Treatments for fragile X syndrome: a closer look at the data

Dev Disabil Res Rev. 2009;15(4):353-60. doi: 10.1002/ddrr.78.

Abstract

Research into the determinants and developmental course of fragile X syndrome (FXS) has made remarkable progress over the last 25 years. However, treatments to ameliorate the symptoms of FXS have been less forthcoming. While there is optimism in the field that the pace of intervention research is quickening, there has been a bias toward psychopharmacological approaches to treatment. A closer look at the data from those investigations reveals a paucity of evidence that medications can improve intellectual and adaptive functioning in FXS, or decrease associated behavioral and/or emotional issues. Work in other related disorders (e.g., autism) has shown that dramatic improvements in intellectual and adaptive functioning, as well as behavioral and emotional problems, can occur if intensive behavioral treatment is begun early in the child's life. It is hoped that future research efforts will evaluate these intensive early intervention strategies in children with FXS, perhaps in combination with pharmacological approaches.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acetylcarnitine / therapeutic use
  • Adrenergic alpha-Agonists / therapeutic use
  • Behavior Therapy
  • Central Nervous System Stimulants / therapeutic use
  • Clonidine / therapeutic use*
  • Dopamine Agonists / therapeutic use
  • Folic Acid / therapeutic use
  • Fragile X Mental Retardation Protein / genetics
  • Fragile X Syndrome / drug therapy
  • Fragile X Syndrome / genetics
  • Fragile X Syndrome / therapy*
  • Humans
  • Memantine / therapeutic use

Substances

  • Adrenergic alpha-Agonists
  • Central Nervous System Stimulants
  • Dopamine Agonists
  • FMR1 protein, human
  • Fragile X Mental Retardation Protein
  • Acetylcarnitine
  • Folic Acid
  • Clonidine
  • Memantine