Abstract

BackgroundPhelan-McDermid syndrome (PMS), also known as the 22q13. 3 deletion syndrome, is a rare neurodevelopmental syndrome with approximately 2,800 patients reported worldwide. Previous pilot study demonstrated that IGF-1 could significantly improve in both social impairment and restrictive behaviors of the patients. However, most of the patients in the developing countries like China cannot afford the high cost of using IGF-1. Our research team speculated that rhGH might serve as a low-cost and more accessible treatment for PMS. Therefore, the purpose of this open-label, cross-over, pilot study was to further investigate the safety and efficiency of rhGH in patients with PMS.MethodsA total of six children with PMS were enrolled in in this open-label, cross-over, pilot study. The children were randomly divided into two different groups. Group A received placebo followed by rhGH, while group B was treated with rhGH first. Neuropsychological and behavior assessments of the patients were performed before the stage I of study and 3 months after the intervention of stage I. After a 4-week period of washout, these assessments were conducted again before the stage II of study and 3 months after the intervention of stage II. Serum insulin-like growth factor-1 (IGF-1) and insulin-like growth factor binding-protein (IGFBP)-3 were also evaluated monthly during the intervention phases of the pilot studyResultsCompared with the placebo, rhGH treatment significantly decreased subscale scores of GDS (P < 0.0085) and trended to improve the total scores of GDS (P < 0.05), while the total scores and subscale scores of SC-ABC significantly decreased (P < 0.0085) following 3-months rhGH treatment. The similar results were also observed in comparison with baseline. Compared with the baseline, the level of serum IGF-1 and IGFBP-3 increased significantly (P < 0.05) following 3-months rhGH treatment, while the placebo group had no significant impact on serum IGF-1 and IGFBP-3 (P > 0.05). One child developed skin allergy the day after the first rhGH treatment, which were resolved later.ConclusionsIn summary, this pilot study involving six PMS children patients reveals that rhGH has a positive treatment effect on PMS. These results encourage the undertaking of a large, randomized placebo-controlled trial to conclusively prove rhGH efficacy and tolerability in PMS, thereby promoting it as a low-cost, more accessible treatment for PMS, as compared to IGF-1.

Highlights

  • Phelan-McDermid syndrome (PMS), known as the 22q13.3 deletion syndrome, is a rare neurodevelopmental syndrome with approximately 2,800 patients reported worldwide [1]

  • The sequence of administration had no significant effect on treatment efficacy, and no statistically significant differences were found on the serum level of insulin-like growth factor-1 (IGF-1) (F = 0.156, P = 0.071), IGFBP-3 (F = 0.687, P = 0.454), total scores of Gesell Development Scale (GDS) (F = 0.643, P = 0.468), and SC-ABC (F = 0.007, P = 0.938) in different orders

  • We found that recombinant human growth hormone (rhGH) was well tolerated by the patients during treatment, with no serious AEs observed

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Summary

Introduction

Phelan-McDermid syndrome (PMS), known as the 22q13.3 deletion syndrome, is a rare neurodevelopmental syndrome with approximately 2,800 patients reported worldwide [1]. PMS is often characterized by seizures, global developmental delay, intellectual disability, severe speech delay, hypotonia, and autism spectrum disorder (ASD) [2, 3]. These children often have minor dysmorphic facial features such as plump flesh, rounded face, long eyelashes, pointed chin, prominent/dysplastic ears, bulbous nose, full lips, dysplastic nails, and dolichocephaly [4]. The purpose of this open-label, cross-over, pilot study was to further investigate the safety and efficiency of rhGH in patients with PMS

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