| Home > In process > Prevalence of Alzheimer's disease pathology in the community. |
| Journal Article | DZNE-2026-00147 |
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2026
Nature Publ. Group
London [u.a.]
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Please use a persistent id in citations: doi:10.1038/s41586-025-09841-y
Abstract: The prevalence of Alzheimer's disease neuropathological changes (ADNCs), the leading cause of cognitive impairment, remains uncertain. Recent blood-based biomarkers enable scalable assessment of ADNCs1. Here we measured phosphorylated tau at threonine 217 in 11,486 plasma samples from a Norwegian population-based cohort of individuals over 57 years of age as a surrogate marker for ADNCs. The estimated prevalence of ADNCs increased with age, from less than 8% in people 58-69.9 years of age to 65.2% in those over 90 years of age. Among participants aged 70 years or older, 10% had preclinical Alzheimer's disease, 10.4% had prodromal Alzheimer's disease and 9.8% had Alzheimer's disease dementia. Furthermore, among those 70 years of age or older, ADNCs were present in 60% of people with dementia, in 32.6% of those with mild cognitive impairment and in 23.5% of the cognitively unimpaired group. Our findings suggest a higher prevalence of Alzheimer's disease dementia in older individuals and a lower prevalence of preclinical Alzheimer's disease in younger groups than previously estimated2.
Keyword(s): Humans (MeSH) ; Alzheimer Disease: epidemiology (MeSH) ; Alzheimer Disease: pathology (MeSH) ; Alzheimer Disease: blood (MeSH) ; Alzheimer Disease: diagnosis (MeSH) ; Aged (MeSH) ; Prevalence (MeSH) ; Aged, 80 and over (MeSH) ; Male (MeSH) ; Female (MeSH) ; tau Proteins: blood (MeSH) ; tau Proteins: chemistry (MeSH) ; Norway: epidemiology (MeSH) ; Cognitive Dysfunction: epidemiology (MeSH) ; Cognitive Dysfunction: blood (MeSH) ; Cognitive Dysfunction: pathology (MeSH) ; Middle Aged (MeSH) ; Phosphorylation (MeSH) ; Cohort Studies (MeSH) ; Biomarkers: blood (MeSH) ; Age Factors (MeSH) ; tau Proteins ; Biomarkers
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