Published online Sep 19, 2022. doi: 10.5498/wjp.v12.i9.1169
Peer-review started: February 28, 2022
First decision: April 18, 2022
Revised: April 24, 2022
Accepted: July 22, 2022
Article in press: July 22, 2022
Published online: September 19, 2022
Processing time: 204 Days and 10 Hours
At present, antipsychotic drug therapy has little effect on the improvement of some psychiatric symptoms in schizophrenia patients, and drug therapy is not acceptable due to the unbearable adverse drug reactions. There is growing evidence that repetitive transcranial magnetic stimulation (rTMS) is effective for both positive and negative symptoms of schizophrenia.
Schizophrenia has brought great burden to the whole society with high morbidity and disability rate. The United Kingdom and the United States spend around 2% of GDP each year on the treatment, care and rehabilitation of people with schizophrenia. In particular, long-term hospitalization of patients wastes a large number of medical resources, and the existence of negative symptoms is one of the important reasons for long-term hospitalization of patients. Therefore, the use of rTMS adjuvant therapy to explore the possibility of improving the negative symptoms of patients, to promote the remission of patients, improve the social function and quality of life of patients, has good social and economic benefits.
In this study, we assessed the therapeutic effects and safety of left dorsolateral prefrontal cortex (DLPFC) high-frequency rTMS on negative symptoms of schizophrenia. We evaluated the efficacy of rTMS on recognition in patients with chronic schizophrenia.
This was a randomized, sham-controlled, double-blinded trial. Patients diagnosed with schizophrenia on stable antipsychotic treatment were randomly assigned to active rTMS treatment group (n = 25) or a sham rTMS treatment group (n = 22). 25 patients in the active rTMS group received 10-Hz 110% motor threshold rTMS, while 22 patients were subjected to sham rTMS, both being given 4-wk treatment (5 d/wk). Efficacy of negative symptom was assessed with the Scale for the Assessment of Negative Symptoms (SANS), the Positive and Negative symptom scale (PANSS) at baseline, the end of 4 and 8 wk. The cognitive function was assessed with Cambridge Neuropsychological Test Automated Battery at baseline, the end of 4 and 8 wk. The side effects were assessed with TESS at baseline and the end of 4 wk.
There were no significant differences in pattern recognition memory (PRM) performance metrics, SANS total score, SANS subscores, PANSS total score, and PANSS subscores between active and sham rTMS groups at the end of the 4-wk treatment period, but PRM performance metrics (percent correct and number correct) and changes in these metrics from baseline were significantly greater in the active rTMS group at week 8 compared to the sham group (all P < 0.05). Active rTMS treatment also significantly reduced SANS score at week 8 compared to sham treatment. Moreover, the improvement in visual memory was correlated with the reduction in negative symptoms at week 8. In contrast, there were no between-group differences in PANSS total score and subscale scores at either week 4 or 8 (all P > 0.05).
High-frequency TMS can improve visual memory and reduce negative symptoms in patients with schizophrenia, but these effects are delayed, potentially due to the requirement for extensive neuroplastic changes within DLPFC networks.
In the future, it is necessary to further explore more scientific treatment parameters and more sensitive assessment tools (such as SANS and neuropsychological assessment kits) for rTMS in the treatment of negative symptoms of schizophrenia, and carry out multicenter, large-sample studies.