Behavior Genetics

, Volume 40, Issue 1, pp 59–75

Biogenic Amines in Rett Syndrome: The Usual Suspects


DOI: 10.1007/s10519-009-9303-y

Cite this article as:
Roux, JC. & Villard, L. Behav Genet (2010) 40: 59. doi:10.1007/s10519-009-9303-y


Rett syndrome (RTT) is a severe postnatal neurological disorder caused by mutations in the methyl-CpG binding protein 2 (MECP2) gene. In affected children, most biological parameters, including brain structure, are normal (although acquired microcephaly is usually present). However, in recent years, a deficit in bioaminergic metabolism has been identified at the cellular and molecular levels, in more than 200 patients. Recently available transgenic mouse strains with a defective Mecp2 gene also show abnormalities, strongly suggesting that there is a direct link between the function of the MECP2 protein and the metabolism of biogenic amines. Biogenic amines appear to have an important role in the pathophysiology of Rett syndrome, for several reasons. Firstly, biogenic amines modulate a large number of autonomic and cognitive functions. Secondly, many of these functions are affected in RTT patients. Thirdly, biogenic amines are the only neurotransmitters that have repeatedly been found to be altered in RTT patients. Importantly, pharmacological interventions can be envisaged to try to counteract the deficits observed. Here, we review the available human and mouse data and present how they have been and could be used in the development of pharmacological treatments for children affected by the syndrome. Given our current knowledge and the tools available, modulating biogenic amine metabolism may prove to be the most promising strategy for improving the life quality of Rett syndrome patients in the short term.


Rett syndrome Biogenic amines Pharmacological intervention 

Copyright information

© Springer Science+Business Media, LLC 2009

Authors and Affiliations

  1. 1.Inserm, U910Marseille Cedex 5France
  2. 2.Aix Marseille Université, Faculté de MédecineMarseilleFrance

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