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. 2020 Jun 29;77(10):1ā€“8. doi: 10.1001/jamaneurol.2020.1941

Table 2. Association of Non-AD Dementia-Associated Brain Pathological Changes With ELCE.

Pathological change No. (%) of participants (nā€‰=ā€‰813)a Association with ELCEb
Odds ratio (95% CI) P value
Cortical Lewy bodies 109 (13) 0.79 (0.57-1.09) .17
TDP-43 protein 1.11 (0.90-1.36) .35
Stage 0 359 (44)
Stage 1 156 (19)
Stage 2 145 (18)
Stage 3 124 (15)
Hippocampal sclerosis 85 (10) 1.17 (0.81-1.69) .40
Macroscopic infarcts 255 (31) 0.90 (0.70-1.16) .43
Cortical macroscopic infarcts 114 (14) 0.97 (0.70-1.33) .83
Subcortical macroscopic infarcts 230 (28) 0.87 (0.68-1.12) .29
Microinfarcts 205 (25) 0.96 (0.73-1.25) .75
Atherosclerosis 1.08 (0.88-1.33) .44
None 170 (21)
Mild 396 (49)
Moderate 194 (24)
Severe 52 (6)
Arteriolosclerosis 1.12 (0.92-1.37) .26
None 243 (30)
Mild 290 (36)
Moderate 218 (27)
Severe 60 (7)
Cerebral amyloid angiopathy 0.84 (0.68-1.02) .08
None 164 (20)
Mild 354 (44)
Moderate 184 (23)
Severe 107 (13)

Abbreviations: AD, Alzheimer disease; ELCE, early-life cognitive enrichment.

a

Owing to missing data, numbers of participants do not total 813.

b

Derived from logistic regression models controlled for age at death, sex, and educational level. In these analyses, ELCE was not associated with any of the examined pathological changes.