Farnesyl diphosphate synthase: a novel genotype association with bone mineral density in elderly women

Maturitas. 2007 Jul 20;57(3):247-52. doi: 10.1016/j.maturitas.2007.01.005. Epub 2007 Mar 26.

Abstract

Objective: We evaluated the association between a single nucleotide polymorphism in the farnesyl diphosphate synthase gene (FDPS), BMD and bone turnover markers.

Methods: Two hundred and eighty-three community-dwelling Caucasian women aged 65 or older were screened from the greater Boston area. A validated FDPS SNP (rs2297480, A/C) was genotyped and evaluated for effect on bone mineral density (spine, hip, forearm) and bone turnover markers (urine N-telopeptide cross-linked collagen type 1, osteocalcin and bone-specific alkaline phosphatase).

Results: BMD was lower at all sites measured in women with the C/C or C/A genotypes. Statistically significant differences (p<0.05) were found at the PA spine, trochanter, distal radius, and proximal ulna after adjustment for age and BMI. No significant differences were found in bone turnover markers.

Conclusion: These findings suggest that a single nucleotide polymorphism in the FDPS gene (rs2297480) may be a genetic marker for lower BMD in postmenopausal Caucasian women.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Alkaline Phosphatase / metabolism
  • Bone Density
  • Boston
  • Collagen Type I / urine
  • Female
  • Genotype
  • Geranyltranstransferase / genetics*
  • Humans
  • Osteocalcin / metabolism
  • Osteoporosis, Postmenopausal / genetics*
  • Polymorphism, Single Nucleotide
  • White People / genetics

Substances

  • Collagen Type I
  • Osteocalcin
  • Geranyltranstransferase
  • Alkaline Phosphatase