[1]马小娜,张 辉,王宏东,等.银屑病患者血浆可溶性尿激酶型纤溶酶原激活物受体(suPAR)与疾病严重程度的关联性研究[J].现代检验医学杂志,2017,32(02):41-44.[doi:10.3969/j.issn.1671-7414.2017.02.011]
 MA Xiao-na,ZHANG Hui,WANG Hong-dong,et al.Correlation between Plasma-soluble Urokinase Plasminogen Activator Receptor(suPAR)Levels and Disease Severity in Psoriasis Patients[J].Journal of Modern Laboratory Medicine,2017,32(02):41-44.[doi:10.3969/j.issn.1671-7414.2017.02.011]
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银屑病患者血浆可溶性尿激酶型纤溶酶原激活物受体(suPAR)与疾病严重程度的关联性研究()
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《现代检验医学杂志》[ISSN:/CN:]

卷:
第32卷
期数:
2017年02期
页码:
41-44
栏目:
论著
出版日期:
2017-03-25

文章信息/Info

Title:
Correlation between Plasma-soluble Urokinase Plasminogen Activator Receptor(suPAR)Levels and Disease Severity in Psoriasis Patients
文章编号:
1671-7414(2017)02-041-04
作者:
马小娜1张 辉1王宏东1韩晓虹1史龙泉1穆 欣2
1.延安大学附属医院皮肤科,陕西延安 716000;
2.西安交通大学第一附属医院皮肤科,西安 710061
Author(s):
MA Xiao-na1ZHANG Hui1WANG Hong-dong1HAN Xiao-hong1SHI Long-quan1MU Xin2
1.Department of Dermatology,Affiliated Hospital of Yan'anUniversity, Shaanxi Yan'an 716000,China;
2.Department of Dermatology, the First Affiliated Hospital of Xi'an Jiaotong University,Xi'an 710061,China
关键词:
银屑病可溶性尿激酶型纤溶酶原激活物受体PASI评分
分类号:
R758.63; R392.11
DOI:
10.3969/j.issn.1671-7414.2017.02.011
文献标志码:
A
摘要:
目的 探索银屑病患者血浆可溶性尿激酶型纤溶酶原激活物受体(suPAR)水平与其疾病严重程度的关联性。方法 选取2013年1月~2015年12月医院就诊的60例银屑病患者(患者组)和60例健康体检者(对照组)。酶联免疫吸附法(ELISA)测定患者组和对照组血浆suPAR水平,Kruskal-Wallis和Mann-Whitney U检验比较血浆suPAR差异。Spearmans's rho分析临床参数与血浆suPAR的相关性。结果 患者组血浆suPAR(3.92±1.04 ng/ml)显著高于对照组(3.03±0.58 ng/ml,Z=13.05,P=0.009)。轻度患者(PASI<10)血浆suPAR(2.67±0.63 ng/ml)显著低于中度(10≤PASI≤20,3.90±1.67 ng/ml,Z=8.00,P=0.035)和重度患者(PASI>20,4.55±1.88 ng/ml,Z=48.5,P=0.031)。患者血浆suPAR与PASI呈正相关(r=0.264,P=0.041)。病程>10年患者(n=35)血浆suPAR(4.43±1.98 ng/ml)显著高于病程<10年患者(n=25,3.41± 0.69 ng/ml,Z=-2.064,P=0.035)。结论 血浆suPAR与银屑病疾病严重程度呈正相关,suPAR可作为银屑病严重程度及疗效评估的指标之一,辅助临床诊断。
Abstract:
Objective To investigate the correlation between plasma-soluble urokinase plasminogen activator receptor(suPAR)levels and disease severity in psoriasis patients.Method 60 psoriasispatients and 60 healthy controls were enrolled from Jan.2013 to Dec.2015 in the hospital.The plasma suPAR of all objects were measured by ELISA.Kruskal-Wallis and Mann-Whitney U test were used to compared plasma suPAR in the difference groups.Correlation between clinical data and plasma suPAR were analyzed by Spearmans's rho method.Result The plasma suPAR of psoriasis patients(3.92±1.74 ng/ml)were higher than controls(3.03±1.08 ng/ml,Z=13.05,P=0.009).The plasma suPAR of mild patients(PASI<10)were lower than moderate patients(10≤PASI≤20, 3.90±1.67 ng/ml,Z=8.00,P=0.035)and severity patients(PASI>20,4.55±1.88 ng/ml,Z=48.5,P=0.031).Positive correlation were found between plasma suPAR and psoriasis area and severity dndex(PASI)score(r=0.264,P=0.041).The plasma suPAR of the patients with disease duration>10 years(n=35,4.43±1.98 ng/ml)were higherthan the patients with disease duration<10 years(n=25,3.41±0.69 ng/ml,Z=-2.064,P=0.035).Conclusion There was a positive correlation between the plasma suPAR and psoriasis disease severity.The Plasma suPAR can be the biomarker of psoriasis disease severity.It facilitate theclinical diagnosis of psoriasis.

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备注/Memo

备注/Memo:
基金项目:陕西省科技攻关项目,项目编号2014K11-02-03-13。
作者简介:马小娜(1975-),女,硕士研究生,副主任医师,研究方向:从事皮肤性病学的临床医疗、教学工作,Tel:13991772860,E-mail:maxiaona197503@163.com。
通讯作者:穆 欣,硕士,主治医师,E-mail:muxin0510@163.com。
更新日期/Last Update: 2017-04-10