TY - JOUR
T1 - Tau Accumulation and Dopamine Transporter Availability in Elderly Adults with Depression
AU - Uchiyama, Shotaro
AU - Arakawa, Ryosuke
AU - Sakayori, Takeshi
AU - Nogami, Tsuyoshi
AU - Ohya, Tomoyuki
AU - Higuchi, Makoto
AU - Tateno, Amane
N1 - Publisher Copyright:
Copyright © 2026 The Medical Association of Nippon Medical School. This is an open access article under the CC BY-NC-ND 4.0 license (https://creativecommons.org/licenses/by-nc-nd/4.0/).
PY - 2026
Y1 - 2026
N2 - Background: Depression in later life is associated with dopaminergic dysfunction and increased risk of neurodegenerative disorders, although the relationship between dopamine transporter (DAT) availability and tau accumulation remains unclear. Although previous studies have linked tau and DAT in neurodegenerative diseases, evidence related to depression is limited. Therefore, this study used positron emission tomography (PET) to investigate the association between tau pathology and DAT availability in elderly adults with depression. Methods: Six patients diagnosed with depression according to ICD-10 criteria underwent PET scans with PET radioligands that enable accurate in vivo assessment, namely, florzolotau (18F) for tau and [^18F]FE-PE2I for DAT. Clinical assessments using the Mini-Mental State Examination (MMSE) and Hamilton Depression Rating Scale (HAM-D) were performed for all patients. Tau standardized uptake value ratios (SUVR) in the striatal and cortical regions and DAT binding potentials (BP_ND) in the striatum were calculated. Results: Tau SUVR in all regions was negatively correlated with DAT BP_ND in the striatum, suggesting that greater tau burden may be linked to dopaminergic dysfunction. Tau SUVR in the striatum was negatively correlated with MMSE, indicating that tau accumulation may be related to subtle cognitive decline. DAT BP_ND in the striatum was not correlated with HAM-D. Conclusions: These preliminary results suggest a link between tau pathology and dopaminergic dysfunction in elderly adults with depression.
AB - Background: Depression in later life is associated with dopaminergic dysfunction and increased risk of neurodegenerative disorders, although the relationship between dopamine transporter (DAT) availability and tau accumulation remains unclear. Although previous studies have linked tau and DAT in neurodegenerative diseases, evidence related to depression is limited. Therefore, this study used positron emission tomography (PET) to investigate the association between tau pathology and DAT availability in elderly adults with depression. Methods: Six patients diagnosed with depression according to ICD-10 criteria underwent PET scans with PET radioligands that enable accurate in vivo assessment, namely, florzolotau (18F) for tau and [^18F]FE-PE2I for DAT. Clinical assessments using the Mini-Mental State Examination (MMSE) and Hamilton Depression Rating Scale (HAM-D) were performed for all patients. Tau standardized uptake value ratios (SUVR) in the striatal and cortical regions and DAT binding potentials (BP_ND) in the striatum were calculated. Results: Tau SUVR in all regions was negatively correlated with DAT BP_ND in the striatum, suggesting that greater tau burden may be linked to dopaminergic dysfunction. Tau SUVR in the striatum was negatively correlated with MMSE, indicating that tau accumulation may be related to subtle cognitive decline. DAT BP_ND in the striatum was not correlated with HAM-D. Conclusions: These preliminary results suggest a link between tau pathology and dopaminergic dysfunction in elderly adults with depression.
KW - aged
KW - depressive disorder
KW - dopamine transporter
KW - positron-emission tomography
KW - tau proteins
UR - https://www.scopus.com/pages/publications/105042673848
UR - https://www.scopus.com/pages/publications/105042673848#tab=citedBy
U2 - 10.1272/jnms.JNMS.2026_93-308
DO - 10.1272/jnms.JNMS.2026_93-308
M3 - Article
C2 - 42366089
AN - SCOPUS:105042673848
SN - 1345-4676
VL - 93
SP - 236
EP - 243
JO - Journal of Nippon Medical School
JF - Journal of Nippon Medical School
IS - 3
ER -