Skip Navigation


Brain Advance Access originally published online on May 6, 2004
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
127/7/1641    most recent
awh179v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (13)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Sleegers, K.
Right arrow Articles by van Duijn, C. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sleegers, K.
Right arrow Articles by van Duijn, C. M.
Social Bookmarking
Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Brain, Vol. 127, No. 7, 1641-1649, July 2004
© 2004 Guarantors of Brain
doi: 10.1093/brain/awh179

Familial clustering and genetic risk for dementia in a genetically isolated Dutch population

K. Sleegers1, G. Roks1,3, J. Theuns5, Y. S. Aulchenko1, R. Rademakers5, M. Cruts5, W. A. van Gool4, C. Van Broeckhoven5, P. Heutink*,1, B. A. Oostra1, J. C. van Swieten2 and C. M. van Duijn1

1 Genetic Epidemiology Unit, Departments of Epidemiology and Biostatistics and Clinical Genetics, and 2 Department of Neurology, Erasmus Medical Centre, Rotterdam, 3 Department of Neurology, St Elisabeth Hospital, Tilburg, and 4 Department of Neurology, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands, and 5 Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Belgium *Present address: Department of Human Genetics, VU University Medical Centre, Amsterdam, The Netherlands

Correspondence to: C. M. van Duijn, PhD, Department of Epidemiology and Biostatistics, Erasmus Medical Centre Rotterdam, PO Box 1738, 3000 DR Rotterdam, The Netherlands E-mail:c.vanduijn{at}erasmusmc.nl

Despite advances in elucidating the genetic epidemiology of Alzheimer’s disease and frontotemporal dementia, the aetiology for most patients with dementia remains unclear. We examined the genetic epidemiology of dementia in a recent genetically isolated Dutch population founded around 1750. The series of 191 patients ascertained comprised 122 probable Alzheimer’s disease patients with late onset and 17 with early onset, and 22 with possible Alzheimer’s disease. It further included 10 patients with vascular dementia, nine with Lewy body dementia and six with frontotemporal dementia. All patients, except those with vascular dementia, were more closely related than healthy individuals from the same area. Clustering was strongest for patients with early-onset Alzheimer’s disease or Lewy body dementia. Although 14% of late-onset Alzheimer’s disease patients had evidence of autosomal dominant disease, consanguinity was found in three late-onset Alzheimer’s disease patients, suggesting a recessive or polygenic model underlying the trait. We found no clustering of vascular dementia, implying a difference in genetic risk for late-onset Alzheimer’s disease and vascular dementia. Mutations in known genes could not explain the occurrence of dementia, but the population attributable proportion of apolipoprotein E gene (APOE*4) was high (45%) due to a high frequency of APOE*4 carriers. Earlier identified regions on chromosomes 10 and 12, nor the effect of the alpha-2-macroglobulin (A2M) I/D polymorphism on Alzheimer’s disease could be confirmed in our study. We did find evidence for association between the A2M D-allele and Lewy body dementia. Our data showed a strong familial clustering of various forms of dementia in this isolated Dutch population. A high percentage of late-onset Alzheimer’s disease could be explained by APOE*4, but 55% of its origin is still unknown.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
 HypertensionHome page
A. L. Berends, C. J.M. de Groot, E. J. Sijbrands, M. P.S. Sie, S. H. Benneheij, R. Pal, R. Heydanus, B. A. Oostra, C. M. van Duijn, and E. A.P. Steegers
Shared Constitutional Risks for Maternal Vascular-Related Pregnancy Complications and Future Cardiovascular Disease
Hypertension, April 1, 2008; 51(4): 1034 - 1041.
[Abstract] [Full Text] [PDF]

Home page
 CMAJHome page
C. Patterson MD, J. W. Feightner MD MSc, A. Garcia MD PhD, G.-Y. R. Hsiung MD MHSc, C. MacKnight MD MSc, and A. D. Sadovnick PhD
Diagnosis and treatment of dementia: 1. Risk assessment and primary prevention of Alzheimer disease
Can. Med. Assoc. J., February 26, 2008; 178(5): 548 - 556.
[Abstract] [Full Text] [PDF]

Home page
 BrainHome page
I. L. Ber, E. Guedj, A. Gabelle, P. Verpillat, M. Volteau, C. Thomas-Anterion, M. Decousus, D. Hannequin, P. Vera, L. Lacomblez, et al.
Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia.
Brain, November 1, 2006; 129(Pt 11): 3051 - 3065.
[Abstract] [Full Text] [PDF]

Home page
 BrainHome page
N. Brouwers, K. Sleegers, S. Engelborghs, V. Bogaerts, S. Serneels, K. Kamali, E. Corsmit, E. D. Leenheir, J.-J. Martin, P. P. De Deyn, et al.
Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease
Brain, November 1, 2006; 129(11): 2984 - 2991.
[Abstract] [Full Text] [PDF]


Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.