Angiotensin-converting enzyme insertion-deletion polymorphism in normotensive and pre-eclamptic pregnancies

Citation
L. Morgan et al., Angiotensin-converting enzyme insertion-deletion polymorphism in normotensive and pre-eclamptic pregnancies, J HYPERTENS, 17(6), 1999, pp. 765-768
Citations number
21
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
JOURNAL OF HYPERTENSION
ISSN journal
02636352 → ACNP
Volume
17
Issue
6
Year of publication
1999
Pages
765 - 768
Database
ISI
SICI code
0263-6352(199906)17:6<765:AEIPIN>2.0.ZU;2-G
Abstract
Objective To investigate the hypothesis that preeclampsia is associated wit h a common insertion-deletion polymorphism in the angiotensin-converting en zyme gene. Design Seventy-two women with pre-eclampsia and 83 normotensive pregnant wo men participated in the study. Pre-eclampsia was defined as a blood pressur e exceeding 140/90 mmHg in a previously normotensive woman, associated with proteinuria in excess of 300 mg/l in a 24 h collection. Samples for fetal genotyping were available from 66 pregnancies complicated by pre-eclampsia and 79 normotensive pregnancies. Methods Maternal and fetal samples were genotyped at the insertion-deletion (I-D) polymorphism in intron 16 of the angiotensin-converting enzyme gene by the polymerase chain reaction followed by agarose electrophoresis. Results Neither the I-D genotype distributions nor the allele frequencies d iffered significantly between preeclamptic and normotensive pregnancies in maternal or fetal samples (chi(2) < 0.3, not significant). The odds ratio f or pre-eclampsia in women with the DD genotype, compared with the ID and II genotype, was 1.09 (95% confidence interval 0.55-2.16), The odds ratio ass ociated with the DD genotype in the fetus was 1.14 (0.56-2.32). Conclusion This study has found no evidence that the insertion-deletion pol ymorphism in the angiotensin-converting enzyme gene is associated with pre- eclampsia. J Hypertens 1999, 17:765-768 (C) Lippincott Williams & Wilkins.