Evidence map›Paper›PMID 39444167›Full record

ArticleEuropean journal of neurology2024

Neuroleptic malignant syndrome in Huntington disease.

Antonio Funcis, Beatrice Ravera, Paola Zinzi, Marcella Solito, Martina Petracca, Paolo Calabresi, Anna Rita Bentivoglio

Abstract readCase Reports
In one paragraph

Article in European journal of neurology, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Neuroleptic malignant syndrome in Huntington disease.European journal of neurology · 2024
    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

7 authors.

Antonio FuncisInstitute of Neurology, Catholic University of the Sacred Heart, Rome, Italy.ORCID 0009-0009-6134-5268
Beatrice RaveraInstitute of Neurology, Catholic University of the Sacred Heart, Rome, Italy.
Paola ZinziInstitute of Neurology, Catholic University of the Sacred Heart, Rome, Italy.
Marcella SolitoInstitute of Neurology, Catholic University of the Sacred Heart, Rome, Italy.
Martina PetraccaInstitute of Neurology, Catholic University of the Sacred Heart, Rome, Italy.
Paolo CalabresiInstitute of Neurology, Catholic University of the Sacred Heart, Rome, Italy.
Anna Rita BentivoglioInstitute of Neurology, Catholic University of the Sacred Heart, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeDespite the wide use of dopamine receptor blocking agents (DRBAs) in Huntington disease (HD), neuroleptic malignant syndrome (NMS) is rarely described in this population. The aim of this study was to assess NMS prevalence in a large cohort of HD patients and explore the main associated risk factors.

methodsIn 2023, an HD patient was admitted to our neurology department due to NMS. Starting from the case description, we performed a narrative review of the literature of NMS cases in HD, reviewed data from the fifth dataset of the Enroll-HD (a longitudinal, observational, global study of families with HD) study (PDS5) selecting HD patients treated with DRBAs and/or tetrabenazine (TBZ) who presented at least one of the core symptoms of NMS (rigidity and hyperthermia), and collected data to investigate prevalence of NMS and identify risk factors.

resultsIn the Enroll-HD PDS5 dataset, we identified 5108 of 11,569 HD patients who were undergoing DRBA and/or TBZ treatment. Only one patient, a Caucasian man of 46 years, undergoing clozapine and valproate treatment, had a registered diagnosis of NMS.

conclusionsNMS in HD patients is seldom described. This could be due to an underestimation of this condition. There are no available objective NMS diagnostic criteria at present, and the existence of atypical forms of NMS further complicates diagnosis. Advanced disease stage, rigid-akinetic phenotype, abrupt therapy changes, polytherapy, and dehydration are key risk factors, most of which are preventable through awareness and caution in managing medications in the HD population.

Indexed as

Huntington DiseaseNeuroleptic Malignant SyndromeAntipsychotic AgentsDopamine AntagonistsHumansMaleMiddle AgedPrevalenceRisk FactorsTetrabenazineAntipsychotic AgentsDopamine AntagonistsTetrabenazinedopamineHuntington diseaseneuroleptic malignant syndromeneurolepticstetrabenazine

Identifiers

PMID39444167
PMCPMC11554869

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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.