Altered bone metabolism in children infected with human immunodeficiency virus

Aim: Data on bone homoeostasis of children infected with human immunodeficiency virus (HIV), at the time of the gain in bone mass, are very rare. To determine possible alterations in bone metabolism, 13 prepubertal vertically HIV‐infected children were studied. Methods: Viral load, CD4 count, interl...

Full description

Saved in:
Bibliographic Details
Published inActa Paediatrica Vol. 92; no. 1; pp. 12 - 16
Main Authors Zamboni, G, Antoniazzi, F, Bertoldo, F, Lauriola, S, Antozzi, L, Tatò, L
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.01.2003
Blackwell
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Aim: Data on bone homoeostasis of children infected with human immunodeficiency virus (HIV), at the time of the gain in bone mass, are very rare. To determine possible alterations in bone metabolism, 13 prepubertal vertically HIV‐infected children were studied. Methods: Viral load, CD4 count, interleukin‐6 (IL‐6), growth hormone, insulin‐like growth factor‐I (IGF‐I), IGF binding protein‐3 (IGFBP‐3), acid‐labile subunit (ALS), IGFBP‐3 proteolysis, osteocalcin in blood and N‐terminal telopeptide of type I collagen in urine were determined. Lumbar spine bone mineral density was examined by dual‐energy X‐ray absorptiometry. Results: Low osteocalcin levels were found in all patients. Low IGF‐I was found in only six children, who had low CD4 count and high IL‐6 levels, with normal levels of IGFBP‐3 and ALS, absent IGFBP‐3 proteolysis and decreased bone mineral density, irrespective of viral load or growth. Conclusion: Low serum osteocalcin levels appear to be an initial warning sign of possible altered bone metabolism in HIV‐infected children. However, only when the immune system becomes more seriously compromised is bone loss measurable by bone densitometry.
Bibliography:ArticleID:APA12
ark:/67375/WNG-FGVVQ1NH-1
istex:32D2503295E9F78C687DED7FCB0E98F7271A8F34
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0803-5253
1651-2227
DOI:10.1111/j.1651-2227.2003.tb00461.x