Bone mineral density in prepubertal children with beta-thalassemia: correlation with growth and hormonal data

Metabolism. 1998 May;47(5):541-8. doi: 10.1016/s0026-0495(98)90237-2.

Abstract

Patients with beta-thalassemia major (beta-thalassemia) frequently have bone disorders of multifactorial etiology. We attempted to analyze the relationship between the bone mineral density ([BMD] measured by dual-photon absorptiometry) and auxanologic parameters, degree of siderosis, function of the growth hormone (GH)/insulin-like growth factor-I (IGF-I)/IGF-binding protein-3 (IGFBP3) axis, calcium-phosphate balance, parathyroid hormone (PTH), and cytokines (interleukin-1beta [IL-1] and tumor necrosis factor-alpha [TNF-alpha]) in 30 prepubertal children with beta-thalassemia major and 15 age-matched children with constitutional short stature (CSS), who have normal glucose tolerance and thyroid function. Children with beta-thalassemia had a significantly decreased BMD and mean BMD% for age and sex (0.75+/-0.24 g/cm2 and 71%+/-10%, respectively) versus children with CSS (1.06+/-0.3 g/cm2 and 92%+/-7%, respectively). Thalassemic patients had significantly lower circulating concentrations of IGF-I and IGFBP3 (49+/-21 ng/mL and 1.2+/-0.25 mg/L, respectively) compared with control children (153+/-42 ng/mL and 2.1+/-0.37 mg/L, respectively). The GH response to provocation by clonidine and glucagon was defective (peak GH < 7 microg/L) in 12 of the 30 thalassemic children. Serum concentrations of IL-1beta and TNF-alpha did not differ among the two study groups. Hypocalcemia was detected in five of the 30 thalassemic patients: hypoparathyroidism was diagnosed in two of the five and rickets in the other three. BMD was highly correlated with the circulating concentrations of IGF-I and IGFBP3, as well as with the auxanologic parameters (age, weight, height, height standard deviation score [HSDS], and body mass index [BMI]). It is suggested that increasing the circulating IGF-I concentration through aggressive nutritional therapy and/or GH/IGF-I therapy with supplementation with vitamin D and/or calcium might improve bone growth and mineralization and prevent the development of osteoporosis and consequent fractures in these patients. Such therapy requires blinded controlled trials.

Publication types

  • Clinical Trial

MeSH terms

  • Absorptiometry, Photon
  • Adolescent
  • Adrenocorticotropic Hormone / administration & dosage
  • Adrenocorticotropic Hormone / blood
  • Adrenocorticotropic Hormone / pharmacology
  • Age Factors
  • Alkaline Phosphatase / blood
  • Alkaline Phosphatase / drug effects
  • Anthropometry
  • Antihypertensive Agents / administration & dosage
  • Antihypertensive Agents / pharmacology
  • Body Height / drug effects
  • Body Height / physiology
  • Body Mass Index
  • Body Weight / drug effects
  • Body Weight / physiology
  • Bone Density / drug effects
  • Bone Density / physiology*
  • Bone and Bones / drug effects
  • Bone and Bones / physiology
  • Calcifediol / blood
  • Calcium / blood
  • Case-Control Studies
  • Child
  • Clonidine / administration & dosage
  • Clonidine / pharmacology
  • Data Interpretation, Statistical
  • Dose-Response Relationship, Drug
  • Female
  • Gastrointestinal Agents / administration & dosage
  • Gastrointestinal Agents / pharmacology
  • Glucagon / administration & dosage
  • Glucagon / pharmacology
  • Growth / drug effects
  • Growth / physiology
  • Growth Hormone / blood
  • Growth Hormone / physiology
  • Hormones / blood
  • Humans
  • Hydrocortisone / blood
  • Hypocalcemia / blood
  • Hypocalcemia / physiopathology
  • Hypothyroidism / blood
  • Hypothyroidism / physiopathology
  • Insulin-Like Growth Factor Binding Protein 3 / blood
  • Insulin-Like Growth Factor Binding Protein 3 / drug effects
  • Insulin-Like Growth Factor I / drug effects
  • Insulin-Like Growth Factor I / metabolism
  • Interleukin-1 / blood
  • Iron / blood
  • Male
  • Parathyroid Hormone / blood
  • Phosphates / blood
  • Puberty
  • Tumor Necrosis Factor-alpha / metabolism
  • beta-Thalassemia / blood
  • beta-Thalassemia / physiopathology*

Substances

  • Antihypertensive Agents
  • Gastrointestinal Agents
  • Hormones
  • Insulin-Like Growth Factor Binding Protein 3
  • Interleukin-1
  • Parathyroid Hormone
  • Phosphates
  • Tumor Necrosis Factor-alpha
  • Insulin-Like Growth Factor I
  • Adrenocorticotropic Hormone
  • Growth Hormone
  • Glucagon
  • Iron
  • Alkaline Phosphatase
  • Clonidine
  • Calcifediol
  • Calcium
  • Hydrocortisone