Evidence map›Paper›PMID 35855480›Full record

ArticleBrain communications2022

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

Alessandra Fanciulli, Fabian Leys, Fabienne Lehner, Victoria Sidoroff, Viktoria C Ruf, Cecilia Raccagni, Philipp Mahlknecht, Demy J S Kuipers, Wilfred F J van IJcken, Heike Stockner and 16 more

Open access · goldAbstract read
In one paragraph

Article in Brain communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Multiple system atrophy: cure and care.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
  2. Comorbid pathologies and their impact on multiple system atrophy: current view.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
  3. Review
  4. Review
  5. Family History for Neurodegeneration in Multiple System Atrophy: Does it Indicate Susceptibility?Movement disorders : official journal of the Movement Disorder Society · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors at 6 institutions in 6 countries.

Alessandra FanciulliDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0002-2854-4179
Fabian LeysDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Fabienne LehnerDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Victoria SidoroffDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Viktoria C RufCenter for Neuropathology and Prion Research, Ludwig-Maximilians-University Munich, Munich, Germany.
Cecilia RaccagniDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Philipp MahlknechtDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0003-0671-0516
Demy J S KuipersDepartment of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Wilfred F J van IJckenCenter for Biomics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-0421-8301
Heike StocknerDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Thomas MusacchioDepartment of Neurology, University of Würzburg, Würzburg, Germany.
Jens VolkmannDepartment of Neurology, University of Würzburg, Würzburg, Germany.
Camelia Maria MonoranuDepartment of Neuropathology, Institute of Pathology, University of Würzburg, Würzburg, Germany.
Iva StankovicNeurology Clinic, Clinical Center of Serbia, University of Belgrade, Belgrade, Serbia.
Guido BreedveldDepartment of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Federico FerraroDepartment of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0003-1365-2529
Christina FevgaDepartment of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Otto WindlCenter for Neuropathology and Prion Research, Ludwig-Maximilians-University Munich, Munich, Germany.
Jochen HermsCenter for Neuropathology and Prion Research, Ludwig-Maximilians-University Munich, Munich, Germany.
Stefan KiechlDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0002-9836-2514
Werner PoeweDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Klaus SeppiDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Nadia StefanovaDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0001-8188-639X
Sonja W ScholzNeurodegenerative Diseases Research Unit, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID https://orcid.org/0000-0002-6623-0429
Vincenzo BonifatiDepartment of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Gregor K WenningDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Innsbruck Medical University · ATErasmus MC · NLLudwig-Maximilians-Universität München · DEUniversity of Würzburg · DEJohns Hopkins University · USUniversity of Belgrade · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

geneticsmultiple system atrophymultiplex pedigreeParkinson’s diseaseParkinson’s disease with dementia

Identifiers

PMID35855480
PMCPMC9291376
OpenAlexW4283791802

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.