Evidence map›Paper›PMID 41908486›Full record

ArticleFrontiers in neuroscience2026

GDF15 - A potential novel biomarker of cognitive impairment in cervical dystonia.

Artur Drużdż, Małgorzata Dudzic, Joanna Poszwa, Anna Rajewska, Aleksandra Mikołajczak, Wojciech Kozubski, Jolanta Dorszewska

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Article in Frontiers in neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Artur DrużdżDepartment of Neurology, Municipal Hospital in Poznan, Poznan, Poland.
Małgorzata DudzicDepartment of Neurology, Municipal Hospital in Poznan, Poznan, Poland.
Joanna PoszwaLaboratory of Neurobiology, Department of Neurology, Poznan University of Medical Sciences, Poznan, Poland.
Anna RajewskaDepartment of Neurology, Municipal Hospital in Poznan, Poznan, Poland.
Aleksandra MikołajczakDepartment of Laboratory Diagnostics, Municipal Hospital in Poznan, Poznan, Poland.
Wojciech KozubskiDepartment of Neurology, Poznan University of Medical Sciences, Poznan, Poland.
Jolanta DorszewskaLaboratory of Neurobiology, Department of Neurology, Poznan University of Medical Sciences, Poznan, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cervical dystonia (CD) is a chronic movement disorder characterized by motor symptoms and a spectrum of non-motor features, including cognitive difficulties, which may affect quality of life. To date, no biomarker exists to identify or monitor cognitive impairment in CD. Growth differentiation factor 15 (GDF15) has been associated with cognitive decline in several neurodegenerative diseases and movement disorders, providing a rationale for its investigation in CD. This study aimed to evaluate whether plasma GDF15 concentrations are associated with cognitive performance in individuals with CD and to assess examine the potential of GDF15 as a biomarker of cognitive decline in CD. Methods: Plasma GDF15 levels were measured in patients with CD before and after botulinum toxin (BoNT) treatment and compared with healthy controls. Correlations between GDF15 concentration, cognitive performance (MoCA total and domain scores), and clinical characteristics-including age, disease duration, and TWSTRS motor severity-were analyzed using Spearman's and Pearson's coefficients. Results: GDF15 concentrations were significantly higher in individuals with CD compared with healthy controls. However, GDF15 levels showed no association with age, disease duration, symptom severity, or treatment response, and remained stable following botulinum toxin administration. No correlations were found between GDF15 and global cognitive performance, with the exception of a correlation with the visuospatial MoCA sub score. Discussion: While GDF15 concentrations were elevated in CD, they did not demonstrate consistent relationships with clinical features or cognitive outcomes. These findings suggest that GDF15 cannot currently be considered a reliable biomarker of cognitive impairment in CD. Given the limited sample size, this study should be regarded as preliminary.

Indexed as

biomarkerbotulinum toxincervical dystoniacognitive declineGDF15

Identifiers

PMID41908486
PMCPMC13017788

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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 Socratic graph.