Key result
First-episode drug-naïve schizophrenia is linked to ~10-fold higher TNF-α levels correlating with negative symptom changes.
Why the study?
The influence of antipsychotic drugs on TNF-α levels and the association between TNF-α and psychotic symptoms in schizophrenia remain unclear.
Do TNF-α levels differ between first-episode drug-naïve schizophrenia patients, chronic patients, and healthy controls, and how do they correlate with psychiatric symptoms before and after risperidone treatment?
Observational (n=217)
No
Do TNF-α levels differ between first-episode drug-naïve schizophrenia patients, chronic patients, and healthy controls, and how do they correlate with psychiatric symptoms before and after risperidone treatment?
Absolute Event Rate: 19% vs 1.98%
p-value: p=<0.001
Increased TNF-α levels in first-episode drug-naïve schizophrenia patients correlate with psychopathology, suggesting a role for inflammatory cytokines in the disease's etiopathogenesis.
TNF-α elevation may link inflammation to negative symptoms in early schizophrenia; hypothesis-generating and requires interventional confirmation.
BACKGROUND: The influence of antipsychotic drugs on tumor necrosis factor-α (TNF-α) levels is unclear, and there is no consensus on the association between TNF-α and psychotic symptoms. This study aimed to investigate the differences in TNF-α levels and clinical correlations in first-episode drug-naïve (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-α levels, were recorded. We used the Positive and Negative Syndrome Scale (PANSS) to measure the psychopathology of all patients. RESULTS: TNF-α 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-α levels of patients with schizophrenia. The TNF-α levels before treatment were significantly positively related to changes in PANSS negative symptoms in FEDN patients. The TNF-α levels in chronic patients were significantly negatively correlated with the general psychopathology subscales and PANSS total scores. CONCLUSIONS: Increased TNF-α 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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Lin et al. (2021) conducted an observational in Schizophrenia (n=217). First-episode drug-naïve schizophrenia vs. Healthy controls and chronic patients was evaluated on Serum TNF-α levels (pg/ml) (p=<0.001). First-episode drug-naïve patients with schizophrenia had significantly higher baseline TNF-α levels compared to healthy controls and chronic patients, which positively correlated with changes in negative symptoms.
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