May April C, Burrows Kaiping, Figueroa-Hall Leandra K, Kirlic Namik, White Evan J, Smith Ryan, Ekhtiari Hamed, Paulus Martin P, Savitz Jonathan, Stewart Jennifer L
San Diego State University/University of California, San Diego Joint Doctoral Program in Clinical Psychology, San Diego, CA, USA; Department of Psychiatry, University of California, San Diego, San Diego, CA, USA.
Laureate Institute for Brain Research, Tulsa, OK, USA.
Drug Alcohol Depend. 2021 Apr 1;221:108610. doi: 10.1016/j.drugalcdep.2021.108610. Epub 2021 Feb 15.
Substance use disorders (SUD) with comorbid depression and anxiety are linked to poor treatment outcome and relapse. Although some depressed individuals exhibit elevated blood-based inflammation (interleukin-6 [IL-6] and C reactive protein [CRP]), few studies have examined whether the presence of SUD exacerbates inflammation.
Treatment-seeking individuals with major depressive disorder (MDD), anxiety disorders, and/or SUD (N = 160; 80 % with MDD) recruited into the Tulsa 1000 study provided blood samples, participated in clinical interviews, and completed a questionnaire battery querying symptoms of current psychopathology and emotional processing. Analyses followed a multistep process. First, groups were created on the presence versus absence of 1+ lifetime SUD diagnoses: SUD+ (37 F, 43 M) and SUD- (60 F, 20 M). Second, a principal component analysis (PCA) of questionnaire data resulted in two factors, one indexing negative emotionality/withdrawal motivation and one measuring positive emotionality/approach motivation. Third, SUD groups, extracted PCA factors, and nuisance covariates (age, body mass index [BMI], nicotine use, psychotropic medication [and hormone/contraception use in females]) were entered as simultaneous predictors of blood-based inflammation (IL-6, IL-8, IL-10, tumor necrosis factor-α, and CRP).
Within females, SUD + exhibited higher IL-8 and IL-10 but lower CRP levels than SUD-. In contrast, SUD was not associated with biomarker levels in males. Across sexes, higher BMI was linked to higher IL-6 and CRP levels, and within the five biomarkers, IL-6 and CRP shared the most variance.
These findings point to sex-specific inflammatory profiles as a function of SUD that may provide new targets for intervention.
伴有共病性抑郁和焦虑的物质使用障碍(SUD)与治疗效果不佳及复发有关。尽管一些抑郁个体表现出血液炎症指标升高(白细胞介素-6 [IL-6] 和C反应蛋白 [CRP]),但很少有研究探讨SUD的存在是否会加剧炎症。
参与塔尔萨1000研究的寻求治疗的重度抑郁症(MDD)、焦虑症和/或SUD患者(N = 160;80%患有MDD)提供了血液样本,参与了临床访谈,并完成了一系列问卷,询问当前精神病理学症状和情绪加工情况。分析采用多步骤过程。首先,根据是否有1次及以上终身SUD诊断创建分组:SUD+组(37名女性,43名男性)和SUD-组(60名女性,20名男性)。其次,对问卷数据进行主成分分析(PCA)得到两个因素,一个指标为负性情绪/退缩动机,另一个衡量正性情绪/趋近动机。第三,将SUD分组、提取的PCA因素以及干扰协变量(年龄、体重指数 [BMI]、尼古丁使用、精神药物 [女性为激素/避孕药物使用])作为血液炎症指标(IL-6、IL-8、IL-10、肿瘤坏死因子-α和CRP)的同时预测因子。
在女性中,SUD+组的IL-8和IL-10水平高于SUD-组,但CRP水平低于SUD-组。相比之下,SUD与男性的生物标志物水平无关。在所有性别中,较高的BMI与较高的IL-6和CRP水平相关,在这五种生物标志物中,IL-6和CRP的变异度最大。
这些发现表明,SUD导致的炎症特征存在性别差异,这可能为干预提供新的靶点。