From the Center for the Prevention of Cardiovascular Disease, Department of Medicine (M.S.G., E.A.F., J.S.B.), New York University School of Medicine, New York.
Leon H. Charney Division of Cardiology, Department of Medicine (M.S.G., T.J.B., S.K., E.A.F., J.S.B.), New York University School of Medicine, New York.
Arterioscler Thromb Vasc Biol. 2019 Apr;39(4):787-798. doi: 10.1161/ATVBAHA.118.312246.
Objective- Psoriasis is an inflammatory skin disease which heightens the risk of cardiovascular disease. This study directly investigated vascular endothelial health and systemically altered pathways in psoriasis and matched controls. Approach and Results- Twenty patients (mean age, 40 years; 50% male) with active psoriasis and 10 age-, sex-matched controls were recruited. To investigate systemically alerted pathways, a deep sequencing omics approach was applied, including unbiased blood transcriptomic and targeted proteomic analysis. Vascular endothelial health was assessed by transcriptomic profiling of endothelial cells obtained from the brachial veins of recruited participants. Blood transcriptomic profiling identified inflammasome signaling as the highest differentially expressed canonical pathway ( Z score 1.6; P=1×10) including upregulation of CASP5 and interleukin ( IL) -1β. Proteomic panels revealed IL-6 as a top differentially expressed cytokine in psoriasis with pathway analysis highlighting IL-1β ( Z score 3.7; P=1.02×10) as an upstream activator of the observed upregulated proteins. Direct profiling of harvested brachial vein endothelial cells demonstrated inflammatory transcript (eg, IL-1β, CXCL10, VCAM-1, IL-8, CXCL1, Lymphotoxin beta, ICAM-1, COX-2, and CCL3) upregulation between psoriasis versus controls. A linear relationship was seen between differentially expressed endothelial inflammatory transcripts and psoriasis disease severity. IL-6 levels correlated with inflammatory endothelial cell transcripts and whole blood inflammasome-associated transcripts, including CASP5 and IL-1β. Conclusions- An unbiased sequencing approach demonstrated the inflammasome as the most differentially altered pathway in psoriasis versus controls. Inflammasome signaling correlated with psoriasis disease severity, circulating IL-6, and proinflammatory endothelial transcripts. These findings help better explain the heightened risk of cardiovascular disease in psoriasis. Clinical Trial Registration- URL: http://www.clinicaltrials.gov . Unique identifier: NCT03228017.
银屑病是一种炎症性皮肤病,会增加心血管疾病的风险。本研究直接研究了银屑病患者和匹配对照者的血管内皮健康和系统性改变的途径。
招募了 20 名(平均年龄 40 岁,50%为男性)活动性银屑病患者和 10 名年龄、性别匹配的对照者。为了研究系统性被激活的途径,应用了一种深度测序组学方法,包括无偏血转录组和靶向蛋白质组分析。通过对招募参与者的肱静脉内皮细胞进行转录组谱分析来评估血管内皮健康。血液转录组谱分析确定炎症小体信号为差异表达最显著的经典途径(Z 分数 1.6;P=1×10),包括 CASP5 和白细胞介素(IL)-1β 的上调。蛋白质组学分析显示,IL-6 是银屑病中差异表达最高的细胞因子,途径分析突出了 IL-1β(Z 分数 3.7;P=1.02×10)作为观察到的上调蛋白的上游激活物。直接分析采集的肱静脉内皮细胞显示炎症转录物(例如,IL-1β、CXCL10、VCAM-1、IL-8、CXCL1、淋巴毒素β、ICAM-1、COX-2 和 CCL3)在银屑病与对照组之间的上调。在银屑病与对照组之间,差异表达的内皮炎症转录物与疾病严重程度之间存在线性关系。IL-6 水平与炎症性内皮细胞转录物和全血炎症小体相关转录物(包括 CASP5 和 IL-1β)相关。
无偏测序方法表明,炎症小体是银屑病与对照组相比差异最显著的途径。炎症小体信号与银屑病疾病严重程度、循环 IL-6 和促炎内皮转录物相关。这些发现有助于更好地解释银屑病患者心血管疾病风险增加的原因。