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. Author manuscript; available in PMC: 2021 Mar 1.
Published in final edited form as: Neurobiol Aging. 2019 Sep 24;87:138.e7–138.e14. doi: 10.1016/j.neurobiolaging.2019.09.007

Table 3.

Association of a mitochondrial PRS and mitochondrial haplogroups (model 1) and their interactions (model 2) with Alzheimer’s disease age of onset

Variable Model 1
Model 2
βa SE p βa SE p
Male −0.21 0.1 0.0034 −0.22 0.1 0.028
APOE status
 ε4+   0.8 0.12 6.50E-12   0.78 0.12 2.70E-11
 ε2+ −0.85 0.39 0.029 −0.86 0.39 0.027
PC1 −0.11 0.06 0.073 −0.1 0.06 0.104
PC2   0.03 0.04 0.525   0.03 0.04 0.509
nMT-PRS   0.36 0.06 3.54E-10   0.37 0.08 2.55E-06
Haplogroup
 I −0.01 0.26 0.958   0.04 0.28 0.879
 J −0.06 0.17 0.707 −0.09 0.19 0.635
 K −0.06 0.18 0.742 −0.05 0.18 0.78
 T −0.31 0.17 0.073 −0.14 0.18 0.422
 U −0.1 0.15 0.528 −0.16 0.17 0.35
 V   0.17 0.28 0.549 −0.26 0.38 0.496
 W   0.38 0.33 0.247   0.38 0.33 0.241
 X   0.08 0.32 0.794   0.16 0.36 0.664
Haplogroup × nMT-PRS
 I - - - −0.14 0.29 0.617
 J - - -   0.08 0.22 0.72
 K - - - −0.06 0.17 0.74
 T - - - −0.48 0.2 0.015
 U - - -   0.14 0.15 0.371
 V - - -   0.82 0.33 0.013
 W - - -   0.13 0.34 0.697
 X - - - −0.13 0.32 0.68

Key: APOE, apolipoprotein E; nMT-PRS, nuclear-encoded mitochondrial polygenic risk score; PC1, principal component 1; PC2, principal component 2.

a

Results in the main text are presented as the exponentiation of the beta.