Abstract

BackgroundEpidermal growth factor (EGF) is implicated in the pathogenesis of schizophrenia, suggesting possible value as a biomarker for disease severity or treatment response. However, basal EGF levels and changes during treatment are inconsistent across studies. The goal of this study is to compare serum EGF in schizophrenia patients before and after treatment with antipsychotics alone or combined with electroconvulsive therapy (ECT).MethodPatients meeting DSM-IV diagnostic criteria for schizophrenia were recruited from June 2013 to December 2015 (n = 186) and followed up after 8 weeks of treatment with antipsychotics alone (n = 119, drug group) or combined with ECT (n = 67, ECT group). Serum EGF levels were measured by ELISA and compared among patients and 74 healthy control subjects. Psychopathology and clinical effects were assessed using the Positive and Negative Syndrome Scale (PANSS).ResultsBasal serum EGF was significantly lower in the entire patient cohort compared to healthy controls (P < 0.05). Repeated-measures ANOVA showed no main effect of time (F = 1.273; P = 0.261), time × group interaction (F = 1.228; P = 0.270), main effect of clinical response (F = 0.191; P = 0.663), or group × clinical interaction (F = 1.765; P = 0.186) on serum EGF. Serum EGF levels did not change significantly following antipsychotic drug or combined therapy (P > 0.05). Additionally, neither basal EGF nor EGF change was associated with the clinical response to drug or combined treatment (P > 0.05). However, baseline serum EGF was weakly associated with PANSS positive score (pretreatment: r = 0.206, posttreatment: r = 0.201) and general symptom score (pretreatment: r = −0.244). Serum EGF was also associated with duration of illness (pretreatment: r = 0.285, posttreatment: r = −0.231).ConclusionsSerum EGF concentration is low in schizophrenia but is unchanged following treatment with antipsychotics alone or combined with ECT, regardless of clinical response. Thus, serum EGF is not a surrogate biomarker for treatment response and is unlikely to be involved in the therapeutic mechanisms of antipsychotics or ECT.

Highlights

  • The cytokine epidermal growth factor (EGF) has been proposed as an important effector molecule in schizophrenia [1,2,3]

  • We measured serum brain derived neurotrophic factor (BDNF) in 160 schizophrenia patients between the ages of 16 and 65 before and after treatment with antipsychotic agents and electroconvulsive therapy (ECT), and we found that both treatments increased serum BDNF [27]

  • Repeated-measures analysis of variance (ANOVA) showed no main effect of time (F = 1.273; P = 0.261), time × group interaction (F =1.228; P =0.270), main effect of clinical response (F = 0.191; P = 0.663), or group × clinical interaction (F = 1.765; P = 0.186) on serum EGF

Read more

Summary

Introduction

The cytokine epidermal growth factor (EGF) has been proposed as an important effector molecule in schizophrenia [1,2,3]. Recent studies have reported the abnormal expression of EGF in Parkinson's disease [11], autism [12, 13], brain injury and limb fracture [14], gastric cancer [15], hepatocellular carcinoma [16, 17], psoriasis [18], endometrial carcinoma [19], and primary ovarian cancer [20]. We speculated that abnormal expression of EGF may contribute to schizophrenia symptoms and (or) treatment efficiency. Epidermal growth factor (EGF) is implicated in the pathogenesis of schizophrenia, suggesting possible value as a biomarker for disease severity or treatment response. The goal of this study is to compare serum EGF in schizophrenia patients before and after treatment with antipsychotics alone or combined with electroconvulsive therapy (ECT)

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call