Postural-motor development, spinal range of movement and caregiver burden in Prader-Willi syndrome-associated scoliosis: an observational study

Published: 22 April 2024
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Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by hypothalamic dysfunction, hypotonia, cognitive deficits, and hyperphagia, primarily resulting from genetic abnormalities on chromosome 15. Among its varied manifestations, musculoskeletal issues, notably scoliosis, pose important challenges in management. This study aims to investigate differences in postural-motor development and spinal range of movement between preadolescents and adolescents with PWS, with and without scoliosis, while also exploring the potential impact of scoliosis on caregiving burden, an aspect yet to be thoroughly explored in existing literature. This observational study evaluated 13 individuals diagnosed with PWS, including 5 with scoliosis (PWS-Sc) and 7 without (PWS-NSc). Inclusion criteria comprised ages 8 to 18 years, confirmed PWS diagnosis through genetic testing, and scoliosis diagnosis. Anamnestic data, physical examinations, and surface measurements were collected, along with parental burden assessments using the Zarit Burden Interview (ZBI). Both groups displayed delays in achieving postural-motor milestones, with the PWS-Sc group exhibiting a more pronounced delay, although statistical significance was not achieved. The main curve magnitude in the PWS-Sc group averaged 31.5° Cobb, with 60% of cases presenting an S-shaped curve. Surface measurements of physiological curves did not differ significantly between groups, but the scoliosis-affected group exhibited lower lumbar extension values (p=0.04). The overall ZBI revealed higher scores in the PWS-Sc group, although statistical significance was not reached. However, significant differences were observed in single questions score evaluating aspects such as social life and caregiver uncertainty (p=0.04 and p=0.03, respectively). Despite the small sample size, delays in achieving postural-motor milestones, particularly in individuals with scoliosis, were observed. The differences recorded in lumbo-pelvic movement suggest that tailored interventions may be beneficial. The heightened caregiving burden in the scoliosis group underscores the need for targeted support. Early intervention and ongoing monitoring should be important for accurate diagnosis and appropriate care, potentially with psychological support for caregivers.

