Posttraumatic stress disorder increases thrombosis risk: Evidence from a biobank data set

IF 10.1 1区 医学 Q1 HEMATOLOGY American Journal of Hematology Pub Date : 2024-08-29 DOI:10.1002/ajh.27468
Hui Chong Lau, Sinead M. Sinnott, Shady Abohashem, Giovanni Civieri, Wesam Aldosoky, Krystel Karam, Maria Khalil, Iqra Qamar, Rachel P. Rosovsky, Michael T. Osborne, Ahmed Tawakol, Antonia V. Seligowski
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Abstract

Depression and anxiety are linked to deep venous thrombosis (DVT) and posttraumatic disorder (PTSD) increases risk of venous thromboembolism in women. However, the mechanisms underlying this relationship remain unknown. We hypothesized that PTSD would associate with increased DVT risk, that neuroimmune mechanisms would mediate the PTSD-DVT link, and that these associations would be stronger in women. This cohort study included N = 106 427 participants from a large biobank. PTSD and DVT were defined using ICD-10 codes. A subset (N = 1520) underwent imaging, from which we assessed stress-associated neural activity (SNA). High-sensitivity C-reactive protein (hs-CRP) levels and heart rate variability (HRV) were used as indicators of systemic inflammation and autonomic activity, respectively. Linear, logistic, and Cox regressions and mediation analyses were used to test our hypotheses. Of 106 427 participants, 4192 (3.9%) developed DVT. PTSD associated with increased DVT risk (HR [95% CI]: 1.66 [1.34, 2.07], p < .001), and this finding remained significant after adjustment for age, sex, and traditional DVT risk factors. When analyzed separately by sex, PTSD was significantly associated with DVT risk in women but not men. Further, heightened SNA and lower HRV mediated the effect of PTSD on DVT risk. Results suggest that individuals with PTSD are at increased risk for DVT, and that risk is higher in women. This relationship was partially driven by alterations in stress-associated neural activity and autonomic function, suggesting potential targets for preventive therapies. Future studies are needed to investigate whether intervening on PTSD-DVT mechanisms has downstream beneficial effects on DVT, especially among women.
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创伤后应激障碍会增加血栓形成风险:来自生物库数据集的证据
抑郁和焦虑与深静脉血栓(DVT)有关,创伤后精神障碍(PTSD)会增加女性静脉血栓栓塞的风险。然而,这种关系的内在机制仍然未知。我们假设创伤后应激障碍会增加深静脉血栓栓塞的风险,神经免疫机制会介导创伤后应激障碍与深静脉血栓栓塞之间的联系,而且这种联系在女性中更为强烈。这项队列研究包括来自一个大型生物库的 106 427 名参与者。创伤后应激障碍和深静脉血栓使用 ICD-10 编码进行定义。一部分人(N = 1520)接受了影像学检查,我们从中评估了压力相关神经活动(SNA)。高敏 C 反应蛋白(hs-CRP)水平和心率变异性(HRV)分别作为全身炎症和自律神经活动的指标。我们使用线性回归、逻辑回归、Cox 回归和中介分析来检验我们的假设。在 106 427 名参与者中,4192 人(3.9%)发生了深静脉血栓。创伤后应激障碍与深静脉血栓风险增加有关(HR [95% CI]:1.66 [1.34, 2.07],p < .001),在对年龄、性别和传统深静脉血栓风险因素进行调整后,这一结果仍然显著。如果按性别单独分析,创伤后应激障碍与女性深静脉血栓风险有显著相关性,但与男性无关。此外,SNA增高和心率变异降低对创伤后应激障碍对深静脉血栓风险的影响具有中介作用。研究结果表明,创伤后应激障碍患者发生深静脉血栓的风险增加,而女性的风险更高。这种关系部分是由应激相关神经活动和自律神经功能的改变引起的,为预防性疗法提供了潜在的目标。未来的研究需要调查干预创伤后应激障碍-深静脉血栓形成机制是否会对深静脉血栓形成产生下游的有益影响,尤其是在女性中。
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来源期刊
CiteScore
15.70
自引率
3.90%
发文量
363
审稿时长
3-6 weeks
期刊介绍: The American Journal of Hematology offers extensive coverage of experimental and clinical aspects of blood diseases in humans and animal models. The journal publishes original contributions in both non-malignant and malignant hematological diseases, encompassing clinical and basic studies in areas such as hemostasis, thrombosis, immunology, blood banking, and stem cell biology. Clinical translational reports highlighting innovative therapeutic approaches for the diagnosis and treatment of hematological diseases are actively encouraged.The American Journal of Hematology features regular original laboratory and clinical research articles, brief research reports, critical reviews, images in hematology, as well as letters and correspondence.
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