Table 4. Association of the genetic variants with the adverse events.
Adverse event (n (%)) | Genetic variant |
Genotypic frequencies (n (%)) |
OR (95% CI) | P | |
---|---|---|---|---|---|
Cases | Controls | ||||
Sexual adverse events | ADRB2 16Gly | 14 (56%) | 21 (25%) | 4.58 (1.72–12.20) | 0.002* |
(25 (22.5%)) | SLC6A4 L/S | 6 (25%) | 44 (53.6%) | 0.22 (0.06–0.75) | 0.015 |
Sleepiness (66 (56.7%)) | DRD3 9Gly | 40 (64.5%) | 22 (45.8%) | 2.47 (1.00–6.09) | 0.050 |
EPS (40 (36%)) | DRD3 9Gly | 18 (45%) | 44 (62.8%) | 0.29 (0.11–0.79) | 0.015 |
Weight gain (40 (36%)) | SLC6A4 S/S | 1 (2.7%) | 17 (24.6%) | 0.07 (0.01–0.66) | 0.020 |
Significant findings (*; P<0.003) and non-significant trends (P<0.05) from the genetic association study after adjusting with the potential confounding variables.
*P<0.003.