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. Author manuscript; available in PMC: 2021 Mar 26.
Published in final edited form as: Mov Disord. 2019 Jun 24;34(9):1325–1332. doi: 10.1002/mds.27773

TABLE 3.

Association between MAPT haplotypes and cortical LB counts

Association With Middle
Frontal LB Count
Association With Superior
Temporal LB Count
Association With Inferior
Parietal LB Count
Association With
Cingulate LB Count
Association With Parahippocampal
LB Count





Haplotype Frequency (%) Regression
Coefficient (95% CI)
P Value Regression
Coefficient (95% CI)
P Value Regression
Coefficient (95% CI)
P Value Regression
Coefficient (95% CI)
P Value Regression
Coefficient (95% CI)
P Value
H1b 16.5 −0.08 (−0.28, 0.11) 0.40 0.00 (−0.23, 0.22) 0.97 −0.05 (−0.24, 0.13) 0.58 −0.07 (−0.27, 0.13) 0.52 −0.10 (−0.34, 0.14) 0.42
H1c 11.9 −0.03 (−0.24, 0.17) 0.72 −0.15 (−0.38, 0.09) 0.20 −0.12 (−0.31, 0.07) 0.21 −0.05 (−0.26, 0.16) 0.62 −0.10 (−0.36, 0.15) 0.38
H1d 7.3 0.07 (−0.21, 0.36) 0.63 0.12 (−0.21, 0.45) 0.50 0.13 (−0.14, 0.39) 0.37 0.11 (−0.18, 0.41) 0.47 0.09 (−0.27, 0.46) 0.65
H1e 8.5 −0.07 (−0.33, 0.18) 0.58 −0.13 (−0.43, 0.16) 0.38 −0.13 (−0.37, 0.11) 0.31 −0.12 (−0.39, 0.14) 0.37 −0.17 (−0.49, 0.14) 0.27
H1fa 1.1 −0.78 (−1.62, 0.07) 0.078 −0.40 (−1.38, 0.58) 0.45 −0.53 (−1.33, 0.26) 0.21 −0.47 (−1.35, 0.41) 0.28
H1g 1.8 0.27 (−0.25, 0.78) 0.33 0.01 (−0.59, 0.60) 0.98 0.37 (−0.12, 0.85) 0.16 0.21 (−0.33, 0.74) 0.45 0.25 (−0.39, 0.90) 0.46
H1h 3.9 0.05 (−0.34, 0.44) 0.81 0.20 (−0.26, 0.65) 0.40 0.21 (−0.15, 0.58) 0.27 0.10 (−0.31, 0.51) 0.63 0.06 (−0.42, 0.55) 0.79
H1i 2.9 0.07 (−0.43, 0.57) 0.73 0.11 (−0.47, 0.69) 0.68 0.03 (−0.44, 0.50) 0.84 0.07 (−0.46, 0.60) 0.75 0.74 (0.13, 1.36) 0.016
H1j 1.3 −0.49 (1.32, 0.34) 0.29 −0.24 (−1.21, 0.72) 0.62 −0.23 (−1.91, 0.55) 0.59 −0.29 (−1.15, 0.58) 0.55 0.13 (−0.86, 1.13) 0.75
H1ka 1.2  —  —  —  — −0.26 (−1.27, 0.75) 0.59
H1l 2.5 −0.06 (−0.53, 0.40) 0.80 0.21 (−0.33, 0.75) 0.44 0.08 (−0.36, 0.51) 0.73 −0.12 (−0.61, 0.37) 0.54 0.21 (−0.47, 0.88) 0.55
H1m 1.9 −0.27 (−0.79, 0.25) 0.32 −0.31 (−0.92, 0.29) 0.32 −0.20 (−0.69, 0.29) 0.41 −0.17 (−0.71, 0.37) 0.54 −0.15 (−0.82, 0.53) 0.67
H1o 2.9 −0.09 (−0.57, 0.39) 0.72 −0.29 (−0.85, 0.27) 0.34 −0.08 (−0.54, 0.37) 0.73 0.00 (−0.50, 0.50) 0.99 −0.51 (−1.11, 0.09) 0.11
H1p 1.2 −0.15 (−0.89, 0.58) 0.69 −0.58 (−1.42, 0.27) 0.19 −0.51 (−1.20, 0.18) 0.13 −0.35 (−1.11, 0.41) 0.37 −0.41 (−1.33, 0.51) 0.43
H1q 1.2 0.48 (−0.13, 1.08) 0.11 0.69 (0.01, 1.38) 0.041 0.42 (−0.15, 0.99) 0.14 0.48 (−0.15, 1.11) 0.12 0.46 (−0.30, 1.21) 0.20
H1r 1.7 0.42 (−0.19, 1.03) 0.14 0.10 (−0.61, 0.81) 0.77 0.49 (−0.08, 1.07) 0.068 0.23 (−0.41, 0.87) 0.47 0.45 (−0.38, 1.29) 0.24
H1s 1.5 −0.27 (−0.79, 0.25) 0.95 −0.31 (−0.92, 0.29) 0.74 −0.20 (−0.69, 0.29) 0.63 −0.17 (−0.71, 0.37) 0.58 −0.15 (−0.82, 0.53) 0.84
H1u 3.0 −0.21 (−0.65, 0.23) 0.38 −0.30 (−0.82, 0.21) 0.27 −0.20 (−0.61, 0.22) 0.37 −0.01 (−0.47, 0.45) 0.99 −0.05 (−0.67, 0.57) 0.94
H1x 1.2 −0.10 (−0.81, 0.60) 0.79 0.07 (−0.75, 0.89) 0.83 −0.22 (−0.88, 0.44) 0.52 −0.23 (−0.99, 0.53) 0.54 −0.31 (−1.22, 0.60) 0.55
H1y 1.5 −0.22 (−0.92, 0.47) 0.42 0.18 (−0.63, 0.99) 0.67 −0.26 (−0.91, 0.40) 0.30 −0.39 (−1.11, 0.34) 0.18 0.14 (−0.72, 0.99) 0.66
H1z 1.1 0.63 (−0.14, 1.41) 0.12 0.57 (−0.33, 1.47) 0.21 0.35 (−0.38, 1.08) 0.33 0.51 (−0.29, 1.32) 0.23 0.50 (−0.49, 1.49) 0.34
H2 22.5 0.10 (−0.05, 0.26) 0.19 0.12 (−0.06, 0.30) 0.18 0.11 (−0.04, 0.25) 0.15 0.12 (−0.04, 0.28) 0.14 0.10 (−0.10, 0.29) 0.33

P values result from score tests of association that were adjusted for age and sex, where haplotypes that occurred in <1% of LBD cases in a given association analysis were excluded from that analysis. Regression coefficients correspond to the change in the mean outcome measure (on the square root scale) for each additional copy of the given haplotype. P values ≤0.0024 were considered to be statistically significant after applying a Bonferroni correction for the 21 tests of association that were performed for each outcome.

a

Indicates a haplotype that was observed at an overall frequency of <1% in a particular analysis and was therefore excluded from that analysis; sample sizes utilized in different analyses varied because of varying missing LB count information in the different cortical regions. Associations between haplotypes and outcomes that had P values ≤0.05 are shown in bold.