Evidence map›Paper›PMID 41052979›Full record

ArticleTranslational psychiatry2025

Salivary mitochondrial DNA is associated with biomarkers of Alzheimer's disease in cognitively normal older adults.

Jose L Cantero, Mercedes Atienza, Petar Podlesniy, Margalida Puigròs, Ramon Trullas

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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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

5 authors.

Jose L CanteroLaboratory of Functional Neuroscience, Pablo de Olavide University, Seville, Spain. jlcanlor@upo.es.ORCID http://orcid.org/0000-0002-2628-7076
Mercedes AtienzaLaboratory of Functional Neuroscience, Pablo de Olavide University, Seville, Spain.
Petar PodlesniyCentro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III, 28029, Madrid, Spain.
Margalida PuigròsCentro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III, 28029, Madrid, Spain.ORCID http://orcid.org/0000-0002-7891-5919
Ramon TrullasCentro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III, 28029, Madrid, Spain.ORCID http://orcid.org/0000-0001-7951-9881

Funding

Ministerio de Economía y Competitividad (Ministry of Economy and Competitiveness) PID2023-149270OB-I00Ministerio de Economía y Competitividad (Ministry of Economy and Competitiveness) PID2023-153168OB-I00
6 · The paper itself

Abstract

A significant body of evidence suggests that mitochondrial dysfunction plays a key role in the development and progression of Alzheimer's disease (AD). However, the absence of peripheral biomarkers for mitochondrial dysfunction limits its clinical applicability. Mitochondrial DNA (mtDNA) copy number, a proxy for mitochondrial function, has shown promise in detecting early stages of AD and predicting AD risk in cerebrospinal fluid (CSF) and blood, respectively. Surprisingly, recent studies have identified mtDNA molecules in human saliva, but their relationship with AD remains unexplored. Here, we investigated potential associations between salivary mtDNA copy number and cortical amyloid-β (Aβ) load measured with PET, and blood AD markers measured with ultrasensitive single molecule array (SIMOA) assays, in cognitively normal older adults. We found that salivary mtDNA copy number was positively correlated with cortical Aβ burden and plasma levels of tau phosphorylated at threonine 181 (pTau-181), and negatively correlated with general cognitive ability. It is worth noting that salivary mtDNA was not significantly associated with other blood-based AD biomarkers, including Aβ

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesDNA, MitochondrialSalivaAgedAged, 80 and overBiomarkersFemaleHumansMaleMiddle AgedNeurofilament ProteinsPositron-Emission Tomographytau ProteinsAmyloid beta-PeptidesBiomarkersDNA, Mitochondrialneurofilament protein LNeurofilament Proteinstau Proteins

Identifiers

PMID41052979
PMCPMC12501003

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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.