CenTauR correlation with amyloid, atrophy and cognition across the Alzheimer's Disease spectrum: A tau imaging study with <sup>18</sup> F‐MK6240 PET

Abstract Background The CenTauR (CTR) standard method for PET measurement of tau provides consistent results across tau tracers. This study establishes regional CTR thresholds for elevated tau and evaluates the CTR relationship with amyloid, neurodegeneration and cognition across the AD spectrum. Method 924 participants from the AIBL‐ADNeT study (448 cognitively unimpaired (CU), 300 MCI, 176 clinical AD), underwent 18 F‐MK6240 tau PET, 18 F‐NAV4694 Aβ PET, MRI and cognitive evaluations. We examined the relationship between global and regional tau quantification using the CTR method, and global Aβ (Centiloid), brain atrophy and cognition. Result From tau scans in A‐ (&lt;25 CL) CU, 2 SD thresholds were 11 CTR in the mesial temporal lobe (MTL) and 15 CTR in the Temporo‐Parietal (TP) cortex. There was a non‐linear relationship between Aβ and tau with cortical tau rare below 60 CL (Figure 1). In clinical AD, 71% had A+ and neocortical tau+ (T TP +), 14% had neither, 14% had only A+. In MCI, 43% had both, 30% had neither and 26% had only A+. In CU, 64% had neither, 27% were A+T‐, and 7% A+T TP +. However 31% of CU, 68% of MCI and 84% of clinical AD were T MTL +. A‐T MTL + was observed in 9% of CU, 8% of MCI and 3% of clinical AD (Figure 2). In A+ MCI and AD, cortical tau was strongly inversely associated with age and cortical volume. No association was found with hippocampal volume when tau was limited to the MTL. The most significant factors associated with worse cognition were age and male sex in CU; Aβ, hippocampal volume and tau in MCI, and tau and hippocampal volume in clinical AD. Cortical tau correlated with worse general cognition, while tau limited to the MTL only affected episodic memory. In the absence of tau, Aβ did not correlate with cognitive decline. Conclusion This study has established regional CTR thresholds and the prevalence of MTL and cortical tau in CU, MCI and clinical AD. It has confirmed that cortical tau is rarely found below 60 CL of Aβ. Cortical CTR strongly correlates with cognitive impairment and atrophy, while tau restricted to the MTL is linked to mild memory impairment.

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Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70856_105321
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
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article

CenTauR correlation with amyloid, atrophy and cognition across the Alzheimer's Disease spectrum: A tau imaging study with 18 F‐MK6240 PET

Vincent Doré, Azadeh Feizpour, Rachel S. Mulligan, Joanne Robertson et al.
Alzheimer s & Dementia
Dementia and Cognitive Impairment Research
article

CenTauR correlation with amyloid, atrophy and cognition across the Alzheimer's Disease spectrum: A tau imaging study with 18 F‐MK6240 PET

Vincent Doré, Azadeh Feizpour, Rachel S. Mulligan, Joanne Robertson, Antoine Leuzy, Christopher C. Rowe, Colin L Masters, Pierrick Bourgeat, Ralph N Martins, Jurgen Fripp, Simon M. Laws, Paul Maruff, Victor L. Villemagne
article en

Abstract

Abstract Background The CenTauR (CTR) standard method for PET measurement of tau provides consistent results across tau tracers. This study establishes regional CTR thresholds for elevated tau and evaluates the CTR relationship with amyloid, neurodegeneration and cognition across the AD spectrum. Method 924 participants from the AIBL‐ADNeT study (448 cognitively unimpaired (CU), 300 MCI, 176 clinical AD), underwent 18 F‐MK6240 tau PET, 18 F‐NAV4694 Aβ PET, MRI and cognitive evaluations. We examined the relationship between global and regional tau quantification using the CTR method, and global Aβ (Centiloid), brain atrophy and cognition. Result From tau scans in A‐ (&lt;25 CL) CU, 2 SD thresholds were 11 CTR in the mesial temporal lobe (MTL) and 15 CTR in the Temporo‐Parietal (TP) cortex. There was a non‐linear relationship between Aβ and tau with cortical tau rare below 60 CL (Figure 1). In clinical AD, 71% had A+ and neocortical tau+ (T TP +), 14% had neither, 14% had only A+. In MCI, 43% had both, 30% had neither and 26% had only A+. In CU, 64% had neither, 27% were A+T‐, and 7% A+T TP +. However 31% of CU, 68% of MCI and 84% of clinical AD were T MTL +. A‐T MTL + was observed in 9% of CU, 8% of MCI and 3% of clinical AD (Figure 2). In A+ MCI and AD, cortical tau was strongly inversely associated with age and cortical volume. No association was found with hippocampal volume when tau was limited to the MTL. The most significant factors associated with worse cognition were age and male sex in CU; Aβ, hippocampal volume and tau in MCI, and tau and hippocampal volume in clinical AD. Cortical tau correlated with worse general cognition, while tau limited to the MTL only affected episodic memory. In the absence of tau, Aβ did not correlate with cognitive decline. Conclusion This study has established regional CTR thresholds and the prevalence of MTL and cortical tau in CU, MCI and clinical AD. It has confirmed that cortical tau is rarely found below 60 CL of Aβ. Cortical CTR strongly correlates with cognitive impairment and atrophy, while tau restricted to the MTL is linked to mild memory impairment.

Alzheimer s & DementiaVol. 21(S2)
Edith Cowan University (AU), The University of Melbourne (AU), University of Pittsburgh (US), Lund University (SE), Florey Institute of Neuroscience and Mental Health (AU), Australian e-Health Research Centre (AU), CSIRO Health and Biosecurity (AU), Austin Health (AU), University of Gothenburg (SE), Macquarie University (AU)
Openalex Percentile: Top 29%
Dementia and Cognitive Impairment Research
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