Fragile X syndrome (FraX) is the most common known cause of inherited mental impairment. FMR1 gene mutations, the cause of FraX, lead to reduced expression of FMR1 protein (FMRP) and increased risk for a particular profile of cognitive, behavioral and emotional dysfunction. Because of the similarity of these features to important (idiopathic) DSM-IV diagnoses, the study of individuals with FraX provides a window of understanding into disorders such as autism, social phobia, depression, and cognitive disability. The study of FraX also is a portal to the realization of innovative interdisciplinary research that spans multiple clinical and basic scientific domains. Such research provides new insights into understanding how genetic and environmental factors contribute to complex variations in typical and atypical human behavior. In this application, we describe plans to build on a unique study of individuals with FraX that has been in existence since 1992. In the first component of our research, we will continue a longitudinal study of 80 well-described individuals with FraX as they reach a critical phase of development - adolescence and young adulthood. Key cognitive, behavioral, neuroendocrinological, genetic and environmental data will be collected, and the relation of these data to functional outcome will be examined. This component of the study will represent the largest comprehensive, prospective investigation of a FraX cohort during adolescence and young adulthood. In the second component of our research, we will extend our investigation into the neurobiology of FraX using novel behavioral studies and advanced, multi-modal neuroimaging experiments to more fully elucidate brain structure, biochemistry, connectivity and function underlying aberrant cognition and behavior. Within the context of the second aim, we also will examine the efficacy of brief intervention trials focused on improving executive function and social behavior. These pilot trials will utilize innovative behavioral and real-time functional magnetic resonance imaging (rtfMRI) strategies and are designed to generate preliminary data to guide the development of new FraX specific treatments in the future. The Center for Interdisciplinary Brain Sciences Research (CIBSR), directed by the PI, Dr. Allan Reiss, represents one of only a handful of sites in the world that has made a long-term commitment to comprehensive, interdisciplinary research on FraX. The work performed in the CIBSR is particularly focused on applied investigation that will provide new knowledge, methods and tools to improve the lives of persons with FraX and their families.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH050047-19
Application #
8097400
Study Section
Child Psychopathology and Developmental Disabilities Study Section (CPDD)
Program Officer
Gilotty, Lisa
Project Start
1993-07-01
Project End
2013-06-30
Budget Start
2011-07-01
Budget End
2013-06-30
Support Year
19
Fiscal Year
2011
Total Cost
$653,442
Indirect Cost
Name
Stanford University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Fung, Lawrence K; Reiss, Allan L (2016) Moving Toward Integrative, Multidimensional Research in Modern Psychiatry: Lessons Learned From Fragile X Syndrome. Biol Psychiatry 80:100-111
Saggar, Manish; Vrticka, Pascal; Reiss, Allan L (2016) Understanding the influence of personality on dynamic social gesture processing: An fMRI study. Neuropsychologia 80:71-78
Quintin, Eve-Marie; Jo, Booil; Hall, Scott S et al. (2016) The cognitive developmental profile associated with fragile X syndrome: A longitudinal investigation of cognitive strengths and weaknesses through childhood and adolescence. Dev Psychopathol 28:1457-1469
Martin, Arianna; Quintin, Eve-Marie; Hall, Scott S et al. (2016) The Role of Executive Function in Independent Living Skills in Female Adolescents and Young Adults With Fragile X Syndrome. Am J Intellect Dev Disabil 121:448-60
Chromik, Lindsay C; Quintin, Eve-Marie; Lepage, Jean-Fran├žois et al. (2015) The Influence of Hyperactivity, Impulsivity, and Attention Problems on Social Functioning in Adolescents and Young Adults With Fragile X Syndrome. J Atten Disord :
Saggar, Manish; Hosseini, S M Hadi; Bruno, Jennifer L et al. (2015) Estimating individual contribution from group-based structural correlation networks. Neuroimage 120:274-84
Hustyi, Kristin M; Hall, Scott S; Quintin, Eve-Marie et al. (2015) The relationship between autistic symptomatology and independent living skills in adolescents and young adults with fragile X syndrome. J Autism Dev Disord 45:1836-44
Hall, Scott S; Frank, Michael C; Pusiol, Guido T et al. (2015) Quantifying naturalistic social gaze in fragile X syndrome using a novel eye tracking paradigm. Am J Med Genet B Neuropsychiatr Genet 168:564-72
Green, Tamar; Barnea-Goraly, Naama; Raman, Mira et al. (2015) Specific effect of the fragile-X mental retardation-1 gene (FMR1) on white matter microstructure. Br J Psychiatry 207:143-8
Romano, David; Nicolau, Monica; Quintin, Eve-Marie et al. (2014) Topological methods reveal high and low functioning neuro-phenotypes within fragile X syndrome. Hum Brain Mapp 35:4904-15

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