Abstract
A growing number of studies have shown that brain-derived neurotrophic factor (BDNF) is associated with weight gain during antipsychotic treatment in schizophrenia patients. However, there is still a lack of research results in the initial stage of antipsychotic treatment. This study aimed to evaluate the relationship between weight gain caused by risperidone monotherapy for 12 weeks and BDNF level in antipsychotic-naive and first-episode (ANFE) patients with schizophrenia, and we hypothesize that this may depend on BDNF Val66Met gene polymorphism. In a 12-week longitudinal trial, 225 ANFE patients were enrolled and treated with risperidone. Body weight was measured at baseline and during the 12-week follow-up. After treatment, the average weight of ANFE patients increased by 2.6 kg. Furthermore, we found that in patients with Val/Val genotype, the increase in serum BDNF levels was negatively correlated with risperidone-induced weight gain (r = −0.44, p = 0.008). Regression analysis showed that the baseline BDNF level was a predictor of weight gain after treatment (β = −0.45, t = −3.0, p = 0.005). Our results suggest that the BDNF signaling may be involved in weight gain caused by risperidone treatment. Furthermore, the negative association between weight gain and increased BDNF levels during risperidone treatment in ANFE schizophrenia depends on the BDNF Val66Met polymorphism.
Highlights
Atypical antipsychotics are the first-line treatment strategy for patients with schizophrenia (SZ), which can alleviate clinical symptoms [1]
Several studies have found that some candidate genes are associated with weight gain induced by antipsychotics, such as brain-derived neurotrophic factor (BDNF), FTO, Dopamine receptor D2 (DRD2), serotonin 2A receptor (HTR2A), serotonin 2C receptor (HTR2C), methylenetetrahydrofolate reductase (MTHFR) and pro-inflammatory cytokine [6,7,8]
After 12 weeks of risperidone monotherapy, the weight of ANFE patients with SZ was significantly increased from baseline
Summary
Atypical antipsychotics are the first-line treatment strategy for patients with schizophrenia (SZ), which can alleviate clinical symptoms [1]. Several studies have found that some candidate genes are associated with weight gain induced by antipsychotics, such as brain-derived neurotrophic factor (BDNF), FTO, Dopamine receptor D2 (DRD2), serotonin 2A receptor (HTR2A), serotonin 2C receptor (HTR2C), methylenetetrahydrofolate reductase (MTHFR) and pro-inflammatory cytokine [6,7,8]. These genetic variations contribute to differences in energy expenditure, thermal effects of food, and energy consumption during exercise. The exact mechanism of antipsychotic-induced weight gain in antipsychotic-naive and first-episode (ANFE) SZ patients remains unclear
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