Association between a dimorphic site on chromosome 12 and clinical diagnosis of hypertension in three independent populations

Clin Genet. 1995 Dec;48(6):284-7. doi: 10.1111/j.1399-0004.1995.tb04110.x.

Abstract

With the aim of identifying putative quantitative trait loci (QTLs) involved in the regulation of blood pressure, we have carried out association studies at a candidate genetic locus-a human pancreatic phospholipase A2 (PLA2) gene localized on chromosome 12. Positive associations were found between the presence of a Taq I dimorphic site localized in the first intron of this gene and hypertension in three sample populations (two from USA and one from Germany). These results indicate that a QTL implicated in determining an individual's genetic susceptibility to hypertension could be present within up to 30 cM of this human PLA2 gene.

MeSH terms

  • Chromosomes, Human, Pair 12*
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Gene Frequency
  • Humans
  • Hypertension / genetics*
  • Leukocytes / physiology
  • Middle Aged
  • Pancreas / chemistry
  • Phospholipases A / genetics*
  • Phospholipases A2
  • Polymorphism, Restriction Fragment Length
  • Population Surveillance

Substances

  • Phospholipases A
  • Phospholipases A2
  • Deoxyribonucleases, Type II Site-Specific
  • TCGA-specific type II deoxyribonucleases