Evidence map›Paper›PMID 42405829›Full record

ArticleClinical nuclear medicine2026

Striatal Tau Pathology Underlies Monoaminergic Disruption in Progressive Supranuclear Palsy.

Chong Dong, Jing-Hong Ma, Hong-Wen Qiao, Wen-Qi Xu, Zhu-Qin Gu, Olivier Barret, Gilles D Tamagnan, Wei Mao, Er-He Xu, Chun Zhang and 3 more

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Article in Clinical nuclear medicine, 2026. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Chong DongDepartments of Neurology.ORCID 0000-0002-1431-7389
Jing-Hong MaDepartments of Neurology.ORCID 0000-0002-3458-1363
Hong-Wen QiaoRadiology and Nuclear Medicine, Xuanwu Hospital, Capital Medical University, Beijing, China.
Wen-Qi XuRadiology and Nuclear Medicine, Xuanwu Hospital, Capital Medical University, Beijing, China.ORCID 0009-0007-7192-4656
Zhu-Qin GuXingImaging LLC, New Haven, CT.
Olivier BarretLaboratory of Neurodegenerative Diseases, Paris-Saclay University Paris-Saclay, CEA, CNRS, MIRCen, Fontenay-aux-Roses, France.ORCID 0000-0003-4247-184
Gilles D TamagnanXingImaging LLC, New Haven, CT.
Wei MaoDepartments of Neurology.
Er-He XuDepartments of Neurology.
Chun ZhangRadiology and Nuclear Medicine, Xuanwu Hospital, Capital Medical University, Beijing, China.
Jie LuRadiology and Nuclear Medicine, Xuanwu Hospital, Capital Medical University, Beijing, China.ORCID 0000-0003-0425-3921
Piu ChanDepartments of Neurology.ORCID 0000-0002-4620-1268
Shu-Ying LiuDepartments of Neurology.ORCID 0000-0001-5787-1163

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeProgressive supranuclear palsy (PSP) is a tauopathy marked by widespread tau aggregation and prominent monoaminergic dysfunction, yet the relationship between regional tau burden and monoaminergic impairment remains unclear. In this study, we determine whether regional tau burden is associated with nigrostriatal monoaminergic dysfunction in PSP using PET imaging. PATIENTS AND

methodsA subset of 20 patients with PSP and monoaminergic impairment, identified by 18 F-FP-DTBZ PET, was recruited and subsequently underwent 18 F-APN-1607 PET to assess tau deposition. All images were spatially normalized and analyzed based on predefined volumes of interest. Erosion-based cerebral white matter was used as the reference region to calculate standardized uptake value ratios (SUVRs) for 18 F-APN-1607 PET.

resultsThe SUVRs of 18 F-APN-1607 PET differed significantly between patients with PSP and healthy controls in the globus pallidus, substantia nigra, subthalamus nucleus, and red nucleus, while a significant difference in 18 F-FP-DTBZ SUVRs was observed in all the striatal regions and substantia nigra. Regression analysis discovered negative associations between tau load and monoaminergic disruption in the putamen and caudate, whereas tau accumulation in the substantia nigra was not significantly associated with nigrostriatal impairment.

conclusionsThe pallido-nigro-luysian axis and nigrostriatal system serve as sensitive targets for detecting tau deposition and monoaminergic disruption in PSP. Local striatal tau pathology and tau burden were associated with monoaminergic disruption in PSP.

Indexed as

NeostriatumSupranuclear Palsy, Progressivetau ProteinsAgedFemaleHumansMaleMiddle AgedPositron-Emission Tomographytau Proteinsmultimodal PETnigrostriatal systempathologyprogressive supranuclear palsytauopathy

Identifiers

PMID42405829
PMCPMC13427346

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