Age-dependent structural connectivity effects in fragile x premutation.

OBJECTIVE To examine the effects of premutation alleles on major brain fiber tracts in males. DESIGN Cross-sectional study performed in 2007-2009. SETTING Institutional practice. PATIENTS Fifteen younger (18-45 years old) carriers, 11 older (>45 years old) unaffected carriers, and 15 older carriers with fragile X-associated tremor/ataxia syndrome, together with 19 younger and 15 older controls matched by age and educational level. MAIN OUTCOME MEASURES Diffusion tensor imaging was performed on all study participants. Eleven fiber tracts important for motor, social, emotional, and cognitive functions were reconstructed and quantified. Complementary tract-based spatial statistical analyses were performed in core white matter. RESULTS In the younger carriers, premutation status was associated with a greater age-related connectivity decline in the extreme capsule. Among older carriers, unaffected individuals did not display structural alterations, whereas the affected carriers showed connectivity loss in 5 fiber tracts and exhibited greater age-related connectivity decline in all 11 tracts compared with the controls. In addition, 9 fiber tracts showed significantly higher variability relative to the controls, and symptom severity explained the variability in 6 measurements from the superior cerebellar peduncle, corpus callosum, and cingulum. CONCLUSIONS The findings revealed widespread alterations in structural connectivity associated with fragile X-associated tremor/ataxia syndrome and preserved or subtle changes in structural connectivity in unaffected carriers. Diffusion tensor imaging is sensitive to pathologic changes in the white matter associated with this neurodegenerative disorder. Wang et al examine the effects of premutation alleles on major brain fiber tracts in males, who are at risk of developing fragile X-associated tremor/ataxia syndrome and may manifest subtle cognitive, social, and emotional disturbances before clinical involvement.

[1]  P. Hagerman,et al.  A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations. , 2008, The Journal of molecular diagnostics : JMD.

[2]  S. Sherman,et al.  New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS) , 2011, neurogenetics.

[3]  D. Loesch,et al.  Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS) , 2006, Journal of the Neurological Sciences.

[4]  P. Hagerman,et al.  Cognitive profile of fragile X premutation carriers with and without fragile X-associated tremor/ataxia syndrome. , 2008, Neuropsychology.

[5]  S. Papapetropoulos Molecular and imaging correlates of the fragile X–associated tremor/ataxia syndrome , 2008 .

[6]  W. Brown,et al.  Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. , 2003, American journal of human genetics.

[7]  Y. Benjamini,et al.  Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .

[8]  P. Basser,et al.  Estimation of the effective self-diffusion tensor from the NMR spin echo. , 1994, Journal of magnetic resonance. Series B.

[9]  W. Brown,et al.  Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction. , 2002, AJNR. American journal of neuroradiology.

[10]  D. Loesch,et al.  Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation , 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[11]  T. Manly,et al.  The emerging fragile X premutation phenotype: Evidence from the domain of social cognition , 2005, Brain and Cognition.

[12]  L. Concha,et al.  Diffusion tensor tractography of the limbic system. , 2005, AJNR. American journal of neuroradiology.

[13]  Stephen M. Smith,et al.  Accurate, Robust, and Automated Longitudinal and Cross-Sectional Brain Change Analysis , 2002, NeuroImage.

[14]  Siddharth Srivastava,et al.  Diffusion tensor imaging in male premutation carriers of the fragile X mental retardation gene , 2011, Movement disorders : official journal of the Movement Disorder Society.

[15]  J. Brunberg,et al.  Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population. , 2004, JAMA.

[16]  P. V. van Zijl,et al.  Three‐dimensional tracking of axonal projections in the brain by magnetic resonance imaging , 1999, Annals of neurology.

[17]  S. Wakana,et al.  Fiber tract-based atlas of human white matter anatomy. , 2004, Radiology.

[18]  Derek K. Jones,et al.  Perisylvian language networks of the human brain , 2005, Annals of neurology.

[19]  Randy L. Gollub,et al.  Reproducibility of quantitative tractography methods applied to cerebral white matter , 2007, NeuroImage.

[20]  M. D. Del Bigio,et al.  Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. , 2002, Brain : a journal of neurology.

[21]  D. Munoz Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. , 2002, Neurology.

[22]  S. Rivera,et al.  A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndrome. , 2011, Brain : a journal of neurology.

[23]  Jane E. Roberts,et al.  Mood and anxiety disorders in females with the FMR1 premutation , 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[24]  J. Sutcliffe,et al.  Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox , 1991, Cell.

[25]  J. R. Augustine Circuitry and functional aspects of the insular lobe in primates including humans , 1996, Brain Research Reviews.

[26]  Daniel Rueckert,et al.  Tract-based spatial statistics: Voxelwise analysis of multi-subject diffusion data , 2006, NeuroImage.

[27]  T. Godfrey,et al.  Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome. , 2000, American journal of human genetics.

[28]  Susumu Mori,et al.  Fiber tracking: principles and strategies – a technical review , 2002, NMR in biomedicine.

[29]  Lexin Li,et al.  Lifespan changes in working memory in fragile X premutation males , 2009, Brain and Cognition.

[30]  Derek K. Jones,et al.  Symmetries in human brain language pathways correlate with verbal recall , 2007, Proceedings of the National Academy of Sciences.

[31]  Hervé Abdi,et al.  A comprehensive reliability assessment of quantitative diffusion tensor tractography , 2012, NeuroImage.

[32]  K. Yau,et al.  Interoception: the sense of the physiological condition of the body , 2003, Current Opinion in Neurobiology.

[33]  E. Crosby,et al.  Correlative Anatomy of the Nervous System , 1962 .

[34]  P. V. van Zijl,et al.  Analysis of noise effects on DTI‐based tractography using the brute‐force and multi‐ROI approach , 2004, Magnetic resonance in medicine.

[35]  J Grigsby,et al.  Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS). , 2006, Brain : a journal of neurology.

[36]  A. Craig,et al.  How do you feel — now? The anterior insula and human awareness , 2009, Nature Reviews Neuroscience.

[37]  Stephen M Smith,et al.  Fast robust automated brain extraction , 2002, Human brain mapping.

[38]  P. Basser,et al.  Microstructural and physiological features of tissues elucidated by quantitative-diffusion-tensor MRI. , 1996, Journal of magnetic resonance. Series B.