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Tauber M, Hoybye C. Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction. Lancet Diabetes Endocrinol 2021;9:4. DOI: https://doi.org/10.1016/S2213-8587(21)00002-4
Höybye C, Tauber M. Approach to the patient With Prader–Willi Syndrome. J Clin Endocrinol Metab 2022;107:1698–705. DOI: https://doi.org/10.1210/clinem/dgac082
Ma VK, Mao R, Toth JN, et al. Prader-Willi and Angelman Syndromes: mechanisms and management. Appl Clin Genet 2023;16:41–52.
Bittel DC, Butler MG. Prader–Willi syndrome: clinical genetics, cytogenetics and molecular biology. Expert Rev Mol Med 2005;7:1–20. DOI: https://doi.org/10.1017/S1462399405009531
Missaglia S, Tommasini E, Vago P, et al. Salivary and serum irisin in healthy adults before and after exercise. Eur J Transl Myol 2023;33:11093. DOI: https://doi.org/10.4081/ejtm.2023.11093
Shim JS, Lee SH, Seo SW, et al. The musculoskeletal manifestations of Prader-Willi Syndrome. J Pediatr Orthop 2010;30:390–5. DOI: https://doi.org/10.1097/BPO.0b013e3181da857d
Nakamura Y, Murakami N, Iida T, et al. The characteristics of scoliosis in Prader–Willi syndrome (PWS): analysis of 58 scoliosis patients with PWS. J Orthop Sci 2015;20:17–22. DOI: https://doi.org/10.1007/s00776-014-0651-y
de Lind van Wijngaarden RFA, de Klerk LWL, Festen DAM, Hokken-Koelega ACS. Scoliosis in Prader-Willi syndrome: prevalence, effects of age, gender, body mass index, lean body mass and genotype. Arch Dis Child 2008;93;1012–16. DOI: https://doi.org/10.1136/adc.2007.123836
van Bosse HJP, Butler MG. Clinical observations and treatment approaches for scoliosis in Prader–Willi Syndrome. Genes (Basel) 2020;11:260. DOI: https://doi.org/10.3390/genes11030260
Odent T, Accadbled F, Koureas G, et al. Scoliosis in patients with Prader-Willi Syndrome. Pediatrics 2008;122:e499–e503. DOI: https://doi.org/10.1542/peds.2007-3487
Butler MG, Hossain W, Hassan M, Manzardo AM. Growth hormone receptor (GHR) gene polymorphism and scoliosis in Prader-Willi syndrome. Growth Horm IGF Res 2018;39:29–33. DOI: https://doi.org/10.1016/j.ghir.2017.12.001
Grootjen LN, Rutges JPHJ, Damen L, et al. Effects of 8 years of growth hormone treatment on scoliosis in children with Prader–Willi syndrome. Eur J Endocrinol 2021;185:47–55. DOI: https://doi.org/10.1530/EJE-21-0211
Tsai LP, Tzeng ST, Hsieh TH, et al. Scoliosis and BMI in patients with Prader–Willi syndrome. J Pediatr Orthop B 2023;32:524–30. DOI: https://doi.org/10.1097/BPB.0000000000001031
van Bosse HJP. Role of body cast application for scoliosis associated with Prader-Willi Syndrome. J Pediatr Orthop 2021;41:e321–e327. DOI: https://doi.org/10.1097/BPO.0000000000001660
Ferraro C, Venturin A, Ferraro M, et al. Hump height in idiopathic scoliosis measured using a humpmeter in growing subjects: relationship between the hump height and the Cobb angle and the effect of age on the hump height. Eur J Phys Rehabil Med 2017;53:3. DOI: https://doi.org/10.23736/S1973-9087.16.04227-1
Gravina A, Ferraro C, Poli P, et al. Goniometric evaluation of the spinal sagittal curves in children and adolescents: A reliability study. J Back Musculoskelet Rehabil 2017;30:325–31. DOI: https://doi.org/10.3233/BMR-160541
Domínguez-Vergara J, Santa-Cruz-Espinoza H, Chávez-Ventura G. Zarit caregiver burden interview: psychometric properties in family caregivers of people with intellectual disabilities. Eur J Investig Heal Psychol Educ 2023;13:391–402. DOI: https://doi.org/10.3390/ejihpe13020029
Kayadjanian N, Schwartz L, Farrar E, et al. High levels of caregiver burden in Prader-Willi syndrome. PLoS One 2018;13:e0194655. DOI: https://doi.org/10.1371/journal.pone.0194655
Crinò A, Armando M, Crostelli M, et al. High Prevalence of Scoliosis in a Large Cohort of Patients with Prader-Willi Syndrome. J Clin Med 2022;11:1574. DOI: https://doi.org/10.3390/jcm11061574
Ehara H, Ohno K, Takeshita K. Growth and developmental patterns in Prader‐Willi syndrome. J Intellect Disabil Res 1993;37:479–85. DOI: https://doi.org/10.1111/j.1365-2788.1993.tb00318.x
Bridges N. What is the value of growth hormone therapy in Prader Willi syndrome? Arch Dis Child 2014;99:166–70. DOI: https://doi.org/10.1136/archdischild-2013-303760
Pansy J, Barones C, Urlesberger B, et al. Early motor and pre-linguistic verbal development in Prader-Willi syndrome – A case report. Res Dev Disabil 2019;88:16–21. DOI: https://doi.org/10.1016/j.ridd.2019.01.012
Vlažná D, Krkoška P, Kuhn M, et al. Assessment of lumbar extensor muscles in the context of trunk function, a pilot study in healthy individuals. Appl Sci 2021;11;9518. DOI: https://doi.org/10.3390/app11209518
Bayartai ME, Luomajoki H, Tringali G, et al. Differences in spinal postures and mobility among adults with Prader-Willi syndrome, essential obesity, and normal-weight individuals. Front. Endocrinol (Lausanne) 2023;14:1235030. DOI: https://doi.org/10.3389/fendo.2023.1235030
Maccarone MC, Masiero S. The important impact of COVID-19 pandemic on the reorganization of a rehabilitation unit in a national healthcare system hospital in Italy. Am J Phys Med Rehabil 2021;100:327–30. DOI: https://doi.org/10.1097/PHM.0000000000001707
Konieczny MR, Hieronymus P, Krauspe R. Time in brace: where are the limits and how can we improve compliance and reduce negative psychosocial impact in patients with scoliosis? A retrospective analysis. Spine J 2017;17:1658–64. DOI: https://doi.org/10.1016/j.spinee.2017.05.010

How to Cite

Maccarone, M. C., Avenia, M., & Masiero, S. (2024). Postural-motor development, spinal range of movement and caregiver burden in Prader-Willi syndrome-associated scoliosis: an observational study . European Journal of Translational Myology, 34(2). https://doi.org/10.4081/ejtm.2024.12533