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Noninvasive Assessment of Skeletal Microstructure and Estimated Bone Strength in Hypoparathyroidism
Author(s) -
Cusano Natalie E,
Nishiyama Kyle K,
Zhang Chengchen,
Rubin Mishaela R,
Boutroy Stephanie,
McMahon Donald J,
Guo X Edward,
Bilezikian John P
Publication year - 2016
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1002/jbmr.2609
Subject(s) - quantitative computed tomography , medicine , hypoparathyroidism , osteoporosis , bone mineral , tibia , bone density , cortical bone , femoral neck , parathyroid hormone , urology , endocrinology , surgery , anatomy , calcium
In hypoparathyroidism, areal bone mineral density (BMD) by dual‐energy X‐ray absorptiometry (DXA) is above average, and skeletal indices by bone biopsy are abnormal. We used high‐resolution peripheral quantitative computed tomography (HRpQCT) and finite element analyses (FEA) to further investigate skeletal microstructure and estimated bone strength. We studied 60 hypoparathyroid subjects on conventional therapy using DXA, HRpQCT, and FEA of the distal radius and tibia compared with normative controls from the Canadian Multicentre Osteoporosis Study. In hypoparathyroid women and men, areal BMD was above average at the lumbar spine and hip sites by DXA; radial BMD was also above average in hypoparathyroid women. Using HRpQCT, cortical volumetric BMD was increased in the hypoparathyroid cohort compared with controls at both the radius and tibia. Cortical porosity was reduced at both sites in pre‐ and postmenopausal women and at the tibia in young men with a downward trend at the radius in men. At the tibia, trabecular number was increased in premenopausal women and men and trabecular thickness was lower in women. Ultimate stress and failure load at both sites for the hypoparathyroid subjects were similar to controls. Using a linear regression model, at both radius and tibia, each increment in age decreased ultimate stress and failure load, whereas each increment in duration of hypoparathyroidism increased these same indices. These results provide additional evidence for the critical role of parathyroid hormone in regulating skeletal microstructure. Longer disease duration may mitigate the adverse effects of age on estimated bone strength in hypoparathyroidism. © 2015 American Society for Bone and Mineral Research.