Evidence map›Paper›PMID 42760397›Full record

ReviewMammalian genome : official journal of the International Mammalian Genome Society2026

The role of impaired mitochondrial function in neurological manifestations of mitochondrial diseases.

Danielle Brister, Mariana Zarate-Mendez, Denisa Hathazi, Rita Horvath

Abstract readReview
PubMed Publisher
In one paragraph

Review in Mammalian genome : official journal of the International Mammalian Genome Society, 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.

Danielle BristerDepartment of Clinical Neurosciences, John van Geest Cambridge Centre for Brain Repair, University of Cambridge, Robinson Way, Cambridge, CB2 0PY, UK.ORCID http://orcid.org/0009-0001-9059-1523
Mariana Zarate-MendezDepartment of Clinical Neurosciences, John van Geest Cambridge Centre for Brain Repair, University of Cambridge, Robinson Way, Cambridge, CB2 0PY, UK.ORCID http://orcid.org/0009-0006-8224-5088
Denisa HathaziDepartment of Clinical Neurosciences, John van Geest Cambridge Centre for Brain Repair, University of Cambridge, Robinson Way, Cambridge, CB2 0PY, UK.ORCID http://orcid.org/0000-0002-0683-7552
Rita HorvathDepartment of Clinical Neurosciences, John van Geest Cambridge Centre for Brain Repair, University of Cambridge, Robinson Way, Cambridge, CB2 0PY, UK. rh732@medschl.cam.ac.uk.ORCID http://orcid.org/0000-0002-9841-170X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria are essential organelles responsible for cellular energy production and the regulation of key metabolic and signalling pathways. Their function depends on the coordinated expression of both mitochondrial and nuclear genomes, and mitochondrial dysfunction leads to a diverse group of mitochondrial diseases. The nervous system is particularly vulnerable to mitochondrial dysfunction due to the high energetic demands and complex morphology of neurons. Neurons rely heavily on mitochondrial ATP production to support processes such as synaptic transmission, axonal transport, and calcium homeostasis, which are tightly regulated by mitochondrial dynamics, intracellular trafficking, and quality control mechanisms. In mitochondrial diseases, impairment of these processes contributes to a range of neurological manifestations, including epilepsy, stroke-like episodes, Leigh syndrome, ataxia, and peripheral neuropathy. Despite the ubiquitous presence of mitochondria, neuronal vulnerability varies between distinct neuronal populations, reflecting differences in neuronal morphology and metabolic demands. This review summarises key mechanisms underlying neuronal susceptibility in mitochondrial disease and highlights how defects in mitochondrial bioenergetics, dynamics, and transport contribute to characteristic neurological phenotypes. Understanding these mechanisms may provide insights into tissue-specific vulnerability and identify potential therapeutic targets to treat mitochondrial diseases and other neurodegenerative disorders associated with mitochondrial mechanisms.

Indexed as

MitochondriaMitochondrial DiseasesNervous System DiseasesAnimalsEnergy MetabolismHumansMitochondrial DynamicsNeurodegenerative DiseasesNeurons

Identifiers

PMID42760397

What OpenQuestion holds

Textmetadata
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.