Department of Anatomy, School of Medicine, Iranshahr University of Medical Sciences, Iranshahr, Iran.
Department of Law, Hatef Higher Education Institute, Zahedan, Iran.
Subst Abuse Treat Prev Policy. 2024 Jan 20;19(1):9. doi: 10.1186/s13011-024-00591-0.
Crack heroin is a novel opiate derivative with highly addictive properties and unfamiliar health consequences. It causes a variety of brain dysfunctions that are mediated by neurochemical alterations and abnormal neuroplasticity. Brain-derived neurotrophic factor (BDNF) is a widely recognized biological marker implicated in the neuropathology of substance use during substance use disorder and withdrawal. Its involvement can significantly contribute to the severity of withdrawal symptoms. Hence, this study aimed to evaluate BDNF levels in crack heroin users before and after withdrawal.
In this cross-sectional study, 148 male participants were recruited and divided into two groups: persons with crack heroin use disorder (n = 74) and the controls (n = 74). The BDNF serum levels were measured in both crack heroin users and control groups upon hospitalization and again after twenty-one days of withdrawal using the enzyme-linked immunosorbent assay.
The results demonstrated that BDNF levels in persons with crack heroin use disorder upon admission were significantly lower than the levels observed upon discharge and in the control group (p < 0.05). Additionally, a significant difference in BDNF levels was found between persons with crack heroin use disorder at admission and discharge (p = 0.038). Furthermore, BDNF levels showed an inverse correlation with the daily dose of substance use (r= -0.420, p = 0.03) and the duration of crack heroin use (r= -0.235, p = 0.001).
A progressive increment in BDNF levels during early detoxification is associated with the daily amount of substance use and the duration of substance use. Our findings suggest that changes in BDNF serum levels during crack heroin use disorder and withdrawal could serve as potential biomarkers for assessing the intensity of withdrawal symptoms and substance use-related behaviors.
冰毒是一种新型阿片类衍生物,具有高度成瘾性和不熟悉的健康后果。它会导致各种大脑功能障碍,这些功能障碍是由神经化学改变和异常神经可塑性介导的。脑源性神经营养因子(BDNF)是一种广泛认可的生物学标志物,与物质使用障碍期间和戒断期间的物质使用的神经病理学有关。其参与可以显著导致戒断症状的严重程度。因此,本研究旨在评估戒断前后冰毒使用者的 BDNF 水平。
在这项横断面研究中,招募了 148 名男性参与者,并将他们分为两组:冰毒使用障碍者(n=74)和对照组(n=74)。使用酶联免疫吸附试验,在住院期间和戒断 21 天后,分别测量两组冰毒使用者和对照组的 BDNF 血清水平。
结果表明,入院时冰毒使用者的 BDNF 水平明显低于出院时和对照组的水平(p<0.05)。此外,入院时和出院时冰毒使用者的 BDNF 水平也存在显著差异(p=0.038)。此外,BDNF 水平与物质使用的每日剂量呈负相关(r=-0.420,p=0.03),与冰毒使用的持续时间呈负相关(r=-0.235,p=0.001)。
早期解毒过程中 BDNF 水平的逐渐增加与物质使用的每日剂量和持续时间有关。我们的发现表明,BDNF 血清水平在冰毒使用障碍和戒断期间的变化可以作为评估戒断症状严重程度和物质使用相关行为的潜在生物标志物。