Journal Article

A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder

Veerle Bogaerts, Sebastiaan Engelborghs, Samir Kumar-Singh, Dirk Goossens, Barbara Pickut, Julie van der Zee, Kristel Sleegers, Karin Peeters, Jean-Jacques Martin, Jurgen Del-Favero, Thomas Gasser, Dennis W. Dickson, Zbigniew K. Wszolek, Peter P. De Deyn, Jessie Theuns and Christine Van Broeckhoven

in Brain

Published on behalf of The Guarantors of Brain

Volume 130, issue 9, pages 2277-2291
Published in print September 2007 | ISSN: 0006-8950
Published online August 2007 | e-ISSN: 1460-2156 | DOI: http://dx.doi.org/10.1093/brain/awm167
A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder

Show Summary Details

Preview

Dementia with Lewy bodies (DLB) represents the second most frequent type of neurodegenerative dementia in the elderly. Although most patients have sporadic DLB, a limited number of DLB families have been described, suggesting that genetic factors may contribute to DLB pathogenesis. Here, we describe a three-generation Belgian family with prominent dementia and parkinsonism, consistent with a diagnosis of DLB, that was autopsy confirmed for the index patient. In a genome-wide scan and subsequent finemapping of candidate loci we obtained significant linkage to 2q35-q36 (Z = 3.01 at D2S1242). Segregation analysis defined a candidate region of 9.2 Mb between D2S433 and chr2q36.3-8, adjacent to the previously reported PARK11 locus. In addition, haplotype sharing studies in another DLB family of close geographical origin with similar clinical and neuropathological features highlighted the specificity of a 2q35-q36 haplotype harbouring a pathogenic mutation that causes DLB in the Belgian family. So far, extensive sequence analysis of five candidate genes within the 2q35-q36 region has not revealed a disease-causing mutation. Together, our data re-emphasize the genetic heterogeneity of DLB, and strongly support the existence of a gene for familial DLB on 2q35-q36. Once identified this will be the first novel causal gene for DLB and can be expected to open new avenues for biological studies of the disease process.

Keywords: dementia with Lewy bodies; autosomal dominant inheritance; linkage analysis; genetic heterogeneity; 2q35-q36

Journal Article.  8169 words.  Illustrated.

Subjects: Neurology ; Neuroscience

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.