Skip to main content

Advertisement

Log in

Anthropometric adjustments are helpful in the interpretation of BMD and BMC Z-scores of pediatric patients with Prader-Willi syndrome

  • Original Article
  • Published:
Osteoporosis International Aims and scope Submit manuscript

Abstract

Summary

Anthropometric adjustments of bone measurements are necessary in Prader-Willi syndrome patients to correctly assess the bone status of these patients. This enables physicians to get a more accurate diagnosis of normal versus abnormal bone, allow for early and effective intervention, and achieve better therapeutic results.

Introduction

Bone mineral density (BMD) is decreased in patients with Prader-Willi syndrome (PWS). Because of largely abnormal body height and weight, traditional BMD Z-scores may not provide accurate information in this patient group. The goal of the study was to assess a cohort of individuals with PWS and characterize the development of low bone density based on two adjustment models applied to a dataset of BMD and bone mineral content (BMC) from dual-energy X-ray absorptiometry (DXA) measurements.

Methods

Fifty-four individuals, aged 5–20 years with genetically confirmed PWS, underwent DXA scans of spine and hip. Thirty-one of them also underwent total body scans. Standard Z-scores were calculated for BMD and BMC of spine and total hip based on race, sex, and age for all patients, as well as of whole body and whole-body less head for those patients with total-body scans. Additional Z-scores were generated based on anthropometric adjustments using weight, height, and percentage body fat and a second model using only weight and height in addition to race, sex, and age.

Results

As many PWS patients have abnormal anthropometrics, addition of explanatory variables weight, height, and fat resulted in different bone classifications for many patients. Thus, 25–70 % of overweight patients, previously diagnosed as normal, were subsequently diagnosed as below normal, and 40–60 % of patients with below-normal body height changed from below normal to normal depending on bone parameter.

Conclusions

This is the first study to include anthropometric adjustments into the interpretation of BMD and BMC in children and adolescents with PWS. This enables physicians to get a more accurate diagnosis of normal versus abnormal BMD and BMC and allows for early and effective intervention.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Cassidy SB, Schwartz S, Miller JL, Driscoll DJ (2012) Prader-Willi syndrome. Genet Med 14:10–26

    Article  CAS  PubMed  Google Scholar 

  2. 2 Prader-Willi Syndrome Association (USA) (2008) Osteoporosis evaluation and therapy in Prader-Willi syndrome. Consensus statement of the PWSA (USA) Clinical Advisory Board. The gathered view (ISSN 1077-9965) 94:3763–3771.

  3. Hirsch HJ, Geva-Eldar T, Benarroch F, Rubinstein O, Gross-Tsur V (2009) Primary testicular dysfunction is a major contributor to abnormal pubertal development in males with Prader-Willi syndrome. J Clin Endocrinol Metab 94:2262–2268

    Article  CAS  PubMed  Google Scholar 

  4. Eldar-Geva T, Hirsch HJ, Benarroch F, Rubinstein O, Gross-Tsur V (2010) Hypogonadism in females with Prader-Willi syndrome from infancy to adulthood: variable combinations of a primary gonadal defect and hypothalamic dysfunction. Eur J Endocrinol 162:377–384

    Article  CAS  PubMed  Google Scholar 

  5. Siemensma EP, de Lind van Wijngaarden RF, Otten BJ, de Jong FH, Hokken-Koelega AC (2012) Testicular failure in boys with Prader-Willi syndrome: longitudinal studies of reproductive hormones. J Clin Endocrinol Metab 97:E452–E459

    Article  CAS  PubMed  Google Scholar 

  6. Radicioni AF, Di Giorgio G, Grugni G, Cuttini M, Losacco V, Anzuini A, Spera S, Marzano C, Lenzi A, Cappa M, Crinò A (2012) Multiple forms of hypogonadism of central, peripheral or combined origin in males with Prader-Willi syndrome. Clin Endocrinol (Oxf) 76:72–77

    Article  CAS  Google Scholar 

  7. Hirsch HJ, Geva-Eldar T, Benarroch F, Pollak Y, Gross-Tsur V (2015) Sexual dichotomy in gonadal function in Prader-Willi syndrome (PWS): a longitudinal study from early infancy through the fourth decade. Hum Reprod 30:2587–2596

    Article  CAS  PubMed  Google Scholar 

  8. Butler MG, Haber L, Mernaugh R, Carlson MG, Price R, Feurer ID (2001) Decreased bone mineral density in Prader-Willi syndrome: comparison with obese subjects. Am J Med Genet 103:216–222

