Abstract
Skeletal growth and changes in body composition during growth present important variations; body mass index and lean body mass related to age show important gender differences. The process of ossification is developed in two different ways, endochondral and intramembraneous. The former is characterised by the formation of bone from growth cartilage. Intramembraneous ossification is characterised by the formation of bone from a mesenchymal structure, as occurs with the flat bones of the skull. During childhood and adolescence and up to the acquisition of adult stature, two phenomenons are produced simultaneously: the synthesis of new bone from growth cartilage due to the process of endochondral ossificaion, and modeling–remodeling of previously synthetised bone. Bone growth and mineralisation of its extracellular matrix are simultaneous phenomenons, the final result being the acquisition and maintenance of body bone mass. A positive calcium balance is necessary during adolescence in order to achieve the maximum peak of bone mass and even with the termination of longitudinal growth of bone, the process of mineralisation can last a further 4 years. Childhood and adolescence are the period of life in which the peak of bone mass must be achieved, and if during this time this does not happen there will be a greater risk for the later development of osteoporosis. Regulation of bone mass is a polygenic process and during recent years studies have been centred on the receptor genes of vitamin D and estrogens. A maximum calcium retention during adolescence may influence the achievement of a high peak of bone mass but at a certain level of calcium intake the calcium retention reaches a plateau. The expression of grams of hydroxyapatite per square centimetre has been used clinically, or expressed in volume as g/cm3. From birth until 3 years, the increase represents approximately 30% of the total increase, from 3 years until the beginning of pubertal development the increase is 20%. During pubertal development there is an increase of 30–40% and from the end of growth until the age of 21 years there is an increase of 15–20%. Both prepubertal boys and girls show a progressive increase of leptin levels during the years prior to the onset of puberty and until Tanner’s stage 11 and higher levels are observed in girls in this period, possibly in relation to their earlier onset of puberty. This increase of leptin in girls during pubertal development suggests that leptin may be a link between adipose tissue and puberty.
European Journal of Clinical Nutrition (2000) 54, Suppl 1, S1–S6
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$259.00 per year
only $21.58 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to the full article PDF.
USD 39.95
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Ballabriga, A. Morphological and physiological changes during growth: an update. Eur J Clin Nutr 54 (Suppl 1), S1–S6 (2000). https://doi.org/10.1038/sj.ejcn.1600976
Published:
Issue date:
DOI: https://doi.org/10.1038/sj.ejcn.1600976
Keywords
This article is cited by
-
New approaches and technical considerations in detecting outlier measurements and trajectories in longitudinal children growth data
BMC Medical Research Methodology (2023)
-
Tributyltin perturbs femoral cortical architecture and polar moment of inertia in rat
BMC Musculoskeletal Disorders (2021)
-
Assessment of the duration of the pubertal growth spurt in patients with skeletal open bite
Journal of Orofacial Orthopedics / Fortschritte der Kieferorthopädie (2021)
-
Ghrelin, adipokines, metabolic factors in relation with weight status in school-children and results of a 1-year lifestyle intervention program
Nutrition & Metabolism (2015)
-
Factors affecting bone mineral density in men
Rheumatology International (2009)

