Bao Yulin, Gu Lingfeng, Chen Jiayi, Wang Hao, Wang Zemu, Wang Huijuan, Wang Sibo, Wang Liansheng
Department of Cardiology, Jiangsu Province Hospital and Nanjing Medical University First Affiliated Hospital, Nanjing, Jiangsu, 210029, China.
Department of Immunology, School of Basic Medical Science, Nanjing Medical University, Nanjing, Jiangsu, 211166, China.
J Transl Autoimmun. 2024 Nov 1;9:100259. doi: 10.1016/j.jtauto.2024.100259. eCollection 2024 Dec.
Autoimmune diseases (AIDs) have been associated with various cardiovascular diseases (CVDs) in observational data. However, the causality of these associations remains uncertain. Therefore, a systematic assessment of the impact of AIDS on cardiovascular risk is required.
We assessed the impact of 19 common AIDs on 14 CVDs using bidirectional Mendelian randomization (MR). Celiac disease (odds ratio [OR] = 2.949, 95 % confidence interval [CI]: 1.111-7.827, P = 0.030) and type 1 diabetes mellitus (T1DM) (OR = 1.044, 95 % CI: 1.021-1.068, P = 1.82e-4) were associated with an increased risk of peripheral arterial disease (PAD). Additionally, celiac disease was linked to an increased risk of arrhythmia (OR = 1.008, 95 % CI: 1.002-1.013, P = 0.004), multiple sclerosis to venous thromboembolism (OR = 1.001, 95 % CI: 1.000-1.001, P = 0.010), and psoriasis to heart failure (OR = 1.048, 95 % CI: 1.021-1.077, P = 0.001). Sensitivity analyses were conducted to enhance the robustness of these findings. Predominantly, immune response and inflammation-related pathways were enriched in the aforementioned associations. Mediation analysis identified human leukocyte antigen-DR positive myeloid dendritic cells as partially mediating the effect of T1DM on PAD, with a mediated proportion of 16.61 % (P = 0.028). Potential therapeutic agents, such as tumor necrosis factor-alpha inhibitors and interferon, may have efficacy in treating AID-related CVDs.
This study presents genetic evidence of certain AIDs impacting specific CVDs and identifies potential mediators and drugs.
在观察性数据中,自身免疫性疾病(AIDs)与多种心血管疾病(CVDs)相关。然而,这些关联的因果关系仍不确定。因此,需要对自身免疫性疾病对心血管风险的影响进行系统评估。
我们使用双向孟德尔随机化(MR)评估了19种常见自身免疫性疾病对14种心血管疾病的影响。乳糜泻(优势比[OR]=2.949,95%置信区间[CI]:1.111 - 7.827,P = 0.030)和1型糖尿病(T1DM)(OR = 1.044,95% CI:1.021 - 1.068,P = 1.82e - 4)与外周动脉疾病(PAD)风险增加相关。此外,乳糜泻与心律失常风险增加有关(OR = 1.008,95% CI:1.002 - 1.013,P = 0.004),多发性硬化症与静脉血栓栓塞有关(OR = 1.001,95% CI:1.000 - 1.001,P = 0.010),银屑病与心力衰竭有关(OR = 1.048,95% CI:1.021 - 1.077,P = 0.001)。进行了敏感性分析以增强这些发现的稳健性。主要地,免疫反应和炎症相关途径在上述关联中富集。中介分析确定人类白细胞抗原 - DR阳性髓样树突状细胞部分介导了T1DM对PAD的影响,介导比例为16.61%(P = 0.028)。潜在的治疗药物,如肿瘤坏死因子 - α抑制剂和干扰素,可能对治疗自身免疫性疾病相关的心血管疾病有效。
本研究提供了某些自身免疫性疾病影响特定心血管疾病的遗传证据,并确定了潜在的介导因素和药物。