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. 2020 Jul 11;24(15):8744–8752. doi: 10.1111/jcmm.15508

TABLE 3.

Association of SNPs of candidate genes and odds ratio to LOPD risk

Candidate gene SNP Effect allele Allele model a Dominant model b Recessive model b Additive model b
P OR (95% CI) P OR (95% CI) P OR (95% CI) P OR (95% CI)
SNCA rs8180209 A .052 0.77 (0.59‐1.00) .146 0.74 (0.49, 1.11) .064 0.94 (0.65, 1.37) .044 0.76 (0.57, 0.99)
MCCC1 rs2270968 G .152 1.23 (0.93‐1.64) .042 1.48 (1.01, 2.16) .822 0.92 (0.46, 1.85) .130 1.26 (0.93, 1.10)
DLG2 rs7479949 C .074 0.77 (0.59‐1.03) .135 0.74 (0.49, 1.10) .015 0.21 (0.06, 0.74) .022 0.66 (0.46, 0.94)
GBF1 rs10748818 G .059 0.77 (0.58‐1.01) .129 0.74 (0.50, 1.09) .075 0.56 (0.30, 1.06) <.001 c 0.41 (0.27, 0.62)
MBNL2 rs4771268 T .015 0.71 (0.54‐0.94) .130 0.74 (0.50, 1.09) .007 0.48 (0.29, 0.82) .015 0.72 (0.55, 0.94)
TRIM40 rs9261484 T .130 1.26 (0.93‐1.70) .039 1.49 (1.02, 2.18) .926 0.96 (0.43, 2.16) .118 1.28 (0.94, 1.75)

Abbreviations: CI, confidence interval;LOPD, late‐onset Parkinson's disease; OR, odds ratio; SNP, single nucleotide polymorphism.

a

Adjusted for age and gender.

b

P value, OR and 95% CI were obtained from risk analysis and refer to the risk allele.

c

The statistical significance remained after using Bonferroni correction.

Bold values are indicate the significant results