Amyloid PET burden

There are 9 papers on amyloid PET burden in aging research: 9 observational studies in people.

Biomarker

9 papers study it15 more mention it6 findings

1 new paper in 30 daysSee all 24

“A non-APOE GRS of top variants was strongly associated with amyloid PET levels in the MCSA (p = 4.34 × 10−9, β = 5.88)”
Combating Genetic Heterogeneity for Polygenic Prediction of Susceptibility to Brain β-Amyloid Deposition: Beyond APOENeurology. Genetics2025doi:10.1212/nxg.0000000000200266
  • Humans9

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1

Hearing loss

no changein humans1

1 study
  1. Hearing loss was not clearly linked with amyloid PET burden in humans (oldest-old individuals) (p=0.7).

    “In oldest-old individuals, hearing function was not associated with amyloid pathology (p=0.7)”

    Humansoldest-old individuals

    Distinct disease mechanisms may underlie cognitive decline related to hearing loss in different age groups

    Journal of neurology, neurosurgery, and psychiatry

Associations

5

Non-APOE GRS

upin humans1

1 study
  1. Non-APOE GRS is associated with amyloid PET burden in APOE ε3/ε3 individuals (β = 5.88, p = 4.34 × 10−9).

    “A non-APOE GRS of top variants was strongly associated with amyloid PET levels in the MCSA (p = 4.34 × 10−9, β = 5.88)”

    Humansin APOE ε3/ε3 individualsbrain

    Combating Genetic Heterogeneity for Polygenic Prediction of Susceptibility to Brain β-Amyloid Deposition: Beyond APOE

    Neurology. Genetics

More on Non-APOE GRS

Hearing loss

upin humans1

1 study
  1. Hearing loss is associated with amyloid PET burden in humans (younger-old individuals) (p=0.0034).

    “in the younger-old individuals hearing loss was associated with higher amyloid burden (p=0.0034).”

    Humansyounger-old individuals

    Distinct disease mechanisms may underlie cognitive decline related to hearing loss in different age groups

    Journal of neurology, neurosurgery, and psychiatry

Non-APOE Alzheimer's disease risk variants

upin humans1

1 study
  1. non-APOE Alzheimer's disease risk variants are associated with amyloid PET burden in humans (MCSA = 2.1%, ADNI = 4.4%).

    “However, in both cohorts the non-APOE variants uniquely contributed only modestly (MCSA = 2.1%, ADNI = 4.4%) to explaining variation in amyloid PET levels.”

    Humansbrain

    Polygenic Scores of Alzheimer's Disease Risk Genes Add Only Modestly to APOE in Explaining Variation in Amyloid PET Burden

    Journal of Alzheimer's disease : JAD

Alzheimer's disease polygenic risk score

upin humans1

1 study
  1. Alzheimer's disease polygenic risk score is associated with amyloid PET burden in humans (p = 1.51×10-50 (MCSA), p = 3.21×10-64 (ADNI)).

    “In aggregate, the AD risk variants were strongly associated with amyloid PET levels in the MCSA (p = 1.51×10-50) and ADNI (p = 3.21×10-64).”

    Humansbrain

    Polygenic Scores of Alzheimer's Disease Risk Genes Add Only Modestly to APOE in Explaining Variation in Amyloid PET Burden

    Journal of Alzheimer's disease : JAD

APOE

upin humans1

1 study
  1. APOE is associated with amyloid PET burden in humans.

    “Known AD risk variants in APOE, PICALM, CR1, and CLU were associated with amyloid PET levels.”

    Humansbrain

    Polygenic Scores of Alzheimer's Disease Risk Genes Add Only Modestly to APOE in Explaining Variation in Amyloid PET Burden

    Journal of Alzheimer's disease : JAD

More on APOE

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