Literature DB >> 16770808

Growth hormone therapy and scoliosis in patients with Prader-Willi syndrome.

T Nagai1, K Obata, T Ogata, N Murakami, Y Katada, A Yoshino, S Sakazume, Y Tomita, R Sakuta, N Niikawa.   

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. Copyright 2006 Wiley-Liss, Inc.

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Year:  2006        PMID: 16770808     DOI: 10.1002/ajmg.a.31295

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  14 in total

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Authors:  L E Polgreen; B S Miller
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3.  Growth hormone supplement treatment reduces the surgical risk for Prader-Willi Syndrome patients.

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Journal:  Scoliosis       Date:  2010-06-15

5.  Inclusion of chiropractic care in multidisciplinary management of a child with Prader-Willi syndrome: a case report.

Authors:  Rebekah A Wittman; Sharon A Vallone
Journal:  J Chiropr Med       Date:  2009-12

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Review 8.  Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.

Authors:  M A Angulo; M G Butler; M E Cataletto
Journal:  J Endocrinol Invest       Date:  2015-06-11       Impact factor: 4.256

9.  Short-term growth hormone treatment in children with Hurler syndrome after hematopoietic cell transplantation.

Authors:  L E Polgreen; M Plog; J D Schwender; J Tolar; W Thomas; P J Orchard; B S Miller; A Petryk
Journal:  Bone Marrow Transplant       Date:  2009-03-02       Impact factor: 5.483

10.  Influence of molecular classes and growth hormone treatment on growth and dysmorphology in Prader-Willi syndrome: A multicenter study.

Authors:  Ranim Mahmoud; Anna Leonenko; Merlin G Butler; Pamela Flodman; June-Anne Gold; Jennifer L Miller; Elizabeth Roof; Elisabeth Dykens; Daniel J Driscoll; Virginia Kimonis
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