Li Yanfei, Duan Ranran, Gong Zhe, Jing Lijun, Zhang Tian, Zhang Yong, Jia Yanjie
Department of Neurology, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Department of Rehabilitation, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Front Psychiatry. 2021 Nov 18;12:754969. doi: 10.3389/fpsyt.2021.754969. eCollection 2021.
Alcohol dependence, a global public health problem, leads to structural and functional damage in the brain. Alcohol dependence patients present complex and varied clinical manifestations and live with general complaints existing in contemporary society, making most people with alcohol dependence hard to identify. Therefore, it is important to find potential biomarkers for the diagnosis and evaluation of alcohol dependence. In the study, we explored potential biomarkers for the diagnosis and monitoring of diseases and evaluated brain structural changes in alcohol dependence patients. Enzyme-linked immunosorbent assay (ELSA) was employed to detect the expression of serum nucleotide-binding oligomerization domain containing 3 (NLRP3) and single-molecule array (Simoa) assay was used to detect the expression of serum neurofilament light (NfL) in 50 alcohol dependence patients and 50 controls with no drinking history. Alcohol consumption was measured by standard drinks. Neuropsychological assessments, including the Montreal cognitive assessment (MoCA), Pittsburgh sleep quality index (PSQI), generalized anxiety disorder (GAD-7), and patient health questionnaire-9 (PHQ-9), were conducted to evaluate cognitive function and psychological state. The degree of white matter lesions (WMLs) was rated using the Fazekas scale based on magnetic resonance imaging analysis. White matter structure was quantified using the voxel-based morphometry method. The correlations between NLRP3 levels, NfL levels, neuropsychological dysfunction, the degree of WMLs, and white matter volume (WMV) were analyzed in alcohol dependence patients. Serum NLRP3 and NfL levels were higher in the alcohol dependence group. NLRP3 levels were irrelevant to monthly alcohol assumption as well as to the MoCA, PSQI, GAD-7, PHQ-9, and Fazekas scale scores and WMV. NfL levels were positively correlated with the PSQI and PHQ-9 scores as well as the degree of WMLs and negatively correlated with the MoCA scores and WMV. No associations were evident between NfL and monthly alcohol assumption and GAD-7 scores in the alcohol dependence group. This study supports the potential value of serum NfL as a non-invasive biomarker in alcohol dependence. The association with neuropsychological dysfunction and degree of WMLs has implications to use NfL as a promising biomarker to assess the severity of brain damage as well as the progression and prognosis of alcohol dependence.
酒精依赖是一个全球性的公共卫生问题,会导致大脑的结构和功能损伤。酒精依赖患者表现出复杂多样的临床表现,且伴有当代社会普遍存在的不适症状,这使得大多数酒精依赖者难以被识别。因此,寻找用于酒精依赖诊断和评估的潜在生物标志物具有重要意义。在本研究中,我们探索了用于疾病诊断和监测的潜在生物标志物,并评估了酒精依赖患者的脑结构变化。采用酶联免疫吸附测定(ELSA)检测50例酒精依赖患者和50例无饮酒史对照者血清中含核苷酸结合寡聚化结构域3(NLRP3)的表达,并用单分子阵列(Simoa)测定法检测血清神经丝轻链(NfL)的表达。饮酒量通过标准饮酒量来衡量。进行了包括蒙特利尔认知评估(MoCA)、匹兹堡睡眠质量指数(PSQI)、广泛性焦虑障碍(GAD - 7)和患者健康问卷9项(PHQ - 9)在内的神经心理学评估,以评估认知功能和心理状态。基于磁共振成像分析,使用 Fazekas量表对白质病变(WMLs)程度进行评分。采用基于体素的形态测量法对白质结构进行量化。分析了酒精依赖患者中NLRP3水平、NfL水平、神经心理功能障碍、WMLs程度和白质体积(WMV)之间的相关性。酒精依赖组血清NLRP3和NfL水平较高。NLRP3水平与每月饮酒量以及MoCA、PSQI、GAD - 7、PHQ - 9和Fazekas量表评分及WMV均无关。NfL水平与PSQI和PHQ - 9评分以及WMLs程度呈正相关,与MoCA评分和WMV呈负相关。在酒精依赖组中,NfL与每月饮酒量和GAD - 7评分之间无明显关联。本研究支持血清NfL作为酒精依赖中非侵入性生物标志物的潜在价值。其与神经心理功能障碍和WMLs程度的关联意味着可将NfL作为一种有前景的生物标志物,用于评估脑损伤的严重程度以及酒精依赖的进展和预后。