Evidence map›Paper›PMID 40877853›Full record

ArticleBMC neurology2025

The potential role of serum and urine galectin-3 values in the diagnosis and staging of Parkinson's disease.

Miray Erdem, Derya Ozdogru, Elif Banu Soker, Burak Ademoglu, Nevzat Unal, Onur Serdar Gencler

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Article in BMC neurology, 2025. 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

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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

6 authors.

Miray ErdemDepartment of Neurology, Adana City Training and Research Hospital, Health Science University, 4522 Street No:1, Yuregir, Adana, Turkey. drmirayerdem85@gmail.com.ORCID http://orcid.org/0000-0001-8369-7816
Derya OzdogruDepartment of Neurology, Adana City Training and Research Hospital, Health Science University, 4522 Street No:1, Yuregir, Adana, Turkey.ORCID http://orcid.org/0000-0003-3567-1317
Elif Banu SokerDepartment of Neurology, Adana City Training and Research Hospital, Health Science University, 4522 Street No:1, Yuregir, Adana, Turkey.ORCID http://orcid.org/0000-0003-0315-901X
Burak AdemogluDepartment of Neurology, Adana City Training and Research Hospital, Health Science University, 4522 Street No:1, Yuregir, Adana, Turkey.ORCID http://orcid.org/0009-0001-9551-3540
Nevzat UnalDepartment of Medical Microbiology, Adana City Training and Research Hospital, Health Science University, Adana, Turkey.ORCID http://orcid.org/0000-0001-5121-3100
Onur Serdar GenclerDepartment of Neurology, Ankara Bilkent City Training and Research Hospital, Health Science University, Ankara, Turkey.ORCID http://orcid.org/0000-0002-1907-892X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParkinson’s disease (PD) is a progressive neurodegenerative disorder characterised by both motor and nonmotor symptoms. Galectin-3, a protein involved in the regulation of inflammatory responses, has emerged as a potential contributor to neurodegenerative processes. This study aimed to measure serum and urinary galectin-3 levels in patients with PD and to evaluate the associations of this biomarker with disease stages and clinical symptoms.

methodsThe present cross-sectional study included 30 PD patients and 29 healthy controls. Galectin-3 levels in serum and urine samples were measured via Enzyme-Linked Immunosorbent Assay (ELISA). The clinical data recorded included demographic information, Hoehn and Yahr (H&Y) stage, Unified Parkinson’s Disease Rating Scale (UPDRS) motor score, nonmotor symptom score (NMS), and total dopaminergic treatment dose parameters. Multivariate analyses were adjusted for age and sex due to demographic differences between groups.

resultsSerum galectin-3 optical density (OD) levels (0.2 [0.1–1.4]) and urinary galectin-3 OD levels (0.2 [0.1–0.6]) were significantly higher in PD patients than in controls (p < 0.050). Serum and urinary galectin-3 concentration (C) values were also elevated in the PD group. A moderate negative correlation was observed between serum galectin-3 levels and both the H&Y stage (r = − 0.418, p = 0.021) and the UPDRS motor score (r = − 0.541, p = 0.002). After adjusting for age and sex, serum galectin-3 C remained independently associated with motor severity. ROC analysis revealed that serum galectin-3 levels demonstrated promising diagnostic performance, with high specificity and sensitivity in distinguishing patients with PD from healthy controls (AUC = 0.716, p = 0.001). The serum/urine galectin-3 concentration ratio also showed significant discriminative value (AUC = 0.722, p = 0.035).

conclusionOur findings suggest that elevated levels of galectin-3 in serum and urine are associated with Parkinson’s disease and may reflect underlying neuroinflammatory mechanisms contributing to its pathophysiology. The diagnostic performance of galectin-3 markers remained robust even after adjusting for age and sex. However, the strict exclusion criteria and the age imbalance between groups may limit the generalizability of these results to broader clinical populations. Therefore, these findings should be considered exploratory and require confirmation through larger, longitudinal studies to determine their diagnostic and prognostic utility.

Indexed as

Galectin 3Parkinson DiseaseAgedBiomarkersCross-Sectional StudiesEnzyme-Linked Immunosorbent AssayFemaleGalectinsHumansMaleMiddle AgedROC CurveSeverity of Illness IndexBiomarkersGalectin 3GalectinsBiomarkerGalectin-3InflammationNeurodegenerationParkinson's disease

Identifiers

PMID40877853
PMCPMC12395917

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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.