Evidence map›Paper›PMID 42194069›Full record

ArticleBiomolecules2026

Oxidative-Nitrosative Stress and Routine Biochemical Parameters in Amyotrophic Lateral Sclerosis: Associations with Clinical Status and Disease Duration-A Pilot Study.

Pavlína Malá, Nela Váňová, Ondřej Malý, Oldřich Vyšata

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Article in Biomolecules, 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Pavlína MaláDepartment of Neurology, University Hospital Hradec Králové, 500 05 Hradec Králové, Czech Republic.
Nela VáňováDepartment of Pharmaceutical Chemistry and Pharmaceutical Analysis, Faculty of Pharmacy in Hradec Králové, Charles University, 500 05 Hradec Králové, Czech Republic.
Ondřej MalýMilitary Faculty of Medicine, University of Defense, 500 01 Hradec Králové, Czech Republic.ORCID 0000-0002-1287-0519
Oldřich VyšataDepartment of Neurology, University Hospital Hradec Králové, 500 05 Hradec Králové, Czech Republic.

Funding

Charles University Cooperatio Program, research area NEURMinistry of Health of the Czech Republic Grant No. DRO-UHHK 00179906
6 · The paper itself

Abstract

backgroundThis pilot study examined whether oxidative-nitrosative stress is associated with clinical status in amyotrophic lateral sclerosis (ALS). We analyzed associations between plasma markers of oxidative-nitrosative imbalance and ALSFRS-R, disease duration, survival, and routine biochemical parameters.

methodsTwenty-nine ALS patients fulfilling the Gold Coast diagnostic criteria were enrolled. Plasma levels of 3-nitrotyrosine (3-NT), 8-oxo-2'-deoxyguanosine (8-oxodG), malondialdehyde (MDA), glutathione (GSH), non-protein thiols (NP-SH), and non-protein disulfides (NP-SS-NP), as well as creatinine, urea, uric acid and BMI, were measured. Associations with ALSFRS-R and disease duration were evaluated using non-parametric correlation analyses and second-order polynomial regression (adjusted R

resultsAt the uncorrected significance level, 3-NT showed a positive correlation with ALSFRS-R and a negative correlation with disease duration, and NP-SH correlated negatively with disease duration; however, these associations did not remain significant after FDR correction (FDR-adjusted

conclusions3-NT and NP-SH exhibited the strongest trends among the investigated markers, but their clinical associations in this small cross-sectional cohort remain exploratory and require confirmation in larger longitudinal studies.

Indexed as

Amyotrophic Lateral SclerosisNitrosative StressOxidative Stress8-Hydroxy-2'-DeoxyguanosineAgedBiomarkersFemaleGlutathioneHumansMaleMalondialdehydeMiddle AgedPilot ProjectsTyrosine3-nitrotyrosine8-Hydroxy-2'-DeoxyguanosineBiomarkersGlutathioneMalondialdehydeTyrosine3–nitrotyrosineamyotrophic lateral sclerosisdisease durationmotor neuron diseaseneurodegenerationnon-protein thiolsoxidative–nitrosative stressoxidative–nitrosative stress biomarkersplasma biomarkers

Identifiers

PMID42194069
PMCPMC13204825

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