Inflammatory markers and cognitive deficits in first-episode psychoses - A cross-sectional study

首发精神病患者的炎症标志物和认知缺陷——一项横断面研究

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Abstract

BACKGROUND: The first episode psychosis (FEP) is diagnosed when an individual exhibits signs of psychosis for the first time in a clinical setting. Various studies have observed elevated inflammatory markers such as C-reactive protein (CRP), Interleukin (IL)-6, IL-1B, Tumor Necrosis Factor (TNF) alpha, erythrocyte sedimentation rate (ESR), and neutrophil-lymphocyte ratio (NLR) in FEP. Cognitive deficits manifest early in patients with psychosis and contribute to poor clinical outcomes. Research indicates that cognitive deficits are linked to increased inflammatory biomarkers IL-6, IL1B, TNF-alpha, CRP). AIM: To evaluate the serum levels of inflammatory markers and severity of cognitive impairment in individuals with first-episode psychoses and to identify any potential associations between inflammatory markers and cognitive decline. METHODS: Fifty drug-naïve patients with FEP visiting the department of Psychiatry at a tertiary care hospital were enrolled following permission from the Institutional Ethics Committee. After obtaining informed consent, they were interviewed using a semi-structured proforma and assessed using DSM-5. The Montreal Cognitive Assessment (MoCA) scale and Mini-Mental Status Examination (MMSE) assessed cognitive deficits. CRP, ESR, and NLR levels were measured, and the data collected were tabulated and statistically analyzed. RESULT: Out of 50 participants, 46% had elevated serum CRP levels, and 90% had elevated Neutrophil Lymphocyte Ratio levels well above clinical cut-offs. Most participants had normal ESR levels, and no vital association was seen between raised inflammatory markers and cognitive deficits. CONCLUSION: Patients with First Episode Psychosis had raised levels of inflammatory markers like CRP and NLR. This could be due to neuroinflammation, contributing to the development of psychosis. The study observed cognitive deficits in First Episode Psychosis to be poorly associated with inflammatory markers.

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