Children with chronic illnesses such as Juvenile Idiopathic Arthritis and Crohn's disease, particularly when taking glucocorticoids, are at significant risk for bone fragility. Furthermore, when childhood illness interferes with achieving normal peak bone mass, life-long fracture risk is increased. Osteopenia and osteoporosis, which is increasingly recognized in pediatric chronic disease, likely results from numerous disease- and treatment-related factors, including glucocorticoid exposure. Diagnosing osteoporosis in childhood is complicated by the limitations of current noninvasive techniques such as DXA, which despite its limitations remains the gold standard. The risk:benefit ratio of treatment is confounded by the potential for spontaneous restitution of bone mass deficits and reshaping of previously fractured vertebral bodies. Bisphosphonates have been used to treat secondary osteoporosis in children, but limited experience and potential long-term toxicity warrant caution in routine use. This article reviews the factors that influence loss of normal bone strength and evidence for effective treatments, in particular in patients with gastrointestinal and rheumatologic disorders who are receiving chronic glucocorticoid therapy.

Glucocorticoid-associated osteoporosis in chronic inflammatory diseases : epidemiology, mechanisms, diagnosis, and treatment / E. Von Scheven, J. Corbin Kathleen, S. Stefano, R. Cimaz. - In: CURRENT OSTEOPOROSIS REPORTS. - ISSN 1544-1873. - 12:3(2014), pp. 289-299. [10.1007/s11914-014-0228-x]

Glucocorticoid-associated osteoporosis in chronic inflammatory diseases : epidemiology, mechanisms, diagnosis, and treatment

R. Cimaz
2014

Abstract

Children with chronic illnesses such as Juvenile Idiopathic Arthritis and Crohn's disease, particularly when taking glucocorticoids, are at significant risk for bone fragility. Furthermore, when childhood illness interferes with achieving normal peak bone mass, life-long fracture risk is increased. Osteopenia and osteoporosis, which is increasingly recognized in pediatric chronic disease, likely results from numerous disease- and treatment-related factors, including glucocorticoid exposure. Diagnosing osteoporosis in childhood is complicated by the limitations of current noninvasive techniques such as DXA, which despite its limitations remains the gold standard. The risk:benefit ratio of treatment is confounded by the potential for spontaneous restitution of bone mass deficits and reshaping of previously fractured vertebral bodies. Bisphosphonates have been used to treat secondary osteoporosis in children, but limited experience and potential long-term toxicity warrant caution in routine use. This article reviews the factors that influence loss of normal bone strength and evidence for effective treatments, in particular in patients with gastrointestinal and rheumatologic disorders who are receiving chronic glucocorticoid therapy.
Bone density; Children; Corticosteroids; Crohn's disease; Glucocorticoids; Juvenile dermatomyositis; Juvenile idiopathic arthritis; Osteoporosis; Pediatric; Rheumatic disease; Systemic lupus erythematosus; Bone Density Conservation Agents; Calcium; Child; Chronic Disease; Crohn Disease; Fractures; Bone; Glucocorticoids; Human Growth Hormone; Humans; Lupus Erythematosus; Systemic; Osteoporosis; Rheumatic Diseases; Vitamin D; Endocrinology; Diabetes and Metabolism; Medicine (all)
Settore MED/16 - Reumatologia
2014
Article (author)
File in questo prodotto:
File Dimensione Formato  
osteoporosisVonScheven2014.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 537.74 kB
Formato Adobe PDF
537.74 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
10.1007_s11914-014-0228-x.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 520.89 kB
Formato Adobe PDF
520.89 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/663328
Citazioni
  • ???jsp.display-item.citation.pmc??? 11
  • Scopus 45
  • ???jsp.display-item.citation.isi??? 39
social impact