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. 2017 Jan 31;5:10. doi: 10.1186/s40478-017-0414-z

Table 1.

Demographics of the two sample sets in this study

CT AD P-value
ROW discovery set
 N 18 27 -
 AAD, yr 76.3 ± 7.1 84.5 ± 8.0 0.001a
 Gender, % (F : M) 27.8 : 72.2 63.0 : 37.0 0.033b
 PMI, hr 9.6 ± 9.4 13.4 ± 11.6 0.158a
 BW, g 1268 ± 127 1156 ± 120 0.003a
 RIN
  TC 7.9 ± 0.8 7.1 ± 1.2 0.006a
 Hemolysis ratio
  Serum 1.9 ± 0.6 1.7 ± 0.5 0.105a
APOE
  Genotype, % (ε3*3 : ε3*4 : ε4*4) 55.6 : 44.4 : 0.0 44.4 : 25.9 : 29.6 0.550c
  Allele, % (ε3 : ε4) 77.8 : 22.2 57.4 : 42.6 0.069c
NIG validation set
 N 22 36 -
 AAE, yr 73.7 ± 8.4 74.7 ± 7.3 0.556a
 Gender, % (F : M) 80.0 : 20.0 63.9 : 36.1 0.333b
 MMSE 29.3 ± 0.7 19.3 ± 5.4 4.8.E-08a
 Hemolysis ratio
  Serum 1.3 ± 0.2 1.3 ± 0.2 0.316a
APOE
  Genotype, % (ε3*3 : ε3*4) 85.7 : 14.3 55.6 : 44.4 0.056c
  Allele, % (ε3 : ε4) 92.9 : 7.1 77.8 : 22.2 0.090c

Abbreviations: AAD age at death, AAE age at examination, AD Alzheimer’s disease, APOE apolipoprotein E, BW brain weight, CT control, F female, g grams, hr hours, M male, MMSE mini-mental state examination, PMI postmortem interval, RIN RNA integrity number, TC temporal cortex, yr years

aCalculated by Mann-Whitney U-test between AD and CT

bCalculated by Fisher’s exact test for gender distribution

cCalculated by Fisher’s exact test for APOE ε4 allele carrier status (ε4 carrier and ε4 non-carrier)

Data are presented as the mean ± standard deviation