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Anthropometric Adjustments Are Helpful in the Interpretation of BMD and BMC Z-scores of Pediatric Patients with Prader-Willi Syndrome

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Journal Osteoporos Int
Date 2016 Jul 6
PMID 27377921
Citations 1
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Abstract

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.

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References
1.
Eldar-Geva T, Hirsch H, Benarroch F, Rubinstein O, Gross-Tsur V . Hypogonadism in females with Prader-Willi syndrome from infancy to adulthood: variable combinations of a primary gonadal defect and hypothalamic dysfunction. Eur J Endocrinol. 2009; 162(2):377-84. DOI: 10.1530/EJE-09-0901. View

2.
Schoenau E, Frost H . The "muscle-bone unit" in children and adolescents. Calcif Tissue Int. 2002; 70(5):405-7. DOI: 10.1007/s00223-001-0048-8. View

3.
Siemensma E, de Lind van Wijngaarden R, Otten B, de Jong F, Hokken-Koelega A . Testicular failure in boys with Prader-Willi syndrome: longitudinal studies of reproductive hormones. J Clin Endocrinol Metab. 2011; 97(3):E452-9. DOI: 10.1210/jc.2011-1954. View

4.
Nakamura Y, Murakami N, Iida T, Asano S, Ozeki S, Nagai T . Growth hormone treatment for osteoporosis in patients with scoliosis of Prader-Willi syndrome. J Orthop Sci. 2014; 19(6):877-82. DOI: 10.1007/s00776-014-0641-0. View

5.
Short D, Gilsanz V, Kalkwarf H, Lappe J, Oberfield S, Shepherd J . Anthropometric models of bone mineral content and areal bone mineral density based on the bone mineral density in childhood study. Osteoporos Int. 2014; 26(3):1099-108. PMC: 4768717. DOI: 10.1007/s00198-014-2916-x. View