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. Author manuscript; available in PMC: 2023 Sep 1.
Published in final edited form as: Neurobiol Aging. 2022 May 28;117:128–138. doi: 10.1016/j.neurobiolaging.2022.05.009

Table 2.

Neuropathologic characteristics of the participants.

Characteristics
N 738
LATE-NC, n (%)
 (stage 0) no TDP-43 inclusions 319 (43.2)
 (stage 1) TDP-43 inclusions in amygdala only 130 (17.6)
 (stage 2) TDP-43 inclusions in amygdala and entorhinal cortex or hippocampus 81 (11)
 (stage 3) TDP-43 inclusions in amygdala, entorhinal cortex or hippocampus, and neocortex 208 (28.2)
AD-NC (NIA-AA criteria), n (%)
 None 61 (8.2)
 Low 132 (17.9)
 Intermediate 346 (46.9)
 High 199 (27)
Lewy bodies, n (%) 217 (29.4)
Gross infarcts, n (%) 298 (40.4)
Microscopic infarcts, n (%) 291 (39.4)
Cerebral amyloid angiopathy, n (%)
 None 145 (19.7)
 Mild 324 (43.9)
 Moderate 181 (24.5)
 Severe 88 (11.9)
Atherosclerosis, n (%)
 None 174 (23.6)
 Mild 394 (53.4)
 Moderate 139 (18.8)
 Severe 31 (4.2)
Arteriolosclerosis, n (%)
 None 273 (37)
 Mild 277 (37.5)
 Moderate 149 (20.2)
 Severe 39 (5.3)

AD-NC, Alzheimer’s Disease neuropathological change; LATE-NC, Limbic predominant age-related transactive response DNA binding protein 43 (TDP-43) encephalopathy neuropathological change; NIA-AA, National Institute on Aging-Alzheimer’s Association.