Regional tau Burden and Multidomain Cognitive Function in Clinically Unimpaired Older Adults: Evidence from the A4 Study


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DEMİRSOY İ., Ozge A.

Haseki Tip Bulteni, cilt.64, sa.3, ss.155-164, 2026 (ESCI, Scopus, TRDizin)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 64 Sayı: 3
  • Basım Tarihi: 2026
  • Doi Numarası: 10.4274/haseki.galenos.2026.99608
  • Dergi Adı: Haseki Tip Bulteni
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, CINAHL, EMBASE, Directory of Open Access Journals, TR DİZİN (ULAKBİM), Academic Search Ultimate (EBSCO), Biomedical Reference Collection: Corporate Edition (EBSCO), Health Research Premium Collection (ProQuest)
  • Sayfa Sayıları: ss.155-164
  • Anahtar Kelimeler: Cognitive dysfunction, Alzheimer's disease, tau proteins, temporal lobe, depression, risk factors
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Uşak Üniversitesi Adresli: Evet

Özet

Aim: We aimed to evaluate how modifiable risk factors influence these relationships and to better understand the drivers of early cognitive changes in regional tau burden in the medial temporal lobe (MTL) versus the neocortex (NEO) during the preclinical stages of Alzheimer’s disease (AD). Methods: In this cross-sectional study, 447 participants in the A4 study (anti-amyloid treatment in asymptomatic AD) underwent tau-positron emission tomography-standardized uptake value ratio evaluations. Cognitive abilities were assessed using the Preclinical Alzheimer’s Cognitive Composite (PACC). Depression, anxiety, and lifestyle factors were analyzed using t-tests, chi-square tests, and multiple linear regression models. Results: The tau-positive cohort was notably older (p=0.002) and significantly more likely to carry APOE4 (p<0.001). Tau-positive groups demonstrated poorer cognitive performance. Negative correlations between tau accumulation and cognitive performance for PACC and its components, with tauMTL/tauNEO associated with worse outcomes. Females were associated with better objective performance but worse informant-reported function, suggesting an early loss of self-awareness. Higher education was protective; depression was linked to decreased memory and executive function, whereas anxiety showed no association. Conclusion: Regional tau pathology is robustly associated with functional decline detectable by informants prior to clinical emergence. The significant interaction between tau and modifiable factors such as depressive symptoms underscores the importance of multifaceted, informant-based assessments in preclinical AD screening.