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. 2015 May 1;10(5):e0125204. doi: 10.1371/journal.pone.0125204

Table 1. Characteristics of Autopsy Subjects.

All autopsies LBD ADLBV AD Control Total
  N 59 68 71 33 231
Male % 71.2 52.9 36.6 54.5 52.8
Age at Dementia (yr)  Mean 66.6 67.6 70.7   68.4
SD 10.3 9.6 8.5   9.5
Age at Death (yr) Mean 78.3 79.1 81.6 70.3 78.4
SD 8.7 8.5 8.6 14.2 10.1
Duration (yr) Mean 11.6 10.3 10.0   10.6
SD 6.1 6.1 4.3   5.5
Education (yr)  Mean 16.6 14.1 13.8 14.2 14.5
SD 2.3 4.1 4.3 3.4 4.0
Ethnicity % White 94.9 86.8 85.9 60.6 84.8
%AJ ancestry N (individuals) 3 7 15 2 27
% AJ (n/total samples with GWAS) 100(3/3) 35 (7/20) 41.67 (15/36) 66.67 (2/3) 43.5** (27/62)
LB Pathology Present % 100.0 100.0 16.9 3.0 60.6
LB Cortical Pathology Present  % 100.0 100.0 0.0 0.0 55.0
LB Subcortical Pathology Present % 64.4 69.1 12.7 0.0 40.7
AD Pathology Present % 79.7 100.0 100.0 33.3 85.3
AD Pathological Diagnosis % 0.0 100.0 100.0 0.0 60.2
GBA mutation N(Individuals) 28 16 6 1 51
% 47.5 23.5 8.5 3.0 22.1
SMPD1 mutation N(Individuals) 12 14 4 3 33
% 20.3 20.6 5.6 9.1 14.3
HEXA mutation N(Individuals) 8 17 8 6 39
% 13.6 25.0 11.3 18.2 16.9
MCOLN1 mutation  N(Individuals) 17 20 17 8 62
% 28.8 29.4 23.9 24.2 26.8
APOE (no E4)* N(Individuals) 33 26 26 24 109
% 66.0 41.9 42.6 77.4 47.2
APOE (one E4) *  N(Individuals) 13 26 25 6 70
% 26.0 41.9 41.0 19.4 30.3
APOE (two E4) * N(Individuals) 4 10 10 1 25
% 8.0 16.1 16.4 3.2 10.8

* APOE missing in 27cases

**%AJ in brain autopsy sample with GWAS data available (n = 62)