Kazmi Narjis, Wallen Gwenyth R, Yang Li, Alkhatib Jenna, Schwandt Melanie L, Feng Dechun, Gao Bin, Diazgranados Nancy, Ramchandani Vijay A, Barb Jennifer J
Translational Biobehavioral and Health Disparities Branch, National Institutes of Health, Clinical Center, Bethesda, MD, United States.
Office of the Clinical Director, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, United States.
Front Psychiatry. 2022 Aug 11;13:931280. doi: 10.3389/fpsyt.2022.931280. eCollection 2022.
High levels of sleep disturbances reported among individuals with alcohol use disorder (AUD) can stimulate inflammatory gene expression, and in turn, may alter pro-inflammatory cytokines levels. We aimed to investigate associations between pro-inflammatory cytokine markers with subjective measures of sleep quality, psychological variables and alcohol consumption among individuals with AUD.
This exploratory study is comprised of individuals with AUD ( = 50) and healthy volunteers ( = 14). Spearman correlation was used to investigate correlations between plasma cytokine levels and clinical variables of interest (liver and inflammatory markers, sleep quality, patient reported anxiety/depression scores, and presence of mood and/or anxiety disorders (DSM IV/5); and history of alcohol use variables.
The AUD group was significantly older, with poorer sleep quality, higher anxiety/depression scores, and higher average drinks per day as compared to controls. Within the AUD group, IL-8 and MCP-1 had positive significant correlations with sleep, anxiety, depression and drinking variables. Specifically, higher levels of MCP-1 were associated with poorer sleep ( = 0.004), higher scores of anxiety ( = 0.006) and depression ( < 0.001), and higher number of drinking days ( = 0.002), average drinks per day ( < 0.001), heavy drinking days ( < 0.001) and total number of drinks ( < 0.001). The multiple linear regression model for MCP-1 showed that after controlling for sleep status and heavy drinking days, older participants ( = 0.003) with more drinks per day ( = 0.016), and higher alkaline phosphatase level ( = 0.001) had higher MCP-1 level.
This exploratory analysis revealed associations with cytokines MCP-1 and IL-8 and drinking consumption, sleep quality, and anxiety and depression in the AUD group. Furthermore, inflammatory and liver markers were highly correlated with certain pro-inflammatory cytokines in the AUD group suggesting a possible relationship between chronic alcohol use and inflammation. These associations may contribute to prolonged inflammatory responses and potentially higher risk of co-morbid chronic diseases.
酒精使用障碍(AUD)患者中报告的高水平睡眠障碍可刺激炎症基因表达,进而可能改变促炎细胞因子水平。我们旨在研究AUD患者中促炎细胞因子标志物与睡眠质量主观测量、心理变量和酒精消费之间的关联。
这项探索性研究由AUD患者(n = 50)和健康志愿者(n = 14)组成。采用Spearman相关性分析来研究血浆细胞因子水平与感兴趣的临床变量(肝脏和炎症标志物、睡眠质量、患者报告的焦虑/抑郁评分以及情绪和/或焦虑障碍(DSM IV/5)的存在情况;以及酒精使用变量的历史记录)之间的相关性。
与对照组相比,AUD组年龄显著更大,睡眠质量更差,焦虑/抑郁评分更高,且每天平均饮酒量更多。在AUD组中,IL-8和MCP-1与睡眠、焦虑、抑郁和饮酒变量呈显著正相关。具体而言,较高水平的MCP-1与较差的睡眠(p = 0.004)、较高的焦虑评分(p = 0.006)和抑郁评分(p < 0.001)以及较多的饮酒天数(p = 0.002)、每天平均饮酒量(p < 0.001)、重度饮酒天数(p < 0.001)和饮酒总量(p < 0.001)相关。MCP-1的多元线性回归模型显示,在控制睡眠状态和重度饮酒天数后,年龄较大的参与者(p = 0.003)、每天饮酒量较多(p = 0.016)以及碱性磷酸酶水平较高(p = 0.001)的参与者MCP-1水平较高。
这项探索性分析揭示了AUD组中细胞因子MCP-1和IL-8与饮酒消费、睡眠质量以及焦虑和抑郁之间的关联。此外,AUD组中的炎症和肝脏标志物与某些促炎细胞因子高度相关,提示慢性酒精使用与炎症之间可能存在关联。这些关联可能导致炎症反应延长,并可能增加共病慢性疾病的风险。