Evidence map›Paper›PMID 40332200›Full record

ArticleInternational journal of molecular sciences2025

Longitudinal Evaluation of the Detection Potential of Serum Oligoelements Cu, Se and Zn for the Diagnosis of Alzheimer's Disease in the 3xTg-AD Animal Model.

Olivia F M Dias, Nicole M E Valle, Javier B Mamani, Cicero J S Costa, Arielly H Alves, Fernando A Oliveira, Gabriel N A Rego, Marta C S Galanciak, Keithy Felix, Mariana P Nucci and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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

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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Olivia F M DiasHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.
Nicole M E ValleHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.ORCID 0000-0003-4523-1753
Javier B MamaniHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.
Cicero J S CostaHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.
Arielly H AlvesHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.ORCID 0000-0003-3570-0827
Fernando A OliveiraHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.ORCID 0000-0002-7226-1694
Gabriel N A RegoHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.ORCID 0000-0003-2011-0373
Marta C S GalanciakHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.ORCID 0009-0006-2924-4262
Keithy FelixHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.ORCID 0009-0007-8856-9654
Mariana P NucciLIM44-Hospital das Clínicas da Faculdade Medicina da Universidade de São Paulo, São Paulo 05403-000, SP, Brazil.ORCID 0000-0002-1502-9215
Lionel F GamarraHospital Israelita Albert Einstein, São Paulo 05652-000, SP, Brazil.ORCID 0000-0002-3910-0047

Funding

CNPq 307318/2023-0FAPESP 2019/21070-3, 2017/17868-4, 2016/21470-3SisNANO 2.0/MCTIC 442539/2019-3
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by the accumulation of β-amyloid (Aβ) and hyperphosphorylated tau, leading to neuroinflammation, oxidative stress, and neuronal death. Early detection of AD remains a challenge, as clinical manifestations only emerge in the advanced stages, limiting therapeutic interventions. Minimally invasive biomarkers are essential for early identification and monitoring of disease progression. This study aims to evaluate the sensitivity of the relationship between serum oligoelement levels as biomarkers and the monitoring of AD progression in the 3xTg-AD model. Transgenic 3xTg-AD mice and C57BL/6 controls were evaluated over 12 months through serum oligoelement quantification using inductively coupled plasma mass spectrometry (ICP-MS), Aβ deposition via immunohistochemistry, and cognitive assessments using memory tests (Morris water maze and novel object recognition test), as well as spontaneous locomotion analysis using the open field test. The results demonstrated that oligoelements (copper, zinc, and selenium) were sensitive in detecting alterations in the AD group, preceding cognitive and motor deficits. Immunohistochemistry was performed for qualitative purposes, confirming the presence of β-amyloid in the CNS of transgenic animals. Up to the third month, labeling was moderate and restricted to neuronal cell bodies; from the fifth month onward, evident extracellular deposits emerged. Behavioral assessment indicated impairments in spatial and episodic memory, as well as altered locomotor patterns in AD mice. These findings reinforce that oligoelement variations may be associated with neurodegenerative processes, including oxidative stress and synaptic dysfunction. Thus, oligoelement analysis emerges as a promising approach for the early diagnosis of AD and the monitoring of disease progression, potentially contributing to the development of new therapeutic strategies.

Indexed as

Alzheimer DiseaseCopperSeleniumZincAmyloid beta-PeptidesAnimalsBiomarkersDisease Models, AnimalDisease ProgressionHumansMaleMiceMice, Inbred C57BLMice, TransgenicAmyloid beta-PeptidesBiomarkersCopperSeleniumZincAlzheimer’s diseaseanimal modelbiomarkersICP-MSoligoelements

Identifiers

PMID40332200
PMCPMC12026877

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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.