AI Article Synopsis

  • Alzheimer's disease (AD) mainly impacts women and shows different neural anatomy and disease mechanisms based on sex, suggesting the need for tailored therapeutic approaches.
  • Previous studies using bulk RNA sequencing identified sex-based differences in molecular pathways related to energy, neurons, and immune response but lacked detailed analysis at the single-cell level.
  • By analyzing nearly 74,000 cells from human brain samples, we found significant sex differences in glial cells in the prefrontal cortex and opposing gene fluctuations in the entorhinal cortex between sexes in AD, highlighting the importance of considering sex in AD research for better treatment development.

Article Abstract

Alzheimer's disease (AD) is a pervasive neurodegenerative disorder that disproportionately affects women. Since neural anatomy and disease pathophysiology differ by sex, investigating sex-specific mechanisms in AD pathophysiology can inform new therapeutic approaches for both sexes. Previous bulk human brain RNA sequencing studies have revealed sex differences in dysregulated molecular pathways related to energy production, neuronal function, and immune response; however, the sex differences in disease mechanisms are yet to be examined comprehensively on a single-cell level. We leveraged nearly 74,000 cells from human prefrontal and entorhinal cortex samples from the first two publicly available single-cell RNA sequencing AD datasets to perform a case versus control sex-stratified differential gene expression analysis and pathway network enrichment in a cell type-specific manner for each brain region. Our examination at the single-cell level revealed sex differences in AD prominently in glial cells of the prefrontal cortex. In the entorhinal cortex, we observed the same genes and networks to be perturbed in opposing directions between sexes in AD relative to healthy state. Our findings contribute to growing evidence of sex differences in AD-related transcriptomic changes, which can fuel the development of therapies that may prove more effective at reversing AD pathophysiology.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8786804PMC
http://dx.doi.org/10.1007/s12035-021-02591-8DOI Listing

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