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Decreased bone mineral density in Prader-Willi syndrome: Comparison with obese subjects

Authors :
Butler, Merlin G.
Haber, Lawrence
Mernaugh, Ray
Carlson, Michael G.
Price, Ron
Feurer, Irene D.
Source :
American Journal of Medical Genetics. Part A; 15 October 2001, Vol. 103 Issue: 3 p216-222, 7p
Publication Year :
2001

Abstract

Bone density, anthropometric data, and markers of bone turnover were collected on 21 subjects diagnosed with Prader-Willi syndrome (PWS) and compared with 9 subjects with obesity of unknown cause. In addition, urinary N-telopeptide levels were obtained in all subjects. N-telopeptides are the peptide fragments of type I collagen, the major bone matrix material. During periods of active bone degradation or high bone turnover, high levels of N-telopeptides are excreted in the urine. However, no significant difference was detected in the urinary N-telopeptide levels when corrected for creatinine excretion (raw or transformed data) between our subjects with obesity or PWS and the observed effect size of the between-group difference was small. Although N-telopeptide levels were higher but not significantly different in the subjects with PWS compared with obese controls, the subjects with PWS had significantly decreased total bone and spine mineral density and total bone mineral content (all Pā€‰<ā€‰0.001). No differences in N-telopeptide levels or bone mineral density were observed between subjects with PWS and chromosome 15q deletion or maternal disomy. Thus, decreased bone mineral density in subjects with PWS may relate to the lack of depositing bone mineral during growth when bones are becoming more dense (e.g., during adolescence), possibly because of decreased production of sex or growth hormones and/or long-standing hypotonia. It may not be caused by loss, or active degradation, of bone matrix measurable by the methods described in this study further supporting the possible need for hormone therapy during adolescence. © 2001 Wiley-Liss, Inc.

Details

Language :
English
ISSN :
15524825 and 15524833
Volume :
103
Issue :
3
Database :
Supplemental Index
Journal :
American Journal of Medical Genetics. Part A
Publication Type :
Periodical
Accession number :
ejs412134