Literature DB >> 18535897

Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers.

Jessica Ezzell Hunter1, Emily Graves Allen, Ann Abramowitz, Michele Rusin, Mary Leslie, Gloria Novak, Debra Hamilton, Lisa Shubeck, Krista Charen, Stephanie L Sherman.   

Abstract

The fragile X disorder spectrum, due to a CGG expansion in FMR1, includes fragile X syndrome (>200 repeats) and the premutation-associated disorders of ovarian insufficiency and tremor/ataxia syndrome (approximately 55-199 repeats). Altered neurobehavioral profiles including variation of phenotypes associated with mood and anxiety may be expected among younger premutation carriers given this spectrum of disorders. However, previous studies have produced conflicting findings, providing the motivation to examine these phenotypes further. We investigated measures of mood and anxiety in 119 males and 446 females age 18-50 ascertained from families with a history of fragile X syndrome and from the general population. Scores were analyzed using a linear model with repeat length as the main predictor, adjusting for potential confounders. Repeat length was not associated with anxiety, but was marginally associated with depression and negative affect in males and negative affect only in females. These results suggest that premutation carriers may be at risk for emotional morbidity; however, phenotypic differences were subtle and of small effect size.

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Year:  2008        PMID: 18535897      PMCID: PMC3696488          DOI: 10.1007/s10519-008-9214-3

Source DB:  PubMed          Journal:  Behav Genet        ISSN: 0001-8244            Impact factor:   2.805


  39 in total

1.  A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other.

Authors:  Dale R Nyholt
Journal:  Am J Hum Genet       Date:  2004-03-02       Impact factor: 11.025

2.  Translational suppression by trinucleotide repeat expansion at FMR1.

Authors:  Y Feng; F Zhang; L K Lokey; J L Chastain; L Lakkis; D Eberhart; S T Warren
Journal:  Science       Date:  1995-05-05       Impact factor: 47.728

3.  Molecular/clinical correlations in females with fragile X.

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Journal:  Am J Med Genet       Date:  1996-08-09

4.  A study of the physical, behavioral, and medical phenotype, including anthropometric measures, of females with fragile X syndrome.

Authors:  C Hull; R J Hagerman
Journal:  Am J Dis Child       Date:  1993-11

Review 5.  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

6.  Behavioral and psychiatric disorders in adult male carriers of fragile X.

Authors:  M B Dorn; M M Mazzocco; R J Hagerman
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1994-02       Impact factor: 8.829

7.  A study of the distributional characteristics of FMR1 transcript levels in 238 individuals.

Authors:  Emily G Allen; Weiya He; Maneesha Yadav-Shah; Stephanie L Sherman
Journal:  Hum Genet       Date:  2004-02-03       Impact factor: 4.132

8.  Neurobehavioral characteristics of CGG amplification status in fragile X females.

Authors:  N M Thompson; M L Gulley; G A Rogeness; R J Clayton; C Johnson; B Hazelton; C G Cho; V T Zellmer
Journal:  Am J Med Genet       Date:  1994-12-15

9.  Absence of expression of the FMR-1 gene in fragile X syndrome.

Authors:  M Pieretti; F P Zhang; Y H Fu; S T Warren; B A Oostra; C T Caskey; D L Nelson
Journal:  Cell       Date:  1991-08-23       Impact factor: 41.582

10.  DNA methylation represses FMR-1 transcription in fragile X syndrome.

Authors:  J S Sutcliffe; D L Nelson; F Zhang; M Pieretti; C T Caskey; D Saxe; S T Warren
Journal:  Hum Mol Genet       Date:  1992-09       Impact factor: 6.150

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  36 in total

1.  Daily health symptoms of mothers of adolescents and adults with fragile x syndrome and mothers of adolescents and adults with autism spectrum disorder.

Authors:  Leann E Smith; Marsha Mailick Seltzer; Jan S Greenberg
Journal:  J Autism Dev Disord       Date:  2012-09

2.  An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS).

Authors:  Ryu-ichiro Hashimoto; Kristina C Backer; Flora Tassone; Randi J Hagerman; Susan M Rivera
Journal:  J Psychiatr Res       Date:  2010-05-31       Impact factor: 4.791

3.  Physiological regulation and social-emotional processing in female carriers of the FMR1 premutation.

Authors:  Molly Winston; Kritika Nayar; Abigail L Hogan; Jamie Barstein; Chelsea La Valle; Kevin Sharp; Elizabeth Berry-Kravis; Molly Losh
Journal:  Physiol Behav       Date:  2019-11-22

4.  Prevalence of CGG expansions of the FMR1 gene in a US population-based sample.

Authors:  Marsha Mailick Seltzer; Mei Wang Baker; Jinkuk Hong; Matthew Maenner; Jan Greenberg; Daniel Mandel
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2012-05-22       Impact factor: 3.568

5.  Maternal well-being and child behavior in families with fragile X syndrome.

Authors:  Claire T Hauser; Sara T Kover; Leonard Abbeduto
Journal:  Res Dev Disabil       Date:  2014-06-29

6.  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

Review 7.  FMR1: a gene with three faces.

Authors:  Ben A Oostra; Rob Willemsen
Journal:  Biochim Biophys Acta       Date:  2009-02-21

8.  Eye movements reveal impaired inhibitory control in adult male fragile X premutation carriers asymptomatic for FXTAS.

Authors:  Ling M Wong; Naomi J Goodrich-Hunsaker; Yingratana McLennan; Flora Tassone; Melody Zhang; Susan M Rivera; Tony J Simon
Journal:  Neuropsychology       Date:  2014-04-28       Impact factor: 3.295

9.  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

10.  Co-occurring diagnoses among FMR1 premutation allele carriers.

Authors:  J E Hunter; J K Rohr; S L Sherman
Journal:  Clin Genet       Date:  2010-01-06       Impact factor: 4.438

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