Elevated C-reactive protein/albumin ratio in patients with methamphetamine use disorder

生物标志物 医学 内科学 甲基苯丙胺 C反应蛋白 逻辑回归 精神科 炎症 生物化学 化学
作者
Ali Baran Tanrıkulu,Hilal Kaya,Zekiye Çatak
出处
期刊:International Journal of Psychiatry in Clinical Practice [Taylor & Francis]
卷期号:27 (4): 351-358
标识
DOI:10.1080/13651501.2023.2237557
摘要

Methamphetamine use disorder causes significant crises, which have individual, familial, and social consequences. Identifying inflammatory biomarkers for methamphetamine use disorder may be useful for following the inflammatory status of patients in clinical assessment. In this study, we aimed to investigate whether neutrophil/lymphocyte ratio (NLR), platelet/lymphocyte ratio (PLR), monocyte/lymphocyte ratio (MLR), C-reactive protein/albumin ratio (CAR) and neutrophil/albumin ratio (NAR) levels can be used as inflammatory biomarkers in methamphetamine use disorder.The sample comprised 139 treatment-seeking participants who met the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria for methamphetamine use disorder and 139 sociodemographically matched controls. Only hospitalised patients were included. An independent sample t-test, Pearson's correlation test, and binominal logistic regression analysis were performed.CAR (p = 0.016) and NAR (p = 0.048) levels were significantly higher in individuals with methamphetamine use disorder when compared with healthy controls. The CAR level was found to be a significant predictor of group membership in regression analysis for methamphetamine use disorder.CAR may be a potential inflammatory biomarker for patients with methamphetamine use disorder. CAR as a relatively easier-to-measure biomarker could be beneficial to follow the inflammatory status and treatment response of patients.This study showed the increased inflammatory response in individuals with methamphetamine use disorder.C- Reactive Protein/Albumin Ratio (CAR) may be a potential inflammatory biomarker in methamphetamine use disorder.CAR may be used to measure the inflammatory status at different phases of treatment and follow treatment response in patients with methamphetamine use disorder.
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