Evidence map›Paper›PMID 40304712›Full record

ReviewHuman molecular genetics2025

Inborn errors of canonical autophagy in neurodegenerative diseases.

Dennis Freisem, Helene Hoenigsperger, Alberto Catanese, Konstantin M J Sparrer

Abstract readReview
In one paragraph

Review in Human molecular genetics, 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. Review
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.

Dennis FreisemInstitute of Molecular Virology, Ulm University Medical Center, Meyerhofstr. 1, Baden-Wuerttemberg, Ulm 89081, Germany.ORCID 0009-0008-9755-2261
Helene HoenigspergerInstitute of Molecular Virology, Ulm University Medical Center, Meyerhofstr. 1, Baden-Wuerttemberg, Ulm 89081, Germany.ORCID 0009-0009-1295-4067
Alberto CataneseGerman Center for Neurodegenerative Diseases, Albert-Einstein-Allee 11, Baden-Wuerttemberg, Ulm 89081, Germany.ORCID 0000-0002-8266-4913
Konstantin M J SparrerInstitute of Molecular Virology, Ulm University Medical Center, Meyerhofstr. 1, Baden-Wuerttemberg, Ulm 89081, Germany.ORCID 0000-0002-8682-1779

Funding

German Research Foundation CA 2915/4-1German Research Foundation CRC1279German Research Foundation CRC1506German Research Foundation SP 1600/7-1German Research Foundation SP 1600/9-1
6 · The paper itself

Abstract

Neurodegenerative disorders (NDDs), characterized by a progressive loss of neurons and cognitive function, are a severe burden to human health and mental fitness worldwide. A hallmark of NDDs such as Alzheimer's disease, Huntington's disease, Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS) and prion diseases is disturbed cellular proteostasis, resulting in pathogenic deposition of aggregated protein species. Autophagy is a major cellular process maintaining proteostasis and integral to innate immune defenses that mediates lysosomal protein turnover. Defects in autophagy are thus frequently associated with NDDs. In this review, we discuss the interplay between NDDs associated proteins and autophagy and provide an overview over recent discoveries in inborn errors in canonical autophagy proteins that are associated with NDDs. While mutations in autophagy receptors seems to be associated mainly with the development of ALS, errors in mitophagy are mainly found to promote PD. Finally, we argue whether autophagy may impact progress and onset of the disease, as well as the potential of targeting autophagy as a therapeutic approach. Concludingly, understanding disorders due to inborn errors in autophagy-"autophagopathies"-will help to unravel underlying NDD pathomechanisms and provide unique insights into the neuroprotective role of autophagy, thus potentially paving the way for novel therapeutic interventions.

Indexed as

AutophagyNeurodegenerative DiseasesAmyotrophic Lateral SclerosisAnimalsHumansMitophagyMutationParkinson DiseaseProteostasisautophagyinnate immunitymonogenic diseasesneurodegenerative diseases

Identifiers

PMID40304712
PMCPMC12501978

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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.