Evidence map›Paper›PMID 39562000›Full record

ArticleBrain : a journal of neurology2025

Synaptic and cognitive impairment associated with L444P heterozygous glucocerebrosidase mutation.

Wudu Lado, Ahrom Ham, Hongyu Li, Hong Zhang, Audrey Yuen Chang, Sergio Pablo Sardi, Roy N Alcalay, Ottavio Arancio, Serge Przedborski, Guomei Tang

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Serum phosphorylated tau 217 inJournal of Parkinson's disease · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. 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

10 authors.

Wudu LadoDepartment of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Ahrom HamDepartment of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Hongyu LiDepartment of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Hong ZhangDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Audrey Yuen ChangDepartment of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Sergio Pablo SardiRare and Neurologic Diseases Research, Sanofi, Cambridge, MA 02141, USA.
Roy N AlcalayDepartment of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Ottavio ArancioDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Serge PrzedborskiDepartment of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Guomei TangDepartment of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.ORCID 0000-0001-9479-5331

Funding

Cellular and Molecular Basis for Cognitive Impairment Associated with Glucocerebrosidase (GBA1) MutationR01NS104390 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TANG, GUOMEI · 2018 to 2022
$1.8M
Mitochondrial dysfunction due to aberrant mTOR-regulated mitophagy in autismK01MH096956 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TANG, GUOMEI · 2013 to 2016
$734k
NIHNIMH NIH HHS K01 MH096956NINDS NIH HHS R01 NS104390
6 · The paper itself

Abstract

Cognitive impairment is a common but poorly understood non-motor aspect of Parkinson's disease, negatively affecting the patient's functional capacity and quality of life. The mechanisms underlying cognitive impairment in Parkinson's disease remain elusive, limiting treatment and prevention strategies. This study investigates the molecular and cellular basis of cognitive impairment associated with heterozygous mutations in GBA1, the strongest risk gene for Parkinson's disease, which encodes glucocerebrosidase, a lysosome enzyme that degrades the glycosphingolipid glucosylceramide into glucose and ceramide. Using a Gba1L444P/+ mouse model, we provide evidence that L444P heterozygous Gba1 mutation (L444P/+) causes hippocampus-dependent spatial and reference memory deficits independently of α-synuclein (αSyn) accumulation, glucocerebrosidase lipid substrate accumulation, dopaminergic dysfunction and motor deficits. The mutation disrupts hippocampal synaptic plasticity and basal synaptic transmission by reducing the density of hippocampal CA3-CA1 synapses, a mechanism that is dissociated from αSyn-mediated presynaptic neurotransmitter release. Using a well-characterized Thy1-αSyn pre-manifest Parkinson's disease mouse model overexpressing wild-type human αSyn, we find that the L444P/+ mutation exacerbates hippocampal synaptic αSyn accumulation, synaptic and cognitive impairment in young Gba1L444P/+:Thy1-αSyn double mutant animals. With age, Thy1-αSyn mice manifest motor symptoms, and the double mutant mice exhibit more exacerbated synaptic and motor impairment than the Thy1-αSyn mice. Taken together, our results suggest that heterozygous L444P GBA1 mutation alone perturbs hippocampal synaptic structure and function, imposing a subclinical pathological burden for cognitive impairment. When co-existing αSyn overexpression is present, heterozygous L444P GBA1 mutation interacts with αSyn pathology to accelerate Parkinson's disease-related cognitive impairment and motor symptoms.

Indexed as

Cognitive DysfunctionGlucosylceramidaseSynapsesalpha-SynucleinAnimalsDisease Models, AnimalHeterozygoteHippocampusHumansMaleMiceMice, Inbred C57BLMice, TransgenicMutationNeuronal PlasticityParkinson Diseasealpha-SynucleinGlucosylceramidaseGBA1-associated Parkinson’s diseasememory deficitneurodegenerationsynapse losssynaptic plasticity

Identifiers

PMID39562000
PMCPMC12073992

What Socratic 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 Socratic graph.