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. 2018 Jan 22;10:7. doi: 10.1186/s13195-017-0334-y

Table 2.

Co-occurring Alzheimer’s disease pathology and clinicopathological correlation, hippocampal neuronal loss, and apolipoprotein E genotype

Identifier Montine Thal Braak CERAD Correlation Hippocampal neuronal loss ApoE genotype
DR2.3 A1B1C1 2 2 1 Low 2 Ɛ2/Ɛ3
DR8.1 A0B1C0 0 1 0 Not 2 Ɛ3/Ɛ3
DR25.1 A0B1C0 0 1 0 Not 1 Ɛ3/Ɛ3
DR25.5 A0B1C0 0 1 0 Not 2 Ɛ3/Ɛ3
DR28.1 A3B1C1 5 1 1 Low 0 Ɛ3/Ɛ4
DR205.1 A2B1C1 3 2 1 Low 1 Ɛ2/Ɛ4
DR31.1 A1B1C1 2 1 1 Low 1 Ɛ2/Ɛ3
DR1207.1 A0B1C0 0 1 0 Not 1 Ɛ3/Ɛ3
DR1213.1 A0B1C0 0 1 0 Not 2 Ɛ3/Ɛ3

ApoE Apolipoprotein E, CERAD Consortium to Establish a Registry for Alzheimer’s Disease

Column 2: Montine classification [39, 83]; column 3: Thal stages for β-amyloid plaques [84]; column 4: Braak stages for neurofibrillary changes [85]; column 5: CERAD stages for senile plaques [86]: 0 = no pathology, 1 = sparse CERAD score; column 6: clinicopathological correlation of Alzheimer’s disease neuropathological changes [39]; column 7: neuronal loss in hippocampal CA1 (scale 0–3): 0 = no pathology, 1 = mild neuronal loss, 2 = moderate neuronal loss; column 8: ApoE genotype