Journal
BMC PSYCHIATRY
Volume 21, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s12888-021-03569-5
Keywords
Schizophrenia; TNF-alpha; Inflammatory cytokines; PANSS
Categories
Funding
- Capital's Funds for Health Improvement and Research [2018-2-2131]
- Beijing Municipal Administration of Hospitals Incubating Program [PX2018066]
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This study found that first-episode drug-naive schizophrenia patients had higher TNF-alpha levels before treatment, which were positively correlated with negative symptoms of the disease. In contrast, TNF-alpha levels in chronic patients were negatively correlated with general psychopathology subscales and total scores.
Background: The influence of antipsychotic drugs on tumor necrosis factor-alpha (TNF-alpha) levels is unclear, and there is no consensus on the association between TNF-alpha and psychotic symptoms. This study aimed to investigate the differences in TNF-alpha levels and clinical correlations in first-episode drug-naive (FEDN) patients with schizophrenia before and after treatment and in chronic patients. Methods: A total of 103 (51 FEDN and 52 chronic) patients and 114 healthy controls were recruited. Demographic and clinical data, including TNF-alpha levels, were recorded. We used the Positive and Negative Syndrome Scale (PANSS) to measure the psychopathology of all patients. Results: TNF-alpha levels before treatment were significantly higher in FEDN patients than in chronic patients and healthy controls. No significant sex differences were found in the TNF-alpha levels of patients with schizophrenia. The TNF-alpha levels before treatment were significantly positively related to changes in PANSS negative symptoms in FEDN patients. The TNF-alpha levels in chronic patients were significantly negatively correlated with the general psychopathology subscales and PANSS total scores. Conclusions: Increased TNF-alpha levels in FEDN patients and their correlation with psychopathology indicate that inflammatory cytokines may play a crucial role in the etiopathogenesis of schizophrenia, and inflammation-directed therapy may, therefore, improve negative symptoms.
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