SuPAR, a potential inflammatory mediator in psoriasis pathogenesis

被引:2
|
作者
Hamie, Lamiaa [1 ]
Eid, Edward [1 ]
Abbas, Ossama [1 ]
Safi, Remi [2 ]
Nammour, Tarak [3 ]
Tamim, Hani [4 ]
Makki, Maha [4 ]
Stephan, Carla [1 ]
Hasbani, Divina [5 ]
Wehbe, Hisham [5 ]
Ghaoui, Nohra [5 ]
Hawa, Mariana [6 ]
Nasser, Nourhan [1 ]
Eid, Assaad [7 ]
Kibbi, Abdul-Ghani [1 ]
Kurban, Mazen [1 ,2 ]
机构
[1] Amer Univ Beirut, Med Ctr, Dept Dermatol, Beirut, Lebanon
[2] Amer Univ Beirut, Dept Biochem & Mol Genet, Beirut, Lebanon
[3] Amer Univ Beirut, Med Ctr, Dept Gastroenterol, Beirut, Lebanon
[4] Amer Univ Beirut, Clin Res Inst, Med Ctr, Beirut, Lebanon
[5] Amer Univ Beirut, Dept Internal Med, Med Ctr, Beirut, Lebanon
[6] Amer Univ Beirut, Fac Med, Beirut, Lebanon
[7] Amer Univ Beirut, Dept Anat Cell Biol & Physiol, Fac Med, Beirut, Lebanon
关键词
biomarker; epidermis; psoriasis; soluble urokinase plasminogen activator receptor (suPAR); PLASMINOGEN-ACTIVATOR RECEPTOR; METABOLIC SYNDROME; DISEASE; MARKER; RISK;
D O I
10.1111/1440-1681.13365
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Psoriasis is an inflammatory skin disorder that is strongly associated with the metabolic syndrome. The sole reliance on clinical examination to guide prognostication and treatment is insufficient at best; accurate diagnostic and prognostic psoriatic molecular biomarkers are needed. Soluble urokinase plasminogen activator receptor (suPAR) has been implicated in inflammation. The aim of this study is to determine whether suPAR plays a role in the pathogenesis of psoriasis and whether an association exists between suPAR levels, disease severity, and other variables like insulin, erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP). This study also compares the pattern of uPAR staining in healthy vs psoriatic skin: 39 psoriatic and 30 control subjects were included. Two biopsies (affected and unaffected skin) and one biopsy were taken from psoriasis patients and healthy controls, respectively, with uPAR staining of all skin biopsies. Blood samples from all subjects were obtained to determine suPAR, ESR, CRP, and fasting insulin levels. uPAR staining was prominent in unaffected skin from psoriasis patients and healthy individuals vs weak/absent uPAR staining in psoriatic skin. CRP, ESR and suPAR levels were not significantly elevated in the mild psoriasis group compared to healthy controls. The loss of epidermal uPAR is suggestive of its tentative role in the pathogenesis of psoriasis. Patients with mild-moderate psoriasis possibly lack the powerful association attributed to metabolic syndrome in psoriatic patients. Further studies on larger cohorts are needed to ascertain the validity of the mentioned conclusions.
引用
收藏
页码:1705 / 1712
页数:8
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