Evidence map›Paper›PMID 42138034›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2026

Heterogenous Neuropathology in a Pedigree with RAB39B-Related Parkinson's Disease.

Caitlin Latimer, Oswaldo Lorenzo-Betancor, Dong-Hui Chen, Kimmy Su, Marika Bogdani, Anna J Park, Minsuh Kim, Joshua Weiss, Malia Callier, Ella H Chiu and 6 more

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder 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

16 authors.

Caitlin Latimer *Veteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-3727-4278
Oswaldo Lorenzo-Betancor *Veteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-5607-8363
Dong-Hui ChenDepartment of Neurology, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-2584-8609
Kimmy SuVeteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-8184-2714
Marika BogdaniDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-4677-7523
Anna J ParkVeteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0009-0004-9737-0709
Minsuh KimVeteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0009-0003-7647-5387
Joshua WeissVeteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0009-0004-1503-0226
Malia CallierVeteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0009-0001-1789-4536
Ella H ChiuVeteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0009-0009-4501-6667
Sarah FishVeteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0009-0004-1664-6292
Jennifer L WittBooth Gardner Parkinson's Care Center, Evergreen Health, Kirkland, Washington, USA.ORCID https://orcid.org/0000-0002-5502-7265
Wendy H RaskindDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0001-8141-9054
Marie Y DavisVeteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-2502-6293
C Dirk KeeneDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-5291-1469
Cyrus P ZabetianVeteran Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-7739-4306

Funding

Translational pharmacoepidemiology: neuroprotection and neurotoxicity of antihypertensives and strong anticholinergicsU19AG066567 · NIA · KAISER FOUNDATION RESEARCH INSTITUTE · PI Paul K Crane, Andrea Z. LaCroix · 2021 to 2026
$80.4M
University of Washington Alzheimer's Disease Research CenterP30AG066509 · NIA · UNIVERSITY OF WASHINGTON · PI Jeffrey J Iliff · 2020 to 2026
$29.0M
Interdisciplinary Research Network on Biologically Active Tau Aggregate Polymorphs from Alzheimer's Disease and Related DementiasU24AG072458 · NIA · UNIVERSITY OF TEXAS MED BR GALVESTON · PI EISENBERG, DAVID, KAYED, RAKEZ · 2021 to 2025
$7.8M
Neuroimaging and clinical Endpoints With High-dimensional analysis Of Pathological Endophenotypes in TBI (NEW-HOPE-TBI)U01NS137484 · NINDS · UNIVERSITY OF WASHINGTON · PI CHRISTOPHER DIRK KEENE, Christine L MacDonald · 2024 to 2026
$6.3M
Transdisciplinary Research Accelerating Neuropathology Studies and Facilitating Open Research Methods in TBI (TRANSFORM-TBI)U01NS137500 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI Edward Byung-Ha Lee, Douglas Hamilton Smith · 2024 to 2026
$5.8M
Molecular Mechanisms of Synergistic TDP-43 and Tau Proteotoxicity in Alzheimer's DiseaseK08AG065426 · NIA · UNIVERSITY OF WASHINGTON · PI LATIMER, CAITLIN SHANNON · 2020 to 2024
$705k
Oligodendrocyte Progenitors and Hyaluronan-mediated Mechanisms of Human Vascular White Matter InjuryR01AG065406 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI BACK, STEPHEN ARTHUR · 2024 to 2024
$667k
CSRD VA I01 CX001702NIA NIH HHS K08 AG065426NIA NIH HHS P30 AG066509NIA NIH HHS R01 AG065406NIA NIH HHS U19 AG066567NIA NIH HHS U24 AG072458NIH HHS K08AG065426NIH HHS P30AG066509NIH HHS R01AG065406NIH HHS U01NS137484NIH HHS U01NS137500NIH HHS U19AG066567NIH HHS U24AG072458NINDS NIH HHS U01 NS137484NINDS NIH HHS U01 NS137500U.S. Department of Defense W81XWH-21-S-TBIPH2U.S. Department of Veterans Affairs I01CX001702
6 · The paper itself

Abstract

backgroundIn 2015, we reported a family with Parkinson's disease resulting from the RAB39B p.G192R (c.574G>A) variant. Since then, two affected brothers from the family have undergone autopsy.

objectivesTo characterize neuropathological findings, assess intracellular distribution of RAB39B protein, and examine the effect of p.G192R on α-synuclein and tau.

methodsDetailed neuropathological assessments were performed on both siblings. Dopaminergic neurons were generated from induced pluripotent stem cells (iPSCs) from an affected and unaffected male in this kindred. Western blots were performed to measure RAB39B, α-synuclein, phospho-α-synuclein, and phospho-tau.

resultsThe younger brother had neocortical stage Lewy body disease (LBD) pathology and an unusual pattern and burden of four-repeat (4R) tau pathology that included neocortical neurofibrillary tangles, pretangles, and neurites in the absence of β-amyloid pathology. The older brother's brain showed a similar pattern of 4R tau pathology but had no LBD pathology. Robust RAB39B immunostaining was seen in p.G192R carriers and non-carriers. In p.G192R iPSC-derived neurons, RAB39B protein was reduced by ~50% and disproportionately diminished in peripheral cell processes compared with cell bodies. Aberrant forms of both α-synuclein and tau were observed in p.G192R neurons.

conclusionsThe intrafamilial pathological heterogeneity observed here is unusual for monogenic parkinsonism and suggests that mechanisms underlying RAB39B-related neurodegeneration might be complex. Our results from iPSC-neurons provide additional support that RAB39B p.G192R promotes α-synuclein and tau co-pathology. Further work in model systems based on RAB39B p.G192R might offer important insights into the interplay between α-synuclein and tau that are applicable to multiple neurodegenerative disorders. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

Indexed as

BrainParkinson Diseaserab GTP-Binding ProteinsAgedalpha-SynucleinDopaminergic NeuronsHumansLewy Body DiseaseMaleMiddle AgedNeurofibrillary TanglesPedigreetau Proteinsalpha-SynucleinRab39B protein, humanrab GTP-Binding Proteinstau ProteinsLewy bodyneuropathologyParkinson's diseaseRAB39Btau

Identifiers

PMID42138034
PMCPMC13518288

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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.