TDP-43 gene analysis in frontotemporal lobar degeneration

被引:42
|
作者
Rollinson, Sara
Snowden, Julie S.
Neary, David
Morrison, Karen E.
Mann, David M. A.
Pickering-Brown, Stuart M.
机构
[1] Univ Manchester, Dept Med, Div Regenerat Med, Manchester M13 9PT, Lancs, England
[2] Univ Manchester, Hope Hosp, Ctr Clin Neurosci, Greater Manchester Neurosci Ctr, Salford M6 8HD, Lancs, England
[3] Univ Birmingham, Sch Med, Div Neurosci, Dept Clin Neurosci, Birmingham B15 2TT, W Midlands, England
[4] Univ Hosp Birmingham, Queen Elizabeth Hosp, NHS Fdn Trust, Birmingham B15 2TH, W Midlands, England
基金
英国医学研究理事会;
关键词
TDP-43; frontotemporal lobar degeneration; FTLD; genetic association; PGRN;
D O I
10.1016/j.neulet.2007.03.044
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It has recently been established that the ubiquitinated neuronal inclusions and neurites observed in frontotemporal lobar degeneration(FTLD) contain the TAR DNA-binding protein, TDP-43. It is not uncommon for genetic variation of genes that encode proteins that accumulate in neurodegenerative conditions to increase risk for disease. We therefore examined whether variation of the TDP-43 locus was associated with an increased risk of disease in the Manchester FTLD cohort. We found no evidence of TDP-43 variation increasing risk for FTLD in this cohort. These data suggest that TDP-43 accumulation is a consequence of the disease process underlying FTLD. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 4
页数:4
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