# Elevated temporal tau PET predicts faster cognitive decline in women than men: A meta‐analysis

**Authors:** Annie Li, Hannah M. Klinger, Mabel Seto, Colin Birkenbihl, Michael J. Properzi, Michelle Farrell, Emma Thibault, Aaron P. Schultz, Diana L. Townsend, Madison Cuppels, Jane A. Brown, Kathryn V. Papp, Rebecca E. Amariglio, Hyun‐Sik Yang, Michael C. Donohue, Robert A. Rissman, Tobey J. Betthauser, Rebecca E. Langhough, Erin M. Jonaitis, Karly Cody, Sterling C. Johnson, Dorene M. Rentz, Keith A. Johnson, Reisa A. Sperling, Rachel F. Buckley, Gillian T. Coughlan

PMC · DOI: 10.1002/alz.71031 · Alzheimer's & Dementia · 2026-02-18

## TL;DR

Women experience faster cognitive decline with higher tau levels than men, suggesting the need for sex-specific Alzheimer's disease strategies.

## Contribution

This study reveals sex-specific differences in cognitive decline related to tau burden, even after adjusting for amyloid levels.

## Key findings

- Higher tau burden in temporal regions is linked to faster cognitive decline in women compared to men.
- Sex differences in tau-related cognitive decline remain consistent after accounting for amyloid burden.
- Female cognitive advantage at low tau levels shifts to vulnerability at higher tau levels.

## Abstract

Women show higher levels of Alzheimer's disease (AD) pathology than men, but the implications for cognitive decline remain unclear. Determining the extent to which tau burden differentially accelerates cognitive decline in men and women will provide critical insights into sex‐specific pathways of disease progression.

We leveraged tau positron emission tomography (PET), amyloid beta (Aβ) PET, apolipoprotein E (APOE) ε4 genotyping, and longitudinal cognitive data over approximately 8.6 (standard deviation [SD] = 3.8) years from 1007 cognitively unimpaired adults across three cohorts. Cognitive trajectories were modeled with linear mixed‐effects regression including sex × tau × time interactions, and results were synthesized using random‐effects meta‐analysis.

Higher tau burden in medial and lateral temporal regions was associated with faster cognitive decline in women than in men.

High tau burden carries a disproportionately greater cognitive cost for women, underscoring the need for sex‐specific approaches to early detection and therapeutic intervention in AD.

A meta‐analysis across three independent cohorts shows that female cognitive advantage at low tau shifts to vulnerability at higher tau.Sex differences in tau‐related cognitive decline were consistent after accounting for amyloid burden.Sex‐specific rates of cognitive decline should be considered in clinical trial design.

A meta‐analysis across three independent cohorts shows that female cognitive advantage at low tau shifts to vulnerability at higher tau.

Sex differences in tau‐related cognitive decline were consistent after accounting for amyloid burden.

Sex‐specific rates of cognitive decline should be considered in clinical trial design.

## Linked entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348]
- **Proteins:** MAPT (microtubule associated protein tau)
- **Diseases:** Alzheimer's disease (MONDO:0004975)

## Full-text entities

- **Genes:** USP11 (ubiquitin specific peptidase 11) [NCBI Gene 8237] {aka UHX1}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}
- **Diseases:** cognitive decline (MESH:D003072), Amyloid (MESH:C000718787), dementia (MESH:D003704), tauopathy (MESH:D024801), PACC (MESH:D058617), AD (MESH:D000544), inflammatory (MESH:D007249), RESEARCH (MESH:D014947), neurodegeneration (MESH:D019636)
- **Chemicals:** PiB (MESH:C475519), CL (-), Solanezumab (MESH:C550616), [18F]Florbetapir (MESH:C545186)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** PACC-96 — Mus musculus (Mouse), Hybridoma (CVCL_U609)

## Full text

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## Figures

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## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12914651/full.md

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Source: https://tomesphere.com/paper/PMC12914651