Genetic studies of GRN and IFT74 in arnyotrophic lateral sclerosis

被引:7
|
作者
Xiao, Shangxi [1 ]
Sato, Christine [1 ]
Kawarai, Toshitaka [1 ]
Goodall, Emily F. [2 ]
Pall, Hardev S. [2 ,3 ]
Zinman, Lorne H. [4 ]
Robertson, Janice [1 ]
Morrison, Karen [2 ,3 ]
Rogaeva, Ekaterina [1 ,5 ]
机构
[1] Univ Toronto, Ctr Res Neurodegenerat Dis, Toronto, ON M5S 3H2, Canada
[2] Univ Birmingham, Dept Clin Neurosci, Inst Biomed Res, Birmingham B15 2TT, W Midlands, England
[3] Univ Birmingham, Queen Elizabeth Hosp, NHS Fdn Trust, Birmingham B15 2TT, W Midlands, England
[4] Univ Toronto, Sunnybrook Hlth Sci Ctr, Toronto, ON, Canada
[5] Univ Toronto, Dept Med, Div Neurol, Toronto, ON M5S 1A1, Canada
基金
加拿大健康研究院;
关键词
amyotrophic lateral sclerosis; single nucleotide polymorphism; progranulin; risk factor;
D O I
10.1016/j.neurobiolaging.2007.02.022
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
There is increasing evidence of a clinical, neuropathological and genetic overlap between frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). We conducted a case-control study using a UK dataset to test the hypothesis that polymorphisms in two FTD-related genes (GRN and FT74) are associated with increased susceptibility to ALS. We evaluated the majority of known genetic variability in IFT74 and GRN. The results revealed that the common variations in IFT74 and GRN neither constitute strong ALS risk factors nor modify the age-at-onset. However, the possibility of a modest risk effect remains to be assessed in large datasets. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1279 / 1282
页数:4
相关论文
共 50 条
  • [41] Genetic approximation in amyotrophic lateral sclerosis
    Cervantes-Aragon, Ivan
    Alberto Ramirez-Garcia, Sergio
    Margarita Baltazar-Rodriguez, Luz
    Garcia-Cruz, Diana
    Castaneda-Cisneros, Gema
    GACETA MEDICA DE MEXICO, 2019, 155 (05): : 513 - 521
  • [42] Genetic epidemiology of amyotrophic lateral sclerosis
    Majoor-Krakauer, D
    Willems, PJ
    Hofman, A
    CLINICAL GENETICS, 2003, 63 (02) : 83 - 101
  • [43] Genetic characterization of primary lateral sclerosis
    Eva M. J. de Boer
    Balint S. de Vries
    Maartje Pennings
    Erik-Jan Kamsteeg
    Jan H. Veldink
    Leonard H. van den Berg
    Michael A. van Es
    Journal of Neurology, 2023, 270 : 3970 - 3980
  • [44] Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome
    Patrick Lorès
    Zine-Eddine Kherraf
    Amir Amiri-Yekta
    Marjorie Whitfield
    Abbas Daneshipour
    Laurence Stouvenel
    Caroline Cazin
    Emma Cavarocchi
    Charles Coutton
    Marie-Astrid Llabador
    Christophe Arnoult
    Nicolas Thierry-Mieg
    Lucile Ferreux
    Catherine Patrat
    Seyedeh-Hanieh Hosseini
    Selima Fourati Ben Mustapha
    Raoudha Zouari
    Emmanuel Dulioust
    Pierre F. Ray
    Aminata Touré
    Human Genetics, 2021, 140 : 1045 - 1045
  • [45] Clinical studies in amyotrophic lateral sclerosis
    Dorst, Johannes
    Genge, Angela
    CURRENT OPINION IN NEUROLOGY, 2022, 35 (05) : 686 - 692
  • [46] VIROLOGICAL STUDIES IN AMYOTROPHIC LATERAL SCLEROSIS
    KASCSAK, RJ
    CARP, RI
    VILCEK, JT
    DONNENFELD, H
    BARTFELD, H
    MUSCLE & NERVE, 1982, 5 (02) : 93 - 101
  • [47] ELECTROMYOGRAPHIC STUDIES IN AMYOTROPHIC LATERAL SCLEROSIS
    LAMBERT, EH
    MULDER, DW
    PROCEEDINGS OF THE STAFF MEETINGS OF THE MAYO CLINIC, 1957, 32 (17): : 441 - 446
  • [48] Polysomnographic studies in amyotrophic lateral sclerosis
    David, WS
    Bundlie, SR
    Mahdavi, Z
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 152 : S29 - S35
  • [49] Invertebrate genetic models of amyotrophic lateral sclerosis
    Zhou, LiJun
    Xu, RenShi
    FRONTIERS IN MOLECULAR NEUROSCIENCE, 2024, 17
  • [50] Amyotrophic lateral sclerosis as a complex genetic disease
    Simpson, Claire L.
    Al-Chalabi, Ammar
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2006, 1762 (11-12): : 973 - 985