Impaired growth plate chondrogenesis in children with chronic illnesses
- PMID: 16627871
- DOI: 10.1203/01.pdr.0000214966.60416.1b
Impaired growth plate chondrogenesis in children with chronic illnesses
Abstract
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.
Similar articles
-
Endocrine regulation of the growth plate.Horm Res. 2005;64(4):157-65. doi: 10.1159/000088791. Epub 2005 Oct 4. Horm Res. 2005. PMID: 16205094 Review.
-
Insulin-Like Growth Factor-Independent Effects of Growth Hormone on Growth Plate Chondrogenesis and Longitudinal Bone Growth.Endocrinology. 2015 Jul;156(7):2541-51. doi: 10.1210/en.2014-1983. Epub 2015 Apr 24. Endocrinology. 2015. PMID: 25910049
-
Promoting growth in chronic inflammatory disease: lessons from studies of the growth plate.Horm Res. 2009 Nov;72 Suppl 1:42-7. doi: 10.1159/000229763. Epub 2009 Nov 27. Horm Res. 2009. PMID: 19940495 Review.
-
Role of Nuclear Factor Kappa B (NF-κB) in Growth Plate Chondrogenesis.Pediatr Endocrinol Rev. 2016 Jun;13(4):720-30. Pediatr Endocrinol Rev. 2016. PMID: 27464415 Review.
-
Physiology and pathophysiology of the growth plate.Birth Defects Res C Embryo Today. 2003 May;69(2):123-43. doi: 10.1002/bdrc.10014. Birth Defects Res C Embryo Today. 2003. PMID: 12955857 Review.
Cited by
-
The role of O-GlcNAcylation in bone metabolic diseases.Front Physiol. 2024 Jun 10;15:1416967. doi: 10.3389/fphys.2024.1416967. eCollection 2024. Front Physiol. 2024. PMID: 38915778 Free PMC article. Review.
-
Pharmacological inhibition of BCL-2 with the FDA-approved drug venetoclax impairs longitudinal bone growth.Sci Rep. 2023 May 17;13(1):8054. doi: 10.1038/s41598-023-34965-4. Sci Rep. 2023. PMID: 37198212 Free PMC article.
-
Closure of the neuro-central synchondrosis and other physes in foal cervical spines.Equine Vet J. 2025 Jan;57(1):217-231. doi: 10.1111/evj.14093. Epub 2024 Apr 9. Equine Vet J. 2025. PMID: 38594893 Free PMC article.
-
The effect of rapamycin on bone growth in rabbits.J Orthop Res. 2009 Sep;27(9):1157-61. doi: 10.1002/jor.20894. J Orthop Res. 2009. PMID: 19382193 Free PMC article.
-
Magnetic resonance imaging is the preferred method to assess treatment-related skeletal changes in children with brain tumors.Pediatr Blood Cancer. 2013 Sep;60(9):1552-6. doi: 10.1002/pbc.24536. Epub 2013 Mar 22. Pediatr Blood Cancer. 2013. PMID: 23526749 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical