Bone mineral density in young adults with Prader-Willi syndrome: A randomized, placebo-controlled, crossover GH trial

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Abstract

Context: The prevalence of osteoporosis is increased in adults with Prader-Willi syndrome (PWS). In children with PWS, growth hormone (GH) treatment has beneficial effects on bone mineral density (BMD). BMD might deteriorate after cessation of GH at adult height (AH), while continuing GH might maintain BMD. Objective: To investigate the effects of GH vs placebo, and furthermore the effects of sex steroid replacement therapy (SSRT), on BMD in GH-treated young adults with PWS who had attained AH. Design: Two-year, randomized, double-blind, placebo-controlled, crossover GH study. Patients: Twenty-seven young adults with PWS were stratified for gender and BMI and then randomly and blindly assigned to receive GH (0.67 mg/m2/day) or placebo for 1 year, after which they crossed over to the alternative treatment for another year. Measurements: Bone mineral density of the total body (BMDTB) and lumbar spine (BMDLS) SDS were measured by dual-energy x-ray absorptiometry. Results: At AH, BMDTBSDS was significantly lower compared to healthy peers (P

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Donze, S. H., Kuppens, R. J., Bakker, N. E., van Alfen-van der Velden, J. A. E. M., & Hokken-Koelega, A. C. S. (2018). Bone mineral density in young adults with Prader-Willi syndrome: A randomized, placebo-controlled, crossover GH trial. Clinical Endocrinology, 88(6), 806–812. https://doi.org/10.1111/cen.13567

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