Pindolol augmentation of selective serotonin reuptake inhibitors: PET evidence that the dose used in clinical trials is too low

Objective: Positron emission tomography (PET) was used to examine whether t he dose of pindolol used to augment antidepressant medication achieves a si gnificant occupancy of the serotonin type 1A (5-HT1A) autoreceptor in depre ssed patients receiving medication. Method: The authors examined eight depressed patients on one of two regimes of pindolol (2.5 mg t.i.d. and 5.0 mg t.i.d.) with PET and [C-11]WAY-10063 5. Results: The 5-mg t.i.d. regime achieved a modest (19%) but significant occ upancy of the 5-HT1A autoreceptor, while the regime used in the vast majori ty of clinical trials (2.5 mg t.i.d.) did not achieve a significant occupan cy. Conclusions: The dose of pindolol used in clinical trials is suboptimal and may explain the inconsistent results. Therefore, a thorough test of pindol ol's efficacy will necessitate doses higher than those used in present clin ical trials.