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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 2.

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

Variable Model 1
Model 2
βa SE p β SE p
Age   0.02 0.02 0.213   0.03 0.02 0.122
Male −0.01 0.22 0.975   −0.09 0.23 0.682
APOE status
 ε4+   1.2 0.24 6.47E-07   1.25 0.25 5.08E-07
 ε2+ −0.7 0.58 0.227 −0.88 0.6 0.142
PC1 −0.14 0.13 0.274 −0.1 0.13 0.423
PC2   0.53 0.55 0.332   0.42 0.55 0.442
nMT-PRS   0.79 0.14 5.58E-09   1.09 0.2 5.68E-08
Haplogroup
 I   0.27 0.62 0.661   0.33 0.63 0.6
 J   0.09 0.4 0.827   0.06 0.44 0.886
 K   0.694 0.35 0.049   0.71 0.34 0.038
 T −0.23 0.4 0.564   0.04 0.38 0.909
 U   0.687 0.35 0.052   0.81 0.38 0.033
 V   0.01 0.63 0.988   0.07 0.76 0.926
 W   0.66 0.9 0.464   0.74 0.86 0.391
 X −1.23 1.13 0.278 −2.04 1.77 0.247
Haplogroup × nMT-PRS
 I - - - −0.38 0.84 0.647
 J - - -   0.28 0.68 0.685
 K - - - −0.8 0.36 0.026
 T - - - −1.51 0.41 2.18E-04
 U - - -   0.07 0.52 0.886
 V - - -   1.01 1.44 0.482
 W - - - −0.68 0.85 0.425
 X - - - −2.31 1.97 0.24

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. p-values are unadjusted.