The urinary excretion of deoxypyridinium cross-links is higher in diabetic than in nondiabetic adolescents

被引:24
作者
Bjorgaas, M [1 ]
Haug, E
Johnsen, HJ
机构
[1] Univ Trondheim Hosp, Dept Clin Chem, N-7006 Trondheim, Norway
[2] Aker Univ Hosp, Hormone Lab, Oslo, Norway
关键词
adolescence; bone resorption; deoxypyridinium crosslinks; diabetes mellitus;
D O I
10.1007/s002239900668
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have measured the urinary excretion of deoxypyridinium (D-Pyr) crosslinks, a sensitive and specific marker of bone resorption, in morning urine in 102 healthy, nonhospitalized, Caucasian subjects (8-18 years) and in Is diabetic subjects (12-17 years). The free D-Pyr crosslinks were measured using the Pyrilinks D-Assay. In the diabetic subjects, plasma glucose was regulated throughout the night by a constant infusion of insulin and a variable infusion of 24% glucose. In the nondiabetic subjects, the excretion of D-Pyr increased until 12-14 years of age, and thereafter decreased, and the excretion of D-Pyr/hour was correlated with the height Z-score. The excretion of D-Pyr/hour and the D-Pyr/creatinine ratio was higher in the diabetic adolescents than in the nondiabetic adolescents. In subjects over the age of 12, the D-pyr/creatinine ratio was higher in males than in females. In conclusion, in healthy children and adolescents, the excretion of D-Pyr peaks at 12-14 years of age. The D-Pyr excretion is higher in diabetic than in nondiabetic adolescents, suggesting increased bone resorption in diabetic adolescents.
引用
收藏
页码:121 / 124
页数:4
相关论文
共 32 条
  • [21] Urinary immunoreactive deoxypyridinoline in children and adolescents: Variations with age, sex and growth velocity
    Rauch, F
    Rauch, R
    Woitge, HW
    Seibel, MJ
    Schonau, E
    [J]. SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1996, 56 (08) : 715 - 719
  • [22] URINARY-EXCRETION OF HYDROXY-PYRIDINIUM CROSS-LINKS OF COLLAGEN REFLECTS SKELETAL GROWTH VELOCITY IN NORMAL-CHILDREN
    RAUCH, F
    SCHONAU, E
    WOITGE, H
    REMER, T
    SEIBEL, M
    [J]. EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY, 1994, 102 (02): : 94 - 97
  • [23] ROBINS SP, 1994, J BONE MINER RES, V9, P1643
  • [24] DIMINUTION OF BONE MASS IN CHILDHOOD DIABETES
    ROSENBLOOM, AL
    LEZOTTE, DC
    WEBER, FT
    GUDAT, J
    HELLER, DR
    WEBER, ML
    KLEIN, S
    KENNEDY, BB
    [J]. DIABETES, 1977, 26 (11) : 1052 - 1055
  • [25] DECREASED CORTICAL THICKNESS AND OSTEOPENIA IN CHILDREN WITH DIABETES-MELLITUS
    SANTIAGO, JV
    MCALISTER, WH
    RATZAN, SK
    BUSSMAN, Y
    HAYMOND, MW
    SHACKELFORD, G
    WELDON, VV
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1977, 45 (04) : 845 - 848
  • [26] HYDROXYPROLINE EXCRETION IS INCREASED IN DIABETES-MELLITUS AND RELATED TO THE PRESENCE OF MICROALBUMINURIA
    SELBY, PL
    SHEARING, PA
    MARSHALL, SM
    [J]. DIABETIC MEDICINE, 1995, 12 (03) : 240 - 243
  • [27] CLINICAL LONGITUDINAL STANDARDS FOR HEIGHT, WEIGHT, HEIGHT VELOCITY, WEIGHT VELOCITY, AND STAGES OF PUBERTY
    TANNER, JM
    WHITEHOUSE, RH
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1976, 51 (03) : 170 - 179
  • [28] OSTEOPOROSIS AND DIABETES - LESSONS FROM THE DIABETIC BB RAT
    VERHAEGHE, J
    VISSER, WJ
    EINHORN, TA
    BOUILLON, R
    [J]. HORMONE RESEARCH, 1990, 34 (5-6) : 245 - 248
  • [29] BONE AND MINERAL METABOLISM IN BB RATS WITH LONG-TERM DIABETES - DECREASED BONE TURNOVER AND OSTEOPOROSIS
    VERHAEGHE, J
    VANHERCK, E
    VISSER, WJ
    SUIKER, AMH
    THOMASSET, M
    EINHORN, TA
    FAIERMAN, E
    BOUILLON, R
    [J]. DIABETES, 1990, 39 (04) : 477 - 482
  • [30] WAALER PE, 1983, ACTA PAEDIATR SC S, V308, P26