Association between brain tau deposition and default mode network connectivity in cognitively normal older adults

Abstract Background Alzheimer’s disease (AD) pathology occurs in the brain before manifestation of significant cognitive decline. Growing evidence suggests that brain networks such as default mode network (DMN) or salience network, identified through resting‐state functional magnetic resonance imaging (MRI), are affected by AD pathology. In this study, we investigated the relationship between network segregation and the key in vivo AD pathologies including beta‐amyloid (Aβ) and tau deposition in old adults with no cognitive impairment. Method A total 283 older adults with normal cognition aging from 55 to 87 were recruited from the Korean Brain Aging Study for the Early Diagnosis and Prediction of Alzheimer’s Disease (KBASE) cohort. The participants underwent comprehensive clinical and neuropsychological assessment, [ 11 C] Pittsburgh Compound B PET for measuring Aβ deposition, [ 18 F] AV‐1451 PET for measuring tau deposition, structural MRI, and resting‐state functional MRI for measuring functional connectivity (FC). For PET scans, standard uptake value ratio (SUVR) was used for the analyses; combined regions of inferior cerebellum and pons were used as the reference region when obtaining SUVRs. For FC, segregation values (ratios between median z‐transformed Pearson correlation of within‐ and between‐network connectivity) for overall and the seven individual resting state networks were computed (Table). The relationships between Aβ or tau deposition and network connectivity segregation were examined through cross‐sectional approach using multiple regression analyses. In the analyses, Aβ or tau deposition was used as an independent variable and segregation values of the networks were used as dependent variables. Result Tau deposition had a significant negative association with the DMN segregation (β = ‐0.249, p = 0.007); but, tau had no relationships with any other networks (Table). Aβ deposition was not associated with any segregation values for the seven brain networks (Table). Conclusion Our finding suggests that impaired functional connectivity of DMN is closely linked to tau deposition even in cognitively unimpaired older individuals.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.090633
Primary Topic
Functional Brain Connectivity Studies
Type
article
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article

Association between brain tau deposition and default mode network connectivity in cognitively normal older adults

Evgeny J. Chumin, Olaf Sporns, Hye‐Jin Ahn, Shannon L. Risacher et al.
Alzheimer s & Dementia
Functional Brain Connectivity Studies
article

Association between brain tau deposition and default mode network connectivity in cognitively normal older adults

Evgeny J. Chumin, Olaf Sporns, Hye‐Jin Ahn, Shannon L. Risacher, Andrew J. Saykin, Min Soo Byun, Joon Hyung Jung, Koung Mi Kang, Yun‐Sang Lee, Dahyun Yi, Kwangsik Nho, Chul‐Ho Sohn, Dong Young Lee, Yoon‐Keun Kim, Woo‐Jin Cha
article en

Abstract

Abstract Background Alzheimer’s disease (AD) pathology occurs in the brain before manifestation of significant cognitive decline. Growing evidence suggests that brain networks such as default mode network (DMN) or salience network, identified through resting‐state functional magnetic resonance imaging (MRI), are affected by AD pathology. In this study, we investigated the relationship between network segregation and the key in vivo AD pathologies including beta‐amyloid (Aβ) and tau deposition in old adults with no cognitive impairment. Method A total 283 older adults with normal cognition aging from 55 to 87 were recruited from the Korean Brain Aging Study for the Early Diagnosis and Prediction of Alzheimer’s Disease (KBASE) cohort. The participants underwent comprehensive clinical and neuropsychological assessment, [ 11 C] Pittsburgh Compound B PET for measuring Aβ deposition, [ 18 F] AV‐1451 PET for measuring tau deposition, structural MRI, and resting‐state functional MRI for measuring functional connectivity (FC). For PET scans, standard uptake value ratio (SUVR) was used for the analyses; combined regions of inferior cerebellum and pons were used as the reference region when obtaining SUVRs. For FC, segregation values (ratios between median z‐transformed Pearson correlation of within‐ and between‐network connectivity) for overall and the seven individual resting state networks were computed (Table). The relationships between Aβ or tau deposition and network connectivity segregation were examined through cross‐sectional approach using multiple regression analyses. In the analyses, Aβ or tau deposition was used as an independent variable and segregation values of the networks were used as dependent variables. Result Tau deposition had a significant negative association with the DMN segregation (β = ‐0.249, p = 0.007); but, tau had no relationships with any other networks (Table). Aβ deposition was not associated with any segregation values for the seven brain networks (Table). Conclusion Our finding suggests that impaired functional connectivity of DMN is closely linked to tau deposition even in cognitively unimpaired older individuals.

Alzheimer s & DementiaVol. 20(S2)
Seoul National University (KR), Seoul National University Hospital (KR), SNUH SMG-SNU Boramae Medical Center (KR), Indiana University Bloomington (US), Chungbuk National University Hospital (KR), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US)
Openalex Percentile: Top 74%
Functional Brain Connectivity Studies
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