Murdough Family Center for Psoriasis, Department of Dermatology, University Hospitals Case Medical Center Cleveland, OH, USA ; Case Western Reserve University School of Medicine Cleveland, OH, USA.
Case Western Reserve University Division of Biostatistics Cleveland, OH, USA.
Am J Transl Res. 2013 Dec 1;6(1):16-27. eCollection 2013.
Recent studies report independent associations between psoriasis, cardiovascular (CV) events and risk factors. Blood Myeloperoxidase (MPO) from activated myeloid cells is associated with CV risk mainly through lipid oxidation, induction of endothelial dysfunction and release of IL-12 from macrophages.
To elucidate associations between psoriasis and conventional CV risk factors.
We performed a cross-sectional study of 100 psoriasis patients and 53 controls, group matched on age, gender and body mass index, to assess levels of MPO in serum, as well as immunohistochemical staining from psoriasis skin lesions, psoriasis uninvolved skin, and normal skin.
Although the groups did not differ on waist circumference, glucose, cholesterol, triglycerides, creatinine or personal history of CV events, psoriasis patients had significantly higher waist-to-hip ratios, blood pressures, proportion of current smokers, and lower high density lipoprotein level than controls. Serum MPO level was elevated 2.5 fold (P<0.001) in psoriasis patients, even after adjusting for the CV risk factors on which the groups differed. MPO did correlate with coronary artery calcification, carotid plaque, carotid intima media thickness and flow mediated dilation, but did not correlate with psoriasis severity. However, MPO was highly expressed in lesional psoriatic skin and colocalized predominantly with CD45(+) CD11b(+) leukocytes. CD11b(+) cell density correlated with circulation MPO levels.
Lesional skin CD11b(+) leukocytes activated to generate MPO may contribute to serum levels of MPO. Lesional CD11b(+) cell activity may be an alternative measure of disease burden to PASI that underlies the MPO biomarker for systemic inflammation related to Cardiovascular Disease.
最近的研究报告指出,银屑病与心血管(CV)事件及其危险因素之间存在独立的关联。来自激活的髓样细胞的血液髓过氧化物酶(MPO)主要通过脂质氧化、诱导内皮功能障碍和巨噬细胞释放 IL-12 与 CV 风险相关。
阐明银屑病与传统 CV 危险因素之间的关系。
我们对 100 例银屑病患者和 53 例对照组进行了横断面研究,这些患者在年龄、性别和体重指数上相匹配,以评估血清中 MPO 的水平,以及银屑病皮损、未受累皮肤和正常皮肤的免疫组织化学染色。
尽管两组在腰围、血糖、胆固醇、甘油三酯、肌酐或个人 CV 事件史方面无差异,但银屑病患者的腰围与臀围比、血压、当前吸烟者比例以及高密度脂蛋白水平明显较低。即使在调整了两组存在差异的 CV 危险因素后,银屑病患者的血清 MPO 水平仍升高了 2.5 倍(P<0.001)。MPO 与冠状动脉钙化、颈动脉斑块、颈动脉内膜中层厚度和血流介导的扩张相关,但与银屑病严重程度无关。然而,MPO 在病变性银屑病皮肤中高度表达,并主要与 CD45(+)CD11b(+)白细胞共定位。CD11b(+)细胞密度与循环 MPO 水平相关。
病变皮肤 CD11b(+)白细胞被激活产生 MPO 可能导致血清 MPO 水平升高。病变性 CD11b(+)细胞活性可能是 PASI 疾病负担的替代指标,PASI 是与心血管疾病相关的全身性炎症的 MPO 生物标志物的基础。