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. 2022 Jun 10;92(6):1606–1612. doi: 10.1038/s41390-022-02132-6

Table 3.

Asymmetric dimethylarginine (ADMA), homocysteine and carotid intima media thickness (CIMT) among the studied groups.

Biomarkers Mean ± SD ANOVA test and P value Post hoc P value
ADMA (μmol/l) P1 < 0.001**
  Valproate-treated patients 4.40 ± 0.75 Test = 630.41 P2 < 0.001**
  Levatiracetam-treated patients 5.56 ± 0.61 P value < 0.001** P3 < 0.001**
  Multidrug-treated patients 5.78 ± 0.62 P4 = 0.06
  Controls 1.27 ± 0.35 P5 < 0.001**
P6 < 0.001**
Homocysteine (μmol/l) P1 = 0.28
  Valproate-treated patients 9.2 ± 1.7 Test = 32.01 P2 = 0.002*
  Levatiracetam-treated patients 8.7 ± 2.1 P value < 0.001** P3 < 0.001**
  Multidrug-treated patients 10.5 ± 3.3 P4 < 0.001**
  Controls 6.4 ± 1.2 P5 < 0.001**
P6 < 0.001**
CIMT (mm) P1 < 0.001**
  Valproate-treated patients 0.33 ± 0.02 Test = 42.88 P2 < 0.001**
  Levatiracetam-treated patients 0.32 ± 0.01 P value < 0.001** P3 < 0.001**
  Multidrug-treated patients 0.35 ± 0.02 P4 < 0.001**
  Controls 0.31 ± 0.02 P5 = 0.09
P6 < 0.001**

P1: valproate-treated patients versus levatiracetam-treated patients; P2: valproate-treated patients versus multidrug-treated patients; P3: valproate-treated patients versus controls; P4: levatiracetam-treated patients versus multidrug-treated patients; P5: levatiracetam-treated patients versus controls; P6: multidrug-treated patients versus controls.

**Highly significant difference.