Evidence map›Paper›PMID 42764280›Full record

ArticleNature communications2026

Drug screen and machine learning predict neuroprotective agents in a preclinical human model of childhood dementia.

Zarina Greenberg, Ella McDonald, Alejandra Noreña Puerta, Manam Inushi De Silva, Cade Christensen, Robert Adams, Jenne Tran, Paris Mazzachi, Sebastian Loskarn, Siti N Mubarokah and 9 more

Abstract read
In one paragraph

Article in Nature communications, 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

19 authors.

Zarina Greenberg *Laboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.
Ella McDonald *Laboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.ORCID http://orcid.org/0009-0006-0852-0723
Alejandra Noreña PuertaLaboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.ORCID http://orcid.org/0009-0001-9531-1180
Manam Inushi De SilvaLaboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.ORCID http://orcid.org/0000-0002-5517-5903
Cade ChristensenLaboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.ORCID http://orcid.org/0000-0001-5661-3787
Robert AdamsLaboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.ORCID http://orcid.org/0000-0001-6254-0385
Jenne TranLaboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.
Paris MazzachiLaboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.ORCID http://orcid.org/0009-0006-5974-7901
Sebastian LoskarnLaboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.ORCID http://orcid.org/0009-0002-4984-5963
Siti N MubarokahFlinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Adelaide, SA, Australia.ORCID http://orcid.org/0009-0002-5029-2198
Leanne WinnerFlinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Adelaide, SA, Australia.ORCID http://orcid.org/0000-0001-5175-4839
Drew NeavinTranslational Genomics, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.ORCID http://orcid.org/0000-0002-1783-6491
Megan MaackSanfilippo Children's Foundation, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0003-0870-0338
Kristina L ElvidgeSanfilippo Children's Foundation, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0002-9763-344X
Lisa MeltonSanfilippo Children's Foundation, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0002-6314-359X
Mark R HutchinsonSchool of Pharmacy and Biomedical Science, Adelaide University, Adelaide, SA, Australia.ORCID http://orcid.org/0000-0003-2154-5950
Kim M HemsleyFlinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Adelaide, SA, Australia.
Nicholas SmithDepartment of Neurology and Clinical Neurophysiology, Women's and Children's Health Network, Adelaide, SA, Australia.ORCID http://orcid.org/0000-0003-2409-9239
Cedric BardyLaboratory for Human Neurophysiology and Genetics, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia. cedric.bardy@flinders.edu.au.ORCID http://orcid.org/0000-0001-8321-0852

Funding

Department of Health | National Health and Medical Research Council (NHMRC) EPCD000025Department of Health | National Health and Medical Research Council (NHMRC) MRF2024419
6 · The paper itself

Abstract

Childhood dementias are a group of paediatric neurodegenerative disorders characterised by neurocognitive decline, and in many cases underpinned by pathophysiological mechanisms similar to adult-onset dementias. In this study, we use patient-derived induced pluripotent stem cells (iPSCs) from children with one of the most prevalent childhood dementias, Mucopolysaccharidosis Type IIIA (MPS IIIA), also known as Sanfilippo syndrome. The derived cortical cultures exhibit lysosomal dysfunction, heparan sulfate accumulation, progressive neurodegeneration and astrocytic reactivity, recapitulating prototypical in-vivo phenotypes. Using a multimodal drug screening platform that integrates machine learning, high-content confocal imaging, single-nuclei transcriptomics and electrophysiology, we identify at least nine repurposed compounds that significantly mitigate these adverse effects within two weeks of treatment in vitro, demonstrating potential for rapid clinical translation. This human preclinical model for MPS IIIA, coupled with a robust multimodal therapeutic interrogation platform, serves as an exemplar for advancing drug discovery for childhood dementias and the broader neurodegenerative disease spectrum.

Indexed as

DementiaMachine LearningMucopolysaccharidosis IIINeuroprotective AgentsChildDrug Evaluation, PreclinicalDrug RepositioningFemaleHeparan SulfateHumansInduced Pluripotent Stem CellsLysosomesHeparan SulfateNeuroprotective Agents

Identifiers

PMID42764280
PMCPMC13590601

What OpenQuestion holds

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Read underepoch 390

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.