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. 2019 Nov 20;5:814–824. doi: 10.1016/j.trci.2019.08.005

Table 2.

Effects of TOMM40-L allele in the risk of PD, PDD, and DLB

Case group, N individuals Control group, N individuals Frequency of effect allele (L)
OR (95% CI) P value P value adjusted for APOE-ε4 effect
Case group, % Reference group, %
PDnD, 84 NC, 86 13.7 10.5 1.15 (0.59–2.26) .69 .58
PDD, 102 NC and PDnD, 170 20.1 12.1 1.69 (1.05–2.76) .033 .73
DLB, 179 NC and PDnD, 170 32.1 12.1 3.61 (2.395.59) 3.23 × 10−9 .66
DLB, 179 PDD, 102 32.1 20.1 2.15 (1.403.38) 6.37 × 10−4 .64
DLB+AD, 46 NC and PDnD, 170 37.0 12.1 4.40 (2.427.99) 1.15 × 10−6 .40
PDD+AD, 15 NC and PDnD, 170 16.7 12.1 1.38 (0.44–3.57) .53 .17
DLB-AD, 47 NC and PDnD, 170 20.2 12.1 1.71 (0.96–3.03) .067 .51
PDD-AD, 49 NC and PDnD, 170 18.4 12.1 1.46 (0.78–2.64) .22 .63

NOTE. The results are reported as odds ratios (ORs) with their 95% confidence intervals (CIs). Model tested: TOMM40-L allele log-additive effect on risk compared with combined effect of other alleles, adjusted for age at death and sex. We also adjusted the same model for the additive effect of APOE-ε4 allele.

Results in bold are statistically significant after correction for multiple testing (P value < .0021).

Abbreviations: NC, normal controls; PDnD, Parkinson's disease without dementia; PDD+AD/PDD-AD, Parkinson's disease with dementia with/without neuropathologically defined Alzheimer's disease; DLB+AD/DLB-AD, dementia with Levy bodies with/without neuropathologically defined AD.