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. 2007 Sep 18:8:62.
doi: 10.1186/1471-2350-8-62.

Genetic variants of complement factor H gene are not associated with premature coronary heart disease: a family-based study in the Irish population

Weihua Meng  1 , Anne Hughes, Chris C Patterson, Christine Belton, Muhammad S Kamaruddin, Paul G Horan, Frank Kee, Pascal P McKeown
Affiliations

Genetic variants of complement factor H gene are not associated with premature coronary heart disease: a family-based study in the Irish population

Weihua Meng et al. BMC Med Genet. .

Abstract

Background: The complement factor H (CFH) gene has been recently confirmed to play an essential role in the development of age-related macular degeneration (AMD). There are conflicting reports of its role in coronary heart disease. This study was designed to investigate if, using a family-based approach, there was an association between genetic variants of the CFH gene and risk of early-onset coronary heart disease.

Methods: We evaluated 6 SNPs and 5 common haplotypes in the CFH gene amongst 1494 individuals in 580 Irish families with at least one member prematurely affected with coronary heart disease. Genotypes were determined by multiplex SNaPshot technology.

Results: Using the TDT/S-TDT test, we did not find an association between any of the individual SNPs or any of the 5 haplotypes and early-onset coronary heart disease.

Conclusion: In this family-based study, we found no association between the CFH gene and early-onset coronary heart disease.

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References

    1. Oksjoki R, Kovanen PT, Pentikainen MO. Role of complement activation in atherosclerosis. Curr Opin Lipidol. 2003;14:477–482. doi: 10.1097/00041433-200310000-00008. - DOI - PubMed
    1. Oksjoki R, Jarva H, Kovanen PT, Laine P, Meri S, Pentikäinen MO. Association between Complement Factor H and Proteoglycans in Early Human Coronary Atherosclerotic Lesions. Arterioscler Thromb Vasc Biol. 2003;23:630–636. doi: 10.1161/01.ATV.0000057808.91263.A4. - DOI - PubMed
    1. Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, Henning AK, SanGiovanni JP, Mane SM, Mayne ST, Bracken MB, Ferris FL, Ott J, Barnstable C, Hoh J. Complement Factor H Polymorphism in Age-Related Macular Degeneration. Science. 2005;308:385–9. doi: 10.1126/science.1109557. - DOI - PMC - PubMed
    1. Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA. Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration. Science. 2005;308:419–421. doi: 10.1126/science.1110359. - DOI - PubMed
    1. Edwards AO, Ritter R, 3rd, Abel KJ, Manning A, Panhuysen C, Farrer LA. Complement factor H polymorphism and age-related macular degeneration. Science. 2005;308:421–424. doi: 10.1126/science.1110189. - DOI - PubMed

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