Literature DB >> 19764075

Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes.

Karen Kuehl1, Christopher Loffredo, Edward J Lammer, David M Iovannisci, Gary M Shaw.   

Abstract

INTRODUCTION: Clark (1996) proposed that abnormal blood flow is related to some congenital cardiovascular malformations (CCVMs), particularly CCVM with obstruction to blood flow. Our hypothesis is that CCVMs may relate to genes that affect blood coagulation or flow. We studied whether polymorphisms of such genes are related to CCVMs; previous association of these SNPs to conotruncal CCVMs is described.
METHODS: We assessed risk of pulmonary stenosis (PS, N = 120), atrial septal defect (ASD, N = 108), aortic stenosis (AS, N = 36), and coarctation of the aorta (CoAo, N = 64), associated with 33 candidate genes, selected for their relationship to blood flow affected by homocysteine metabolism, coagulation, cell-cell interaction, inflammation, or blood pressure regulation.
RESULTS: Effects were specific to cardiac phenotype and race. CoAo was associated with MTHFR (-667) C>T (odds ratio [OR] for TT 3.5, 95% confidence limits [CI] 1.4-8.6). AS was associated with a polymorphism of SERPINE1, G5>G4, OR = 5.6 for the homozygote with 95% CI 1.4-22.9. Unique polymorphisms were associated with increased risk of ASD and PS: NPPA 664G>A with ASD (OR of 2.4, 95%CI 1.3-4.4) and NOS3 (-690) C>T with PS (OR 6.1; 95% CI 1.6-22.6 in the African American population only). For ASD, the NPPA (-664) G>A SNP there was increased risk from the variant genotype only in maternal smokers (OR 2.6; 95% CI 1.0-7.2).
CONCLUSIONS: Genes affecting vascular function and coagulation appear to be promising candidates for the etiology of cardiac malformations and warrant further study.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 19764075      PMCID: PMC2857411          DOI: 10.1002/bdra.20630

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN: 1542-0752


  58 in total

1.  Cardiovascular malformations: epidemiologic study presages endothelial cell origin.

Authors:  C Ferencz
Journal:  Teratology       Date:  2000-11

Review 2.  Heart development: an introduction.

Authors:  J M Opitz; E B Clark
Journal:  Am J Med Genet       Date:  2000

3.  Functional inference of the methylenetetrahydrofolate reductase 677C > T and 1298A > C polymorphisms from a large-scale epidemiological study.

Authors:  Arve Ulvik; Per M Ueland; Ase Fredriksen; Klaus Meyer; Stein Emil Vollset; Geir Hoff; Jørn Schneede
Journal:  Hum Genet       Date:  2006-11-18       Impact factor: 4.132

4.  Association of the 4G/5G polymorphism in the promoter region of plasminogen activator inhibitor-1 with abdominal aortic aneurysms.

Authors:  J I Rossaak; A M Van Rij; G T Jones; E L Harris
Journal:  J Vasc Surg       Date:  2000-05       Impact factor: 4.268

5.  Maternal hyperhomocysteinaemia is a risk factor for congenital heart disease.

Authors:  A C Verkleij-Hagoort; M Verlinde; N T C Ursem; J Lindemans; W A Helbing; J Ottenkamp; F M H Siebel; A C Gittenberger-de Groot; R de Jonge; M M Bartelings; E A P Steegers; R P M Steegers-Theunissen
Journal:  BJOG       Date:  2006-12       Impact factor: 6.531

Review 6.  Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.

Authors:  Kathy J Jenkins; Adolfo Correa; Jeffrey A Feinstein; Lorenzo Botto; Amy E Britt; Stephen R Daniels; Marsha Elixson; Carole A Warnes; Catherine L Webb
Journal:  Circulation       Date:  2007-05-22       Impact factor: 29.690

7.  Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation.

Authors:  Ingrid M van Beynum; Livia Kapusta; Martin den Heijer; Sita H H M Vermeulen; Margreet Kouwenberg; Otto Daniëls; Henk J Blom
Journal:  Eur Heart J       Date:  2006-03-07       Impact factor: 29.983

8.  Genetic and environmental influences on plasma homocysteine: results from a Danish twin study.

Authors:  Lise Bathum; Inge Petersen; Lene Christiansen; Agnieszka Konieczna; Thorkild I A Sørensen; Kirsten O Kyvik
Journal:  Clin Chem       Date:  2007-04-05       Impact factor: 8.327

9.  Endothelial nitric oxide synthase gene expression during murine embryogenesis: commencement of expression in the embryo occurs with the establishment of a unidirectional circulatory system.

Authors:  Anouk-Martine Teichert; Jeremy A Scott; G Brett Robb; Yu-Qing Zhou; Su-Ning Zhu; Melissa Lem; Angela Keightley; Brent M Steer; Andre C Schuh; S Lee Adamson; Myron I Cybulsky; Philip A Marsden
Journal:  Circ Res       Date:  2008-06-12       Impact factor: 17.367

10.  Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease.

Authors:  D Girelli; C Russo; P Ferraresi; O Olivieri; M Pinotti; S Friso; F Manzato; A Mazzucco; F Bernardi; R Corrocher
Journal:  N Engl J Med       Date:  2000-09-14       Impact factor: 91.245

View more
  6 in total

1.  Polymorphism 677C → T MTHFR gene in Mexican mothers of children with complex congenital heart disease.

Authors:  Norma A Balderrábano-Saucedo; Rocio Sánchez-Urbina; José A Sierra-Ramírez; Normand García-Hernández; Adriana Sánchez-Boiso; Miguel Klunder-Klunder; Diego Arenas-Aranda; Gabriela Bravo-Hernández; Penelope Noriega-Zapata; Alfredo Vizcaíno-Alarcón
Journal:  Pediatr Cardiol       Date:  2012-06-04       Impact factor: 1.655

2.  Fitting homocysteine to disease models, as well as adjusting the models to the disease.

Authors:  Friedrich C Luft
Journal:  J Mol Med (Berl)       Date:  2015-06       Impact factor: 4.599

3.  Gene Expression in Experimental Aortic Coarctation and Repair: Candidate Genes for Therapeutic Intervention?

Authors:  John F LaDisa; Serdar Bozdag; Jessica Olson; Ramani Ramchandran; Judy R Kersten; Thomas J Eddinger
Journal:  PLoS One       Date:  2015-07-24       Impact factor: 3.240

4.  Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329 cases and 15,076 controls.

Authors:  Chao Xuan; Hui Li; Jin-Xia Zhao; Hong-Wei Wang; Yi Wang; Chun-Ping Ning; Zhen Liu; Bei-Bei Zhang; Guo-Wei He; Li-Min Lun
Journal:  Sci Rep       Date:  2014-12-04       Impact factor: 4.379

5.  "Association of MTHFR and MS/MTR gene polymorphisms with congenital heart defects in North Indian population (Jammu and Kashmir): a case-control study encompassing meta-analysis and trial sequential analysis".

Authors:  Jyotdeep Kour Raina; Rakesh Kumar Panjaliya; Vikas Dogra; Sushil Sharma; Parvinder Kumar
Journal:  BMC Pediatr       Date:  2022-04-25       Impact factor: 2.567

6.  MTHFR C677T polymorphism and risk of congenital heart defects: evidence from 29 case-control and TDT studies.

Authors:  Wei Wang; Yujia Wang; Fangqi Gong; Weihua Zhu; Songling Fu
Journal:  PLoS One       Date:  2013-03-11       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.