Literature DB >> 18563710

Risk of cognitive impairment in female premutation carriers of fragile X premutation: analysis by means of robust segmented linear regression models.

Mónica Mínguez1, Berta Ibáñez, Maria-Pilar Ribate, Feliciano Ramos, Eva García-Alegría, Aránzazu Fernández-Rivas, Eduardo Ruiz-Parra, Marisa Poch, Angel Alonso, Cristina Martinez-Bouzas, Elena Beristain, Maria-Isabel Tejada.   

Abstract

This report describes a study focused on the relationship between CGG repeat length, FMRP, mRNA levels and cognitive functioning in premutation carriers (PM) carriers of Fragile X Syndrome (FXS). We studied 60 females-43 with PM and 17 with normal (N) alleles-from 25 FXS Spanish families. The Wechsler scales were administered to all subjects and new blood samples and hair roots were taken to study mRNA and FMRP levels. Using lowess curves together with segmented models we showed that within the premutation range, IQ scores tend to decrease when the number of CGG repeats increases and the FMRP values decrease. Furthermore, we discovered cut-off points in the molecular variables that seem to change the probability of having some cognitive impairment. Specifically, for those PM females in the upper premutation range (CGG > or = 100) and with FMRP expression < 60% in hair roots, a 10% decrement of FMRP expression represents a significant decrease in IQ scores of about six points, which is more evident for Full-Scale IQ (P-value = 0.035) and Performance IQ (P-value = 0.045) than for Verbal IQ (P-value = 0.074). On the contrary, we did not find any significant correlation between FMR1 mRNA levels and the IQ scores, probably due to the fact that mRNA levels were measured in blood. In conclusion, our findings suggest that the PM can have some effect on cognitive ability in female carriers, although these effects may be subtle. In these cases, it would be advisable to carry out a hair root analysis of FMRP. 2008 Wiley-Liss, Inc.

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Year:  2009        PMID: 18563710     DOI: 10.1002/ajmg.b.30803

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  6 in total

1.  COGNITIVE DYSFUNCTION IN FMR1 PREMUTATION CARRIERS.

Authors:  Andreea Seritan; Jennifer Cogswell; Jim Grigsby
Journal:  Curr Psychiatry Rev       Date:  2013-02

2.  Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women.

Authors:  Kim M Cornish; Claudine M Kraan; Quang Minh Bui; Mark A Bellgrove; Sylvia A Metcalfe; Julian N Trollor; Darren R Hocking; Howard R Slater; Yoshimi Inaba; Xin Li; Alison D Archibald; Erin Turbitt; Jonathan Cohen; David E Godler
Journal:  Neurology       Date:  2015-03-25       Impact factor: 9.910

3.  Trajectories and predictors of the development of very young boys with fragile X syndrome.

Authors:  Jane E Roberts; Jean B Mankowski; John Sideris; Barbara Davis Goldman; Deborah D Hatton; Penny L Mirrett; Grace T Baranek; J Steven Reznick; Anna C J Long; Donald B Bailey
Journal:  J Pediatr Psychol       Date:  2008-12-12

Review 4.  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

5.  No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50.

Authors:  Jessica Ezzell Hunter; Emily Graves Allen; Ann Abramowitz; Michele Rusin; Mary Leslie; Gloria Novak; Debra Hamilton; Lisa Shubeck; Krista Charen; Stephanie L Sherman
Journal:  Am J Hum Genet       Date:  2008-11-20       Impact factor: 11.025

Review 6.  Increasing our understanding of human cognition through the study of Fragile X Syndrome.

Authors:  Denise Cook; Erin Nuro; Keith K Murai
Journal:  Dev Neurobiol       Date:  2013-07-30       Impact factor: 3.964

  6 in total

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