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本文引用的文献

1
Chronic skin-specific inflammation promotes vascular inflammation and thrombosis.慢性皮肤特异性炎症可促进血管炎症和血栓形成。
J Invest Dermatol. 2012 Aug;132(8):2067-75. doi: 10.1038/jid.2012.112. Epub 2012 May 10.
2
Endothelial dysfunction is associated with increased levels of biomarkers in essential hypertension.内皮功能障碍与原发性高血压患者生物标志物水平升高有关。
J Hum Hypertens. 2010 Jun;24(6):373-9. doi: 10.1038/jhh.2009.91. Epub 2009 Nov 26.
3
IL-6 signaling in psoriasis prevents immune suppression by regulatory T cells.银屑病中的白细胞介素-6信号传导可防止调节性T细胞介导的免疫抑制。
J Immunol. 2009 Sep 1;183(5):3170-6. doi: 10.4049/jimmunol.0803721. Epub 2009 Jul 31.
4
Contribution of myeloperoxidase to smoking-dependent vascular inflammation.髓过氧化物酶对吸烟依赖的血管炎症的作用。
Proc Am Thorac Soc. 2008 Dec 1;5(8):820-3. doi: 10.1513/pats.200807-063TH.
5
Abdominal adipose tissue: early metabolic dysfunction associated to insulin resistance and oxidative stress induced by an unbalanced diet.腹部脂肪组织:与不均衡饮食诱导的胰岛素抵抗和氧化应激相关的早期代谢功能障碍。
Horm Metab Res. 2008 Nov;40(11):794-800. doi: 10.1055/s-2008-1081502. Epub 2008 Jul 11.
6
Psoriasis treatment patterns: results of a cross-sectional survey of dermatologists.银屑病治疗模式:皮肤科医生横断面调查结果
J Am Acad Dermatol. 2008 Jun;58(6):964-9. doi: 10.1016/j.jaad.2008.02.048. Epub 2008 Apr 18.
7
Smoking is associated with epicardial coronary endothelial dysfunction and elevated white blood cell count in patients with chest pain and early coronary artery disease.吸烟与胸痛和早期冠状动脉疾病患者的心外膜冠状动脉内皮功能障碍及白细胞计数升高有关。
Circulation. 2007 May 22;115(20):2621-7. doi: 10.1161/CIRCULATIONAHA.106.641654. Epub 2007 May 7.
8
Myeloperoxidase as a marker of increasing systemic inflammation in smokers without severe airway symptoms.髓过氧化物酶作为无严重气道症状吸烟者全身炎症加重的标志物。
Respir Med. 2007 May;101(5):888-95. doi: 10.1016/j.rmed.2006.09.023. Epub 2006 Nov 13.
9
Poor agreement between self-reported and dermatologists' diagnoses for five common dermatoses.对于五种常见皮肤病,自我报告的诊断结果与皮肤科医生的诊断结果之间一致性较差。
Br J Dermatol. 2006 Nov;155(5):1006-12. doi: 10.1111/j.1365-2133.2006.07402.x.
10
Risk of myocardial infarction in patients with psoriasis.银屑病患者发生心肌梗死的风险
JAMA. 2006 Oct 11;296(14):1735-41. doi: 10.1001/jama.296.14.1735.

银屑病与心血管危险因素:皮损中 CD11b(+) CD68(+) 巨噬细胞血清髓过氧化物酶升高及相应免疫细胞过度表达。

Psoriasis and cardiovascular risk factors: increased serum myeloperoxidase and corresponding immunocellular overexpression by Cd11b(+) CD68(+) macrophages in skin lesions.

机构信息

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.

出版信息

Am J Transl Res. 2013 Dec 1;6(1):16-27. eCollection 2013.

PMID:24349618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3853421/
Abstract

BACKGROUND

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.

OBJECTIVES

To elucidate associations between psoriasis and conventional CV risk factors.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

目的

阐明银屑病与传统 CV 危险因素之间的关系。

方法

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。

结果

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。

结论

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。