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Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population

BACKGROUND: The etiology of pre-eclampsia (PE) is unknown; but it is accepted that normal pregnancy represents a distinctive challenge to the maternal immune system. C-reactive protein is a prominent component of the innate immune system; and we previously reported an association between PE and the...

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Autores principales: Best, Lyle G., Saxena, Richa, Anderson, Cindy M., Barnes, Michael R., Hakonarson, Hakon, Falcon, Gilbert, Martin, Candelaria, Castillo, Berta Almoguera, Karumanchi, Ananth, Keplin, Kylie, Pearson, Nichole, Lamb, Felicia, Bercier, Shellee, Keating, Brendan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3733916/
https://www.ncbi.nlm.nih.gov/pubmed/23940726
http://dx.doi.org/10.1371/journal.pone.0071231
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author Best, Lyle G.
Saxena, Richa
Anderson, Cindy M.
Barnes, Michael R.
Hakonarson, Hakon
Falcon, Gilbert
Martin, Candelaria
Castillo, Berta Almoguera
Karumanchi, Ananth
Keplin, Kylie
Pearson, Nichole
Lamb, Felicia
Bercier, Shellee
Keating, Brendan J.
author_facet Best, Lyle G.
Saxena, Richa
Anderson, Cindy M.
Barnes, Michael R.
Hakonarson, Hakon
Falcon, Gilbert
Martin, Candelaria
Castillo, Berta Almoguera
Karumanchi, Ananth
Keplin, Kylie
Pearson, Nichole
Lamb, Felicia
Bercier, Shellee
Keating, Brendan J.
author_sort Best, Lyle G.
collection PubMed
description BACKGROUND: The etiology of pre-eclampsia (PE) is unknown; but it is accepted that normal pregnancy represents a distinctive challenge to the maternal immune system. C-reactive protein is a prominent component of the innate immune system; and we previously reported an association between PE and the CRP polymorphism, rs1205. Our aim was to explore the effects of additional CRP variants. The IBC (Cardiochip) genotyping microarray focuses on candidate genes and pathways related to the pathophysiology of cardiovascular disease. METHODS: This study recruited 140 cases of PE and 270 matched controls, of which 95 cases met criteria as severe PE, from an American Indian community. IBC array genotypes from 10 suitable CRP SNPs were analyzed. A replication sample of 178 cases and 427 controls of European ancestry was also genotyped. RESULTS: A nominally significant difference (p value <0.05) was seen in the distribution of discordant matched pairs for rs3093068; and Bonferroni corrected differences (P<0.005) were seen for rs876538, rs2794521, and rs3091244. Univariate conditional logistic regression odds ratios (OR) were nominally significant for rs3093068 and rs876538 models only. Multivariate logistic models with adjustment for mother's age, nulliparity and BMI attenuated the effect (OR 1.58, P = 0.066, 95% CI 0.97–2.58) for rs876538 and (OR 2.59, P = 0.050, 95% CI 1.00–6.68) for rs3093068. An additive risk score of the above two risk genotypes shows a multivariate adjusted OR of 2.04 (P = 0.013, 95% CI 1.16–3.56). The replication sample also demonstrated significant association between PE and the rs876538 allele (OR = 1.55, P = 0.01, 95% CI 2.16–1.10). We also show putative functionality for the rs876538 and rs3093068 CRP variants. CONCLUSION: The CRP variants, rs876538 and rs3093068, previously associated with other cardiovascular disease phenotypes, show suggestive association with PE in this American Indian population, further supporting a possible role for CRP in PE.
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spelling pubmed-37339162013-08-12 Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population Best, Lyle G. Saxena, Richa Anderson, Cindy M. Barnes, Michael R. Hakonarson, Hakon Falcon, Gilbert Martin, Candelaria Castillo, Berta Almoguera Karumanchi, Ananth Keplin, Kylie Pearson, Nichole Lamb, Felicia Bercier, Shellee Keating, Brendan J. PLoS One Research Article BACKGROUND: The etiology of pre-eclampsia (PE) is unknown; but it is accepted that normal pregnancy represents a distinctive challenge to the maternal immune system. C-reactive protein is a prominent component of the innate immune system; and we previously reported an association between PE and the CRP polymorphism, rs1205. Our aim was to explore the effects of additional CRP variants. The IBC (Cardiochip) genotyping microarray focuses on candidate genes and pathways related to the pathophysiology of cardiovascular disease. METHODS: This study recruited 140 cases of PE and 270 matched controls, of which 95 cases met criteria as severe PE, from an American Indian community. IBC array genotypes from 10 suitable CRP SNPs were analyzed. A replication sample of 178 cases and 427 controls of European ancestry was also genotyped. RESULTS: A nominally significant difference (p value <0.05) was seen in the distribution of discordant matched pairs for rs3093068; and Bonferroni corrected differences (P<0.005) were seen for rs876538, rs2794521, and rs3091244. Univariate conditional logistic regression odds ratios (OR) were nominally significant for rs3093068 and rs876538 models only. Multivariate logistic models with adjustment for mother's age, nulliparity and BMI attenuated the effect (OR 1.58, P = 0.066, 95% CI 0.97–2.58) for rs876538 and (OR 2.59, P = 0.050, 95% CI 1.00–6.68) for rs3093068. An additive risk score of the above two risk genotypes shows a multivariate adjusted OR of 2.04 (P = 0.013, 95% CI 1.16–3.56). The replication sample also demonstrated significant association between PE and the rs876538 allele (OR = 1.55, P = 0.01, 95% CI 2.16–1.10). We also show putative functionality for the rs876538 and rs3093068 CRP variants. CONCLUSION: The CRP variants, rs876538 and rs3093068, previously associated with other cardiovascular disease phenotypes, show suggestive association with PE in this American Indian population, further supporting a possible role for CRP in PE. Public Library of Science 2013-08-05 /pmc/articles/PMC3733916/ /pubmed/23940726 http://dx.doi.org/10.1371/journal.pone.0071231 Text en © 2013 Best 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
Best, Lyle G.
Saxena, Richa
Anderson, Cindy M.
Barnes, Michael R.
Hakonarson, Hakon
Falcon, Gilbert
Martin, Candelaria
Castillo, Berta Almoguera
Karumanchi, Ananth
Keplin, Kylie
Pearson, Nichole
Lamb, Felicia
Bercier, Shellee
Keating, Brendan J.
Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population
title Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population
title_full Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population
title_fullStr Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population
title_full_unstemmed Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population
title_short Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population
title_sort two variants of the c-reactive protein gene are associated with risk of pre-eclampsia in an american indian population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3733916/
https://www.ncbi.nlm.nih.gov/pubmed/23940726
http://dx.doi.org/10.1371/journal.pone.0071231
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