Evidence map›Paper›PMID 38404049›Full record

ArticleMovement disorders clinical practice2024

Neuroenergetic Changes in Patients with X-Linked Dystonia-Parkinsonism and Female Carriers.

Jannik Prasuhn, Julia Henkel, Shela Marie Algodon, Jan Uter, Raymond L Rosales, Christine Klein, Julia Steinhardt, Cid C Diesta, Norbert Brüggemann

Abstract read
In one paragraph

Article in Movement disorders clinical practice, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. Article
4 · The record

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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

9 authors.

Jannik PrasuhnDepartment of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.ORCID 0000-0003-4184-9409
Julia HenkelDepartment of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Shela Marie AlgodonInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Jan UterDepartment of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Raymond L RosalesDepartment of Neurology and Psychiatry, University of Santo Thomas, Manila, Philippines.
Christine KleinInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Julia SteinhardtDepartment of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.ORCID 0000-0002-4175-8112
Cid C DiestaMakati Medical Center, Makati City, Philippines.
Norbert BrüggemannDepartment of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.ORCID 0000-0001-5969-6899

Funding

Collaborative Center for X-linked Dystonia-ParkinsonismDeutsche Forschungsgemeinschaft BR4328/2-2Deutsche Forschungsgemeinschaft GRK1957
6 · The paper itself

Abstract

backgroundX-linked dystonia-parkinsonism (XDP) is a rare movement disorder characterized by profound neurodegeneration in the basal ganglia. The molecular consequences and the bioenergetic state of affected individuals remain largely unexplored.

objectivesTo investigate the bioenergetic state in male patients with XDP and female carriers using

methodsWe examined the levels of high-energy phosphorus-containing metabolites (HEP) in the basal ganglia and cerebellum of five male patients with XDP, 10 asymptomatic female heterozygous carriers, and 10 SVA-insertion-free controls.

resultsHEP levels were reduced in the basal ganglia of patients with XDP (PwXDP) compared to controls, but increased in the cerebellum of both male patients and female carriers.

conclusionsOur findings suggest a potential compensatory mechanism in the cerebellum of female carriers regardless of sex. Our study highlights alterations in HEP levels in PwXDP patients and female carriers.

Indexed as

Basal GangliaCerebellumDystonic DisordersGenetic Diseases, X-LinkedHeterozygoteAdultEnergy MetabolismFemaleHumansMagnetic Resonance SpectroscopyMaleMiddle AgedYoung Adult31‐phosphorus magnetic resonance spectroscopy imaging (31P‐MRSI)neuroimagingTAF1X‐linked dystonia‐parkinsonism (XDP)

Identifiers

PMID38404049
PMCPMC11078482

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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.