Concerning the ApoE4 variant, regardless of AD diagnosis, older adults that are ApoE4 + display a greater level of A accumulation that is not evident in ApoE3 + or ApoE2 + individuals (Lim et al., 2017), and AD patients with the ApoE4 genotype ( +/+ or +/ ) display higher levels of intraneuronal A accumulation compared to controls, indicating a baseline detrimental cognitive effect (Yamazaki et al., 2019)
Importantly, their ability to undergo OXPHOS and to form tumors was effectively restored by genetic replacement of their mt-DNA [5]
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