Intermediate FMR1 alleles and cognitive and/or behavioural phenotypes

被引:0
作者
Irene Madrigal
Mar Xunclà
Maria Isabel Tejada
Francisco Martínez
Isabel Fernández-Carvajal
Luís Alberto Pérez-Jurado
Laia Rodriguez-Revenga
Montserrat Milà
机构
[1] Hospital Clínic,CIBER de Enfermedades Raras and Biochemistry and Molecular Genetics Department
[2] Fundació Clinic per a la Recerca Biomèdica,Biochemistry Department
[3] Molecular Genetics Laboratory,undefined
[4] Cruces Hospital,undefined
[5] GIRMOGEN (Spanish Network for Mental Retardation),undefined
[6] Spain,undefined
[7] Unidad de Genética,undefined
[8] Hospital Universitario La Fe,undefined
[9] Instituto de Biología y Genética Molecular (IBGM),undefined
[10] Universidad de Valladolid,undefined
[11] Centro Superior de Investigaciones Científicas (CSIC),undefined
[12] CIBER de Enfermedades Raras,undefined
[13] Genetics Unit,undefined
[14] Universitat Pompeu Fabra,undefined
[15] Program in Molecular Medicine,undefined
[16] Institut d’Investigacions Biomèdiques August Pi i Sunyer,undefined
来源
European Journal of Human Genetics | 2011年 / 19卷
关键词
intermediate alleles; cognitive and behavioural phenotypes; FMR1; ASD; ADHD;
D O I
暂无
中图分类号
学科分类号
摘要
During the last few years, several studies have reported an excess of intermediate FMR1 alleles in patients with cognitive and/or behavioural phenotypes. Here, we report the frequency of intermediate alleles (IAs) in three pathologies, intellectual disabilities (IDs), attention-deficit/hyperactivity disorder and autism, from different Spanish regions. We found 142 IAs among 9015 patients with ID (1.6%), 4 among the 415 ADHD patients (0.96%) and 4 among the 300 autistic patients (1.3%), similar to the frequency reported in our control population. No evidence was found of an excess of IA at the FRAXA locus in any of the study populations, although geographical variability was detected. Moreover, the analysis of 100 transmissions of IAs showed that 95% of these alleles were stable. Only 3% expanded within the same range and 2% expanded to a full mutation in two generations. No evidence of an association between IAs and behavioural or cognitive phenotypes was found, suggesting that IAs are not clearly implicated in these pathologies.
引用
收藏
页码:921 / 923
页数:2
相关论文
共 50 条
  • [41] Spontaneous rescue of a FMR1 repeat expansion and review of deletions in the FMR1 non-coding region
    Erbs, Emilie
    Fenger-Gron, Jesper
    Jacobsen, Cecilie Mondrup
    Lildballe, Dorte Launholt
    Rasmussen, Maria
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2021, 64 (08)
  • [42] The Spectrum of Neurological and White Matter Changes and Premutation Status Categories of Older Male Carriers of the FMR1 Alleles Are Linked to Genetic (CGG and FMR1 mRNA) and Cellular Stress (AMPK) Markers
    Loesch, Danuta Z.
    Trost, Nicholas
    Bui, Minh Q.
    Hammersley, Eleanor
    Lay, Sui T.
    Annesley, Sarah J.
    Sanislav, Oana
    Allan, Claire Y.
    Tassone, Flora
    Chen, Zhi-Ping
    Ngoei, Kevin R. W.
    Kemp, Bruce E.
    Francis, David
    Fisher, Paul R.
    Storey, Elsdon
    FRONTIERS IN GENETICS, 2018, 9
  • [43] Fragile X syndrome with FMR1 and FMR2 deletion
    Moore, SJ
    Strain, L
    Cole, GF
    Miedzybrodzka, Z
    Kelly, KF
    Dean, JCS
    JOURNAL OF MEDICAL GENETICS, 1999, 36 (07) : 565 - 566
  • [44] Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian age
    Kline, Jennie K.
    Kinney, Ann M.
    Levin, Bruce
    Brown, Stephen A.
    Hadd, Andrew G.
    Warburton, Dorothy
    MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY, 2014, 21 (07): : 740 - 748
  • [45] Postnatal downregulation of Fmr1 in microglia promotes microglial reactivity and causes behavioural alterations in female mice
    Hooshmandi, Mehdi
    Ho-Tieng, David
    Lister, Kevin C.
    Cai, Weihua
    Wong, Calvin
    Brown, Nicole
    Fan, Jonathan
    Hovhannisyan, Volodya
    Uttam, Sonali
    Prager-Khoutorsky, Masha
    Sonenberg, Nahum
    Gkogkas, Christos G.
    Khoutorsky, Arkady
    MOLECULAR AUTISM, 2025, 16 (01):
  • [46] Associated features in females with an FMR1 premutation
    Wheeler, Anne C.
    Bailey, Donald B., Jr.
    Berry-Kravis, Elizabeth
    Greenberg, Jan
    Losh, Molly
    Mailick, Marsha
    Mila, Montserrat
    Olichney, John M.
    Rodriguez-Revenga, Laia
    Sherman, Stephanie
    Smith, Leann
    Summers, Scott
    Yang, Jin-Chen
    Hagerman, Randi
    JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2014, 6
  • [47] Relationships between Mitochondrial Function, AMPK, and TORC1 Signaling in Lymphoblasts with Premutation Alleles of the FMR1 Gene
    Fisher, Paul R.
    Allan, Claire Y.
    Sanislav, Oana
    Atkinson, Anna
    Ngoei, Kevin R. W.
    Kemp, Bruce E.
    Storey, Elsdon
    Loesch, Danuta Z.
    Annesley, Sarah J.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (19)
  • [48] Premature ovarian failure and the FMR1 gene
    Murray, A
    SEMINARS IN REPRODUCTIVE MEDICINE, 2000, 18 (01) : 59 - 66
  • [49] FMR1 gene and fragile X syndrome
    Bardoni, B
    Mandel, JL
    Fisch, GS
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 97 (02): : 153 - 163
  • [50] From dynamic FMR1 mutation to variable phenotypes: A case series from a large Tunisian family
    Ketata, Imen
    Ellouz, Emna
    NEUROLOGY AND CLINICAL NEUROSCIENCE, 2025, 13 (02): : 107 - 114