Literature DB >> 20735728

Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK men.

G Ken-Dror1, F Drenos, S E Humphries, P J Talmud, A D Hingorani, M Kivimäki, M Kumari, K A Bauer, J H Morrissey, H A Ireland.   

Abstract

BACKGROUND: Evidence for the associations of single nucleotide polymorphisms (SNPs) in the F7 gene and factor (F)VII levels and with risk of coronary heart disease (CHD) is inconsistent. We examined whether F7 tagging SNPs (tSNPs) and haplotypes were associated with FVII levels, coagulation activation markers (CAMs) and CHD risk in two cohorts of UK men.
METHODS: Genotypes for eight SNPs and baseline levels of FVIIc, FVIIag and CAMs (including FVIIa) were determined in 2773 healthy men from the Second Northwick Park Heart Study (NPHS-II). A second cohort, Whitehall II study (WH-II, n = 4055), was used for replication analysis of FVIIc levels and CHD risk.
RESULTS: In NPHS-II the minor alleles of three SNPs (rs555212, rs762635 and rs510317; haplotype H2) were associated with higher levels of FVIIag, FVIIc and FVIIa, whereas the minor allele for two SNPs (I/D323 and rs6046; haplotype H5) was associated with lower levels. Adjusted for classic risk factors, H2 carriers had a CHD hazard ratio of 1.34 [95% confidence interval (CI): 1.12-1.59; independent of FVIIc], whereas H5 carriers had a CHD risk of 1.29 (95% CI: 1.01-1.56; not independent of FVIIc) and significantly lower CAMs. Effects of haplotypes on FVIIc levels were replicated in WH-II, as was the association of H5 with higher CHD risk [pooled-estimate odds ratio (OR) 1.16 (1.00-1.36), P = 0.05], but surprisingly, H2 exhibited a reduced risk for CHD.
CONCLUSION: tSNPs in the F7 gene strongly influence FVII levels. The haplotype associated with low FVIIc level, with particularly reduced functional activity, was consistently associated with increased risk for CHD, whereas the haplotype associated with high FVIIc level was not.
© 2010 International Society on Thrombosis and Haemostasis.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20735728      PMCID: PMC3226948          DOI: 10.1111/j.1538-7836.2010.04035.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  50 in total

1.  A new statistical method for haplotype reconstruction from population data.

Authors:  M Stephens; N J Smith; P Donnelly
Journal:  Am J Hum Genet       Date:  2001-03-09       Impact factor: 11.025

2.  Comparison of novel hemostatic factors and conventional risk factors for prediction of coronary heart disease.

Authors:  J A Cooper; G J Miller; K A Bauer; J H Morrissey; T W Meade; D J Howarth; S Barzegar; J P Mitchell; R D Rosenberg
Journal:  Circulation       Date:  2000-12-05       Impact factor: 29.690

3.  Factor VII polymorphisms and myocardial infarction: what is special in Italians? REGRESS study group. Regression Growth Evaluation Statin Study.

Authors:  R J Nederhand; M P de Maat; J W Jukema
Journal:  Thromb Haemost       Date:  2001-04       Impact factor: 5.249

4.  The genetics of haemostasis: a twin study.

Authors:  M de Lange; H Snieder; R A Ariëns; T D Spector; P J Grant
Journal:  Lancet       Date:  2001-01-13       Impact factor: 79.321

5.  Factor VII gene polymorphism, factor VII levels, and prevalent cardiovascular disease: the Framingham Heart Study.

Authors:  D Feng; G H Tofler; M G Larson; C J O'Donnell; I Lipinska; C Schmitz; P A Sutherland; M T Johnstone; J E Muller; R B D'Agostino; D Levy; K Lindpaintner
Journal:  Arterioscler Thromb Vasc Biol       Date:  2000-02       Impact factor: 8.311

6.  APOE/C1/C4/C2 gene cluster genotypes, haplotypes and lipid levels in prospective coronary heart disease risk among UK healthy men.

Authors:  Gie Ken-Dror; Philippa J Talmud; Steve E Humphries; Fotios Drenos
Journal:  Mol Med       Date:  2010-05-20       Impact factor: 6.354

7.  Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

Authors:  Philippa J Talmud; Fotios Drenos; Sonia Shah; Tina Shah; Jutta Palmen; Claudio Verzilli; Tom R Gaunt; Jacky Pallas; Ruth Lovering; Kawah Li; Juan Pablo Casas; Reecha Sofat; Meena Kumari; Santiago Rodriguez; Toby Johnson; Stephen J Newhouse; Anna Dominiczak; Nilesh J Samani; Mark Caulfield; Peter Sever; Alice Stanton; Denis C Shields; Sandosh Padmanabhan; Olle Melander; Claire Hastie; Christian Delles; Shah Ebrahim; Michael G Marmot; George Davey Smith; Debbie A Lawlor; Patricia B Munroe; Ian N Day; Mika Kivimaki; John Whittaker; Steve E Humphries; Aroon D Hingorani
Journal:  Am J Hum Genet       Date:  2009-11       Impact factor: 11.025

8.  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

9.  Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Authors:  Fotios Drenos; Philippa J Talmud; Juan P Casas; Liam Smeeth; Jutta Palmen; Steve E Humphries; Aroon D Hingorani
Journal:  Hum Mol Genet       Date:  2009-03-31       Impact factor: 6.150

10.  Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies.

