Growth Standards of Infants With Prader-Willi Syndrome

Author:

Butler Merlin G.1,Sturich Jennifer1,Lee Jaehoon2,Myers Susan E.34,Whitman Barbara Y.4,Gold June-Anne56,Kimonis Virginia5,Scheimann Ann7,Terrazas Norma8,Driscoll Daniel J.9

Affiliation:

1. Departments of Psychiatry, Behavioral Sciences and Pediatrics, Kansas University Medical Center, Kansas City, Kansas;

2. Center for Research Methods and Data Analysis, University of Kansas, Lawrence, Kansas;

3. Division of Endocrinology,

4. Department of Pediatrics, St Louis University School of Medicine, St Louis, Missouri;

5. Division of Genetics and Metabolism, Department of Pediatrics, University of California, Irvine, California;

6. Division of Medical Genetics and Metabolism, Department of Pediatrics, Loma Linda University Medical School, Loma Linda, California;

7. Division of Pediatric Nutrion and Gastroenterology, Johns Hopkins School of Medicine, Baltimore, Maryland;

8. Section of Gastroenterology, Hepatology, and nutrition, Texas Children's Hospital, Houston, Texas; and

9. Division of Genetics and Metabolism, Department of Pediatrics, University of Florida, Gainesville, Florida

Abstract

OBJECTIVE: To generate and report standardized growth curves for weight, length, head circumference, weight/length, and BMI for non–growth hormone–treated white infants (boys and girls) with Prader-Willi syndrome (PWS) between 0 and 36 months of age. The goal was to monitor growth and compare data with other infants with PWS. METHODS: Anthropometric measures (N = 758) were obtained according to standard methods and analyzed from 186 non–growth hormone–treated white infants (108 boys and 78 girls) with PWS between 0 and 36 months of age. Standardized growth curves were developed and the 3rd, 10th, 25th, 50th, 75th, 90th, and 97th percentiles were calculated by using the LMS (refers to λ, μ, and σ) smoothing procedure method for weight, length, head circumference, weight/length, and BMI along with the normative 50th percentile using Centers for Disease Control and Prevention national growth data from 2003. The data were plotted for comparison purposes. RESULTS: Five separate standardized growth curves (weight, length, head circumference, weight/length, and BMI) representing 7 percentile ranges were developed from 186 non–growth hormone–treated white male and female infants with PWS aged 0 to 36 months, and the normative 50th percentile was plotted on each standardized infant growth curve. CONCLUSIONS: We encourage the use of these growth standards when examining infants with PWS and evaluating growth for comparison purposes, monitoring for growth patterns, nutritional assessment, and recording responses to growth hormone therapy, commonly used in infants and children with PWS.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

Reference24 articles.

1. A syndrome characterized by obesity, small stature, Cryptorchidism and oligophrenia following a myotonia-like status in infancy [in German];Prader;Schweiz Med Wochensshr,1956

2. Prader-Willi syndrome: Current understanding of cause and diagnosis;Butler;Am J Med Genet,1990

3. Management of Prader-Willi Syndrome

4. Recommendations for the diagnosis and management of Prader-Willi syndrome;Goldstone;J Clin Endocrinol Metab,2008

5. Prader-Willi syndrome;Cassidy;Eur J Hum Genet,2009

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