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. 2022 Oct 22;4(1):vdac152. doi: 10.1093/noajnl/vdac152

Table 2.

Multivariable Logistic Regression Model with Significant Clinical Risk Factors and Dose Effect of Top SNPs

Characteristics Cases Controls OR 95% Wald CI P-value
No. % No. %
Final Clinical Model (n = 591)
Treatment arm .0243
 TMZ+placebo 54 40.3 239 52.3 1
 TMZ+BEV 80 59.7 218 47.7 1.60 1.06 2.38
Gender <.0001
 Male 52 38.8 308 67.4 1
 Female 82 61.2 149 32.6 2.98 2.00 4.45
Anticonvulsants .0386
 No 29 21.6 133 29.1 1
 Yes 105 78.4 324 70.9 1.65 1.03 2.65
Final Clinical+SNP Model (n = 367)
Treatment arm .0441
 TMZ+placebo 30 36.1 153 53.9 1
 TMZ+BEV 53 63.9 131 46.1 1.82 1.02 3.27
Gender <.0001
 Male 31 37.4 194 68.3 1
 Female 52 62.7 90 31.7 4.45 2.45 8.08
Anticonvulsants .1442
 No 20 24.1 88 31.1 1
 Yes 63 75.9 196 69.0 1.64 0.85 3.18
Top SNPs dose effect, number at-risk alleles Median = 6, IQR = 4–7 Median = 3, IQR = 1–5 1.64 1.43 1.89 <.0001

Abbreviations: BEV, bevacizumab; CI, confidence interval; IQR, inter-quartile range; OR, odds ratio; SNP, single nucleotide polymorphism; TMZ, temozolomide.