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      Oxytocin treatment in children with Prader–Willi syndrome: A double-blind, placebo-controlled, crossover study

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          Abstract

          Prader–Willi syndrome (PWS) is a rare, complex multisystem genetic disorder which includes hypothalamic dysfunction, hyperphagia, cognitive and behavioral problems, increased anxiety, and compulsive behaviors. Individuals with PWS have a deficit of oxytocin producing neurons in the paraventricular nucleus of the hypothalamus. Oxytocin plays a role in regulation of feeding behaviors, social interactions, and emotional reactivity, which are all issues that significantly affect the quality of life for individuals with this syndrome. We performed a double-blind, placebo-controlled, crossover study in 24 children with PWS at three academic institutions using 5 days of intranasal oxytocin (IN-OT) or 5 days of intranasal placebo spray, followed by a 4 week washout period, and then patients returned for 5 days of treatment with the alternate source. Questionnaires, including the Aberrant Behavior Checklist, Social Responsiveness Scale, Repetitive Behavior Scale − Revised, and the Hyperphagia Questionnaire, as well as Clinical Global Impression scales were administered. Blood testing for sodium, potassium, and glucose levels on days 2, 4, and 6, and a 24 hr diet recall. All scales factor improvement from Day 3 to Day 6 favored oxytocin over placebo. No single factor showed a statistically significant difference ( P < 0.05) between groups at Day 6. The drug effect appeared to be diminished at Day 14. There was no evidence of a difference between oxytocin and placebo in safety lab parameters, 60 min post dose vital signs, weight, or diet parameters. The results from this study suggest that low dose intranasal oxytocin is safe for individuals with PWS and may result in reduction in appetite drive, and improvements in socialization, anxiety, and repetitive behaviors. Further, long-term studies with a larger population of participants are necessary to confirm these findings. The results of this study are encouraging that oxytocin may be a safe and effective treatment for many of the issues that negatively impact individuals with PWS.

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          Author and article information

          Journal
          101235741
          32200
          Am J Med Genet A
          Am. J. Med. Genet. A
          American journal of medical genetics. Part A
          1552-4825
          1552-4833
          21 February 2018
          30 March 2017
          May 2017
          01 May 2018
          : 173
          : 5
          : 1243-1250
          Affiliations
          [1 ]Department of Pediatrics College of Medicine, University of Florida, Gainesville, Florida
          [2 ]Health Informatics Institute, University of South Florida, Tampa, Florida
          [3 ]Departments of Psychiatry and Behavioral Sciences and Pediatrics, Kansas University Medical Center, Kansas City, Kansas
          [4 ]Division of Genetics and Genomics, Department of Pediatrics, University of California Irvine, Irvine, California
          [5 ]Department of Pediatrics, Division of Genetics and Metabolism, Loma Linda University Medical school, Loma Linda, California
          [6 ]Center for Epigenetics, College of Medicine, University of Florida, Gainesville, Florida
          Author notes
          Correspondence. Jennifer Miller MD, PO Box 100296, Department of Pediatrics, College of Medicine, University of Florida, Gainesville, 320610 FL. millejl@ 123456peds.ufl.edu
          Article
          PMC5828021 PMC5828021 5828021 nihpa944925
          10.1002/ajmg.a.38160
          5828021
          28371242
          da887d65-8d46-4d5e-b78a-ddd41842696d
          History
          Categories
          Article

          hyperphagia,oxytocin,Prader–Willi syndrome
          hyperphagia, oxytocin, Prader–Willi syndrome

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