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. Author manuscript; available in PMC: 2017 Jun 1.
Published in final edited form as: J Neural Transm (Vienna). 2016 Apr 20;123(6):583–588. doi: 10.1007/s00702-016-1552-3

Table 1.

Association between MAPT haplotype, demographic factors, and pathological measures in PD patients

Genotype p value

H1/H1 H2
N= 51 20
Male, N (%) 37 (73) 16 (80) 0.76
Age at death, mean (SD) 76 (7) 77 (8) 0.87
Disease durationa, years, mean (SD) 18.4 (8.4) 15.8 (9.7) 0.54
Braak LB stage 0.10
  4 7 (14 %) 6 (30 %)
  5 17 (33 %) 7 (35 %)
  6 27 (53 %) 7 (35 %)
CERAD scoreb 0.39
  0 22 (44 %) 5 (26 %)
  A 16 (32 %) 8 (42 %)
  B 5 (10 %) 6 (32 %)
  C 7 (14 %) 0
Braak NFT stageb 0.52
  0 7 (14 %) 0
  I–II 8 (16 %) 3 (16 %)
  III–IV 20 (40 %) 12 (63 %)
  V–VI 15 (30 %) 4 (21 %)

Wilcoxon rank sum test was used to compare Braak LB stage, Braak NFT stage, and CERAD score between H1/H1 and H2 carriers. Fisher’s exact test was used to compare the gender, and a t test was used to compare age at death and disease duration

LB Lewy body, CERAD consortium to establish a registry for Alzheimer’s Disease, NFT neurofibrillary tangle

a

For disease duration, data were available for 18 H1/H1 and 6 H2 cases

b

For CERAD and NFT scores, 50 H1/H1 and 19 H2 cases were assessed