Khandaker Golam M, Zammit Stanley, Lewis Glyn, Jones Peter B
Department of Psychiatry, University of Cambridge, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK.
Centre for Mental Health, Addiction and Suicide Research, School of Social and Community Medicine, University of Bristol, UK; Institute of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK.
Neurobiol Stress. 2016 Oct;4:55-61. doi: 10.1016/j.ynstr.2016.02.003.
Animal studies suggest a role of inflammation in the pathophysiology of anxiety, but human studies of inflammatory markers and anxiety disorders are scarce. We report a study of serum C-reactive protein (CRP) and generalised anxiety disorder (GAD) from the general population-based ALSPAC birth cohort.
DSM-IV diagnosis of GAD was obtained from 5365 cohort members during face-to-face clinical assessment at age 16 years, of which 3392 also provided data on serum high sensitivity CRP levels. Logistic regression calculated odds ratio (OR) for GAD among individuals in top and middle thirds of CRP distribution compared with the bottom third. Effect of comorbid depression was assessed. Age, sex, body mass, ethnicity, social class, maternal education, maternal age at delivery, and family history of inflammatory conditions were included as potential confounders.
Forty participants met DSM-IV criteria for GAD (0.74%). CRP levels were higher in GAD cases compared with the rest of the cohort (P = 0.005). After adjusting for potential confounders, participants in the top third of CRP values compared with the bottom third were more likely to have GAD; adjusted OR 5.06 (95% CI, 1.31-19.59). The association between CRP and GAD was consistent with a linear dose-response relationship. The pattern of association between CRP and GAD remained unchanged after excluding cases with co-morbid depression.
The findings are consistent with a role of inflammation in anxiety disorders. Longitudinal studies of inflammatory markers, subsequent anxiety taking into account current and past psychological stress are required to understand this association further.
动物研究表明炎症在焦虑症的病理生理学中起作用,但关于炎症标志物与焦虑症的人体研究较少。我们报告了一项基于人群的阿冯纵向父母与儿童发育研究(ALSPAC)出生队列中血清C反应蛋白(CRP)与广泛性焦虑症(GAD)的研究。
在16岁的面对面临床评估中,从5365名队列成员中获得了GAD的《精神疾病诊断与统计手册》第四版(DSM-IV)诊断,其中3392人还提供了血清高敏CRP水平的数据。逻辑回归计算了CRP分布处于上三分之一和中三分之一的个体与下三分之一个体相比患GAD的比值比(OR)。评估了共病抑郁症的影响。将年龄、性别、体重、种族、社会阶层、母亲教育程度、母亲分娩年龄和炎症性疾病家族史作为潜在混杂因素纳入分析。
40名参与者符合GAD的DSM-IV标准(0.74%)。GAD患者的CRP水平高于队列中的其他成员(P = 0.005)。在调整潜在混杂因素后,CRP值处于上三分之一的参与者与下三分之一相比更有可能患GAD;调整后的OR为5.06(95%可信区间,1.31 - 19.59)。CRP与GAD之间的关联符合线性剂量反应关系。排除共病抑郁症的病例后,CRP与GAD之间的关联模式保持不变。
这些发现与炎症在焦虑症中的作用一致。需要对炎症标志物进行纵向研究,并考虑当前和过去的心理压力对后续焦虑的影响,以进一步了解这种关联。