A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson’s disease with dementia

Author:

Fanciulli Alessandra1ORCID,Leys Fabian1,Lehner Fabienne1,Sidoroff Victoria1,Ruf Viktoria C2,Raccagni Cecilia13,Mahlknecht Philipp1ORCID,Kuipers Demy J S4,van IJcken Wilfred F J5ORCID,Stockner Heike1,Musacchio Thomas6,Volkmann Jens6,Monoranu Camelia Maria7,Stankovic Iva8,Breedveld Guido4,Ferraro Federico4ORCID,Fevga Christina4,Windl Otto2,Herms Jochen2,Kiechl Stefan1ORCID,Poewe Werner1,Seppi Klaus1,Stefanova Nadia1ORCID,Scholz Sonja W910ORCID,Bonifati Vincenzo4,Wenning Gregor K1

Affiliation:

1. Department of Neurology, Medical University of Innsbruck , Innsbruck , Austria

2. Center for Neuropathology and Prion Research, Ludwig-Maximilians-University Munich , Munich , Germany

3. Department of Neurology, Regional General Hospital Bolzano , Bolzano , Italy

4. Department of Clinical Genetics, Erasmus MC, University Medical Center , Rotterdam , the Netherlands

5. Center for Biomics, Erasmus MC, University Medical Center , Rotterdam , the Netherlands

6. Department of Neurology, University of Würzburg , Würzburg , Germany

7. Department of Neuropathology, Institute of Pathology, University of Würzburg , Würzburg , Germany

8. Neurology Clinic, Clinical Center of Serbia, University of Belgrade , Belgrade , Serbia

9. Neurodegenerative Diseases Research Unit, National Institute of Neurological Disorders and Stroke , Bethesda, MD , USA

10. Department of Neurology, Johns Hopkins University Medical Center , Baltimore, MD , USA

Abstract

Abstract Multiple system atrophy is considered a sporadic disease, but neuropathologically confirmed cases with a family history of parkinsonism have been occasionally described. Here we report a North-Bavarian (colloquially, Lion’s tail region) six-generation pedigree, including neuropathologically confirmed multiple system atrophy and Parkinson’s disease with dementia. Between 2012 and 2020, we examined all living and consenting family members of age and calculated the risk of prodromal Parkinson’s disease in those without overt parkinsonism. The index case and one paternal cousin with Parkinson’s disease with dementia died at follow-up and underwent neuropathological examination. Genetic analysis was performed in both and another family member with Parkinson’s disease. The index case was a female patient with cerebellar variant multiple system atrophy and a positive maternal and paternal family history for Parkinson’s disease and dementia in multiple generations. The families of the index case and her spouse were genealogically related, and one of the spouse's siblings met the criteria for possible prodromal Parkinson’s disease. Neuropathological examination confirmed multiple system atrophy in the index case and advanced Lewy body disease, as well as tau pathology in her cousin. A comprehensive analysis of genes known to cause hereditary forms of parkinsonism or multiple system atrophy lookalikes was unremarkable in the index case and the other two affected family members. Here, we report an extensive European pedigree with multiple system atrophy and Parkinson`s disease suggesting a complex underlying α-synucleinopathy as confirmed on neuropathological examination. The exclusion of known genetic causes of parkinsonism or multiple system atrophy lookalikes suggests that variants in additional, still unknown genes, linked to α-synucleinopathy lesions underlie such neurodegenerative clustering.

Funder

Stichting ParkinsonFonds

Multiple System Atrophy Coalition

Publisher

Oxford University Press (OUP)

Subject

General Earth and Planetary Sciences,General Environmental Science

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