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PMID: 9500549 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

Nature genetics ·Vol. 18 ·No. 3 ·1998-03-00 ·Pages 262-5

Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD

Abstract

Parkinson's disease (PD) is a common degenerative neurologic disorder, which is pathologically characterized by a selective degeneration of dopaminergic neurons of the substantia nigra pars compacta, and the presence of characteristic eosinophilic inclusions, known as Lewy-bodies in affected brain areas. The cause of PD is unknown but, in recent years, genetic factors have been implicated in the aetiology of the disease. Firstly, clinico-genetic, epidemiologic and twin studies revealed inheritable effects and questioned earlier studies which had denied such influences. Secondly, several family studies suggested autosomal-dominant inheritance of syndromes which, to variable degrees, resembled sporadic PD clinically and in some cases also neuropathologically. Recently, a disease locus has been mapped to chromosome 4q21-22 in a large Mediterranean pedigree, in which disease expression is clinically and pathologically within the spectrum of sporadic PD; being atypical only for a relatively young mean age at onset of 46 years and rapid course of 10 years from onset to death. In affected individuals of this family and of three unrelated Greek kindreds, a putative disease-causing mutation has been identified in the gene encoding alpha-synuclein. With the first variant being defined, genetic heterogeneity has become apparent, as in other families parkinsonism was not linked to the 4q-locus and was not associated with the alpha-synuclein mutation (unpublished data). We describe a different genetic locus that appears to be involved in the development of parkinsonism closely resembling sporadic PD including a similar mean age of onset (59 years in the families, 59.7 years in sporadic PD; ref. 12). This locus was detected in a group of families of European origin. In two of these families, there is genetic evidence for a common founder. The penetrance of the mutation appears to be low, most likely below 40%. This is compatible with a possible role of this locus not only in familial, but also in typical (sporadic) PD.

MeSH Terms
Adult Age of Onset Aged Aged, 80 and over Chromosomes, Human, Pair 2 Disease Susceptibility Female Genes, Dominant Genetic Linkage Genetic Markers Haplotypes Humans Lod Score Male Middle Aged Parkinson Disease/genetics Pedigree
Chemicals
Genetic Markers
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Gasser T
Neurologische Klinik, Klinikum Grosshadern, Ludwig-Maximilians-Universität, München, Germany. tgasser@brain.nefo.med.uni-muenchen.de
Müller-Myhsok B
Wszolek Z K
Oehlmann R
Calne D B
Bonifati V
Bereznai B
Fabrizio E
Vieregge P
Horstmann R D
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
1998-03-00
Pages
262-5
Language
English
Region
United States
NLM ID
9216904
Subset
IM
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