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
  • [31] FMR1 premutation as a rare cause of late onset ataxia -: Evidence for FXTAS in female carriers
    Zühlke, C
    Budnik, A
    Gehlken, U
    Dalski, A
    Purmann, S
    Naumann, M
    Schmidt, M
    Bürk, K
    Schwinger, E
    JOURNAL OF NEUROLOGY, 2004, 251 (11) : 1418 - 1419
  • [32] Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene
    Nobile, Veronica
    Palumbo, Federica
    Lanni, Stella
    Ghisio, Valentina
    Vitali, Alberto
    Castagnola, Massimo
    Marzano, Valeria
    Maulucci, Giuseppe
    De Angelis, Claudio
    De Spirito, Marco
    Pacini, Laura
    D'Andrea, Laura
    Ragno, Rino
    Stazi, Giulia
    Valente, Sergio
    Mai, Antonello
    Chiurazzi, Pietro
    Genuardi, Maurizio
    Neri, Giovanni
    Tabolacci, Elisabetta
    HUMAN GENETICS, 2020, 139 (02) : 227 - 245
  • [33] Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene
    Nobile, V.
    Palumbo, F.
    Lanni, S.
    Ghisio, V.
    Vitali, A.
    Marzano, V.
    Castagnola, M.
    Maulucci, G.
    De Angelis, C.
    De Spirito, M.
    Pacini, L.
    D'Andrea, L.
    Ragno, R.
    Stazi, G.
    Valente, S.
    Mai, A.
    Chiurazzi, P.
    Genuardi, M.
    Neri, G.
    Tabolacci, E.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 336 - 337
  • [34] Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene
    Veronica Nobile
    Federica Palumbo
    Stella Lanni
    Valentina Ghisio
    Alberto Vitali
    Massimo Castagnola
    Valeria Marzano
    Giuseppe Maulucci
    Claudio De Angelis
    Marco De Spirito
    Laura Pacini
    Laura D’Andrea
    Rino Ragno
    Giulia Stazi
    Sergio Valente
    Antonello Mai
    Pietro Chiurazzi
    Maurizio Genuardi
    Giovanni Neri
    Elisabetta Tabolacci
    Human Genetics, 2020, 139 : 227 - 245
  • [35] Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing
    Ardui, Simon
    Race, Valerie
    Zablotskaya, Alena
    Hestand, Matthew S.
    Van Esch, Hilde
    Devriendt, Koenraad
    Matthijs, Gert
    Vermeesch, Joris R.
    HUMAN MUTATION, 2017, 38 (03) : 324 - 331
  • [36] Expansion to full mutation of a FMR1 intermediate allele over two generations
    Terracciano, A
    Pomponi, MG
    Marino, GME
    Chiurazzi, P
    Rinaldi, MM
    Dobosz, M
    Neri, G
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2004, 12 (04) : 333 - 336
  • [37] Expansion to full mutation of a FMR1 intermediate allele over two generations
    Alessandra Terracciano
    Maria Grazia Pomponi
    Grazia Maria Elisabetta Marino
    Pietro Chiurazzi
    Maria Michela Rinaldi
    Marina Dobosz
    Giovanni Neri
    European Journal of Human Genetics, 2004, 12 : 333 - 336
  • [38] Strong similarities of the FMR1 mutation in multiple tissues:: Postmortem studies of a male with a full mutation and a male carrier of a premutation
    Tassone, F
    Hagerman, RJ
    Gane, LW
    Taylor, AK
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 84 (03): : 240 - 244
  • [39] Delineating the Relationships Between Motor, Cognitive-Executive and Psychiatric Symptoms in Female FMR1 Premutation Carriers
    Hocking, Darren R.
    Loesch, Danuta Z.
    Stimpson, Paige
    Tassone, Flora
    Atkinson, Anna
    Storey, Elsdon
    FRONTIERS IN PSYCHIATRY, 2021, 12
  • [40] Characterization of the Metabolic, Clinical and Neuropsychological Phenotype of Female Carriers of the Premutation in the X-Linked FMR1 Gene
    Napoli, Eleonora
    McLennan, Yingratana Amabel
    Schneider, Andrea
    Tassone, Flora
    Hagerman, Randi J.
    Giulivi, Cecilia
    FRONTIERS IN MOLECULAR BIOSCIENCES, 2020, 7