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Genetic associations between fibrinogen and cognitive performance in three Scottish cohorts.

Authors :
Marioni RE
Deary IJ
Murray GD
Lowe GD
Strachan MW
Luciano M
Houlihan LM
Gow AJ
Harris SE
Rumley A
Stewart MC
Fowkes FG
Price JF
Source :
Behavior genetics [Behav Genet] 2011 Sep; Vol. 41 (5), pp. 691-9. Date of Electronic Publication: 2011 Jan 23.
Publication Year :
2011

Abstract

There is increasing evidence to suggest that elevated plasma levels of fibrinogen are associated with late-life cognitive performance. This study tested the association of single nucleotide polymorphisms in the fibrinogen α (FGA) and β (FGB) genes with cognitive performance. Data were analysed from three community-dwelling populations of older persons (>50 years) in central Scotland: the Aspirin for Asymptomatic Atherosclerosis (AAA) Trial (n = 2,091), the Edinburgh Type 2 Diabetes Study (ET2DS, n = 1,066), and the Lothian Birth Cohort 1936 (LBC1936, n = 1,091). Cognition was assessed using a battery of five, seven, and four psychometric tests, respectively. This information was used to derive a general cognitive factor. Weakly significant associations were found between the rs4220 (FGB), and rs2227412 (FGB) SNPs and a single test of cognitive performance in the AAA Trial (p < 0.05). These findings did not replicate in the LBC1936 or ET2DS cohorts, except for the rs2227412 SNP, which was significantly associated with the general cognitive factor in the ET2DS (p = 3.3 × 10(-4)). A summary term that combined results from all three studies suggested that the rs2227412 genotype associated with reduced cognitive ability also associated with higher plasma fibrinogen levels. These findings suggest a tentative role for fibrinogen as a determinant of late-life cognitive performance and justify further attempts at replication in older persons.

Details

Language :
English
ISSN :
1573-3297
Volume :
41
Issue :
5
Database :
MEDLINE
Journal :
Behavior genetics
Publication Type :
Academic Journal
Accession number :
21258858
Full Text :
https://doi.org/10.1007/s10519-011-9449-2