4.5 Article

Effect of concomitant vitamin D deficiency or insufficiency on lumbar spine volumetric bone mineral density and trabecular bone score in primary hyperparathyroidism

Journal

OSTEOPOROSIS INTERNATIONAL
Volume 27, Issue 10, Pages 3063-3071

Publisher

SPRINGER LONDON LTD
DOI: 10.1007/s00198-016-3637-0

Keywords

Central quantitative computed tomography; Primary hyperparathyroidism; Trabecular bone score; Vitamin D deficiency; Volumetric bone density

Funding

  1. NIH [R01 DK084986, K24 DK074457]
  2. Joseph Weintraub Family Foundation

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Lower vitamin D and higher parathyroid hormone (PTH) levels are associated with higher volumetric BMD and bone strength at the lumbar spine as measured by central quantitative computed tomography in primary hyperparathyroidism (PHPT), but there are no differences in bone microarchitecture as measured by trabecular bone score (TBS). The purpose of this study was to evaluate the association between 25-hydroxyvitamin D (25OHD) and volumetric bone mineral density (vBMD) and the TBS at the lumbar spine (LS) in PHPT. This is a cross-sectional analysis of PHPT patients with and without low 25OHD. We measured vBMD with quantitative computed tomography (cQCT) and TBS by dual-energy X-ray absorptiometry (DXA) at the LS in 52 and 88 participants, respectively. In the cQCT cohort, those with lower vitamin D (< 20 vs. 20-29 vs. aeyen30 ng/ml) tended to be younger (p = 0.05), were less likely to use vitamin D supplementation (p < 0.01), and had better renal function (p = 0.03). Those with 25OHD < 20 ng/ml had 80 and 126 % higher serum PTH levels respectively vs. those with 25OHD 20-29 ng/ml (p = 0.002) and 25OHD aeyen30 ng/ml (p < 0.0001). Covariate-adjusted integral and trabecular vBMD were higher in those with 25OHD 20-29 vs. those with 25OHD aeyen30 ng/ml, but those with 25OHD < 20 did not differ. Because there were few participants with 25OHD deficiency, we also compared those with vitamin D < 30 vs. aeyen30 ng/ml. Covariate-adjusted integral and trabecular vBMD were 23 and 30 % higher respectively (both p < 0.05) in those with vitamin D < 30 vs. aeyen30 ng/ml. TBS was in the partially degraded range but did not differ by vitamin D status. In mild PHPT, lower 25OHD is associated with higher PTH, but vitamin D deficiency and insufficiency using current clinical thresholds did not adversely affect lumbar spine skeletal health in PHPT. Further work is needed to determine if higher vBMD in those with lower vitamin D is due to an anabolic effect of PTH.

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