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类风湿关节炎患者的脑血管风险:来自帕拉塞尔苏斯一万研究中颈动脉粥样硬化的见解。

Cerebrovascular risk in rheumatoid arthritis patients: insights from carotid artery atherosclerosis in the Paracelsus 10,000 study.

作者信息

Ausserwinkler Mathias, Gensluckner Sophie, Frey Vanessa, Gostner Isabella, Paulweber Bernhard, Trinka Eugen, Langthaler Patrick, Datz Christian, Iglseder Bernhard, Thiel Jens, Neumann Hans-Joerg, Flamm Maria, Aigner Elmar, Wernly Bernhard

机构信息

Department of Internal Medicine, Elisabethinen Hospital Klagenfurt, Klagenfurt, Austria.

First Department of Medicine, Paracelsus Medical University, Salzburg, Austria.

出版信息

Rheumatol Int. 2025 Jan 18;45(2):33. doi: 10.1007/s00296-024-05781-4.

Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune disease marked by systemic inflammation. While RA primarily affects the joints, its systemic effects may lead to an increased cerebro- and cardiovascular risk. Atherosclerosis of the carotid arteries is a significant risk factor for cerebrovascular events and serves as a surrogate marker for cardiovascular risk. This study explores the link between RA and carotid artery atherosclerosis with data from the Paracelsus 10,000 Study. Baseline assessments were conducted on individuals randomly selected from Salzburg and its surrounding regions. Participants diagnosed with RA based on ACR-EULAR classification criteria and who underwent carotid artery ultrasound were included. Data were gathered from a total of 9729 participants, among whom 299 were diagnosed with RA. Carotid arteries were examined using ultrasound imaging. The primary endpoint was the difference in the prevalence of plaque presence between the RA and non-RA groups. One univariate (Model I) and three multivariate analyses were conducted, with adjustments in Model II incorporating SCORE 2, while Model III accounted for metabolic syndrome, age and sex. Additionally, Model IV included further adjustments for high-sensitivity C-reactive protein (hs-CRP). Plaque presence was defined as the ultrasound detection of plaque formation larger than 0 mm, regardless of whether it was unilateral or bilateral. Additional assessments included carotid stenosis, intima-media thickness (IMT) and total plaque area (TPA). RA patients had a higher prevalence of plaque (50%) compared to non-RA individuals (38%). The odds ratio (OR) for plaque presence in RA patients versus non-RA individuals was 1.64 (95% CI 1.30-2.06). This association persisted after adjusting for SCORE2, with an adjusted odds ratio (aOR) of 1.65 (95% CI 1.26-2.15). The association remained significant when adjusting for metabolic syndrome, age and sex (aOR = 1.32, 95% CI 1.02-1.72) and also in Model IV, which included further adjustment for hs-CRP (OR = 1.33, 95% CI 1.02-1.74). The findings underscore an increased risk of cerebrovascular disease associated with RA. This study highlights the importance of thorough cerebrovascular and cardiovascular risk assessments, along with proactive management, for RA patients to reduce this risk. Recognizing the substantial impact of RA on stroke and cerebrovascular disease is important for enhancing patient care strategies. Carotid ultrasound appears to be an effective method for atherosclerosis screening in RA patients.

摘要

类风湿关节炎(RA)是一种以全身炎症为特征的慢性自身免疫性疾病。虽然RA主要影响关节,但其全身影响可能导致脑血管和心血管风险增加。颈动脉粥样硬化是脑血管事件的重要危险因素,也是心血管风险的替代标志物。本研究利用帕拉塞尔苏斯万人研究的数据,探讨RA与颈动脉粥样硬化之间的联系。对从萨尔茨堡及其周边地区随机选取的个体进行基线评估。纳入根据美国风湿病学会(ACR)-欧洲抗风湿病联盟(EULAR)分类标准诊断为RA且接受过颈动脉超声检查的参与者。共收集了9729名参与者的数据,其中299人被诊断为RA。使用超声成像检查颈动脉。主要终点是RA组和非RA组斑块存在率的差异。进行了一项单变量分析(模型I)和三项多变量分析,模型II的调整纳入了SCORE 2,而模型III考虑了代谢综合征、年龄和性别。此外,模型IV对高敏C反应蛋白(hs-CRP)进行了进一步调整。斑块存在定义为超声检测到大于0 mm的斑块形成,无论其为单侧还是双侧。额外的评估包括颈动脉狭窄、内膜中层厚度(IMT)和总斑块面积(TPA)。与非RA个体(38%)相比,RA患者的斑块患病率更高(50%)。RA患者与非RA个体相比斑块存在的比值比(OR)为1.64(95%可信区间1.30-2.06)。在对SCORE2进行调整后,这种关联仍然存在,调整后的比值比(aOR)为1.65(95%可信区间1.26-2.15)。在对代谢综合征、年龄和性别进行调整时,这种关联仍然显著(aOR = 1.32,95%可信区间1.02-1.72),在模型IV中也是如此,该模型对hs-CRP进行了进一步调整(OR = 1.33,95%可信区间1.02-1.74)。这些发现强调了与RA相关的脑血管疾病风险增加。本研究强调了对RA患者进行全面的脑血管和心血管风险评估以及积极管理以降低这种风险的重要性。认识到RA对中风和脑血管疾病的重大影响对于加强患者护理策略很重要。颈动脉超声似乎是RA患者动脉粥样硬化筛查的有效方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb26/11742769/4bf3fd688b82/296_2024_5781_Fig1_HTML.jpg

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