    Article  CAS  PubMed  Google Scholar 

  9. Vestergaard P, Kristensen K, Bruun JM, Østergaard JR, Heickendorff L, Mosekilde L, Richelsen B (2004) Reduced bone mineral density and increased bone turnover in Prader-Willi syndrome compared with controls matched for sex and body mass index—a cross-sectional study. J Pediatr 144:614–619

    Article  PubMed  Google Scholar 

  10. Rizzoli R, Cooper C, Reginster JY, Abrahamsen B, Adachi JD, Brandi ML, Bruyère O, Compston J, Ducy P, Ferrari S, Harvey NC, Kanis JA, Karsenty G, Laslop A, Rabenda V, Vestergaard P (2012) Antidepressant medications and osteoporosis. Bone 51:606–613

    Article  CAS  PubMed  Google Scholar 

  11. Khare M, Gold JA, Wencel M, Billimek J, Surampalli A, Duarte B, Pontello A, Galassetti P, Cassidy S, Kimonis VE (2014) Effect of genetic subtypes and growth hormone treatment on bone mineral density in Prader-Willi syndrome. J Pediatr Endocrinol Metabol 27:511–518

    Article  CAS  Google Scholar 

  12. Bakker NE, Kuppens RJ, Siemensma EP, van Wijngaarden RF T-de L, Festen DA, Bindels-de Heus GC, Bocca G, Haring DA, Hoorweg-Nijman JJ, Houdijk EC, Jira PE, Lunshof L, Odink RJ, Oostdijk W, Rotteveel J, Van Alfen AA, Van Leeuwen M, Van Wieringen H, Wegdam-den Boer ME, Zwaveling-Soonawala N, Hokken-Koelega AC (2015) Bone mineral density in children and adolescents with Prader-Willi syndrome: a longitudinal study during puberty and 9 years of growth hormone treatment. J Clin Endocrinol Metab 100:1609–1618

    Article  CAS  PubMed  Google Scholar 

  13. Schoenau E, Frost HM (2002) The “muscle-bone unit” in children and adolescents. Calcif Tissue Int 70:405–407

    Article  CAS  PubMed  Google Scholar 

  14. Short DF, Gilsanz V, Kalkwarf HJ, Lappe JM, Oberfield S, Shepherd JA, Winer KK, Zemel BS, Hangartner TN (2015) Anthropometric models of bone mineral content and areal bone mineral density based on the Bone Mineral Density in Childhood Study. Osteoporos Int 26:1099–1108

    Article  CAS  PubMed  Google Scholar 

  15. 15 World Health Organization (2015) Growth reference data for 5–19 years. http://www.who.int/growthref/en/; accessed 25 September 2015.

  16. De Lind van Wijngaarden RFA, Festen DAM, Otten BJ, van Mil EGAH, Rotteveel J, Odink RJ, van Leeuwen M, Haring DAJP, Bocca G, Houdijk AM, Hokken-Koelega ACS (2009) Bone mineral density and effects of growth hormone treatment in prepubertal children with Prader-Willi syndrome: a randomized clinical trial. J Clin Endocrinol Metab 94:3763–3771

    Article  Google Scholar 

  17. Rubin DA, Cano-Sokoloff N, Castner DL, Judelson DA, Wright P, Duran A, Haqq AM (2013) Update on body composition and bone density in children with Prader-Willi syndrome. Horm Res Paediatr 79:271–276

    Article  CAS  PubMed  Google Scholar 

  18. Nakamura Y, Murakami N, Ilda T, Asano S, Ozeki S, Nagal T (2014) Growth hormone treatment for osteoporosis in patients with scoliosis of Prader-Willi syndrome. J Orthop Sci 19:877–882

    Article  CAS  PubMed  Google Scholar 

  19. Gordon CM, Leonard MB, Zemel BS (2014) 2013 Pediatric position development conference: executive summary and reflections. J Clin Densitom 17:219–224

    Article  PubMed  Google Scholar 

  20. International Society for Clinical Densitometry 2013 ISCD Official Positions—Pediatric. http://www.iscd.org/official-positions/2013-iscd-official-positions-pediatric/

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to T. N. Hangartner.

Ethics declarations

Conflicts of interest

None.

Electronic supplementary material

Below is the link to the electronic supplementary material.

ESM 1

(PDF 296 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hangartner, T.N., Short, D.F., Eldar-Geva, T. et al. Anthropometric adjustments are helpful in the interpretation of BMD and BMC Z-scores of pediatric patients with Prader-Willi syndrome. Osteoporos Int 27, 3457–3464 (2016). https://doi.org/10.1007/s00198-016-3671-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00198-016-3671-y

Keywords

Navigation