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Published on: February 10, 2026
Growth hormone therapy and scoliosis in patients with Prader-Willi syndrome
1Department of Pediatrics, Dokkyo University School of Medicine Koshigaya Hospital, Saitama, Japan. t-nagai@dokkyomed.ac.jp
Insights
Growth hormone (GH) therapy for Prader-Willi syndrome (PWS) does not increase scoliosis risk. Early GH treatment in PWS patients may not worsen spinal curvature, with some cases showing improvement.
Area of Science:
- Pediatrics
- Endocrinology
- Orthopedics
Background:
- Growth hormone (GH) therapy is used for short stature in Prader-Willi syndrome (PWS).
- Concerns exist regarding potential GH therapy-induced scoliosis progression in PWS patients.
Purpose of the Study:
- To investigate the association between GH therapy and scoliosis development/progression in PWS patients.
- To determine if accelerated height velocity from GH therapy influences scoliosis.
Main Methods:
- Retrospective analysis of 72 PWS patients (41 on GH therapy, 31 not).
- Assessed scoliosis prevalence (Cobb angle >10 degrees) and progression.
- Compared height velocity and treatment initiation age between scoliotic and non-scoliotic groups.
Main Results:
- Scoliosis prevalence was similar between GH-treated (48.8%) and non-treated (41.9%) groups (P=0.56).
- Accelerated height velocity in the first year of GH therapy did not correlate with scoliosis development (P<0.001).
- Scoliosis progression occurred with age, independent of GH therapy; some patients showed improvement during treatment.
Conclusions:
- GH therapy increases height velocity in PWS patients but does not necessarily cause or worsen scoliosis.
- Early initiation of GH therapy does not appear to be an exacerbating factor for scoliosis in PWS.
- Scoliosis management in PWS patients on GH therapy should consider age-related progression and potential for improvement.
Abstract:
Growth hormone (GH) therapy for short stature in patients with Prader-Willi syndrome (PWS) has started worldwide, and various favorable effects have been reported. However, the possibility of progression of scoliosis arises as a new problem of the GH therapy. In this study, we analyzed whether 72 patients who have been followed up in our hospital have such a problem. They included 46 males and 26 females (41 patients with the GH therapy and 31 without it) aged from one to 49 years. Consequently, 33 (45.8%) of 72 patients had scoliosis with the Cobb angle of >10 degrees. Twenty (48.8%) of forty-one patients who received a GH therapy and 13 (41.9%) of 31 patients without the therapy had scoliosis, the frequency of scoliosis between the two groups showing no statistical difference (P = 0.56). Height velocity of scoliotic and non-scoliotic patients during the first year of the therapy was 8.59 +/- 1.92 and 10.70 +/- 2.54 cm, respectively, showing a significant difference (P < 0.001). This shows that accelerated height velocity may not induce scoliosis. Comparison of starting age of a GH treatment revealed that non-scoliotic patients received the therapy earlier than scoliotic patients (P = 0.021). Among 20 scoliotic patients who received the GH therapy, the degree of scoliosis progressed during the therapy in six patients, improved in three and fluctuated in one. Many patients showed progression of scoliosis with age irrespective of the use of GH, and some patients improved their scoliosis during the GH therapy. These findings showed that a GH therapy increases height velocity of PWS patients but does not necessarily develop scoliosis, and early start of the therapy may not be an exacerbating factor of scoliosis.
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