Evidence map›Paper›PMID 34493736›Full record

ArticleNPJ Parkinson's disease2021

Heterogeneity of prodromal Parkinson symptoms in siblings of Parkinson disease patients.

Luca Baldelli, Sebastian Schade, Silvia Jesús, Sebastian R Schreglmann, Luisa Sambati, Pilar Gómez-Garre, Claire Halsband, Giovanna Calandra-Buonaura, Astrid Daniela Adarmes-Gómez, Friederike Sixel-Döring and 12 more

Open access · goldAbstract read
In one paragraph

Article in NPJ Parkinson's disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. 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

22 authors at 17 institutions in 5 countries.

Luca BaldelliDepartment of Biomedical and NeuroMotor Sciences (DiBiNeM), University of Bologna, Bologna, Italy.
Sebastian SchadeDepartment of Clinical Neurophysiology, University Medical Center Göttingen, Göttingen, Germany.ORCID http://orcid.org/0000-0002-6316-6804
Silvia JesúsUnidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.
Sebastian R SchreglmannUniversity College London (UCL), Institute of Neurology, London, United Kingdom.
Luisa SambatiDepartment of Biomedical and NeuroMotor Sciences (DiBiNeM), University of Bologna, Bologna, Italy.
Pilar Gómez-GarreUnidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.ORCID http://orcid.org/0000-0002-0437-6182
Claire HalsbandDepartment of Clinical Neurophysiology, University Medical Center Göttingen, Göttingen, Germany.
Giovanna Calandra-BuonauraDepartment of Biomedical and NeuroMotor Sciences (DiBiNeM), University of Bologna, Bologna, Italy.
Astrid Daniela Adarmes-GómezUnidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.
Friederike Sixel-DöringParacelsus-Elena-Klinik Kassel, Kassel, Germany.
Corrado ZenesiniIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Chiara PirazziniIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Paolo GaragnaniDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
Maria Giulia BacaliniIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Kailash P BhatiaUniversity College London (UCL), Institute of Neurology, London, United Kingdom.
Pietro CortelliDepartment of Biomedical and NeuroMotor Sciences (DiBiNeM), University of Bologna, Bologna, Italy.
Brit MollenhauerParacelsus-Elena-Klinik Kassel, Kassel, Germany.
Claudio FranceschiIRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
PROPAG-AGEING consortium
Pablo MirUnidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.ORCID http://orcid.org/0000-0003-1656-302X
Claudia TrenkwalderDepartment of Neurosurgery, University Medical Center Göttingen, Göttingen, Germany.
Federica ProviniDepartment of Biomedical and NeuroMotor Sciences (DiBiNeM), University of Bologna, Bologna, Italy. federica.provini@unibo.it.ORCID http://orcid.org/0000-0001-9063-2658
Istituto delle Scienze Neurologiche di Bologna · ITBiomedical Research Networking Center on Neurodegenerative Diseases · ESKarolinska Institutet · SELondon Library · GBUniversity of Bologna · ITUniversitätsmedizin Göttingen · DEUniversity College London · GBUniversity of Cambridge · GBUniversity of Florence · ITUniversity of Verona · ITAzienda Sanitaria Unità Locale di Reggio Emilia · ITAzienda USL di Bologna · ITConsorzio Roma Ricerche · ITGiotto Biotech (Italy) · ITPhilipps University of Marburg · DEUniversity of L'Aquila · ITUniversity of Oxford · GB

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 634821
6 · The paper itself

Abstract

A prodromal phase of Parkinson's disease (PD) may precede motor manifestations by decades. PD patients' siblings are at higher risk for PD, but the prevalence and distribution of prodromal symptoms are unknown. The study objectives were (1) to assess motor and non-motor features estimating prodromal PD probability in PD siblings recruited within the European PROPAG-AGEING project; (2) to compare motor and non-motor symptoms to the well-established DeNoPa cohort. 340 PD siblings from three sites (Bologna, Seville, Kassel/Goettingen) underwent clinical and neurological evaluations of PD markers. The German part of the cohort was compared with German de novo PD patients (dnPDs) and healthy controls (CTRs) from DeNoPa. Fifteen (4.4%) siblings presented with subtle signs of motor impairment, with MDS-UPDRS-III scores not clinically different from CTRs. Symptoms of orthostatic hypotension were present in 47 siblings (13.8%), no different to CTRs (p = 0.072). No differences were found for olfaction and overall cognition; German-siblings performed worse than CTRs in visuospatial-executive and language tasks. 3/147 siblings had video-polysomnography-confirmed REM sleep behavior disorder (RBD), none was positive on the RBD Screening Questionnaire. 173/300 siblings had <1% probability of having prodromal PD; 100 between 1 and 10%, 26 siblings between 10 and 80%, one fulfilled the criteria for prodromal PD. According to the current analysis, we cannot confirm the increased risk of PD siblings for prodromal PD. Siblings showed a heterogeneous distribution of prodromal PD markers and probability. Additional parameters, including strong disease markers, should be investigated to verify if these results depend on validity and sensitivity of prodromal PD criteria, or if siblings' risk is not elevated.

Identifiers

PMID34493736
PMCPMC8423761
OpenAlexW3197687946

What OpenQuestion holds

Textmetadata
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.