期刊
BONE
卷 35, 期 1, 页码 312-319出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.bone.2004.02.003
关键词
calcium; vitamin D; secondary hyperparathyroidism; osteoporosis; bone turnover
It is evident from several studies that not all patients with hypovitaminosis D develop secondary hyperparathyroidism. What this means for bone biochemistry and bone mineral density (BMD) remains unclear. The aim of this study was to investigate the effects of hypovitaminosis D (defined as a 25OHD less than or equal to 30 nmol/l) and patients with a blunted PTH response (defined arbitrarily as a PTH within the standard laboratory reference range in the presence of a 25OHD :5 30 nmol/l) in comparison to patients with hypovitaminosis D and secondary hyperparathyroidism, (defined arbitrarily as a PTH above the standard laboratory reference range in the presence of a 25OHD less than or equal to 30 nmol/l) and vitamin D-replete subjects (25OHD > 30 nmol/l). Four hundred twenty-one postmenopausal women (mean age: 71.2 years) with established vertebral osteoporosis were evaluated by assessing mean serum calcium, 25OHD, 1,25(OH)(2)D, bone turnover markers, and BMD. The prevalence of hypovitaminosis D was 39%. Secondary hyperparathyroidism was found in only one-third of these patients who maintained calcium homeostasis at the expense of increased bone turnover relative to the vitamin D-replete subjects (bone ALP mean difference: 43.9 IU/I [95% Cl: 24.8, 59.1], osteocalcin: 1.3 ng/ml [95% Cl: 1.1, 2.5], free deoxypyridinoline mean difference: 2.6 nmol/nmol creatinine [95% CI: 2.5, 4.8]) and bone loss (total hip BMD mean difference: 0.11 g/cm(2) [95% CI: 0.09, 0.12]). Patients with hypovitaminosis D and a blunted PTH response were characterized by a lower serum calcium (mean difference: 0.07 mmol/l [95% CI: 0.08, 0.2]), a reduction in bone turnover (bone ALP mean difference: 42.4 IU/I [95% Cl: 27.8, 61.9], osteocalcin: 1.6 ng/ml [95% Cl: 0.3, 3.1], free-deoxypyridinoline mean difference: 3.0 nmol/nmol creatinine [95% Cl: 1.9, 5.9]), but protection in bone density (total hip BMD mean difference: 0.10 g/cm(2), [95% CI: 0.08, 0.11]) as compared to those with hypovitaminosis D and secondary hyperparathyroidism. This study identifies a distinct group of patients with hypovitaminosis D and a blunted PTH response who show a disruption in calcium homeostasis but protected against PTH-mediated bone loss. This has clinical implications with respect to disease definition and may be important in deciding the optimal replacement therapy in patients with hypovitaminosis D but a blunted PTH response. (C) 2004 Elsevier Inc. All rights reserved.
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