An escalating continuum of learning and attention difficulties from premutation to full mutation in female carriers of FMR1 expansion

被引:4
|
作者
Gabis, Lidia V. [1 ,2 ,3 ]
Shaham, Meirav [4 ]
Attia, Odelia Leon [3 ]
Kowal, Tamar [5 ]
David, Sivan [6 ]
Banet-Levi, Yonit [7 ]
Shefer, Shahar [8 ]
Gabis, Daniel [9 ]
Mula-Topf, Dana [7 ]
Avrech Bar, Michal [6 ]
Bart, Orit [6 ]
Segal, Osnat [5 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[2] Maccabi Healthcare, Tel Aviv, Israel
[3] Keshet Autism Ctr Maccabi Wolfson, Holon, Israel
[4] Univ Haifa, Dept Stat, Haifa, Israel
[5] Tel Aviv Univ, Sackler Fac Med, Dept Commun Disorders, Tel Aviv, Israel
[6] Tel Aviv Univ, Sackler Fac Med, Sch Hlth Profess, Dept Occupat Therapy, Tel Aviv, Israel
[7] Weinberg Child Dev Ctr Safra Childrens Hosp, Sheba Med Ctr, Ramat Gan, Israel
[8] Coll Management, Rishon Leziyyon, Israel
[9] Tel Aviv Sourasky Med Ctr Ichilov, Tel Aviv, Israel
来源
FRONTIERS IN NEUROLOGY | 2023年 / 14卷
关键词
Fragile X; FXS; FMR1; Fragile X carriers; learning disabilities (LD); attention deficit and hyperactivity disorder (ADHD); premutation; FRAGILE-X; TREMOR/ATAXIA SYNDROME; CLINICAL PHENOTYPE; ASSOCIATION; DEPRESSION; SYMPTOMS; CHILDREN; ANXIETY; MOTHERS; STRESS;
D O I
10.3389/fneur.2023.1135630
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ObjectiveCarriers of Fragile X premutation may have associated medical comorbidities, such as Fragile X-associated tremor and ataxia (FXTAS) and Fragile X-associated premature ovarian insufficiency (FXPOI). We examined the Fragile X premutation effect on cognition, and we assumed that there is a direct correlation between the continuous spectrum of specific learning and attention deficits to the number of CGG repeats on the FMR1 gene. MethodsA total of 108 women were referred to our center due to a related Fragile X syndrome (FXS) patient, 79 women carried a premutation of 56-199 repeats, and 19 women carried a full mutation of more than 200 CGG repeats on FMR1 gene. Genetic results of CGG repeats, demographic information, structured questionnaires for ADHD, learning disabilities of language and mathematics, and independence level were analyzed in women carrying the FMR1 premutation and compared to the group carrying the full mutation. Women with FXS and FXTAS were excluded. ResultsWhen analyzed as a continuum, there was a significant increase in the following complaints which were associated with a higher number of repeats: specific daily function skills such as driving a car, writing checks, disorientation in directions, and also specific learning difficulties such as spelling and math difficulties. Additionally, when tested as a categorical independent variable, we observe that women with the full mutation were more likely to have ADHD or other learning disability diagnoses in the past than during premutation (<200 CGG repetitions). ConclusionSpecific learning and attention difficulties and resulting daily function difficulties correlate with an increased number of CGG repeats and are more likely to be associated as a common feature of premutation and full mutation in a female premutation carrier. Despite evidence of learning and attention difficulties, it is encouraging that most female carriers of the premutation and full mutation function well in most areas. Nevertheless, they face significant difficulties in specific areas of functioning such as driving, and confusion in times and schedules. Those daily function skills are mostly impacted by dyscalculia, right and left disorientation, and attention difficulties. This may aid to design specific interventions to address specific learning deficits in order to improve daily function skills and quality of life.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] Analysis of FMR1 gene expression in female premutation carriers using robust segmented linear regression models
    Garcia-Alegria, Eva
    Ibanez, Berta
    Minguez, Monica
    Poch, Marisa
    Valiente, Alberto
    Sanz-Parra, Arantza
    Martinez-Bouzas, Cristina
    Beristain, Elena
    Tejada, Maria-Isabel
    RNA, 2007, 13 (05) : 756 - 762
  • [42] Evidence for Three Subgroups of Female FMR1 Premutation Carriers Defined by Distinct Neuropsychiatric Features: A Pilot Study
    Schmitt, Lauren M.
    Dominick, Kelli C.
    Liu, Rui
    Pedapati, Ernest V.
    Ethridge, Lauren E.
    Smith, Elizabeth
    Sweeney, John A.
    Erickson, Craig A.
    FRONTIERS IN INTEGRATIVE NEUROSCIENCE, 2022, 15
  • [43] Expansion of an FMR1 Grey-Zone Allele to a Full Mutation in Two Generations
    Fernandez-Carvajal, Isabel
    Lopez Posadas, Blanca
    Pan, Ruiqin
    Raske, Christopher
    Hagerman, Paul J.
    Tassone, Flora
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2009, 11 (04): : 306 - 310
  • [44] Mosaicism for FMR1 gene full mutation and deletion in a fragile X female.
    Fan, H
    Booker, JK
    McCandless, SE
    Shashi, V
    Farber, RA
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 585 - 585
  • [45] Both cis and trans-acting genetic factors drive somatic instability in female carriers of the FMR1 premutation
    Ye Hyun Hwang
    Bruce Eliot Hayward
    Marwa Zafarullah
    Jay Kumar
    Blythe Durbin Johnson
    Peter Holmans
    Karen Usdin
    Flora Tassone
    Scientific Reports, 12
  • [46] Both cis and trans-acting genetic factors drive somatic instability in female carriers of the FMR1 premutation
    Hwang, Ye Hyun
    Hayward, Bruce Eliot
    Zafarullah, Marwa
    Kumar, Jay
    Johnson, Blythe Durbin
    Holmans, Peter
    Usdin, Karen
    Tassone, Flora
    SCIENTIFIC REPORTS, 2022, 12 (01)
  • [47] Delineation of the working memory profile in female FMR1 premutation carriers: The effect of cognitive load on ocular motor responses
    Shelton, Annie L.
    Cornish, Kim M.
    Godler, David E.
    Clough, Meaghan
    Kraan, Claudine
    Minh Bui
    Fielding, Joanne
    BEHAVIOURAL BRAIN RESEARCH, 2015, 282 : 194 - 200
  • [48] Expansion to full mutation of a FMR1 gray zone allele over two generations.
    Terracciano, A
    Pomponi, MG
    Marino, GME
    Neri, G
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 564 - 564
  • [49] Fragile X Syndrome in a Female With Homozygous Full-Mutation Alleles of the FMR1 Gene
    Vafaeie, Farzane
    Alerasool, Masoome
    Mojaver, Nasrin Kaseb
    Mojarrad, Majid
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2021, 13 (07)
  • [50] Impaired Response Inhibition Is Associated With Self-Reported Symptoms of Depression, Anxiety, and ADHD in Female FMR1 Premutation Carriers
    Kraan, Claudine M.
    Hocking, Darren R.
    Georgiou-Karistianis, Nellie
    Metcalfe, Sylvia A.
    Archibald, Alison D.
    Fielding, Joanne
    Trollor, Julian
    Bradshaw, John L.
    Cohen, Jonathan
    Cornish, Kim M.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2014, 165 (01) : 41 - 51