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银屑病患者替代补体途径的组成部分。

Components of the alternative complement pathway in patients with psoriasis.

作者信息

Sereflican Betul, Bugdayci Guler

机构信息

Department of Dermatology, Medical Faculty, Abant İzzet Baysal University, Bolu, Turkey.

Department of Biochemistry, Medical Faculty, Abant İzzet Baysal University, Bolu, Turkey.

出版信息

Acta Dermatovenerol Alp Pannonica Adriat. 2017 Jun;26(2):37-40. doi: 10.15570/actaapa.2017.11.

Abstract

INTRODUCTION

Psoriasis is a chronic inflammatory skin disease. Adipose tissue plays important roles in the events that regulate body metabolism. This study determined the levels of complement 3 ( C3), acylation-stimulating protein (ASP), and adipsin, which take part in the alternate complement pathway, and are synthesized in and secreted by adipose tissue.

METHODS

Thirty-two patients with psoriasis were matched with 22 controls in terms of age, sex, body mass index, and lipid profiles. Serum C3, ASP, and adipsin levels were measured in both groups.

RESULTS

The serum C3 level was higher and ASP and adipsin levels were lower in the patient group, but these differences were not significant (p = 0.708, p = 0.628, and p = 0.218, respectively). ASP and adipsin levels were correlated positively in patients with psoriasis (p = 0.029).

CONCLUSION

To our knowledge, this study is the first to evaluate ASP and adipsin levels in patients with psoriasis. The roles of ASP and adipsin in the etiopathogenesis of psoriasis are unclear. Although not statistically significant, the lower ASP and adipsin levels in the patient group suggest a potential anti-inflammatory role of these proteins in psoriasis. Further studies should examine the relationships between ASP/adipsin and psoriasis.

摘要

引言

银屑病是一种慢性炎症性皮肤病。脂肪组织在调节身体代谢的过程中发挥着重要作用。本研究测定了参与替代补体途径、在脂肪组织中合成并分泌的补体3(C3)、酰化刺激蛋白(ASP)和脂肪酶的水平。

方法

32例银屑病患者与22例对照者在年龄、性别、体重指数和血脂谱方面进行匹配。测量两组患者的血清C3、ASP和脂肪酶水平。

结果

患者组血清C3水平较高,ASP和脂肪酶水平较低,但这些差异无统计学意义(分别为p = 0.708、p = 0.628和p = 0.218)。银屑病患者的ASP和脂肪酶水平呈正相关(p = 0.029)。

结论

据我们所知,本研究首次评估了银屑病患者的ASP和脂肪酶水平。ASP和脂肪酶在银屑病发病机制中的作用尚不清楚。尽管无统计学意义,但患者组较低的ASP和脂肪酶水平提示这些蛋白在银屑病中可能具有抗炎作用。进一步的研究应探讨ASP/脂肪酶与银屑病之间的关系。

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