Abstract

BackgroundCardiovascular disease (CVD) risk factors such as dyslipidemia and systemic aberrant inflammatory processes may occur in patients with psychotic disorders, which may cause increased mortality. The interplay between immune and metabolic markers and its contribution to the clinical symptoms of schizophrenia (SCZ) remain unclear. This study aimed to examine the association of a series of inflammatory factors, plasma biochemical indicators, and SCZ clinical symptomatology with the severity of SCZ symptoms.MethodsA total of 115 participants, including 79 first-episode drug-naïve patients with SCZ and 36 healthy controls, were enrolled in this study. Semi-structured interviews were used to collect sociodemographic data, family history of SCZ, and medical and psychiatric history. The Brief Psychiatric Rating Scale (BPRS) and the Positive and Negative Syndrome Scale (PANSS) were administered by a clinical psychiatrist to evaluate the symptom severity of patients with SCZ. Plasma inflammatory cytokines were measured by a fully automated electrochemiluminescent immunoassay (Meso Scale Discovery).ResultsBlood routine, biochemical, and inflammation cytokine test results showed that the levels of white blood cell count, neutrophil count, natrium, CRP, IL-8, IL-6, IL-13, and IL-16 significantly increased in the case group than in the healthy controls (p < 0.05), whereas levels of red blood cell count, hemoglobin concentration, mean corpuscular hemoglobin concentration, total protein, albumin, total bile acid, high-density lipoprotein (HDL), apolipoprotein A1, blood urea nitrogen, kalium and IL-15 were lower than in the healthy controls (p < 0.05). Correlation network analysis results shown that the natrium, HDL and red blood cell count were the top 3 factors closely to with BPRS and PANSS related clinical symptoms among of correlation network (degree = 4). ROC curve analysis explored the IL-16, IL-8, IL-13, IL-15, natrium, and HDL had highly sensitivity and specificity to the predictive validity and effectiveness for SCZ symptoms.ConclusionOur study revealed a complex interactive network correlation among the cardiovascular risk factors, biological immunity profiles, and psychotic symptoms in first-episode patients. Abnormal inflammatory factors and CVD risk factors had high sensitivity and specificity for predicting SCZ symptoms. Generally, our study provided novel information on the immune-related mechanisms involved in early CVD risk in patients with psychotic disorders.

Highlights

  • Schizophrenia (SCZ) is a chronic mental illness with a lifetime prevalence of nearly 1% of the world population [1]

  • We found that hemoglobin concentration, mean corpuscular hemoglobin concentration, red blood cell count, high-density lipoprotein (HDL), total bile acid, total protein, albumin, apolipoprotein A1, blood urea nitrogen, and kalium were lower in the case group than in the healthy controls (Figures 1A–C,F–L, respectively; p < 0.05)

  • Results showed that the plasma levels of C-reactive protein (CRP), IL-8, IL-16, IL-6, IL-13, IL-10, and IL-15 significantly increased in the case group than in the healthy controls (Figures 1N–R,T,U, respectively; p < 0.05), whereas IL-7 levels were significantly lower than in the healthy controls (Supplementary Figure 1; p < 0.05)

Read more

Summary

Introduction

Schizophrenia (SCZ) is a chronic mental illness with a lifetime prevalence of nearly 1% of the world population [1]. Numerous pathophysiological processes have been identified in SCZ, including immune-mediated responses, biochemical metabolism, and white blood cell (WBC) count. These anomalous phenomena can be considered as risk factors for disease progression. Previous studies have shown heterogeneous features for immune dysfunction in SCZ, leading to difficulty in determining the clear biological markers in this patient group [8, 9]. These conditions pose a great challenge to clinicians to use the biological markers as guiding tools in the clinical evaluation of psychosis together with metabolic syndromes. This study aimed to examine the association of a series of inflammatory factors, plasma biochemical indicators, and SCZ clinical symptomatology with the severity of SCZ symptoms

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

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