Evidence map›Paper›PMID 42274583›Full record

ReviewCells2026

Mitochondrial Dysfunction in Alzheimer's Disease and Mitochondria-Targeted Therapeutics.

Jasbir Bisht, Priyanka Rawat, Andrew C Shin, Vijay Hegde

Abstract readReview
In one paragraph

Review in Cells, 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
–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

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

4 authors.

Jasbir BishtObesity and Metabolic Health Laboratory, Department of Nutritional Sciences, Texas Tech University, Lubbock, TX 79409, USA.ORCID 0009-0005-1612-407X
Priyanka RawatObesity and Metabolic Health Laboratory, Department of Nutritional Sciences, Texas Tech University, Lubbock, TX 79409, USA.
Andrew C ShinNeurobiology of Nutrition Laboratory, Department of Nutritional Sciences, Texas Tech University, Lubbock, TX 79409, USA.ORCID 0000-0002-4748-5135
Vijay HegdeObesity and Metabolic Health Laboratory, Department of Nutritional Sciences, Texas Tech University, Lubbock, TX 79409, USA.ORCID 0000-0003-4160-2764

Funding

Serotonin modulated mitochondrial dysfunction in Depression Diabetes and Dementia (3Ds)R01AG071560 · NIA · TEXAS TECH UNIVERSITY · PI Vijay Karkal Hegde, Andrew Changhun Shin · 2022 to 2026
$2.1M
NIH HHS R01 AG071560
6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most prevalent form of dementia and is characterized by progressive cognitive decline due to the loss of neurons. The accumulation of extracellular senile plaques (Aβ) and intracellular tau neurofibrillary tangles (NFTs) is a key pathological feature of AD. Mitochondrial dysfunction is implicated in all key AD pathologies, whether as a cause or a consequence of disease progression. Growing evidence indicates that mitochondrial impairment plays a central role in AD pathogenesis by disrupting cellular homeostasis, promoting oxidative stress, and contributing to progressive neuronal death. Therefore, targeting mitochondria may offer promising insights into the development of disease-modifying therapies. In this review, we summarize current evidence on the role of mitochondrial dysfunction in the pathophysiology of AD and on its therapeutic potential.

Indexed as

Alzheimer DiseaseMitochondriaAnimalsHumansNeuronsOxidative StressAlzheimer’s diseasemitochondrial dysfunctionmitochondrial therapeuticsneurodegenerative diseaseneuronal lossoxidative stress

Identifiers

PMID42274583
PMCPMC13256190

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.