The relationship between vitamin D and parathyroid hormone: calcium homeostasis, bone turnover, and bone mineral density in postmenopausal women with established osteoporosis

被引:181
作者
Sahota, O
Mundey, MK
San, P
Godber, IM
Lawson, N
Hosking, DJ
机构
[1] Univ Nottingham Hosp, Queens Med Ctr, Dept Hlth Care Elderly, Nottingham NG7 2UH, England
[2] Univ Nottingham Hosp, Sch Biomed Sci, Queens Med Ctr, Nottingham NG7 2UH, England
[3] City Hosp Nottingham, Div Mineral Metab, Nottingham, England
[4] Wishaw Gen Hosp, Clin Labs, Wishaw, Lancs, England
[5] City Hosp Nottingham, Dept Clin Chem, Nottingham, England
关键词
calcium; vitamin D; secondary hyperparathyroidism; osteoporosis; bone turnover;
D O I
10.1016/j.bone.2004.02.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:312 / 319
页数:8
相关论文
共 33 条
[1]   Low vitamin D levels in outpatient postmenopausal women from a rheumatology clinic in Madrid, Spain:: Their relationship with bone mineral density [J].
Aguado, P ;
del Campo, MT ;
Garcés, MV ;
González-Casaús, ML ;
Bernad, M ;
Gijón-Baños, J ;
Mola, EM ;
Torrijos, A ;
Martínez, ME .
OSTEOPOROSIS INTERNATIONAL, 2000, 11 (09) :739-744
[2]   Rationale for active vitamin D analog therapy in senile osteoporosis [J].
Akesson, K ;
Lau, KHW ;
Baylink, DJ .
CALCIFIED TISSUE INTERNATIONAL, 1997, 60 (01) :100-105
[3]   High prevalence of hypovitaminosis D among free-living postmenopausal women referred to an osteoporosis outpatient clinic in Northern Italy for initial screening [J].
Bettica, P ;
Bevilacqua, M ;
Vago, T ;
Norbiato, G .
OSTEOPOROSIS INTERNATIONAL, 1999, 9 (03) :226-229
[4]   Prevalence of vitamin D insufficiency in an adult normal population [J].
Chapuy, MC ;
Preziosi, P ;
Maamer, M ;
Arnaud, S ;
Galan, P ;
Hercberg, S ;
Meunier, PJ .
OSTEOPOROSIS INTERNATIONAL, 1997, 7 (05) :439-443
[5]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[6]  
CONNOLLY TM, 1985, J BIOL CHEM, V260, P7868
[7]   1,25-dihydroxyvitamin D3 in the pathogenesis and treatment of osteoporosis [J].
Deluca, HF .
OSTEOPOROSIS INTERNATIONAL, 1997, 7 (Suppl 3) :24-29
[8]   RENAL IMPAIRMENT AND ITS EFFECTS ON CALCIUM-METABOLISM IN ELDERLY WOMEN [J].
FRANCIS, RM ;
PEACOCK, M ;
BARKWORTH, SA .
AGE AND AGEING, 1984, 13 (01) :14-20
[9]   VITAMIN-D DEFICIENCY IN HOMEBOUND ELDERLY PERSONS [J].
GLOTH, FM ;
GUNDBERG, CM ;
HOLLIS, BW ;
HADDAD, JG ;
TOBIN, JD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 274 (21) :1683-1686
[10]   Vitamin D status during puberty in French healthy male adolescents [J].
Guillemant, J ;
Taupin, P ;
Le, HT ;
Taright, N ;
Allemandou, A ;
Pérès, G ;
Guillemant, S .
OSTEOPOROSIS INTERNATIONAL, 1999, 10 (03) :222-225