Tian Xiaoyuan, Yang Xianglin, Cao Ying, Qu Zhenan, Zhang Bocheng
Department of Orthopaedics, Second Affiliated Hospital, Dalian Medical University, Dalian, China.
Department of Orthopaedics, Affiliated Zhongshan Hospital, Dalian University, Liaoning, Dalian, China.
Front Immunol. 2025 Aug 19;16:1590483. doi: 10.3389/fimmu.2025.1590483. eCollection 2025.
To investigate the association between depression and cardiovascular disease (CVD) risk in arthritis patients and evaluate the modifying role of systemic inflammation.
Using data from the China Health and Retirement Longitudinal Study (CHARLS), we conducted a prospective cohort analysis of 2,571 arthritis patients without baseline CVD. Depression severity was assessed using the 10-item CES-D scale, with scores ≥12 defining depression. Multivariable logistic regression and restricted cubic spline (RCS) models analyzed dose-response relationships. We utilized C-reactive protein (CRP) to assess whether inflammatory status in arthritis patients modify this relationship. Sensitivity analyses included multiple imputation and complete-case approaches.
Each 1-point increase in CES-D score elevated CVD risk by 2.8% (OR=1.028, 95% CI 1.012-1.044). High inflammation amplified CVD risk exclusively in depressed patients (OR=1.52 vs. OR=1.32 in low-inflammation depressed group), with no significant association in non-depressed individuals. Diabetes mellitus synergistically intensified this relationship (OR=2.83 in diabetic vs. OR=1.21 in non-diabetic depressed patients, P = 0.03 for interaction). Results remained robust across sensitivity analyses.
Depression linearly increases CVD risk in arthritis patients, with systemic inflammation selectively potentiating this association in depressed individuals. The diabetes-depression-CVD interaction highlights shared pathophysiological pathways. These findings underscore the imperative for integrated clinical strategies targeting both psychological health and inflammatory pathways to reduce cardiovascular morbidity in arthritis populations.
探讨关节炎患者抑郁与心血管疾病(CVD)风险之间的关联,并评估全身炎症的调节作用。
利用中国健康与养老追踪调查(CHARLS)的数据,我们对2571例无基线CVD的关节炎患者进行了前瞻性队列分析。使用10项CES-D量表评估抑郁严重程度,得分≥12定义为抑郁。多变量逻辑回归和受限立方样条(RCS)模型分析剂量反应关系。我们利用C反应蛋白(CRP)评估关节炎患者的炎症状态是否会改变这种关系。敏感性分析包括多重插补和完整病例法。
CES-D评分每增加1分,CVD风险升高2.8%(OR=1.028,95%CI 1.012-1.044)。高炎症仅在抑郁患者中增加CVD风险(高炎症抑郁组OR=1.52,低炎症抑郁组OR=1.32),在非抑郁个体中无显著关联。糖尿病协同增强了这种关系(糖尿病抑郁患者OR=2.83,非糖尿病抑郁患者OR=1.21,交互作用P=0.03)。敏感性分析结果保持稳健。
抑郁使关节炎患者的CVD风险呈线性增加,全身炎症在抑郁个体中选择性地增强了这种关联。糖尿病-抑郁-CVD相互作用突出了共同的病理生理途径。这些发现强调了针对心理健康和炎症途径的综合临床策略对于降低关节炎人群心血管发病率的必要性。