Cargando…

Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: Evidence of Small-Study Bias

BACKGROUND: Inappropriate activation of the renin–angiotensin system may play a part in the development of preeclampsia. An insertion/deletion polymorphism within the angiotensin-I converting enzyme gene (ACE-I/D) has shown to be reliably associated with differences in angiotensin-converting enzyme...

Descripción completa

Detalles Bibliográficos
Autores principales: Serrano, Norma C, Díaz, Luis A, Páez, Maria C, Mesa, Clara M, Cifuentes, Rodrigo, Monterrosa, Alvaro, González, Adriana, Smeeth, Liam, Hingorani, Aroon D, Casas, Juan P
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1716194/
https://www.ncbi.nlm.nih.gov/pubmed/17194198
http://dx.doi.org/10.1371/journal.pmed.0030520
_version_ 1782131322148356096
author Serrano, Norma C
Díaz, Luis A
Páez, Maria C
Mesa, Clara M
Cifuentes, Rodrigo
Monterrosa, Alvaro
González, Adriana
Smeeth, Liam
Hingorani, Aroon D
Casas, Juan P
author_facet Serrano, Norma C
Díaz, Luis A
Páez, Maria C
Mesa, Clara M
Cifuentes, Rodrigo
Monterrosa, Alvaro
González, Adriana
Smeeth, Liam
Hingorani, Aroon D
Casas, Juan P
author_sort Serrano, Norma C
collection PubMed
description BACKGROUND: Inappropriate activation of the renin–angiotensin system may play a part in the development of preeclampsia. An insertion/deletion polymorphism within the angiotensin-I converting enzyme gene (ACE-I/D) has shown to be reliably associated with differences in angiotensin-converting enzyme (ACE) activity. However, previous studies of the ACE-I/D variant and preeclampsia have been individually underpowered to detect plausible genotypic risks. METHODS AND FINDINGS: A prospective case-control study was conducted in 1,711 unrelated young pregnant women (665 preeclamptic and 1,046 healthy pregnant controls) recruited from five Colombian cities. Maternal blood was obtained to genotype for the ACE-I/D polymorphism. Crude and adjusted odds ratio (OR) and 95% confidence interval (CI) using logistic regression models were obtained to evaluate the strength of the association between ACE-I/D variant and preeclampsia risk. A meta-analysis was then undertaken of all published studies to February 2006 evaluating the ACE-I/D variant in preeclampsia. An additive model (per-D-allele) revealed a null association between the ACE-I/D variant and preeclampsia risk (crude OR = 0.95 [95% CI, 0.81–1.10]) in the new case-control study. Similar results were obtained after adjusting for confounders (adjusted per-allele OR = 0.90 [95% CI, 0.77–1.06]) and using other genetic models of inheritance. A meta-analysis (2,596 cases and 3,828 controls from 22 studies) showed a per-allele OR of 1.26 (95% CI, 1.07–1.49). An analysis stratified by study size showed an attenuated OR toward the null as study size increased. CONCLUSIONS: It is highly likely that the observed small nominal increase in risk of preeclampsia associated with the ACE D-allele is due to small-study bias, similar to that observed in cardiovascular disease. Reliable assessment of the origins of preeclampsia using a genetic approach may require the establishment of a collaborating consortium to generate a dataset of adequate size.
format Text
id pubmed-1716194
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-17161942007-03-24 Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: Evidence of Small-Study Bias Serrano, Norma C Díaz, Luis A Páez, Maria C Mesa, Clara M Cifuentes, Rodrigo Monterrosa, Alvaro González, Adriana Smeeth, Liam Hingorani, Aroon D Casas, Juan P PLoS Med Research Article BACKGROUND: Inappropriate activation of the renin–angiotensin system may play a part in the development of preeclampsia. An insertion/deletion polymorphism within the angiotensin-I converting enzyme gene (ACE-I/D) has shown to be reliably associated with differences in angiotensin-converting enzyme (ACE) activity. However, previous studies of the ACE-I/D variant and preeclampsia have been individually underpowered to detect plausible genotypic risks. METHODS AND FINDINGS: A prospective case-control study was conducted in 1,711 unrelated young pregnant women (665 preeclamptic and 1,046 healthy pregnant controls) recruited from five Colombian cities. Maternal blood was obtained to genotype for the ACE-I/D polymorphism. Crude and adjusted odds ratio (OR) and 95% confidence interval (CI) using logistic regression models were obtained to evaluate the strength of the association between ACE-I/D variant and preeclampsia risk. A meta-analysis was then undertaken of all published studies to February 2006 evaluating the ACE-I/D variant in preeclampsia. An additive model (per-D-allele) revealed a null association between the ACE-I/D variant and preeclampsia risk (crude OR = 0.95 [95% CI, 0.81–1.10]) in the new case-control study. Similar results were obtained after adjusting for confounders (adjusted per-allele OR = 0.90 [95% CI, 0.77–1.06]) and using other genetic models of inheritance. A meta-analysis (2,596 cases and 3,828 controls from 22 studies) showed a per-allele OR of 1.26 (95% CI, 1.07–1.49). An analysis stratified by study size showed an attenuated OR toward the null as study size increased. CONCLUSIONS: It is highly likely that the observed small nominal increase in risk of preeclampsia associated with the ACE D-allele is due to small-study bias, similar to that observed in cardiovascular disease. Reliable assessment of the origins of preeclampsia using a genetic approach may require the establishment of a collaborating consortium to generate a dataset of adequate size. Public Library of Science 2006-12 2006-12-26 /pmc/articles/PMC1716194/ /pubmed/17194198 http://dx.doi.org/10.1371/journal.pmed.0030520 Text en © 2006 Serrano et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Serrano, Norma C
Díaz, Luis A
Páez, Maria C
Mesa, Clara M
Cifuentes, Rodrigo
Monterrosa, Alvaro
González, Adriana
Smeeth, Liam
Hingorani, Aroon D
Casas, Juan P
Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: Evidence of Small-Study Bias
title Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: Evidence of Small-Study Bias
title_full Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: Evidence of Small-Study Bias
title_fullStr Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: Evidence of Small-Study Bias
title_full_unstemmed Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: Evidence of Small-Study Bias
title_short Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: Evidence of Small-Study Bias
title_sort angiotensin-converting enzyme i/d polymorphism and preeclampsia risk: evidence of small-study bias
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1716194/
https://www.ncbi.nlm.nih.gov/pubmed/17194198
http://dx.doi.org/10.1371/journal.pmed.0030520
work_keys_str_mv AT serranonormac angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias
AT diazluisa angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias
AT paezmariac angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias
AT mesaclaram angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias
AT cifuentesrodrigo angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias
AT monterrosaalvaro angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias
AT gonzalezadriana angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias
AT smeethliam angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias
AT hingoraniaroond angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias
AT casasjuanp angiotensinconvertingenzymeidpolymorphismandpreeclampsiariskevidenceofsmallstudybias