Anxiety and depression are associated with heightened risk of incident deep vein thrombosis: Mediation through stress‐related neural mechanisms

Abstract Controversy exists as to whether anxiety and depression increase deep vein thrombosis (DVT) risk, and the mechanisms mediating potential links remain unknown. We aimed to evaluate the association between anxiety and depression and DVT risk and determine whether upregulated stress‐related neural activity (SNA), which promotes chronic inflammation, contributes to this link. Our retrospective study included adults ( N = 118 871) enrolled in Mass General Brigham Biobank. A subset ( N = 1520) underwent clinical 18 F‐FDG‐PET/CT imaging. SNA was measured as the ratio of amygdalar to cortical activity (AmygA C ). High‐sensitivity C‐reactive protein (hs‐CRP) and heart rate variability (HRV) were also obtained. Median age was 58 [interquartile range (IQR) 42–70] years with 57% female participants. DVT occurred in 1781 participants (1.5%) over median follow‐up of 3.6 years [IQR 2.1–5.2]. Both anxiety and depression independently predicted incident DVT risk after robust adjustment (HR [95% CI]: 1.53 [1.38–1.71], p < .001; and 1.48 [1.33–1.65], p < .001, respectively). Additionally, both anxiety and depression associated with increased AmygA C (standardized beta [95% CI]: 0.16 [0.04–0.27], p = .007, and 0.17 [0.05–0.29], p = .006, respectively). Furthermore, AmygA C associated with incident DVT (HR [95% CI]: 1.30 [1.07–1.59], p = .009). Mediation analysis demonstrated that the link between anxiety/depression and DVT was mediated by: (1) higher AmygA C , (2) higher hs‐CRP, and (3) lower HRV ( < .05 for each). Anxiety and depression confer an attributable risk of DVT similar to other traditional DVT risk factors. Mechanisms appear to involve increased SNA, autonomic system activity, and inflammation. Future studies are needed to determine whether treatment of anxiety and depression can reduce DVT risk.