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Alzheimer's & dementia : the journal of the Alzheimer's Association
Published

Biomarkers

Authors

Colin Groot, Emma M Coomans, Christopher C Rowe, Vincent Dore, Azadeh Feizpour, Elsmarieke van de Giessen, Wiesje M van der Flier, Yolande A L Pijnenburg, Pieter Jelle Visser, Anouk den Braber, Michael J Pontecorvo, Samantha C Burnham, Ian A Kennedy, Ming Lu, William J Jagust, Suzanne L Baker, Theresa M Harrison, Juan Domingo Gispert, Mahnaz Shekari, Carolina Minguillón, Ruben Smith, Niklas Mattsson-Carlgren, Sebastian Palmqvist, Olof Strandberg, Erik Stomrud, Adam Brickman, José A Luchsinger, Jennifer J Manly, Patrick J Lao, William Charles Kreisl, Maura Malpetti, John T O'Brien, James B Rowe, Elena Jäger, Gérard N Bischof, Alexander Drzezga, Fang Xie, Xiaoxie Mao, Yihui Guan, Valentina Garibotto, Giovanni B Frisoni, Débora E Peretti, Michael Schöll, Ingmar Skoog, Silke Kern, Reisa A Sperling, Keith A Johnson, Shannon Risacher, Andrew J Saykin, Maria C Carrillo, Brad Dickerson, Liana G Apostolova, Gil D Rabinovici, Henryk Barthel, Michael Rullmann, Konstantin Messerschmidt, Rik Vandenberghe, Koen Van Laere, Laure Spruyt, Ronald Petersen, Clifford R Jack, Nicolai Franzmeier, Matthias Brendel, Johannes Gnörich, Tammie Benzinger, Julien Lagarde, Marie Sarazin, Michel Bottlaender, Sylvia Villeneuve, Judes Poirier, Sang Won Seo, Yuna Gu, Jun Pyo Kim, Beth Mormino, Christina B Young, Hillary Vossler, Pedro Rosa-Neto, Joseph Therriault, Nesrine Rahmouni, William Coath, David M Cash, Jonathan M Schott, Bernard J Hanseeuw, Yasmine Salman, Vincent Malotaux, Willemijn J Jansen, Renaud La Joie, Howard J Rosen, Sterling C Johnson, Bradley T Christian, Tobey J Betthauser, Susan M Landau, Sid E O'Bryant, Oskar Hansson, Rik Ossenkoppele, ADNI, ADNI‐DOD, A‐Study, MCSA, Prevent‐AD

Abstract

Alzheimers Dement. 2025 Dec;21 Suppl 2:e105387. doi: 10.1002/alz70856_105387.

ABSTRACT

BACKGROUND: Sex, education and race/ethnicity are all associated with risk of Alzheimer's disease dementia. Here, we assess the effects of self-reported sex, educational attainment and race/ethnicity on amyloid-positivity, and tau-PET-positivity in 12,048 (7,394 cognitively unimpaired [CU], 2,177 MCI, and 2,477 dementia) individuals from 42 cohorts worldwide.

METHOD: Logistic generalized estimating equations were used to estimate frequency of amyloid-positivity (using cohort-specific thresholds for amyloid-PET [84%] or CSF) and tau-PET-positivity (cohort-specific thresholds of 2SD above mean temporal uptake in amyloid-negative controls). We assessed: i) sex and APOEε4 (N = 10,098) associations, to complement earlier findings of a higher frequency of tau-positivity in females, ii) effects of lower/higher education (N = 10,970; cohort-specific median-split), and iii) effects of race/ethnicity (non-Hispanic White [hereafter: White], N = 4880; Asian, N = 116; Black or African-American [hereafter: Black], N = 353; Hispanic, N = 356, only from Northern-American cohorts). Outcomes were frequency of amyloid-positivity in CU individuals only, and tau-PET-positivity in both amyloid-positive (AB+) CU and cognitively impaired (CI, i.e. MCI and dementia) individuals. Interaction effects on the relationship between age and amyloid/tau-positivity were assessed and only retained in the models when significant.

RESULT: Female sex was associated with an APOEε4-independent increased frequency of amyloid-positivity (β=0.51[0.22], p = 0.02) in CU and increase of tau-positivity in both AB+CU (β=0.27[0.08]) and AB+CI (β=0.37[0.08], both p <0.01). Remarkably, tau-positivity frequencies of female APOEε4 non-carriers were equivalent to male APOEε4 carriers in AB+CI (Figure 1). No significant sex*APOE interactions were observed. In CU, higher education was associated with lower amyloid-positivity frequency (β=-0.12[0.05], p = 0.02). In contrast, among AB+CU, there was an age*education interaction effect that indicated more pronounced age effects on tau-positivity in individuals with higher education (age*education:βinteraction=0.03[0.01], p <0.01). There were no education effects in AB+CI (Figure 2). In CU, an age*race/ethnicity interaction effect was observed across all non-White groups compared to White (Hispanic:βinteraction=-0.05[0.01], p <0.01; Black:-0.04[0.01], p <0.01; Asian:-0.02[0.01], p = 0.04). This suggests that the impact of age on amyloid-positivity was less pronounced in non-White groups. Furthermore, in AB+CI, Hispanic ethnicity was related to higher tau-positivity frequency than White (β=0.51[0.22], p = 0.02; Figure 3).

CONCLUSION: In this multi-center initiative comprised of clinical and community-based cohorts, we observed that self-reported sex, educational attainment and race/ethnicity were related to positivity-frequencies of Alzheimer's disease pathology.

PMID:41505496 | DOI:10.1002/alz70856_105387

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Dr Maura Malpetti

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Using specialist brain scans and novel blood tests to measure inflammation and accelerate the development of new treatments

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