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. 2016 Jun 9;6:27524. doi: 10.1038/srep27524

Table 2. Individual patient characteristics.

No Code Group Age/Sex Ante-mortem assessment of brain disease/mental state Cause of death Braak Stage (Amyloid load) PMD (h) Brain Wt (g)
1 H155 Control 61/M No brain disease or dementia Ischemic heart disease 0 (0) 7.0 1258
2 H121 Control 64/F No brain disease or dementia Pulmonary embolism 0 (0) 5.5 1260
3 H132 Control 63/F No brain disease or dementia Ruptured aorta 0 (0) 12.0 1280
4 H122 Control 72/F No brain disease or dementia Emphysema 0 (0) 9.0 1230
5 H204 Control 66/M No brain disease or dementia Ischemic heart disease 0 (0) 9.0 1461
6 H241 Control 76/F No brain disease or dementia Metastatic carcinoma II (A3, B1, C1) 12.0 1094
7 H164 Control 73/M No brain disease or dementia Ischemic heart disease 0 (0) 13.0 1315
8 H123 Control 78/M No brain disease or dementia Ruptured aortic aneurysm 0 (0) 7.5 1260
9 H150 Control 78/M No brain disease or dementia Ruptured MI 0 (0) 12.0 1416
10 AZ42 AD 60/M Alzheimer’s dementia Alzheimer’s disease VI (3/3) 7.0 1020
11 AZ71 AD 62/F Alzheimer’s dementia Alzheimer’s disease VI (3/3) 6.0 831
12 AZ48 AD 63/F Alzheimer’s dementia Bronchopneumonia VI (2/3) 7.0 1080
13 AZ72 AD 70/F Alzheimer’s dementia Lung cancer V (3/3) 7.0 1044
14 AZ90 AD 73/M Alzheimer’s dementia GI hemorrhage IV (3/3) 4.0 1287
15 AZ96 AD 74/F Alzheimer’s dementia Metastatic cancer V (3/3) 8.5 1062
16 AZ39 AD 74/M Alzheimer’s dementia Pseudomonas bacteremia VI (2/3) 12.0 1355
17 AZ80 AD 77/M Alzheimer’s dementia Myocardial infarction VI (3/3) 4.5 1180
18 AZ38 AD 80/M Alzheimer’s dementia Bronchopneumonia/ pulmonary oedema V (3/3) 5.5 1039

Abbreviations: GI, gastrointestinal; MI, myocardial infarction; PMD, post-mortem delay; wt, weight. Cause of death was determined by post-mortem examination, and brain pathology and Braak Stage were determined by specialist neuropathological examination. All AD cases had ‘Age-Related Plaque’ scores of “C”. Causes of death were the primary causes listed on the death certificate. Patient H241 had post-mortem signs consistent with AD and was therefore diagnosed with preclinical disease: the corresponding data have been retained in the main analysis presented in the manuscript, and removed from the control group for the secondary analysis. Control patient H241 (preclinical AD) was described as A3, B1, C1 using the ‘ABC’ criteria for AD neuropathologic change that incorporates histopathological assessments of Aβ deposits (A), staging of neurofibrillary tangles (B), and scoring of neuritic plaques (C)2.