Literature DB >> 22101959

The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance.

Jessica Ezzell Hunter1, Michael P Epstein, Stuart W Tinker, Ann Abramowitz, Stephanie L Sherman.   

Abstract

We recently reported elevated symptoms associated with attention-deficit hyperactivity disorder (ADHD) among adult female carriers of the FMR1 premutation. To gain insight into the contribution of this mutation in the context of polygenes, we examined the proportion of variation in these symptoms due to residual genetic factors after adjustment for the effect of the premutation. To accomplish this, we performed a familial aggregation analysis of ADHD symptoms among 231 females from 82 pedigrees using scores from the Connors Adult ADHD Rating Scales. Results indicate that after accounting for the effect of FMR1, there are significant residual polygenic effects on self-reported symptoms of ADHD, as measured by the ADHD Index (p = 0.0117) and problems with self-concept (p = 0.0110), one specific symptom domain associated with ADHD. For both measures, FMR1 accounts for ~5% of the variance while polygenes account for ~50% of the residual variance, suggesting that the premutation acts in concert with additional genetic loci to influence the severity of ADHD symptoms.

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Year:  2011        PMID: 22101959      PMCID: PMC3696489          DOI: 10.1007/s10519-011-9520-z

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


  38 in total

Review 1.  Phenotypic and measurement influences on heritability estimates in childhood ADHD.

Authors:  Christine M Freitag; Luis A Rohde; Thomas Lempp; Marcel Romanos
Journal:  Eur Child Adolesc Psychiatry       Date:  2010-03-07       Impact factor: 4.785

2.  Genetic and environmental influences on ADHD symptom dimensions of inattention and hyperactivity: a meta-analysis.

Authors:  Molly A Nikolas; S Alexandra Burt
Journal:  J Abnorm Psychol       Date:  2010-02

Review 3.  Molecular genetics of attention-deficit/hyperactivity disorder: an overview.

Authors:  Tobias Banaschewski; Katja Becker; Susann Scherag; Barbara Franke; David Coghill
Journal:  Eur Child Adolesc Psychiatry       Date:  2010-02-10       Impact factor: 4.785

4.  Co-occurring conditions associated with FMR1 gene variations: findings from a national parent survey.

Authors:  Donald B Bailey; Melissa Raspa; Murrey Olmsted; David B Holiday
Journal:  Am J Med Genet A       Date:  2008-08-15       Impact factor: 2.802

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

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:  Behav Genet       Date:  2008-06-06       Impact factor: 2.805

6.  Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.

Authors:  Sarah L Nolin; W Ted Brown; Anne Glicksman; George E Houck; Alice D Gargano; Amy Sullivan; Valérie Biancalana; Karen Bröndum-Nielsen; Helle Hjalgrim; Elke Holinski-Feder; Frank Kooy; John Longshore; James Macpherson; Jean-Louis Mandel; Gert Matthijs; Francois Rousseau; Peter Steinbach; Marja-Leena Väisänen; Harriet von Koskull; Stephanie L Sherman
Journal:  Am J Hum Genet       Date:  2003-01-14       Impact factor: 11.025

7.  Mood and anxiety disorders in females with the FMR1 premutation.

Authors:  Jane E Roberts; Donald B Bailey; Jean Mankowski; Amy Ford; John Sideris; Leigh Anne Weisenfeld; T Morgan Heath; Robert N Golden
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2009-01-05       Impact factor: 3.568

8.  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

9.  Child and genetic variables associated with maternal adaptation to fragile X syndrome: a multidimensional analysis.

Authors:  Donald B Bailey; John Sideris; Jane Roberts; Deborah Hatton
Journal:  Am J Med Genet A       Date:  2008-03-15       Impact factor: 2.802

Review 10.  Genome-wide association studies in ADHD.

Authors:  Barbara Franke; Benjamin M Neale; Stephen V Faraone
Journal:  Hum Genet       Date:  2009-04-22       Impact factor: 4.132

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  23 in total

1.  Improving Health Education for Women Who Carry an FMR1 Premutation.

Authors:  Whitney Espinel; Krista Charen; Lillie Huddleston; Jeannie Visootsak; Stephanie Sherman
Journal:  J Genet Couns       Date:  2015-07-16       Impact factor: 2.537

2.  PSYCHIATRIC DISORDERS ASSOCIATED WITH FXTAS.

Authors:  Andreea L Seritan; Melina Ortigas; Stefan Seritan; James A Bourgeois; Randi J Hagerman
Journal:  Curr Psychiatry Rev       Date:  2013

Review 3.  Implications of the FMR1 Premutation for Children, Adolescents, Adults, and Their Families.

Authors:  Anne Wheeler; Melissa Raspa; Randi Hagerman; Marsha Mailick; Catharine Riley
Journal:  Pediatrics       Date:  2017-06       Impact factor: 7.124

4.  Health knowledge of women with a fragile X premutation: Improving understanding with targeted educational material.

Authors:  Liana Smolich; Krista Charen; Stephanie L Sherman
Journal:  J Genet Couns       Date:  2020-01-30       Impact factor: 2.537

5.  The emergence and stability of attention deficit hyperactivity disorder in boys with fragile X syndrome.

Authors:  M Grefer; K Flory; K Cornish; D Hatton; J Roberts
Journal:  J Intellect Disabil Res       Date:  2015-11-27

6.  Abnormal semantic processing in females with fragile X-associated tremor/ataxia syndrome.

Authors:  J-C Yang; C Simon; A Schneider; A L Seritan; L Hamilton; P J Hagerman; R J Hagerman; J M Olichney
Journal:  Genes Brain Behav       Date:  2013-12-26       Impact factor: 3.449

Review 7.  Fragile X-associated tremor/ataxia syndrome - features, mechanisms and management.

Authors:  Randi J Hagerman; Paul Hagerman
Journal:  Nat Rev Neurol       Date:  2016-06-24       Impact factor: 42.937

8.  Phenotypes of hypofrontality in older female fragile X premutation carriers.

Authors:  Jin-Chen Yang; Christa Simon; Yu-Qiong Niu; Mark Bogost; Andrea Schneider; Flora Tassone; Andreea Seritan; Jim Grigsby; Paul J Hagerman; Randi J Hagerman; John M Olichney
Journal:  Ann Neurol       Date:  2013-08       Impact factor: 10.422

Review 9.  Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome.

Authors:  Randi Hagerman; Paul Hagerman
Journal:  Lancet Neurol       Date:  2013-08       Impact factor: 44.182

10.  Towards an Understanding of Neuropsychiatric Manifestations in Fragile X Premutation Carriers.

Authors:  Aaron D Besterman; Scott A Wilke; Tua-Elisabeth Mulligan; Stephen C Allison; Randi Hagerman; Andreea L Seritan; James A Bourgeois
Journal:  Future Neurol       Date:  2014-03
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