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Insular volume reduction in fragile X syndrome.
Cohen, Jeremy D; Nichols, Taylor; Brignone, Laura; Hall, Scott S; Reiss, Allan L.
Afiliação
  • Cohen JD; Center for Interdisciplinary Brain Sciences Research, Stanford University School of Medicine, Stanford, CA 94305, USA. jcohen@xula.edu
Int J Dev Neurosci ; 29(4): 489-94, 2011 Jun.
Article em En | MEDLINE | ID: mdl-21291994
ABSTRACT
Fragile X syndrome (FraX) is the most common form of inherited mental deficit and is caused by mutations of the Fragile X Mental Retardation 1 (FMR1) gene on the X chromosome. While males and females with the full FMR1 mutation are affected differently because the disorder is X-linked, both suffer from varying degrees of cognitive impairment, attention deficits and social anxiety. The insula is a sensory integrative region that has been increasingly suggested as a critical area involved in anxiety manifestation. The current study was designed to examine possible changes in insular volume in FraX compared to age- and gender-matched typically developing healthy controls (HC) as well as age-, gender-, and intelligence-matched developmentally delayed controls (DD). An established native-space, manual morphometry method was utilized to quantify total and regional insular volumes using structural magnetic resonance imaging. Total, anterior and posterior insular volumes were found to be reduced in FraX compared to both HC and DD. The current data add to a growing literature concerning brain abnormalities in FraX and suggests that significant volume reduction of the insula is a component of the FraX neuroanatomical phenotype. This finding also provides an intriguing potential neural correlate for hyperarousal and gaze aversion, which are prominent behavioral symptoms of FraX.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Córtex Cerebral / Síndrome do Cromossomo X Frágil Idioma: En Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Córtex Cerebral / Síndrome do Cromossomo X Frágil Idioma: En Ano de publicação: 2011 Tipo de documento: Article