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Amyloid deposition is associated with different patterns of hippocampal connectivity in men versus women.

Minjie Wu | Rebecca C Thurston | Dana L Tudorascu | Helmet T Karim | Chester A Mathis | Brian J Lopresti | M Ilyas Kamboh | Ann D Cohen | Beth E Snitz | William E Klunk | Howard J Aizenstein
Neurobiology of aging | 2019

Compared to men, women are disproportionally affected by Alzheimer's disease (AD) and have an accelerated trajectory of cognitive decline and disease progression. Neurobiological factors underlying gender differences in AD remain unclear. This study investigated brain beta-amyloid (Aβ)-related neural system differences in cognitively normal older men and women (N = 61; 41 females, 65-93 years old). We found that men and women showed different associations between Aβ load and hippocampal functional connectivity. During associative memory encoding, in men greater Aβ burden was accompanied by greater hippocampus-prefrontal connectivity (i.e., more synchronized activities), whereas in women hippocampal connectivity did not vary by Aβ burden. For resting-state data, the interaction of gender × Aβ on hippocampal connectivity did not survive multiple comparison in the whole-brain analyses. In the region of interest-based analyses, resting-state hippocampal-prefrontal connectivity was positively correlated with Aβ load in men and was negatively correlated with Aβ load in women. The observed Aβ-related neural differences may explain the accelerated trajectory of cognitive decline and AD progression in women.

Pubmed ID: 30711677

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Associated grants

  • Agency: NIA NIH HHS, United States
    Id: RF1 AG025516
  • Agency: NIA NIH HHS, United States
    Id: R01 AG030653
  • Agency: NIA NIH HHS, United States
    Id: R01 AG041718
  • Agency: NHLBI NIH HHS, United States
    Id: K24 HL123565
  • Agency: NIA NIH HHS, United States
    Id: P01 AG025204

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