OBJECTIVE
To identify pharmacogenetic markers of the effectiveness and safety of sertraline pharmacotherapy at polymorphic loci (−1438G>A, rs6311), (102c>T, rs6313), (1354C/T, rs6314), (rs7997012 G>A) of the HTR2A gene in patients with mixed anxiety-depressive disorder from the Republic of Bashkortostan.
MATERIAL AND METHODS
The study included 100 patients treated with sertraline. The effectiveness and safety of sertraline therapy in patients were assessed using standardized psychometric scales on the day before the start of therapy and then for 42 days. Four polymorphic loci, rs6311, rs6313, rs6314, and rs7997012, of the HTR2A gene were tested using real-time polymerase chain reaction (PCR).
RESULTS
Significant differences in the severity of depressive symptoms were found between carriers of different rs6311 genotypes of the HTR2A gene at the beginning of the study (p<0.05) and on day 42 of the study (p<0.001). More severe depressive symptoms were observed in carriers of the rs6311*A/A (p<0.05) and rs6313*T/T (p<0.001) genotypes. Statistically significant differences were observed between carriers of different rs6311 and rs6313 genotypes of the HTR2A gene in the severity of anxiety symptoms on all study days. More severe anxiety symptoms were observed in carriers of the rs6311*A/A (p<0.001) and rs6313*T/T (p<0.001) genotypes. The rs6311*A/A and rs6313*T/T genotypes can be considered markers of low effectiveness for anxiety and depressive symptoms and markers of risk of adverse reactions (ADRs) when taking sertraline. The rs6314*C/T and rs7997012*G/G genotypes can be considered markers of the ADR risk during sertraline therapy.
CONCLUSION
The study showed that the studied polymorphic variants of the HTR2A gene can be predictors of the effectiveness and safety of sertraline in the treatment of mixed anxiety-depressive disorder.