Effects of 8 years of growth hormone treatment on scoliosis in children with Prader-Willi syndrome

L.N. (Lionne) Grootjen*, J.P.H.J. (Joost) Rutges, L (Layla) Damen, Stephany Donze, A.F. (Alicia) Juriaans, Gerthe Kerkhof, Anita Koelega

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Objective
Scoliosis is frequently seen in children with Prader–Willi syndrome (PWS). There is still concern that growth hormone (GH) treatment might increase the risk of onset or progression of scoliosis. Short-term data suggested no adverse effects of GH on scoliosis, but long-term effects of GH treatment on development of scoliosis in PWS are unknown. This study investigated the effects of 8 years of GH treatment on scoliosis in children with PWS.

Design
Open-label, prospective cohort study in 103 children with PWS receiving GH for 8 years was analyzed. Prevalence and severity of scoliosis were compared to a group of 23 age-matched GH-untreated children with PWS.

Methods
Spine X-rays and DEXA-scans were performed, and Cobb angel was measured by two independent observers.

Results
After 8 years of GH treatment, at median age of 10.8 years, prevalence of scoliosis was 77.7%. No difference in prevalence or severity of scoliosis was found between GH-treated and age-matched untreated children with PWS (P = 0.409 and P = 0.709, respectively). Height SDS and trunkLBM were significantly higher in GH-treated children. Higher bone mineral density of the lumbar spine was found in children without scoliosis after 8 years of GH. Bone mineral apparent density of lumbar spine (BMADLS) SDS was associated with lower Cobb angle (r = −0.270, P = 0.008).

Conclusions
Eight years of GH treatment has no adverse effects on the prevalence and severity of scoliosis in children with PWS until 11 years of age. As BMADLS SDS is inversely associated with Cobb angle, it is pivotal to optimize the BMD status in children with PWS.
Original languageEnglish
Pages (from-to)47-55
Number of pages9
JournalEuropean Journal of Endocrinology
Volume185
Issue number1
DOIs
Publication statusPublished - 21 May 2021

Bibliographical note

Funding:
This study was an investigator-initiated study, supported by an independent research grant from Pfizer.
Pfizer was not involved in the conception or design of the study, nor in the collection, analysis or interpretation of
data, writing the manuscript, or decision to submit the manuscript for publication.

© 2021 European Society of Endocrinology

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