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抑郁是导致伴有和不伴有心房颤动的患者治疗范围内时间不足和痴呆的驱动力。

Depression as a Driving Force for Low Time in Therapeutic Range and Dementia in Patients With and Without Atrial Fibrillation.

机构信息

Department of Medicine, School of Medicine, University of Utah, Salt Lake City, Utah.

Intermountain Medical Center Heart Institute, Intermountain Medical Center, Murray, Utah.

出版信息

Am J Cardiol. 2021 Aug 15;153:58-64. doi: 10.1016/j.amjcard.2021.05.021. Epub 2021 Jun 25.

DOI:10.1016/j.amjcard.2021.05.021
PMID:34176597
Abstract

Both time in therapeutic range (TTR) for anticoagulation and depression are associated with dementia risk. The purposes of this study were to examine the impact of depression on TTR and to describe the partitioned contribution of depression and TTR on long-term dementia risk. We studied 14,953 patients anticoagulated with warfarin (target INR 2-3) for atrial fibrillation (AF), venous thromboembolism (VTE), or a mechanical heart valve from 2003 to 2015. We excluded patients with a diagnosis of dementia before or within 6 months of warfarin initiation. We examined the association of depression with TTR using finite mixture modeling and logistic regression and utilized multivariable Cox hazard regression to determine the association of TTR and depression with incident dementia at 3 and 13 years. Forty % (n = 6055) of patients were diagnosed with depression before or while on warfarin. Patients with depression had significantly lower TTR and were 1.37 times more likely to have TTR <50% than non-depressed patients (p <0.0001). During follow-up, 4.2% of patients received the diagnosis of dementia within 3 years as compared to 12% during all-time follow up. The 3-year risk of dementia was highest for patients with a ≤50% TTR regardless of depression status. The 3-year dementia risk was associated with TTR (p <0.0001) but not depression. However, for all-time dementia both TTR (p <0.0001) and depression (p <0.0001) as well as their interaction (p = 0.049) were associated with dementia. Depression increased the risk of long-term dementia by 1.69 fold (95% CI: 1.33, 2.15) for patients with the lowest TTR. Depression is prevalent in patients managed with warfarin and is associated with significant decreases in TTR. In conclusion, decreased TTR appears to increase 3-year dementia risk and both low TTR and depression interact to increase risk for all-time dementia in patients taking warfarin.

摘要

抗凝治疗的治疗范围时间(TTR)和抑郁均与痴呆风险相关。本研究的目的是探讨抑郁对 TTR 的影响,并描述抑郁和 TTR 对长期痴呆风险的划分贡献。我们研究了 2003 年至 2015 年间接受华法林抗凝治疗(目标 INR 2-3)的 14953 例房颤(AF)、静脉血栓栓塞(VTE)或机械心脏瓣膜患者。我们排除了在开始使用华法林之前或之后 6 个月内患有痴呆症的患者。我们使用有限混合模型和逻辑回归检查了抑郁与 TTR 的关系,并利用多变量 Cox 风险回归来确定 TTR 和抑郁与 3 年和 13 年时发生痴呆的关系。40%(n=6055)的患者在开始使用华法林之前或使用期间被诊断为抑郁症。与非抑郁患者相比,抑郁患者的 TTR 明显更低,TTR<50%的可能性高 1.37 倍(p<0.0001)。在随访期间,4.2%的患者在 3 年内被诊断为痴呆,而在整个随访期间这一比例为 12%。无论抑郁状态如何,TTR≤50%的患者 3 年痴呆风险最高。TTR(p<0.0001)与抑郁(p<0.0001)与 3 年痴呆风险相关。然而,对于所有时间的痴呆,TTR(p<0.0001)和抑郁(p<0.0001)以及它们的相互作用(p=0.049)都与痴呆相关。对于 TTR 最低的患者,抑郁使长期痴呆的风险增加了 1.69 倍(95%CI:1.33,2.15)。在接受华法林治疗的患者中,抑郁较为普遍,且与 TTR 显著降低相关。总之,TTR 降低似乎会增加 3 年痴呆风险,并且低 TTR 和抑郁相互作用会增加服用华法林的患者发生所有时间痴呆的风险。

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