[Impact of CYP3A7*1C polymorphism on bone mineral content in postmenopausal women]

Orv Hetil. 2007 Jul 8;148(27):1273-80. doi: 10.1556/OH.2007.28102.
[Article in Hungarian]

Abstract

Introduction: CYP3A7*1C polymorphism has been shown to be associated with lower levels of serum dehydroepiandrosterone sulphate in men. The age-related decline of dehydroepiandrosterone sulphate levels is believed to contribute to the development of osteoporosis. We hypothesized that CYP3A7*1C may lead to bone loss through decreased levels of dehydroepiandrosterone sulphate in postmenopausal women.

Patients and methods: 319 postmenopausal women were studied and divided into two subgroups: 217 women with osteoporosis and 102 aged-matched women without osteoporosis. The CYP3A7*1C polymorphism was genotyped. Serum dehydroepiandrosterone sulphate levels and bone mineral density were measured.

Results: Homozygous CYP3A7*1C carriers had significantly lower bone mineral density at lumbar spine than that of wild type (T-score with CYP3A7*1C mutant type: -3.27 +/- 1.02, T-score with wild type: -1.35 +/- 1.53, p = 0.041) after adjusting for age and DHEAS levels. No association was found between genotypes and dehydroepiandrosterone sulphate levels.

Conclusion: Our data suggest that CYP3A7 polymorphism might have an influence on bone mass at the lumbar spine independently of serum dehydroepiandrosterone sulphate concentrations.

MeSH terms

  • Aged
  • Aryl Hydrocarbon Hydroxylases / genetics*
  • Bone Density* / genetics
  • Case-Control Studies
  • Cytochrome P-450 CYP3A
  • Dehydroepiandrosterone Sulfate / blood
  • Female
  • Genotype
  • Humans
  • Lumbar Vertebrae / metabolism
  • Middle Aged
  • Osteoporosis, Postmenopausal / blood
  • Osteoporosis, Postmenopausal / enzymology*
  • Osteoporosis, Postmenopausal / genetics*
  • Polymorphism, Genetic*
  • Risk Factors

Substances

  • Dehydroepiandrosterone Sulfate
  • Aryl Hydrocarbon Hydroxylases
  • CYP3A7 protein, human
  • Cytochrome P-450 CYP3A