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 angiotensinconverting enzyme (A...

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Autores:
Norma C. Serrano
Luis A. DÍaz
Maria C. Páez
Clara M. Mesa
Rodrigo Cifuentes
Alvaro Monterrosa
Adriana González
Liam Smeeth
Aroon D. Hingorani
Juan P. Casas
Tipo de recurso:
Article of journal
Fecha de publicación:
2006
Institución:
Universidad de Cartagena
Repositorio:
Repositorio Universidad de Cartagena
Idioma:
spa
OAI Identifier:
oai:repositorio.unicartagena.edu.co:11227/18368
Acceso en línea:
https://hdl.handle.net/11227/18368
Palabra clave:
investigación educativa
Educación Medicina
Enseñanza
3. Ciencias Médicas y de la Salud
Rights
openAccess
License
Derechos reservados, Universidad de Cartagena.
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network_name_str Repositorio Universidad de Cartagena
repository_id_str
dc.title.none.fl_str_mv 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.
spellingShingle Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: evidence of small-study bias.
investigación educativa
Educación Medicina
Enseñanza
3. Ciencias Médicas y de la Salud
title_short 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_sort Angiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: evidence of small-study bias.
dc.creator.fl_str_mv Norma C. Serrano
Luis A. DÍaz
Maria C. Páez
Clara M. Mesa
Rodrigo Cifuentes
Alvaro Monterrosa
Adriana González
Liam Smeeth
Aroon D. Hingorani
Juan P. Casas
dc.contributor.author.none.fl_str_mv Norma C. Serrano
Luis A. DÍaz
Maria C. Páez
Clara M. Mesa
Rodrigo Cifuentes
Alvaro Monterrosa
Adriana González
Liam Smeeth
Aroon D. Hingorani
Juan P. Casas
dc.subject.armarc.none.fl_str_mv investigación educativa
Educación Medicina
Enseñanza
topic investigación educativa
Educación Medicina
Enseñanza
3. Ciencias Médicas y de la Salud
dc.subject.ocde.none.fl_str_mv 3. Ciencias Médicas y de la Salud
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 angiotensinconverting 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 ¼ 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 OR¼0.90 [95% CI, 0.77–1.06]) and using other genetic models of inheritance. A metaanalysis (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.
publishDate 2006
dc.date.issued.none.fl_str_mv 2006
dc.date.accessioned.none.fl_str_mv 2024-09-18T21:02:09Z
dc.date.available.none.fl_str_mv 2024-09-18T21:02:09Z
dc.type.none.fl_str_mv Artículo de revista
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dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/11227/18368
url https://hdl.handle.net/11227/18368
dc.language.iso.none.fl_str_mv spa
language spa
dc.relation.ispartofjournal.none.fl_str_mv PLoS MEDICINE
dc.relation.citationendpage.none.fl_str_mv 13
dc.relation.citationissue.none.fl_str_mv 3
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dc.relation.citationvolume.none.fl_str_mv 3
dc.relation.references.none.fl_str_mv 1. World Health Organization International Collaborative Study of Hypertensive Disorders of Pregnancy (1988) Geographic variation in the incidence of hypertension in pregnancy. Am J Obstet Gynecol 158: 80–83.
2. Khan KS, Wojdyla D, Say L, Gulmezoglu AM, Van Look PF (2006) WHO analysis of causes of maternal death: A systematic review. Lancet 367: 1066– 1074
3. Sibai B, Dekker G, Kupferminc M (2005) Pre-eclampsia. Lancet 365: 785– 799.
4. Villar J, Abalos E, Nardin JM, Merialdi M, Carroli G (2004) Strategies to prevent and treat preeclampsia: Evidence from randomized controlled trials. Semin Nephrol 24: 607–615.
5. Duckitt K, Harrington D (2005) Risk factors for pre-eclampsia at antenatal booking: Systematic review of controlled studies. BMJ 330: 565–567.
dc.rights.none.fl_str_mv Derechos reservados, Universidad de Cartagena.
dc.rights.uri.none.fl_str_mv https://creativecommons.org/licenses/by-nc/4.0/
dc.rights.license.none.fl_str_mv Atribución-NoComercial 4.0 Internacional (CC BY-NC 4.0)
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rights_invalid_str_mv Derechos reservados, Universidad de Cartagena.
https://creativecommons.org/licenses/by-nc/4.0/
Atribución-NoComercial 4.0 Internacional (CC BY-NC 4.0)
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dc.format.extent.none.fl_str_mv 13 paginas
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dc.publisher.none.fl_str_mv Universidad de Cartagena.
dc.publisher.place.none.fl_str_mv Cartagena de Indias.
publisher.none.fl_str_mv Universidad de Cartagena.
dc.source.none.fl_str_mv texto
institution Universidad de Cartagena
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spelling Norma C. SerranoLuis A. DÍazMaria C. PáezClara M. MesaRodrigo CifuentesAlvaro MonterrosaAdriana GonzálezLiam SmeethAroon D. HingoraniJuan P. Casas2024-09-18T21:02:09Z2024-09-18T21:02:09Z2006https://hdl.handle.net/11227/18368Background 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 angiotensinconverting 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 ¼ 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 OR¼0.90 [95% CI, 0.77–1.06]) and using other genetic models of inheritance. A metaanalysis (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.13 paginasapplication/pdfspaUniversidad de Cartagena.Cartagena de Indias.PLoS MEDICINE133131. World Health Organization International Collaborative Study of Hypertensive Disorders of Pregnancy (1988) Geographic variation in the incidence of hypertension in pregnancy. Am J Obstet Gynecol 158: 80–83.2. Khan KS, Wojdyla D, Say L, Gulmezoglu AM, Van Look PF (2006) WHO analysis of causes of maternal death: A systematic review. Lancet 367: 1066– 10743. Sibai B, Dekker G, Kupferminc M (2005) Pre-eclampsia. Lancet 365: 785– 799.4. Villar J, Abalos E, Nardin JM, Merialdi M, Carroli G (2004) Strategies to prevent and treat preeclampsia: Evidence from randomized controlled trials. Semin Nephrol 24: 607–615.5. Duckitt K, Harrington D (2005) Risk factors for pre-eclampsia at antenatal booking: Systematic review of controlled studies. BMJ 330: 565–567.Derechos reservados, Universidad de Cartagena.https://creativecommons.org/licenses/by-nc/4.0/Atribución-NoComercial 4.0 Internacional (CC BY-NC 4.0)http://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccesstextoAngiotensin-Converting Enzyme I/D Polymorphism and Preeclampsia Risk: evidence of small-study bias.Artículo de revistainfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1Textinfo:eu-repo/semantics/articlehttp://purl.org/redcol/resource_type/ARTOTRinvestigación educativaEducación MedicinaEnseñanza3. 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