The 4G5G polymorphism in the gene for PAI-1 and the circadian oscillation of plasma PAI-1

DOI PDF 4 Citations
  • Johanna G. van der Bom
    From the Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht; Van Creveldkliniek, University Medical Center Utrecht; Gaubius Laboratory, TNO-PG, Leiden; and the Department of Epidemiology and Biostatistics, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Michiel L. Bots
    From the Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht; Van Creveldkliniek, University Medical Center Utrecht; Gaubius Laboratory, TNO-PG, Leiden; and the Department of Epidemiology and Biostatistics, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Frits Haverkate
    From the Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht; Van Creveldkliniek, University Medical Center Utrecht; Gaubius Laboratory, TNO-PG, Leiden; and the Department of Epidemiology and Biostatistics, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Cornelis Kluft
    From the Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht; Van Creveldkliniek, University Medical Center Utrecht; Gaubius Laboratory, TNO-PG, Leiden; and the Department of Epidemiology and Biostatistics, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Diederick E. Grobbee
    From the Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht; Van Creveldkliniek, University Medical Center Utrecht; Gaubius Laboratory, TNO-PG, Leiden; and the Department of Epidemiology and Biostatistics, Erasmus University Medical Center, Rotterdam, the Netherlands.

Abstract

<jats:p>Plasminogen activator inhibitor type I (PAI-1) antigen concentrations follow a circadian oscillation peaking in the morning. Some individuals show no apparent circadian rhythm, while others show up to a 10-fold variation in PAI-1 over 24 hours. Results from experimental studies suggest that a polymorphism in the promoter of the gene for PAI-1 (4G5G) directly influences the circadian expression of the PAI-1 gene. We studied whether the diurnal variation of PAI-1 antigen differs for the genotypes of the4G5G polymorphism. A population-based, cross-sectional study was performed among 263 subjects selected from the Rotterdam Study, a population-based cohort of 7983 men and women aged 55 years and older. The 4G allele was associated with a more pronounced circadian expression of PAI-1 antigen. Morning PAI-1 antigen concentrations were 79 ng/mL (95% confidence interval [CI], 68-92) in subjects homozygous for 4G, 62 ng/mL (95% CI, 54-72) in heterozygous subjects, and 59 ng/mL (95% CI, 49-71) in subjects homozygous for 5G. While respective PAI-1 antigen concentrations in the afternoon were 40 ng/mL (95% CI, 33-49), 41 ng/mL (95% CI, 37-47), and 40 ng/mL (95% CI, 49-71). These findings suggest that the morning increase in PAI-1 antigen concentration is more pronounced among subjects homozygous for the4G allele compared with the morning increase among the other genotypes. Additionally, these findings show that homozygosity for the 4G allele is associated with increased PAI-1 levels during the morning only.</jats:p>

Journal

  • Blood

    Blood 101 (5), 1841-1844, 2003-03-01

    American Society of Hematology

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