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. 2022 Nov 9;23(22):13781. doi: 10.3390/ijms232213781

Table 4.

Lymphotoxin alpha (LTA) and superoxide dismutase 1 (SOD1) and 2 (SOD2) genetic polymorphisms and corresponding genotype frequencies in 172 migraine patients with (n = 38) or without (n = 134) white matter hyperintensities (WMHs).

Genotype Frequencies *
Allele Frequencies Without WMHs With WMHs
Rs SNP Without WMHs With WMHs WT HET HOM WT HET HOM OR (C.I.) AIC p
LTA
rs2071590 C→T 0.61 0.39 0.55 0.45 0.37 0.49 0.14 0.21 0.68 0.11 2.23 (1.04–4.79) 181 0.034
rs2844482 A→G 0.12 0.88 0.14 0.86 0.02 0.20 0.78 0.00 0.29 0.71 1.69 (0.74–3.85) 184 0.22
SOD1
rs2234694 A→C 0.97 0.03 0.87 0.13 0.94 0.06 0.00 0.76 0.21 0.03 4.89 (1.74–13.8) 177 0.003
SOD2
rs4880 C→T 0.51 0.49 0.45 0.55 0.27 0.43 0.30 0.21 0.47 0.32 0.92 (0.42–2.01) 185 0.84

* Eleven patients with cerebrovascular lesions were excluded from the analysis.  p value for SNP association with WMHs in an over-dominant model.  p value for SNP association with WMHs in a dominant model. SNP, single nucleotide polymorphism; WT, wild type; HET, heterozygous; HOM, homozygous; AIC: Akaike information criterion.