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. 2024 Mar 18;20(5):3203–3210. doi: 10.1002/alz.13747

TABLE 2.

Linear regression models examining the cross‐sectional associations of fractal regulation with neuropathologies.

Neuropathology α 1 α 2
Estimate (95% CI) p value Estimate (95% CI) p value
Amyloid β −0.008 (−0.106, 0.090) 0.871 0.047 (−0.052, 0.146) 0.349
PHFtau tangles 0.003 (−0.108, 0.115) 0.953 −0.063 (−0.176, 0.049) 0.270
Odds ratio (95% CI) p value Odds ratio (95% CI) p value
Lewy body disease 0.790 (0.627, 0.996) 0.047 0.996 (0.780, 1.270) 0.972
LATE‐NC 0.994 (0.831, 1.188) 0.945 0.992 (0.829, 1.187) 0.929
Hippocampal sclerosis 0.804 (0.600, 1.078) 0.144 0.980 (0.730, 1.318) 0.896
Gross chronic infarcts 0.773 (0.648, 0.923) 0.005 0.893 (0.748, 1.066) 0.210
Chronic microinfarcts 0.813 (0.678, 0.974) 0.025 1.021 (0.851, 1.224) 0.822
Atherosclerosis 0.862 (0.710, 1.047) 0.134 0.989 (0.811, 1.206) 0.916
Arteriolosclerosis 0.795 (0.658, 0.960) 0.017 1.028 (0.852, 1.241) 0.769
Cerebral amyloid angiopathy 1.111 (0.927, 1.331) 0.255 1.043 (0.871, 1.250) 0.643
Sensitivity analysis Estimate (95% CI) p value Estimate (95% CI) p value
Amyloid β −0.090 (−0.217, 0.037) 0.164 0.002 (−0.124, 0.127) 0.978
PHFtau tangles −0.072 (−0.192, 0.047) 0.233 −0.118 (−0.235, −0.001) 0.049
Odds ratio (95% CI) p value Odds ratio (95% CI) p value
Lewy body disease 0.694 (0.504, 0.955) 0.025 0.975 (0.700, 1.359) 0.881
LATE‐NC 1.076 (0.854, 1.355) 0.533 0.995 (0.796, 1.244) 0.965
Hippocampal sclerosis 1.109 (0.721, 1.705) 0.637 0.850 (0.562, 1.286) 0.439
Gross chronic infarcts 0.774 (0.618, 0.970) 0.026 0.910 (0.732, 1.131) 0.392
Chronic microinfarcts 0.743 (0.587, 0.941) 0.014 1.007 (0.803, 1.262) 0.954
Atherosclerosis 0.833 (0.654, 1.062) 0.140 1.014 (0.797, 1.289) 0.909
Arteriolosclerosis 0.802 (0.632, 1.017) 0.069 1.064 (0.847, 1.338) 0.592
Cerebral amyloid angiopathy 1.056 (0.836, 1.335) 0.646 1.105 (0.880, 1.389) 0.390

Note: Models were adjusted for age at death, sex, and education. Results represent changes in the level (for continuous outcomes) or the odds (for dichotomized outcomes) for each 1 standard deviation increase in α 1 or α 2. Sensitivity analysis was performed in participants with the time interval between last actigraphy and death of ≤2 years. Detailed results are summarized in Tables S1 and S2. LATE‐NC, limbic‐predominant age‐related TDP‐43 encephalopathy neuropathological change; PHF, paired helical filament.