Wnt5a-a potential factor linking psoriasis to metabolic complications

被引:17
作者
Gerdes, Sascha [1 ]
Laudes, Matthias [2 ,3 ]
Neumann, Katrin [2 ]
Baurecht, Hansjoerg [4 ]
Mrowietz, Ulrich [1 ,3 ]
机构
[1] Univ Med Ctr Schleswig Holstein, Dept Dermatol, Psoriasis Ctr, Kiel, Germany
[2] Univ Med Ctr Schleswig Holstein, Dept Internal Med 1, Kiel, Germany
[3] Univ Med Ctr Schleswig Holstein, Cluster Excellence Inflammat Interfaces, Kiel, Germany
[4] Univ Med Ctr Schleswig Holstein, Dept Dermatol, Kiel, Germany
关键词
comorbidity; obesity; psoriasis; sFRP5; wnt5a; DISEASE; OBESITY; MANAGEMENT; EXPRESSION; SMOKING;
D O I
10.1111/exd.12413
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Psoriasis is associated with comorbidity including obesity, insulin resistance and diabetes mellitus type 2. In obesity, the protein wingless-type MMTV integration site Family, Member 5a (wnt5a) is released from adipose tissue macrophages and was shown to be of importance in the development of insulin resistance. As wnt5a was also shown to be upregulated in psoriatic skin lesions, we investigated whether wnt5a and its counterpart secreted frizzled-related protein 5 are altered in the circulation of lean and obese patients with psoriasis compared with lean and obese healthy volunteers by measuring serum concentrations of both proteins. Our results showed that wnt5a was significantly higher in lean patients with psoriasis (0.096ng/ml; SD 0.12) compared with lean healthy controls (0.020ng/ml; SD 0.04; P0.01) as well as in obese patients (0.177ng/ml; SD 0.14) compared with obese healthy controls (0.011ng/ml; SD 0.03; P0.001). Therefore, we suggest that in psoriasis, an increase in wnt5a may contribute to the development of metabolic comorbidity.
引用
收藏
页码:438 / 440
页数:3
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