Impaired growth plate chondrogenesis in children with chronic illnesses

被引:33
作者
De Luca, F [1 ]
机构
[1] Drexel Univ, Coll Med, Dept Pediat, St Christophers Hosp Children,Sect Endocrinol & D, Philadelphia, PA 19134 USA
关键词
D O I
10.1203/01.pdr.0000214966.60416.1b
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
In mammals, statural growth is primarily accomplished by endochondral ossification, which takes place at the growth plate. Growth plate chondrocyte proliferation, hypertrophy/differentiation, apoptosis, and cartilage matrix synthesis all contribute to chondrogenesis or cartilage formation, a process tightly coupled to the Simultaneous remodeling of the cartilage into bone at the metaphyseal border of the growth plate. Growth plate chondrogenesis is regulated by the complex interaction of molecular signals acting systemically as well locally within the growth plate. This network is often dysregulated during chronic illnesses, thus resulting in impaired growth plate chondrogenesis and, in turn, growth failure. The principal events responsible for altered growth plate chondrogenesis in chronic illness are inflammation, protein/calorie deprivation, uremia/metabolic acidosis, glucocorticoids, and impaired GH/IGF-I axis.
引用
收藏
页码:625 / 629
页数:5
相关论文
共 78 条
[1]
The localization of the functional glucocorticoid receptor α in human bone [J].
Abu, EO ;
Horner, A ;
Kusec, V ;
Triffitt, JT ;
Compston, JE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (02) :883-889
[2]
Growth suppression by glucocorticoid therapy [J].
Allen, DB .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1996, 25 (03) :699-&
[3]
ALLEN LH, 1995, J NUTR, V125, pS1119
[4]
INTERACTIONS BETWEEN GROWTH-HORMONE AND DEXAMETHASONE IN SKELETAL GROWTH AND BONE-STRUCTURE OF THE YOUNG-MOUSE [J].
ALTMAN, A ;
HOCHBERG, Z ;
SILBERMANN, M .
CALCIFIED TISSUE INTERNATIONAL, 1992, 51 (04) :298-304
[5]
CHANGES IN RAT EPIPHYSEAL CARTILAGE AFTER TREATMENT WITH DEXAMETHASONE AND GLYCOSAMINOGLYCAN-PEPTIDE COMPLEX [J].
ANNEFELD, M .
PATHOLOGY RESEARCH AND PRACTICE, 1992, 188 (4-5) :649-652
[6]
Fundamental mechanisms of growth failure in inflammatory bowel disease [J].
Ballinger, A .
HORMONE RESEARCH, 2002, 58 :7-10
[7]
Ballinger AB, 2000, GUT, V46, P694, DOI 10.1136/gut.46.5.695
[8]
THE ONTOGENY OF GROWTH-HORMONE RECEPTORS IN THE RABBIT TIBIA [J].
BARNARD, R ;
HAYNES, KM ;
WERTHER, GA ;
WATERS, MJ .
ENDOCRINOLOGY, 1988, 122 (06) :2562-2569
[9]
BARON J, 1992, AM J PHYSIOL, V263, pE489
[10]
GROWTH-PATTERN AND DIETARY INTAKE OF CHILDREN WITH CHRONIC RENAL-INSUFFICIENCY [J].
BETTS, PR ;
MAGRATH, G .
BMJ-BRITISH MEDICAL JOURNAL, 1974, 2 (5912) :189-193