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

被引:21
作者
Best, Lyle G. [1 ,2 ]
Saxena, Richa [3 ]
Anderson, Cindy M. [4 ]
Barnes, Michael R. [5 ]
Hakonarson, Hakon [6 ]
Falcon, Gilbert [1 ]
Martin, Candelaria [1 ]
Castillo, Berta Almoguera [6 ]
Karumanchi, Ananth [7 ]
Keplin, Kylie [1 ]
Pearson, Nichole [1 ]
Lamb, Felicia [1 ]
Bercier, Shellee [1 ]
Keating, Brendan J. [6 ]
机构
[1] Turtle Mt Community Coll, Dept Sci, Belcourt, ND USA
[2] Univ N Dakota, Sch Med & Hlth Sci, Grand Forks, ND 58201 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Human Genet Res, Boston, MA USA
[4] Univ N Dakota, Coll Nursing, Grand Forks, ND 58201 USA
[5] Barts & London Queen Marys Sch Med & Dent, William Harvey Res Inst, London, England
[6] Childrens Hosp Philadelphia, Ctr Appl Genom, Philadelphia, PA 19104 USA
[7] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Vasc Biol Res Ctr, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
MATERNAL SUSCEPTIBILITY LOCUS; HYPERTENSIVE DISORDERS; PREGNANCY; CRP; MARKERS; FETAL; POLYMORPHISMS; EXPRESSION; ECLAMPSIA; INNATE;
D O I
10.1371/journal.pone.0071231
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
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.
引用
收藏
页数:10
相关论文
共 62 条
[1]
ACOG Committee on Obstetric Practice, 2002, Int J Gynaecol Obstet, V77, P67
[2]
A map of human genome variation from population-scale sequencing [J].
Altshuler, David ;
Durbin, Richard M. ;
Abecasis, Goncalo R. ;
Bentley, David R. ;
Chakravarti, Aravinda ;
Clark, Andrew G. ;
Collins, Francis S. ;
De la Vega, Francisco M. ;
Donnelly, Peter ;
Egholm, Michael ;
Flicek, Paul ;
Gabriel, Stacey B. ;
Gibbs, Richard A. ;
Knoppers, Bartha M. ;
Lander, Eric S. ;
Lehrach, Hans ;
Mardis, Elaine R. ;
McVean, Gil A. ;
Nickerson, DebbieA. ;
Peltonen, Leena ;
Schafer, Alan J. ;
Sherry, Stephen T. ;
Wang, Jun ;
Wilson, Richard K. ;
Gibbs, Richard A. ;
Deiros, David ;
Metzker, Mike ;
Muzny, Donna ;
Reid, Jeff ;
Wheeler, David ;
Wang, Jun ;
Li, Jingxiang ;
Jian, Min ;
Li, Guoqing ;
Li, Ruiqiang ;
Liang, Huiqing ;
Tian, Geng ;
Wang, Bo ;
Wang, Jian ;
Wang, Wei ;
Yang, Huanming ;
Zhang, Xiuqing ;
Zheng, Huisong ;
Lander, Eric S. ;
Altshuler, David L. ;
Ambrogio, Lauren ;
Bloom, Toby ;
Cibulskis, Kristian ;
Fennell, Tim J. ;
Gabriel, Stacey B. .
NATURE, 2010, 467 (7319) :1061-1073
[3]
[Anonymous], J PERINAT MED, DOI [10.1515/jpm-2011-0190, DOI 10.1515/JPM-2011-0190]
[4]
A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13 [J].
Arngrímsson, R ;
Siguróardóttir, S ;
Frigge, ML ;
Bjarnadóttir, RI ;
Jónsson, T ;
Stefánsson, H ;
Baldursdóttir, A ;
Einarsdóttir, AS ;
Palsson, B ;
Snorradóttir, S ;
Lachmeijer, AMA ;
Nicolae, D ;
Kong, A ;
Bragason, BT ;
Gulcher, JR ;
Geirsson, RT ;
Stefánsson, K .
HUMAN MOLECULAR GENETICS, 1999, 8 (09) :1799-1805
[5]
GENETIC AND FAMILIAL PREDISPOSITION TO ECLAMPSIA AND PREECLAMPSIA IN A DEFINED POPULATION [J].
ARNGRIMSSON, R ;
BJORNSSON, S ;
GEIRSSON, RT ;
BJORNSSON, H ;
WALKER, JJ ;
SNAEDAL, G .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1990, 97 (09) :762-769
[6]
Pre-eclampsia: Clinical manifestations and molecular mechanisms [J].
Baumwell, Suzanne ;
Karumanchi, S. Ananth .
NEPHRON CLINICAL PRACTICE, 2007, 106 (02) :C72-C81
[7]
Genome-wide association with select biomarker traits in the Framingham Heart Study [J].
Benjamin, Emelia J. ;
Dupuis, Josee ;
Larson, Martin G. ;
Lunetta, Kathryn L. ;
Booth, Sarah L. ;
Govindaraju, Diddahally R. ;
Kathiresan, Sekar ;
Keaney, John F., Jr. ;
Keyes, Michelle J. ;
Lin, Jing-Ping ;
Meigs, James B. ;
Robins, Sander J. ;
Rong, Jian ;
Schnabel, Renate ;
Vita, Joseph A. ;
Wang, Thomas J. ;
Wilson, Peter W. F. ;
Wolf, Philip A. ;
Vasan, Ramachandran S. .
BMC MEDICAL GENETICS, 2007, 8
[8]
Genetic determination of acute phase reactant levels: The strong heart study [J].
Best, LG ;
North, KE ;
Tracy, RP ;
Lee, ET ;
Howard, BV ;
Palmieri, V ;
MacCluer, JW .
HUMAN HEREDITY, 2004, 58 (02) :112-116
[9]
Genetic Variants, Immune Function, and Risk of Pre-Eclampsia among American Indians [J].
Best, Lyle G. ;
Nadeau, Melanie ;
Davis, Kylie ;
Lamb, Felicia ;
Bercier, Shellee ;
Anderson, Cindy M. .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2012, 67 (02) :152-159
[10]
Inflammatory bio-markers and cardiovascular risk prediction [J].
Blake, GJ ;
Ridker, PM .
JOURNAL OF INTERNAL MEDICINE, 2002, 252 (04) :283-294