ABCB1 C1236T , G2677TA and C3435T Genetic Polymorphisms and Antidepressant Response Phenotypes: Results from a Portuguese Major Depressive Disorder Cohort.
Marlene SantosLuis LimaSerafim CarvalhoAndreia BrandãoFátima BarrosoAgostinho CruzRui MedeirosPublished in: International journal of molecular sciences (2024)
P-glycoprotein (P-GP) is a transporter molecule expressed on the apical surface of capillary endothelial cells of the Blood-Brain Barrier (BBB), whose activity heavily influences drug distribution, including antidepressants. This transporter is encoded by ABCB1 gene, and genetic variations within ABCB1 gene have been proposed to affect drug efflux and have been previously associated with depression. In this context, we aimed to evaluate the role of C1236T , G2677TA and C3435T ABCB1 genetic polymorphisms in antidepressant treatment phenotypes from a cohort of patients harboring Major Depressive Disorder. Patients enrolled in the study consisted of 80 individuals with Major Depressive Disorder, who took part in a 27-month follow-up study at HML, Portugal. To investigate the correlation between ABCB1 polymorphisms and antidepressant response phenotypes, DNA was extracted from peripheral blood, and C1236T , C3435T and G2677TA polymorphisms were genotyped with TaqMan ® SNP Genotyping Assays. Despite the fact that the evaluated polymorphisms ( C1236T , C3435T and G2677TA ) were not associated with treatment resistant depression, or relapse, we observed that patients carrying TT genotype of the C3435T polymorphism remit earlier than the ones carrying CC or CT genotypes (10.2 weeks vs. 14.9 and 21.3, respectively, p = 0.028, Log-rank test). Since we found an association with C3435T and time to remission, and not to the absence of remission, we suggest that this polymorphism could have an impact on antidepressant drug distribution, and thus influence on the time to remission will occur, without influencing the risk of remission itself.
Keyphrases
- major depressive disorder
- bipolar disorder
- end stage renal disease
- ejection fraction
- genome wide
- chronic kidney disease
- newly diagnosed
- endothelial cells
- peripheral blood
- peritoneal dialysis
- depressive symptoms
- magnetic resonance imaging
- high throughput
- disease activity
- systemic lupus erythematosus
- computed tomography
- copy number
- single cell
- circulating tumor
- sleep quality
- genetic diversity
- replacement therapy
- patient reported
- image quality