Bone Health in Pediatric Patients With Crohn Disease

ABSTRACT Objective: The aim of our study was to examine longitudinal changes in bone mineral density (BMD) of children and adolescents with Crohn disease (CD), and risk factors related to low BMD. Patients and methods: All patients ages from 2 to 18 years with CD who underwent dual‐energy X‐ray abso...

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Veröffentlicht in:Journal of pediatric gastroenterology and nutrition 2021-08, Vol.73 (2), p.231-235
Hauptverfasser: Rozes, Sylvana, Guilmin‐Crepon, Sophie, Alison, Marianne, Thomas, Edouard, Hugot, Jean‐Pierre, Viala, Jerome, Martinez‐Vinson, Christine
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Sprache:eng
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Zusammenfassung:ABSTRACT Objective: The aim of our study was to examine longitudinal changes in bone mineral density (BMD) of children and adolescents with Crohn disease (CD), and risk factors related to low BMD. Patients and methods: All patients ages from 2 to 18 years with CD who underwent dual‐energy X‐ray absorptiometry (DXA) at diagnosis and at the end of follow‐up between 1999 and 2018 were considered for inclusion in this retrospective study. Factors related to changes in BMD at diagnosis and during follow‐up were investigated. Results: One hundred and ninety‐three patients had the two DXA required. At diagnosis, 36 patients (18.7%) had a low BMD. At the end of follow‐up, 31 patients (16%). One hundred and sixty‐four patients did not have the two DXA required. In included CD, BMD values were lower in the lumbar spine (LS) than in total body less head (TBLH), as well at diagnosis (P < 0.0001) or at the end of follow‐up (P = 0.001). At diagnosis, only growth impairment or low BMI was associated with low BMD (P < 0.0001), only cumulative dose of corticosteroid at the end of follow‐up (P = 0.01). Conclusion: The high prevalence of low BMD in children and adolescents with IBD highlights the importance of evaluating BMD in these patients at the time of diagnosis and throughout the course of their treatment. Special attention must be given to patients with height delay or low BMI at diagnosis. Long‐term glucocorticoid therapy is the main clinical risk factor associated with low BMD at the end of follow‐up.
ISSN:0277-2116
1536-4801
DOI:10.1097/MPG.0000000000003132