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...
- 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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|
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 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.version.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.coarversion.none.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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http://purl.org/coar/resource_type/c_6501 |
dc.type.content.none.fl_str_mv |
Text |
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info:eu-repo/semantics/article |
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http://purl.org/redcol/resource_type/ARTOTR |
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http://purl.org/coar/resource_type/c_6501 |
status_str |
publishedVersion |
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 |
dc.relation.citationstartpage.none.fl_str_mv |
1 |
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) |
dc.rights.coar.none.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.accessrights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
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) http://purl.org/coar/access_right/c_abf2 |
eu_rights_str_mv |
openAccess |
dc.format.extent.none.fl_str_mv |
13 paginas |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
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 |
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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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