Evidence map›Paper›PMID 40509569›Full record

ArticleAnnals of clinical and translational neurology2025

Stage-Dependent Inhibitory Connectivity in Striatal-Motor Circuit in Huntington's Disease.

Yinghua Jing, Imis Dogan, Rena Theda Overbeck, Kathrin Reetz, Sandro Romanzetti

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Article in Annals of clinical and translational neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yinghua JingDepartment of Neurology, RWTH Aachen University, Aachen, Germany.ORCID 0000-0001-5387-6063
Imis DoganDepartment of Neurology, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-6632-197X
Rena Theda OverbeckDepartment of Neurology, RWTH Aachen University, Aachen, Germany.ORCID 0009-0008-9781-1518
Kathrin ReetzDepartment of Neurology, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-9730-9228
Sandro RomanzettiDepartment of Neurology, RWTH Aachen University, Aachen, Germany.ORCID 0000-0001-8519-1309

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundElucidating dysfunctional connectivity patterns among key brain regions in Huntington's disease (HD) underlying progression may have implications for developing treatment and therapeutic evaluation.

objectiveExplore the relationship between abnormal spontaneous resting-state activity and atrophy in HD-specific brain regions and clarify effective connectivity changes among them across different stages of HD.

methodsAmplitude of low-frequency fluctuation (ALFF) analysis was used to detect abnormal spontaneous neural activity; voxel-based morphometry analysis was applied to assess atrophy; spectral dynamic causal model (DCM) was conducted to estimate regional effective connectivity between HD participants and healthy controls, as well as between preclinical mutation carriers and symptomatic patients.

resultsVoxel-wise whole-brain ALFF analysis identified the bilateral caudate nucleus, putamen, and motor cortex as HD-specific brain regions. ALFF changes in the caudate nucleus and putamen correlated with their respective volumetric atrophy, whereas ALFF changes in the motor cortex preceded its atrophy in the HD preclinical stage. Subsequently, DCM revealed increased inhibitory connectivity from the bilateral caudate nucleus to the motor cortex in HD participants compared to controls. Moreover, compared to preclinical mutation carriers, symptomatic patients showed decreased inhibitory connectivity from the right putamen to the bilateral caudate nucleus, with nonlinear relationships with motor scores.

conclusionsOur results indicate that striatal atrophy and hyper-inhibition of caudate-motorial connectivity might contribute to the regional function alterations in HD. Furthermore, disruption of inhibitory connectivity in the striatal-motor circuit may play an important role in the emergence of motor symptoms.

Indexed as

Caudate NucleusCorpus StriatumHuntington DiseaseMotor CortexNerve NetPutamenAdultAtrophyFemaleHumansMagnetic Resonance ImagingMaleMiddle Agedamplitude of low‐frequency fluctuationdynamic causal modeleffective connectivityHuntington's diseasestructure atrophy

Identifiers

PMID40509569
PMCPMC12343314

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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.