Authors:  Brendan J Keating; Sam Tischfield; Sarah S Murray; Tushar Bhangale; Thomas S Price; Joseph T Glessner; Luana Galver; Jeffrey C Barrett; Struan F A Grant; Deborah N Farlow; Hareesh R Chandrupatla; Mark Hansen; Saad Ajmal; George J Papanicolaou; Yiran Guo; Mingyao Li; Stephanie Derohannessian; Paul I W de Bakker; Swneke D Bailey; Alexandre Montpetit; Andrew C Edmondson; Kent Taylor; Xiaowu Gai; Susanna S Wang; Myriam Fornage; Tamim Shaikh; Leif Groop; Michael Boehnke; Alistair S Hall; Andrew T Hattersley; Edward Frackelton; Nick Patterson; Charleston W K Chiang; Cecelia E Kim; Richard R Fabsitz; Willem Ouwehand; Alkes L Price; Patricia Munroe; Mark Caulfield; Thomas Drake; Eric Boerwinkle; David Reich; A Stephen Whitehead; Thomas P Cappola; Nilesh J Samani; A Jake Lusis; Eric Schadt; James G Wilson; Wolfgang Koenig; Mark I McCarthy; Sekar Kathiresan; Stacey B Gabriel; Hakon Hakonarson; Sonia S Anand; Muredach Reilly; James C Engert; Deborah A Nickerson; Daniel J Rader; Joel N Hirschhorn; Garret A Fitzgerald
Journal:  PLoS One       Date:  2008-10-31       Impact factor: 3.240

View more
  9 in total

1.  Factor VII R353Q genetic polymorphism is associated with altered warfarin sensitivity among CYP2C9 *1/*1 carriers.

Authors:  Liat Mlynarsky; Idit Bejarano-Achache; Mordechai Muszkat; Yoseph Caraco
Journal:  Eur J Clin Pharmacol       Date:  2011-11-10       Impact factor: 2.953

2.  A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium.

Authors:  Kira C Taylor; Leslie A Lange; Delilah Zabaneh; Ethan Lange; Brendan J Keating; Weihong Tang; Nicholas L Smith; Joseph A Delaney; Meena Kumari; Aroon Hingorani; Kari E North; Mika Kivimaki; Russell P Tracy; Christopher J O'Donnell; Aaron R Folsom; David Green; Steve E Humphries; Alexander P Reiner
Journal:  Hum Mol Genet       Date:  2011-06-15       Impact factor: 6.150

3.  Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.

Authors:  José A Guerrero; José Rivera; Teresa Quiroga; Angel Martinez-Perez; Ana Isabel Antón; Constantino Martínez; Olga Panes; Vicente Vicente; Diego Mezzano; José-Manuel Soria; Javier Corral
Journal:  Haematologica       Date:  2011-05-05       Impact factor: 9.941

4.  Associations of activated coagulation factor VII and factor VIIa-antithrombin levels with genome-wide polymorphisms and cardiovascular disease risk.

Authors:  N C Olson; L M Raffield; L A Lange; E M Lange; W T Longstreth; G Chauhan; S Debette; S Seshadri; A P Reiner; R P Tracy
Journal:  J Thromb Haemost       Date:  2017-12-08       Impact factor: 5.824

5.  Genetic predictors of severe intraventricular hemorrhage in extremely low-birthweight infants.

Authors:  Courtney D Thornburg; Stephen W Erickson; Grier P Page; Erin A S Clark; Margaret M DeAngelis; M Elizabeth Hartnett; Ricki F Goldstein; John M Dagle; Jeffrey C Murray; Brenda B Poindexter; Abhik Das; C Michael Cotten
Journal:  J Perinatol       Date:  2020-09-25       Impact factor: 2.521

6.  Can Genetic Analysis of Putative Blood Alzheimer's Disease Biomarkers Lead to Identification of Susceptibility Loci?

Authors:  Robert C Barber; Nicole R Phillips; Jeffrey L Tilson; Ryan M Huebinger; Shantanu J Shewale; Jessica L Koenig; Jeffrey S Mitchel; Sid E O'Bryant; Stephen C Waring; Ramon Diaz-Arrastia; Scott Chasse; Kirk C Wilhelmsen
Journal:  PLoS One       Date:  2015-12-01       Impact factor: 3.240

7.  Efficient haplotype block partitioning and tag SNP selection algorithms under various constraints.

Authors:  Wen-Pei Chen; Che-Lun Hung; Yaw-Ling Lin
Journal:  Biomed Res Int       Date:  2013-11-11       Impact factor: 3.411

8.  Coagulation factor VII gene polymorphisms are not associated with the occurrence or the survival of hepatocellular carcinoma: a report of 37 cases.

Authors:  Chih-Che Lin; Chun-Hsien Wu; Li-Yu Chen; Ming-Chao Tsai; Ahmed M Elsarawy; Kuang-Tzu Huang
Journal:  Cancer Biol Med       Date:  2018-08       Impact factor: 4.248

Review 9.  Biochemical, molecular and clinical aspects of coagulation factor VII and its role in hemostasis and thrombosis.

Authors:  Francesco Bernardi; Guglielmo Mariani
Journal:  Haematologica       Date:  2021-02-01       Impact factor: 9.941

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.