Title of article :
The Effect of Naltrexone on Memory Deficit Followed by Electroconvulsive
Therapy: A Randomized, Double-Blind, Placebo-Controlled Trial
Author/Authors :
SHAMS JAMAL نويسنده , Jafari Reyhaneh نويسنده Department of Microbiology, Falavarjan Branch, Islamic Azad University, Isfahan, Iran. Jafari Reyhaneh , Zahiroddin Alireza نويسنده Behavioral Science Research Center, Shahid Beheshti
University of Medical Sciences, Tehran, IR Iran , Noorbakhsh Simasadat نويسنده Behavioral Sciences Research Center, Imam Hoseyn Hospital,
Shahid Beheshti University of Medical Sciences, Tehran, IR
Iran , Motazedian Somayeh نويسنده MD, Department of Psychiatry, Dr Ali Shariati Hospital,
Fasa University of Medical Sciences, Fasa, IR Iran , Faghihimohamadi Mohamadmahdi نويسنده M.Sc. Candidate, Behavioral Sciences Research Center,
Shahid Beheshti University of Medical Sciences, Tehran, IR
Iran
Abstract :
Background Electroconvulsive therapy (ECT) is famously known as a
treatment for depression; however, memory impairments have always been a
point of concern. The use of opioid antagonists may protect against the
development of memory deficits after ECT. The current study aimed at
assessing the effect of Naltrexone in diminishing memory impairments.
Methods This randomized, double-blinded, placebo-controlled clinical
trial took place at Imam Hossein hospital of Tehran/Iran. Patients
diagnosed with MDD, were assigned to either Naltrexone or placebo and
received 6 sessions of ECT within 2 weeks. Wechsler Memory Scale was
performed the day before the first session of ECT, as well as 2 weeks, 1
and 3 months after finishing the 6th session. The Hamilton depression
rating scale was performed 2 times to examine the possible interference
caused by depression or to relapse as a confounding variable. Results
Patients receiving Naltrexone and placebo showed no significant
difference in WMS scores. However, after further assessment, changes of
WMS scores in every round were compared; the results showed that after 2
weeks from baseline, the amount of the reduction of total WMS scores
from baseline was significantly lower in the Naltrexone group (P =
0.04). Conclusions This study suggests that Naltrexone as compared to
placebo has no advantageous effect on attenuating memory deficits in the
long term. It is a smaller degree of memory decline that makes
Naltrexone superior to placebo.