Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

被引:299
作者
Houlden, H
Baker, M
Morris, HR
MacDonald, N
Pickering-Brown, S
Adamson, J
Lees, AJ
Rossor, MN
Quinn, NP
Kertesz, A
Khan, MN
Hardy, J
Lantos, PL
George-Hyslop, PS
Munoz, DG
Mann, D
Lang, AE
Bergeron, C
Bigio, EH
Litvan, I
Bhatia, KP
Dickson, D
Wood, NW
Hutton, M
机构
[1] Mayo Clin Jacksonville, Jacksonville, FL 32224 USA
[2] Inst Neurol, Clin Neurol & Dementia Res Grp, London WC1N 3BG, England
[3] St Bartholomews Hosp, Dept Gynaecol Oncol, London, England
[4] Univ Manchester, Sch Biol Sci, Manchester M13 9PL, Lancs, England
[5] Univ Manchester, Dept Med, Manchester M13 9PL, Lancs, England
[6] Inst Psychiat, Dept Neuropathol, London SE5 8AF, England
[7] Univ Western Ontario, Dept Neuropathol, London, ON N6A 3K7, Canada
[8] Dept Neurol, Toronto, ON, Canada
[9] Univ Texas, SW Med Sch, Dept Pathol, Dallas, TX 75230 USA
[10] NINDS, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1212/WNL.56.12.1702
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To analyze the association of polymorphisms in the tau gene with pathologically confirmed corticobasal degeneration (CBD). Background: The authors previously described an extended tau haplotype (H1) that covers the human tau gene and is associated with the development of progressive supranuclear palsy (PSP). The authors now extend this analysis to CBD, a neurodegenerative condition with clinical and neuropathologic similarities to PSP. Like PSP, CBD is associated with accumulation of aggregates containing the 4-repeat isoforms of tau. Because of difficulty in diagnosis of CBD, the authors only analyzed cases with pathologically confirmed CBD. Methods: The authors collected 57 unrelated, neuropathologically confirmed cases of CBD. Tau sequencing in these cases failed to show the presence of pathogenic mutations. Polymorphisms that spanned the tau gene were analyzed in all CBD cases and controls. Results: Analyzing tau polymorphisms in CBD cases showed that the frequency of H1 and H1/H1 was significantly increased when analyzing all cases and when separating by country of origin. H1 frequency in all CBD cases was 0.921, compared with a control frequency of 0.766 (X-2 = 9.1, P = 0.00255 [1df], OR 3.56 [8.43 > CI 95% > 1.53]). The H1/H1 frequency was also significantly higher at 0.842 compared with 0.596 in age-matched controls (X-2 = 17.42,p = 0.00016, 2df), OR 3.61 [7.05 > CI 95% > 1.851). Conclusions: The CBD tau association described here suggests that PSP and CBD share a similar cause, although the pathogenic mechanism behind the two diseases leads to a different clinical and pathologic phenotype.
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页码:1702 / 1706
页数:5
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