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Medial amygdalar tau is associated with anxiety symptoms in preclinical Alzheimer's disease.
Li, Joyce S; Tun, Samantha M; Ficek-Tani, Bronte; Xu, Wanwan; Wang, Selena; Horien, Corey L; Toyonaga, Takuya; Nuli, Shreya S; Zeiss, Caroline J; Powers, Albert R; Zhao, Yize; Mormino, Elizabeth C; Fredericks, Carolyn A.
Afiliação
  • Li JS; Department of Neurology, Yale School of Medicine, New Haven, CT.
  • Tun SM; Department of Neurology, Yale School of Medicine, New Haven, CT.
  • Ficek-Tani B; University of Washington School of Medicine, Seattle, WA.
  • Xu W; Department of Biostatistics, Yale School of Medicine, New Haven, CT.
  • Wang S; Department of Biostatistics, Yale School of Medicine, New Haven, CT.
  • Horien CL; Yale School of Medicine, New Haven, CT.
  • Toyonaga T; Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT.
  • Nuli SS; Yale University, New Haven, CT.
  • Zeiss CJ; Department of Comparative Medicine, Yale School of Medicine, New Haven, CT.
  • Powers AR; Department of Psychiatry, Yale School of Medicine, New Haven, CT.
  • Zhao Y; Department of Biostatistics, Yale School of Medicine, New Haven, CT.
  • Mormino EC; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA.
  • Fredericks CA; Department of Neurology, Yale School of Medicine, New Haven, CT.
bioRxiv ; 2024 Jun 03.
Article em En | MEDLINE | ID: mdl-38895308
ABSTRACT

BACKGROUND:

While the amygdala receives early tau deposition in Alzheimer's disease (AD) and is involved in social and emotional processing, the relationship between amygdalar tau and early neuropsychiatric symptoms in AD is unknown. We sought to determine whether focal tau binding in the amygdala and abnormal amygdalar connectivity were detectable in a preclinical AD cohort and identify relationships between these and self-reported mood symptoms.

METHODS:

We examined n=598 individuals (n=347 amyloid-positive (58% female), n=251 amyloid-negative (62% female); subset into tau PET and fMRI cohorts) from the A4 Study. In our tau PET cohort, we used amygdalar segmentations to examine representative nuclei from three functional divisions of the amygdala. We analyzed between-group differences in division-specific tau binding in the amygdala in preclinical AD. We conducted seed-based functional connectivity analyses from each division in the fMRI cohort. Finally, we conducted exploratory post-hoc correlation analyses between neuroimaging biomarkers of interest and anxiety and depression scores.

RESULTS:

Amyloid-positive individuals demonstrated increased tau binding in medial and lateral amygdala (F(4,442)=14.61, p=0.00045; F(4,442)=5.83, p=0.024, respectively). Across amygdalar divisions, amyloid-positive individuals had relatively increased regional connectivity from amygdala to other temporal regions, insula, and orbitofrontal cortex. There was an interaction by amyloid group between tau binding in the medial and lateral amygdala and anxiety. Medial amygdala to retrosplenial connectivity negatively correlated with anxiety symptoms (rs=-0.103, p=0.015).

CONCLUSIONS:

Our findings suggest that preclinical tau deposition in the amygdala may result in meaningful changes in functional connectivity which may predispose patients to mood symptoms.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article