ASSESSMENT OF BONE-RESORPTION WITH A NEW MARKER OF COLLAGEN DEGRADATION IN PATIENTS WITH METABOLIC BONE-DISEASE

被引:174
作者
GARNERO, P
GINEYTS, E
RIOU, JP
DELMAS, PD
机构
[1] HOP EDOUARD HERRIOT, INSERM, U403, F-69437 LYON 03, FRANCE
[2] HOP EDOUARD HERRIOT, DEPT ENDOCRINOL DIABETOL & NUTR, LYON, FRANCE
关键词
D O I
10.1210/jc.79.3.780
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have used a new enzyme-linked immunoassay (ELISA) to meas ure the urinary excretion of type I collagen peptides (CrossLaps) released during bone matrix degradation in a sample of healthy adults comprising 146 women and 60 men, aged 31-89 yr, and in patients with metabolic bone disease. The intra- and interassay coefficients of variation were less than 10% and 13%, respectively. The recovery of CrossLaps antigen from urine samples ranged from 92-115%, and the ELISA was linear for serial sample dilutions. The CrossLaps assay does not cross-react with either free pyridinoline (Pyr) or free deoxypyridinoline (D-Pyr). CrossLaps measured by ELISA and the total excretion of Pyr measured by high performance liquid chromatography were highly correlated in normal women (n = 91; r = 0.73; P < 0.001). Urinary CrossLaps excretion increased with age in women, but not in men. In women, the menopause was reflected by a mean 141% increase in CrossLaps excretion [from an average 217 to 524 mu g/mmol creatinine (Cr)] that was higher than the mean increase in total D-Pyr (+91%) and total Pyr (+47%) measured by HPLC and the mean increase in bone alkaline phophatase (+48 %) and osteocalcin (+41%). Urinary CrossLaps excretion was increased from control values in Paget's disease (n = 32; mean, 1810 +/- 2300 mu g/mmol Cr; P < 0.001), in patients with primary hyperparathyroidism (n = 10; mean, 780 +/- 380 mu g/mmol Cr; P < 0.001), and in patients with hyperthyroidism (n = 27; mean, 1280 +/- 970 mu g/mmol Cr; P < 0.001), with Z-scores (number of so from the mean of sex- and age-matched controls) of 4.4 +/- 6.6, 1.5 +/- 1.2, and 6.7 +/- 6.5, respectively. In patients with Paget's disease, CrossLaps values were highly correlated with urinary hydroxyproline levels (r = 0.91; P < 0.001), and the decrease in urinary CrossLaps excretion was greater than that in urinary hydroxyproline (-71% vs. -17%; P < 0.001) after 3 days of iv treatment with the bisphosphonate pamidronate. In patients with hyperthyroidism, CrossLaps excretion was elevated above the normal range in most patients (78%) and returned to normal within 1 month of treatment for hyperthyroidism. It is concluded that this new convenient assay represents a sensitive and specific index of the bone resorption rate, and that it should be useful for the clinical investigation and therapeutic monitoring of patients with osteoporosis and other metabolic bone diseases.
引用
收藏
页码:780 / 785
页数:6
相关论文
共 31 条
[1]   QUANTITATIVE-ANALYSIS OF THE PYRIDINIUM CROSSLINKS OF COLLAGEN IN URINE USING ION-PAIRED REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
BLACK, D ;
DUNCAN, A ;
ROBINS, SP .
ANALYTICAL BIOCHEMISTRY, 1988, 169 (01) :197-203
[2]   URINARY PYRIDINIUM CROSS-LINKS AS MARKERS OF BONE-RESORPTION IN TUMOR-ASSOCIATED HYPERCALCEMIA [J].
BODY, JJ ;
DELMAS, PD .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 74 (03) :471-475
[3]  
BONDE M, IN PRESS CLIN CHEM
[4]  
DANILOFF GY, 1993, J BONE MINER RES, V8, pS357
[5]  
Delmas P. D., 1988, OSTEOPOROSIS ETIOLOG, P297
[6]   INCREASE IN SERUM BONE GAMMA-CARBOXYGLUTAMIC ACID PROTEIN WITH AGING IN WOMEN - IMPLICATIONS FOR THE MECHANISM OF AGE-RELATED BONE LOSS [J].
DELMAS, PD ;
STENNER, D ;
WAHNER, HW ;
MANN, KG ;
RIGGS, BL .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 71 (05) :1316-1321
[7]  
DELMAS PD, 1993, J BONE MINER RES, V8, P643
[8]  
DELMAS PD, 1991, J BONE MINER RES, V6, P639
[9]  
DELMAS PD, 1993, J BONE MINER RES, V8, pS549
[10]   BONE-FORMATION RATE IN OLDER NORMAL WOMEN - CONCURRENT ASSESSMENT WITH BONE HISTOMORPHOMETRY, CALCIUM KINETICS, AND BIOCHEMICAL MARKERS [J].
EASTELL, R ;
DELMAS, PD ;
HODGSON, SF ;
ERIKSEN, EF ;
MANN, KG ;
RIGGS, BL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 67 (04) :741-748