Impairment of bone status in patients with central diabetes insipidus

被引:21
作者
Pivonello, R
Colao, A
Di Somma, C
Facciolli, G
Klain, M
Faggiano, A
Salvatore, M
Lombardi, G
机构
[1] Univ Naples Federico II, Dept Mol & Clin Endocrinol & Oncol, I-80131 Naples, Italy
[2] CNR, I-80125 Naples, Italy
关键词
D O I
10.1210/jc.83.7.2275
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of the current study was to evaluate the biochemical parameters of bone metabolism and the bone mineral density (BMD) in patients with central diabetes insipidus, either treated or not treated with endonasal desmopressin. Eighteen patients with central diabetes insipidus and 18 sex- and age-matched healthy subjects entered the study. The patients were divided into 2 groups: patients who did not receive treatment with desmopressin for at least 1 yr (group 1), and patients chronically treated with desmopressin since the diagnosis of diabetes insipidus (group 2). Serum osteocalcin and urinary cross-linked N-telopeptide of type I collagen levels were measured in all patients and controls using RIA and enzyme-linked immunosorbent assay kits, respectively. BMD was measured at the lumbar spine (L1-L4) and at the femoral neck in all subjects, using a Hologic QDR 1000 analyzer (Hologic Inc., Waltham, MA). Serum osteocalcin concentrations were significantly lower, both in patients of group 1 and group 2, compared with healthy subjects (5.1 +/- 0.6 and 4.5 +/- 0.3 vs. 7.9 +/- 0.2 mu g/L, P < 0.05), whereas urinary cross-linked N-telopeptide of type I collagen concentrations were similar in the three groups of subjects (72.8 +/- 2.2, 71.6 +/- 2.7, and 64.6 +/- 1.7 nmol bone collagen equivalent/mmol creatinine). BMD was significantly decreased in patients of groups 1 and 2, compared with controls, both at lumbar spine (0.84 +/- 0.06 and 0.87 +/- 0.04 vs. 1.01 +/- 0.02 g/cm(2), P < 0.05) and femoral neck (0.78 +/- 0.06 and 0.80 +/- 0.04 us. 0.93 +/- 0.02 g/cm2, P < 0.05). A significant inverse correlation was found between disease duration and BMD values, evaluated as T scores, both at lumbar spine (group 1: r = -0.952, P < 0.005; group 2: r = -0.921, P < 0.001) and at femoral neck (group 1: r = -0.914, P < 0.05; group 2: r = -0.683, P < 0.05). In conclusion, patients with central diabetes insipidus had a significant bone impairment, compared with healthy subjects. Replacement with endonasal desmopressin at standard doses was not able to prevent or reverse the bone impairment. These findings suggest that, in patients with central diabetes insipidus, bone status analysis is mandatory; and a bone-loss preventing treatment might be beneficial.
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页码:2275 / 2280
页数:6
相关论文
共 20 条
[1]  
Baylis P, 1989, ENDOCRINOLOGY, P213
[2]  
Cooper C L, 1985, Adv Prostaglandin Thromboxane Leukot Res, V15, P437
[3]  
DALSKY G P, 1989, Comprehensive Therapy, V15, P30
[4]   EPIDEMIOLOGY OF FRACTURES OF THE PROXIMAL FEMUR ASSOCIATED WITH OSTEOPOROSIS IN BARCELONA, SPAIN [J].
DIEZ, A ;
PUIG, J ;
MARTINEZ, MT ;
DIEZ, JL ;
AUBIA, J ;
VIVANCOS, J .
CALCIFIED TISSUE INTERNATIONAL, 1989, 44 (06) :382-386
[5]   VASOPRESSIN ANALOG DDAVP IN DIABETES-INSIPIDUS - CLINICAL AND LABORATORY STUDIES [J].
EDWARDS, CRW ;
KITAU, MJ ;
CHARD, T ;
BESSER, GM .
BRITISH MEDICAL JOURNAL, 1973, 3 (5876) :375-378
[6]   Effect of plasma osmolality on pituitary-adrenal responses to corticotropin-releasing hormone and atrial natriuretic peptide changes in central diabetes insipidus [J].
Elias, LLK ;
AntunesRodrigues, J ;
Elias, PCL ;
Moreira, AC .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (04) :1243-1247
[7]   NEW CLUES INTO THE ETIOLOGY OF OSTEOPOROSIS - THE EFFECTS OF PROSTAGLANDINS (E2 AND F2-ALPHA) ON BONE [J].
GOLDE, B .
MEDICAL HYPOTHESES, 1992, 38 (02) :125-131
[8]  
GUYTON AC, 1986, TXB MED PHYSL, P411
[9]  
GUYTON AC, 1986, TXB MED PHYSL, P884
[10]  
JARD S, 1988, INT CONGR SER, V799, P1183