"Genetic Variation in Hyaluronan Metabolism Loci Is Associated with Pla" by Matthew B. Lanktree, Christopher T. Johansen et al.
 

Department of Medicine Publications

Genetic Variation in Hyaluronan Metabolism Loci Is Associated with Plasma Plasminogen Activator Inhibitor-1 Concentration

Document Type

Article

Publication Date

9-23-2010

Journal

Blood

Volume

116

Issue

12

First Page

2160

Last Page

2163

URL with Digital Object Identifier

http://dx.doi.org/10.1182/blood-2010-02-269902

Abstract

Elevated plasma plasminogen activator inhibitor-1 (PAI-1) concentration is associated with cardiovascular disease risk. PAI-1 is the primary inhibitor of fibrinolysis within both the circulation and the arterial wall, playing roles in both atherosclerosis and thrombosis. To define the heritable component, subjects within the population-based SHARE (Study of Health Assessment and Risk in Ethnic groups) and SHARE-AP (Study of Health Assessment and Risk Evaluation in Aboriginal Peoples) studies, composed of Canadians of South Asian (n = 298), Chinese (n = 284), European (n = 227), and Aboriginal (n = 284) descent, were genotyped using the gene-centric Illumina HumanCVD BeadChip. After imputation, more than 150,000 single nucleotide polymorphisms (SNPs) in more than 2000 loci were tested for association with plasma PAI-1 concentration. Marginal association was observed with the PAI-1 locus itself (SERPINE1; P < .05). However, 5 loci (HABP2, HSPA1A, HYAL1, MBTPS1, TARP) were associated with PAI-1 concentration at a P < 1 × 10(-5) threshold. The protein products of 2 of these loci, hyaluronan binding protein 2 (HABP2) and hyaluronoglucosaminidase 1 (HYAL1), play key roles in hyaluronan metabolism, providing genetic evidence to link these pathways.

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