Evidence map›Paper›PMID 38353748›Full record

ArticleJournal of neurology2024

The comorbidity profiles and medication issues of patients with multiple system atrophy: a systematic cross-sectional analysis.

Lan Ye, Stephan Greten, Florian Wegner, Johanna Doll-Lee, Lea Krey, Johanne Heine, Florin Gandor, Annemarie Vogel, Luise Berger, Doreen Gruber and 38 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Comorbid pathologies and their impact on multiple system atrophy: current view.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
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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

48 authors at 10 institutions in 3 countries.

Lan Ye *Department of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Stephan Greten *Department of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany. Greten.Stephan@mh-hannover.de.ORCID http://orcid.org/0000-0003-0638-8571
Florian WegnerDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Johanna Doll-LeeDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Lea KreyDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Johanne HeineDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Florin GandorNeurologisches Fachkrankenhaus für Bewegungsstörungen/Parkinson, Kliniken Beelitz, 14547, Beelitz-Heilstätten, Germany.
Annemarie VogelNeurologisches Fachkrankenhaus für Bewegungsstörungen/Parkinson, Kliniken Beelitz, 14547, Beelitz-Heilstätten, Germany.
Luise BergerNeurologisches Fachkrankenhaus für Bewegungsstörungen/Parkinson, Kliniken Beelitz, 14547, Beelitz-Heilstätten, Germany.
Doreen GruberNeurologisches Fachkrankenhaus für Bewegungsstörungen/Parkinson, Kliniken Beelitz, 14547, Beelitz-Heilstätten, Germany.
Johannes LevinDepartment of Neurology, University Hospital of Munich, Ludwig-Maximilians-Universität (LMU) Munich, Munich, Germany.
Sabrina KatzdoblerDepartment of Neurology, University Hospital of Munich, Ludwig-Maximilians-Universität (LMU) Munich, Munich, Germany.
Oliver PetersGerman Center for Neurodegenerative Diseases (DZNE), Berlin, Germany.
Eman DashtiDepartment of Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Josef PrillerGerman Center for Neurodegenerative Diseases (DZNE), Berlin, Germany.
Eike Jakob SpruthGerman Center for Neurodegenerative Diseases (DZNE), Berlin, Germany.
Andrea A KühnGerman Center for Neurodegenerative Diseases (DZNE), Berlin, Germany.
Patricia KrauseMovement Disorder and Neuromodulation Unit, Department of Neurology, Charité, University Medicine Berlin, Charité, Berlin, Germany.
Annika SpottkeGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Anja SchneiderGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Aline BeyleGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Okka KimmichGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Markus DonixGerman Center for Neurodegenerative Diseases (DZNE), Dresden, Germany.
Robert HaussmannDepartment of Psychiatry and Psychotherapy, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Moritz BrandtGerman Center for Neurodegenerative Diseases (DZNE), Dresden, Germany.
Elisabeth DinterGerman Center for Neurodegenerative Diseases (DZNE), Dresden, Germany.
Jens WiltfangGerman Center for Neurodegenerative Diseases (DZNE), Goettingen, Germany.
Björn H SchottGerman Center for Neurodegenerative Diseases (DZNE), Goettingen, Germany.
Inga ZerrGerman Center for Neurodegenerative Diseases (DZNE), Goettingen, Germany.
Mathias BährGerman Center for Neurodegenerative Diseases (DZNE), Goettingen, Germany.
Katharina BuergerGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Daniel JanowitzGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Robert PerneczkyGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Boris-Stephan RauchmannGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Endy WeidingerDepartment of Neurology, University Hospital of Munich, Ludwig-Maximilians-Universität (LMU) Munich, Munich, Germany.
Emrah DüzelGerman Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany.
Wenzel GlanzGerman Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany.
Stefan TeipelGerman Center for Neurodegenerative Diseases (DZNE), Rostock-Greifswald, Germany.
Ingo KilimannGerman Center for Neurodegenerative Diseases (DZNE), Rostock-Greifswald, Germany.
Isabel WursterGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Kathrin BrockmannGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Daniel C HoffmannGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Thomas KlockgetherGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Olaf KrauseDIAKOVERE Henriettenstift and Department of General Medicine and Palliative Care, Center for Medicine of the Elderly, Hannover Medical School, Carl-Neuberg-Straße 1, 30625, Hannover, Germany.
Johannes HeckInstitute for Clinical Pharmacology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625, Hannover, Germany.
PROMESA study group
Günter U HöglingerDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Martin KlietzDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
German Center for Neurodegenerative Diseases · DEMedizinische Hochschule Hannover · DEUniversity Hospital Bonn · DENeurologisches Fachkrankenhaus für Bewegungsstörungen/Parkinson · DECharité - Universitätsmedizin Berlin · DELMU Klinikum · DEMunich Cluster for Systems Neurology · DEUniversity Hospital Carl Gustav Carus · DEUniversity of Aveiro · PTUniversity of Rostock · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple system atrophy (MSA) is a complex and fatal neurodegenerative movement disorder. Understanding the comorbidities and drug therapy is crucial for MSA patients' safety and management.

objectivesTo investigate the pattern of comorbidities and aspects of drug therapy in MSA patients.

methodsCross-sectional data of MSA patients according to Gilman et al. (2008) diagnostic criteria and control patients without neurodegenerative diseases (non-ND) were collected from German, multicenter cohorts. The prevalence of comorbidities according to WHO ICD-10 classification and drugs administered according to WHO ATC system were analyzed. Potential drug-drug interactions were identified using AiDKlinik®.

resultsThe analysis included 254 MSA and 363 age- and sex-matched non-ND control patients. MSA patients exhibited a significantly higher burden of comorbidities, in particular diseases of the genitourinary system. Also, more medications were prescribed MSA patients, resulting in a higher prevalence of polypharmacy. Importantly, the risk of potential drug-drug interactions, including severe interactions and contraindicated combinations, was elevated in MSA patients. When comparing MSA-P and MSA-C subtypes, MSA-P patients suffered more frequently from diseases of the genitourinary system and diseases of the musculoskeletal system and connective tissue.

conclusionsMSA patients face a substantial burden of comorbidities, notably in the genitourinary system. This, coupled with increased polypharmacy and potential drug interactions, highlights the complexity of managing MSA patients. Clinicians should carefully consider these factors when devising treatment strategies for MSA patients.

Indexed as

ComorbidityDrug InteractionsMultiple System AtrophyPolypharmacyAgedCross-Sectional StudiesFemaleGermanyHumansMaleMiddle AgedPrevalenceComorbiditiesDrug-drug interactionsGenitourinary system diseasesMultiple system atrophyPolypharmacy

Identifiers

PMID38353748
PMCPMC11055732
OpenAlexW4391809696

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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.