AI Article Synopsis

  • FTLD-MND is a condition marked by the presence of TDP-43 in neurons, and apoE4 is linked to increased brain atrophy in those affected.
  • A study of two siblings with a specific genetic mutation showed that the sibling with the apoE4 variant experienced more severe cognitive and behavioral issues and brain atrophy compared to the other sibling.
  • The findings suggest that apoE4 may worsen brain pathology in FTLD-MND due to creating harmful fragments and interacting with TDP-43, although such differences in siblings could still be coincidental.

Article Abstract

Frontotemporal lobar degeneration with motor neuron disease (FTLD-MND) is characterized by neuronal cytoplasmic inclusions containing TDP-43. Apolipoprotein E4 (apoE4), derived from the apoE ϵ4 allele, enhances brain atrophy in FTLD through unknown mechanisms. Here, we studied two siblings with C9ORF72-linked familial FTLD-MND, an apoE ϵ4 homozygote and an apoE ϵ3 homozygote. The apoE ϵ4 homozygote had more cognitive-behavioral symptoms, fronto-insulo-temporal atrophy, and apoE fragments and aggregates in the anterior cingulate cortex. ApoE formed complexes with TDP-43 that were more abundant in the apoE ϵ4 homozygote. Although differences seen in a sibling pair could arise due to chance, these findings raise the possibility that apoE4 exacerbates brain pathology in FTLD through formation of neurotoxic apoE fragments and interactions with TDP-43.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655113PMC
http://dx.doi.org/10.1080/13554794.2012.667124DOI Listing

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