Literature DB >> 12949966

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis.

D Z Loesch1, R M Huggins, Q M Bui, A K Taylor, C Pratt, J Epstein, R J Hagerman.   

Abstract

The effect of the fragile X pre-mutation and full mutation categories, and FMRP deficits in these categories, on neurocognitive status, have been assessed in fragile X individuals from 144 extended families, which included fragile X individuals, as well as their non-fragile X relatives. Neuropsychological status was assessed by the Wechsler summary and subtest test scores. A modification of the maximum likelihood estimators for pedigree data that is resistant to outliers was used to analyze the data. The results have demonstrated the effect of large expansions of CGG repeat in the FMR1 (fragile X mental retardation 1) gene (full mutation) in decreasing full scale IQ (FSIQ), as well as several FSIQ-adjusted subtest scores in the performance domain. Moreover, the results have demonstrated significant cognitive deficits in male individuals with pre-mutation. FMRP depletion correlates strongly with neurocognitive status in the full mutation subjects. Evidence for the effect of FMRP in smaller expansions (pre-mutation) in reducing FSIQ, Performance and Verbal scores, as well as subtest scores in males, has also been obtained. The results are also suggestive of factors other than FMRP deficit which may determine some specific cognitive deficits in fragile X pre-mutation carriers. Genetic variance estimated from the models accounts for less than half of the total variance in FSIQ, and it varies widely between individual Wechsler subtests. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 12949966     DOI: 10.1002/ajmg.a.20214

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  14 in total

1.  A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis.

Authors:  Mei Qin; Ali Entezam; Karen Usdin; Tianjian Huang; Zhong-Hua Liu; Gloria E Hoffman; Carolyn B Smith
Journal:  Neurobiol Dis       Date:  2011-01-08       Impact factor: 5.996

2.  Broad clinical involvement in a family affected by the fragile X premutation.

Authors:  Weerasak Chonchaiya; Agustini Utari; Gabriela Marques Pereira; Flora Tassone; David Hessl; Randi J Hagerman
Journal:  J Dev Behav Pediatr       Date:  2009-12       Impact factor: 2.225

Review 3.  Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X.

Authors:  Danuta Z Loesch; Quang M Bui; Cheryl Dissanayake; Sally Clifford; Emma Gould; Danuta Bulhak-Paterson; Flora Tassone; Annette K Taylor; David Hessl; Randi Hagerman; Richard M Huggins
Journal:  Neurosci Biobehav Rev       Date:  2006-11-09       Impact factor: 8.989

Review 4.  What can we learn about autism from studying fragile X syndrome?

Authors:  Dejan B Budimirovic; Walter E Kaufmann
Journal:  Dev Neurosci       Date:  2011-09-01       Impact factor: 2.984

5.  Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice.

Authors:  Adam J Iliff; Abigail J Renoux; Amy Krans; Karen Usdin; Michael A Sutton; Peter K Todd
Journal:  Hum Mol Genet       Date:  2012-12-18       Impact factor: 6.150

Review 6.  Gene, brain, and behavior relationships in fragile X syndrome: evidence from neuroimaging studies.

Authors:  Amy A Lightbody; Allan L Reiss
Journal:  Dev Disabil Res Rev       Date:  2009

Review 7.  The fragile-X premutation: a maturing perspective.

Authors:  Paul J Hagerman; Randi J Hagerman
Journal:  Am J Hum Genet       Date:  2004-03-29       Impact factor: 11.025

Review 8.  The changing impact of genes and environment on brain development during childhood and adolescence: initial findings from a neuroimaging study of pediatric twins.

Authors:  Rhoshel K Lenroot; Jay N Giedd
Journal:  Dev Psychopathol       Date:  2008

Review 9.  Unstable mutations in the FMR1 gene and the phenotypes.

Authors:  Danuta Loesch; Randi Hagerman
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

Review 10.  Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature.

Authors:  Jessica Ezzell Hunter; Ann Abramowitz; Michele Rusin; Stephanie L Sherman
Journal:  Genet Med       Date:  2009-02       Impact factor: 8.822

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