Decreased bone mineral density in young adults treated with SCT in childhood: the role of 25-hydroxyvitamin D
We measured bone mineral density (BMD) with dual-energy X-ray absorptiometry in the total body, at the lumbar spine, at the femoral neck and in the total hip, in 18 young adults with a median of 18.2 years after SCT. Fifteen patients had undergone auto-SCT and all patients had received TBI. The pati...
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Published in | Bone marrow transplantation (Basingstoke) Vol. 47; no. 5; pp. 657 - 662 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.05.2012
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | We measured bone mineral density (BMD) with dual-energy X-ray absorptiometry in the total body, at the lumbar spine, at the femoral neck and in the total hip, in 18 young adults with a median of 18.2 years after SCT. Fifteen patients had undergone auto-SCT and all patients had received TBI. The patients had significantly lower BMD in the total body, at the femoral neck, and in the total hip compared with age- and sex-matched controls. Six of 18 patients (33%) had low bone mass (
z
-score <−1) at one or more measurement sites, as opposed to two of the controls (11%,
P
=0.29). We found no significant influence of growth hormone levels or of untreated hypogonadism on BMD variables. Levels of 25-hydroxy (25(OH)) vitamin D were lower among the patients (35.2 vs 48.8 nmol/L,
P
=0.044) and were significantly correlated with total body BMD in the patient group (r=0.55,
P
=0.021). All six patients with low bone mass had hypovitaminosis D (⩽37 nmol/L as opposed to 4 of the 11 (36%) patients without low bone mass (
P
=0.035). In conclusion, we found decreased BMD in SCT survivors, which may in part be caused by 25(OH) vitamin D deficiency. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0268-3369 1476-5365 1476-5365 |
DOI: | 10.1038/bmt.2011.147 |