Systemic treatment and narrowband ultraviolet B differentially affect cardiovascular risk markers in psoriasis

被引:32
作者
Sigurdardottir, Gunnthorunn [1 ]
Ekman, Anna-Karin [1 ]
Stahle, Mona [2 ]
Bivik, Cecilia [1 ]
Enerback, Charlotta [1 ]
机构
[1] Linkoping Univ, Fac Hlth Sci, Ingrid Asp Psoriasis Res Ctr, Dept Clin & Expt Med, SE-58185 Linkoping, Sweden
[2] Karolinska Inst, Dept Med, Unit Dermatol & Venereol, Stockholm, Sweden
基金
英国医学研究理事会;
关键词
cardiovascular risk; matrix metalloproteinase-9; myeloperoxidase; psoriasis; soluble E-selectin; soluble intercellular adhesion molecule-1; soluble vascular cell adhesion molecule-1; total plasminogen activator inhibitor-1; tumor necrosis factor-alfa inhibitor; ultraviolet B; PLASMINOGEN-ACTIVATOR INHIBITOR-1; ENDOTHELIAL GROWTH-FACTOR; CORONARY-ARTERY-DISEASE; CELL-ADHESION MOLECULES; ANTI-TNF-ALPHA; PATHOGENIC MECHANISMS; MYOCARDIAL-INFARCTION; RHEUMATOID-ARTHRITIS; VASCULAR-DISEASES; THERAPY;
D O I
10.1016/j.jaad.2013.12.044
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Psoriasis is associated with a systemic inflammation and an increased frequency of the metabolic syndrome, both of which are believed to link psoriasis to an increased risk of cardiovascular disease. Objective: The study aimed to investigate the systemic expression of markers of cardiovascular risk and determine their response to ultraviolet B therapy and treatment with the tumor necrosis factor-alfa inhibitor, etanercept. Methods: Six markers of cardiovascular risk were measured in 28 patients with psoriasis and 28 control subjects. Results: Five of the 6 investigated markers were elevated in patients with psoriasis. Four of these correlated to the body mass index and waist-hip ratio, suggesting a link to the metabolic syndrome. Total plasminogen activator inhibitor-1 remained elevated independently of these factors. The levels of the investigated risk markers decreased considerably after tumor necrosis factor-alfa inhibitor treatment but remained unaffected by ultraviolet therapy. Limitations: A relatively limited study population and nonrandomization are limitations. Conclusion: These findings suggest that the choice of treatment in psoriasis may influence the cardiovascular risk in patients with psoriasis and the metabolic syndrome.
引用
收藏
页码:1067 / 1075
页数:9
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