Immobility as a major cause of bone remodeling in residents of a long-staygeriatric ward

Citation
H. Bischoff et al., Immobility as a major cause of bone remodeling in residents of a long-staygeriatric ward, CALCIF TIS, 64(6), 1999, pp. 485-489
Citations number
33
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
CALCIFIED TISSUE INTERNATIONAL
ISSN journal
0171967X → ACNP
Volume
64
Issue
6
Year of publication
1999
Pages
485 - 489
Database
ISI
SICI code
0171-967X(199906)64:6<485:IAAMCO>2.0.ZU;2-L
Abstract
Residents of a long-stay geriatric ward at the University Hospital Basel we re included in a study to investigate the effects of hypovitaminosis D and immobility. All 91 women (mean age 82.5 years) and 92 men (mean age 78.7 ye ars) were enrolled in the study. Measurements in eluded bone resorption, as measured by urinary deoxypyridinoline (dpd), serum 25-hydroxyvitamin D (25 0HD), serum intact parathyroid hormone (iPTH), and their correlations with a four grade mobility score. Mobility score reflected the degree of weight bearing, ranging from walking independently to primarily bed bound. Ire 86% of all residents, serum 250HD levels were below the normal limit of 12 ng/ ml. Secondary hyperparathyroidism (HPT) was detected in 24% of all patients , using 55 pg/ml as the upper limit for serum iPTH. No significant correlat ion was found between urinary dpd and serum 250HD or serum iPTH. Mobility i ndex and both urinary dpd (f: P = 0.001, r = 0.37; m: P < 0.0001, r = 0.47) and serum calcium (female: P = 0.007, r = 0.28; male: P = 0.02, r = 0.24) were positively related. In institutionalized elderly people with a high pr evalence of vitamin D deficiency serum intact PTH levels did not correlate with bone resorption as measured by urinary deoxypyridinolin. However, more immobile subjects had significantly higher excretion rates for urinary dpd and higher serum calcium levels. Our results suggest that in elderly peopl e immobility may contribute to bone loss that might preempt the development of secondary HPT through elevation of serum calcium.