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. 2020 Aug 31;29(4):198–201. doi: 10.1136/ejhpharm-2020-002367

Table 3.

Effects of the CYP2C19 and CYP2C9 genotypes on standardised VPA concentrations in the patients with epilepsy

Genotypes N (%) Mean age
(years)
Mean VPA dose
(mg/kg per day)
Mean VPA concentration
(μg/mL)
CDRV
(μg·kg/mL·mg)
P value
CYP2C19 G681A/ G636A
EMs* 37 (44.6%) 50.70±17.91 16.28±7.50 48.73±24.08 3.33±1.78 EMs vs IMs p=0.013§
EMs vs PMs p=0.000§
IMs vs PMs
p=0.000§
IMs† 33 (39.8%) 48.73±19.05 12.80±5.02 57.15±25.07 4.45±1.42
PMs‡ 13 (15.6%) 51.15±24.62 11.54±3.12 75.55±25.58 6.64±1.06
CYP2C9 T269C
Non-carriers¶ 75 49.72±22.98 14.14±6.50 56.21±26.40 4.08±1.97 p=0.809††
Carriers** 8 52.50±17.17 14.25±4.52 56.92±24.64 3.91±0.99

*EM: extensive metaboliser genotype: CYP2C19 *1/*1.

†IM intermediate metaboliser genotype: CYP2C19 *1/*2 (n=31) and CYP2C19 *1/*3 (n=2).

‡Poor metabolizer genotype: CYP2C19 *2/*2 (n=11), CYP2C19 *3/*3 (n=1) and CYP2C19 *2/*3 (n=1).

§Games–Howell test, mean difference is significant at the 0.05 level.

¶Non-carriers: CYP2C9*1/*1.

**Carriers: *1/*13 (n=7) and *13/*13 (n=1).

††Independent sample t-test, mean difference is significant at the 0.05 level.

EMs, extensive metabolisers; IMs, intermediate metabolisers; PMs, poor metabolisers; VPA, valproic acid.