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Farnesyl diphosphate synthase: a novel genotype association with bone mineral density in elderly women
Matthew E Levy1, Robert A Parker, Robert E Ferrell
1Division of Endocrinology and Metabolism and Division of Geriatrics, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, United States. levyme2@upmc.edu
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.
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