/deletion polymorphism with history of foetal loss Journal of the Renin-Angiotensin-Aldosterone System |
author_facet |
Larisa Bukreeva Alexander Grigorov Holger Kiesewetter Berthold Hoppe |
author_sort |
Larisa Bukreeva |
title |
Association of angiotensin-converting enzyme intron 16 insertion/deletion polymorphism with history of foetal loss |
title_short |
Association of angiotensin-converting enzyme intron 16 insertion/deletion polymorphism with history of foetal loss |
title_full |
Association of angiotensin-converting enzyme intron 16 insertion/deletion polymorphism with history of foetal loss |
title_fullStr |
Association of angiotensin-converting enzyme intron 16 insertion/deletion polymorphism with history of foetal loss |
title_full_unstemmed |
Association of angiotensin-converting enzyme intron 16 insertion/deletion polymorphism with history of foetal loss |
title_sort |
association of angiotensin-converting enzyme intron 16 insertion/deletion polymorphism with history of foetal loss |
publisher |
Hindawi - SAGE Publishing |
series |
Journal of the Renin-Angiotensin-Aldosterone System |
issn |
1470-3203 |
publishDate |
2009-12-01 |
description |
Introduction. The angiotensin-converting enzyme (ACE) intron 16 insertion/deletion (I/D) polymorphism is associated with ACE activity and has been discussed as a risk factor for pre-eclampsia. Disturbances of uteroplacental circulation are involved in the pathogenesis of pre-eclampsia. In this study, we tested whether the ACE I/D genotype is associated with history of foetal loss (FL) or uteroplacental dysfunction (UPD). Patients and methods. ACE I/D genotype was determined in 312 women presenting with a history of FL and 112 women admitted because of UPD. The association of the ACE I/D genotype with FL or UPD was assessed in a case-control study using 527 patients with diagnoses other than FL or UPD. To exclude potential biases due to associations of this genotype with other diagnoses, we additionally performed a case-control study using 553 healthy controls. Results. ACE I/D genotype was significantly associated with history of FL in both case-control studies (patient controls: odds ratio 1.52, p<0.02; healthy controls: odds ratio 1.48, p=0.02). There was no evidence for allele-dose dependency. No association of the ACE I/D genotype with UPD could be detected. Conclusions. The ACE I/D genotype exhibits a statistically significant association with a history of FL. These results corroborate an involvement of the renin-angiotensin system in pregnancy complications. |
url |
https://doi.org/10.1177/1470320309343813 |
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