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Cell-type-specific Alzheimer’s disease polygenic risk scores are associated with distinct disease processes in Alzheimer’s disease

Author

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  • Hyun-Sik Yang

    (Brigham and Women’s Hospital
    Massachusetts General Hospital
    Harvard Medical School
    Broad Institute of MIT and Harvard)

  • Ling Teng

    (Brigham and Women’s Hospital
    Broad Institute of MIT and Harvard)

  • Daniel Kang

    (Massachusetts General Hospital)

  • Vilas Menon

    (Columbia University Irving Medical Center
    Columbia University Irving Medical Center)

  • Tian Ge

    (Harvard Medical School
    Broad Institute of MIT and Harvard
    Center for Genomic Medicine, Massachusetts General Hospital
    Massachusetts General Hospital)

  • Hilary K. Finucane

    (Harvard Medical School
    Broad Institute of MIT and Harvard
    Massachusetts General Hospital)

  • Aaron P. Schultz

    (Massachusetts General Hospital
    Harvard Medical School)

  • Michael Properzi

    (Massachusetts General Hospital)

  • Hans-Ulrich Klein

    (Columbia University Irving Medical Center
    Columbia University Irving Medical Center)

  • Lori B. Chibnik

    (Massachusetts General Hospital
    Broad Institute of MIT and Harvard
    Harvard T.H. Chan School of Public Health)

  • Julie A. Schneider

    (Rush University Medical Center)

  • David A. Bennett

    (Rush University Medical Center)

  • Timothy J. Hohman

    (Vanderbilt University Medical Center)

  • Richard P. Mayeux

    (Columbia University Irving Medical Center)

  • Keith A. Johnson

    (Brigham and Women’s Hospital
    Massachusetts General Hospital
    Harvard Medical School
    Massachusetts General Hospital)

  • Philip L. Jager

    (Columbia University Irving Medical Center
    Columbia University Irving Medical Center)

  • Reisa A. Sperling

    (Brigham and Women’s Hospital
    Massachusetts General Hospital
    Harvard Medical School)

Abstract

Many of the Alzheimer’s disease (AD) risk genes are specifically expressed in microglia and astrocytes, but how and when the genetic risk localizing to these cell types contributes to AD pathophysiology remains unclear. Here, we derive cell-type-specific AD polygenic risk scores (ADPRS) from two extensively characterized datasets and uncover the impact of cell-type-specific genetic risk on AD endophenotypes. In an autopsy dataset spanning all stages of AD (n = 1457), the astrocytic ADPRS affected diffuse and neuritic plaques (amyloid-β), while microglial ADPRS affected neuritic plaques, microglial activation, neurofibrillary tangles (tau), and cognitive decline. In an independent neuroimaging dataset of cognitively unimpaired elderly (n = 2921), astrocytic ADPRS was associated with amyloid-β, and microglial ADPRS was associated with amyloid-β and tau, connecting cell-type-specific genetic risk with AD pathology even before symptom onset. Together, our study provides human genetic evidence implicating multiple glial cell types in AD pathophysiology, starting from the preclinical stage.

Suggested Citation

  • Hyun-Sik Yang & Ling Teng & Daniel Kang & Vilas Menon & Tian Ge & Hilary K. Finucane & Aaron P. Schultz & Michael Properzi & Hans-Ulrich Klein & Lori B. Chibnik & Julie A. Schneider & David A. Bennett, 2023. "Cell-type-specific Alzheimer’s disease polygenic risk scores are associated with distinct disease processes in Alzheimer’s disease," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43132-2
    DOI: 10.1038/s41467-023-43132-2
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    References listed on IDEAS

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