Evidence map›Paper›PMID 41758045›Full record

ArticleJournal of cellular and molecular medicine2026

Specific Lipid Peroxidation Products in Erythrocytes and Their Relationship to the Pathogenesis of Alzheimer's Disease.

Lenka Martináková, Zuzana Chmátalová, Kateřina Veverová, Vanesa Jurášová, Alžběta Katonová, Martina Laczó, Jan Laczó, Martin Vyhnálek, Jakub Hort, Alice Skoumalová

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Lenka MartinákováDepartment of Medical Chemistry and Clinical Biochemistry, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.ORCID https://orcid.org/0009-0001-2317-1174
Zuzana ChmátalováDepartment of Medical Chemistry and Clinical Biochemistry, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Kateřina VeverováMemory Clinic, Department of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Vanesa JurášováMemory Clinic, Department of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Alžběta KatonováMemory Clinic, Department of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Martina LaczóMemory Clinic, Department of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Jan LaczóMemory Clinic, Department of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Martin VyhnálekMemory Clinic, Department of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Jakub HortMemory Clinic, Department of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Alice SkoumalováDepartment of Medical Chemistry and Clinical Biochemistry, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.

Funding

Grantová Agentura, Univerzita Karlova 180221Ministry of Health - DRO FNM,00064203NextGenerationEU LX22NPO5107
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a highly complex and multifactorial disorder in which oxidative stress acts as a key amplifying mechanism in the disease progression. Lipofuscin-like pigments (LFP), end products of lipid peroxidation, reflect oxidative damage and are capable of crossing the blood-brain barrier into the circulation. Thus, erythrocyte-derived LFP may serve as peripheral indicators of brain-specific processes. In this study, we aimed to assess the specificity of previously identified LFP for AD pathology. We analysed erythrocyte-derived LFP in individuals with biomarker-verified AD pathology (n = 40) and non-AD cognitive disorders (n = 21) across the prodromal and dementia stages, and in cognitively unimpaired individuals (n = 19). AD individuals showed significantly higher LFP levels compared with both healthy controls (p < 0.003) and the non-AD group (p ≤ 0.001). Furthermore, LFP levels correlated with established AD biomarkers in CSF, including amyloid-beta (r > -0.566) and phosphorylated tau 181 (r < 0.477). Our findings suggest that LFP may serve as potential blood-based biochemical markers reflecting oxidative stress-related processes associated with AD pathology.

Indexed as

Alzheimer DiseaseErythrocytesLipid PeroxidationAgedAged, 80 and overAmyloid beta-PeptidesBiomarkersFemaleHumansLipofuscinMaleOxidative Stresstau ProteinsAmyloid beta-PeptidesBiomarkersLipofuscintau Proteinsalzheimer's diseasecerebrospinal fluid biomarkerslipofuscin‐like pigmentsneurodegenerationoxidative stress

Identifiers

PMID41758045
PMCPMC12947772

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Registered trials

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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.