Association between cognition and gene polymorphisms involved in thrombosis and haemostasis

被引:0
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作者
Terence J. Quinn
Jahad Alghamdi
Sandosh Padmanabhan
David J. Porteous
Blair H. Smith
Lynne Hocking
Ian J. Deary
John Gallacher
Martina Messow
David J. Stott
机构
[1] University of Glasgow,Institute of Cardiovascular and Medical Sciences
[2] New Lister Building,Centre for Integrative Physiology, Medical Genetics Section
[3] Glasgow Royal Infirmary,School of Medicine
[4] University of Edinburgh,Institute of Medical Sciences
[5] University of Dundee,Centre for Cognitive Ageing and Cognitive Epidemiology
[6] University of Aberdeen,Institute of Primary Care and Public Health
[7] University of Edinburgh,Robertson Centre for Biostatistics
[8] Cardiff University,undefined
[9] University of Glasgow,undefined
来源
AGE | 2015年 / 37卷
关键词
Cognition disorders; Dementia; Haemostasis; Genomics; Mendelian randomization analysis;
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学科分类号
摘要
An association between blood markers of thrombosis and haemostasis and cognitive decline has been described. These results may be confounded by lifestyle and environmental factors. We used a Mendelian randomisation approach to describe the association between thrombosis/haemostasis genotypes and cognition. We studied the genetic variants (single nucleotide polymorphisms) of circulating markers of thrombosis and haemostasis. Our chosen blood factors and associated polymorphisms were D-dimer [rs12029080], fibrinogen [rs1800789], plasminogen activator inhibitor [rs2227631], and von Willebrand factor [rs1063857]. We described association with multidomain cognitive test scores using data from the Scottish Family Health Study. Cognitive data were analysed for individual tests and combined to give a general cognitive factor. In 20,288 subjects, we found no evidence of association between cognitive function (individual tests and combined scores) and any of the above-mentioned single nucleotide polymorphisms. Lower scores on cognitive measures were associated with increasing age, socioeconomic deprivation, blood pressure, waist-hip ratio, smoking, and vascular comorbidity (all p < 0.001). In a post hoc sensitivity analysis restricted to those aged over 50 years, there was still no signal of association. Our data add to our understanding of determinants of cognition but are not definitive; the variation in blood levels explained by SNPs was modest and our sample size may have been insufficient to detect a modest association.
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