医学分子生物学杂志 ›› 2026, Vol. 23 ›› Issue (5): 549-555.doi: 10.3870/j.issn.1672-8009.2026.05.009

• 论著 • 上一篇    下一篇

中重度斑块型银屑病患者血清白介素-17、抗菌肽LL-37水平与颈动脉粥样硬化的关系

赵旭明1, 柴琴琴2, 李亚维1, 景晓蕾1, 刘晓静1, 杨晓静1, 孟昭影1   

  1. 河北北方学院附属第一医院 1皮肤科, 2神经内科 河北省张家口, 075000
  • 收稿日期:2025-12-14 出版日期:2026-09-30 发布日期:2026-09-30
  • 通讯作者: 孟昭影(E-mail:1076502992@qq.com)
  • 基金资助:
    河北省卫生健康委员会医学科学研究课题计划(No.20260800)

Relationship Between Serum Interleukin-17, Cathelicidin Antimicrobial Peptide 37 Levels and Carotid Atherosclerosis in Patients with Moderate-to-Severe Plaque Psoriasis

ZHAO Xuming1, CHAI Qinqin2, LI Yawei1, JING Xiaolei1, LIU Xiaojing1, YANG Xiaojing1, MENG Zhaoying1   

  1. 1Departement of Dermatology, 2Departement of Neurology, the First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei, 075000, China
  • Received:2025-12-14 Online:2026-09-30 Published:2026-09-30
  • Contact: MENG Zhaoying(E-mail:1076502992@qq.com)
  • Supported by:
    Medical Research Program of the Hebei Provincial Health Commission(No.20260800)

摘要: 目的 研究中重度斑块型银屑病患者血清白介素-17(interleukin-17,IL-17)、抗菌肽LL-37 水平与颈动脉粥样硬化的关系。方法 选择2023年6月~2024年12月收治的168例中重度斑块型银屑病患者,检测血清IL-17和LL-37水平。根据颈动脉内膜中层厚度(intima-media thickness,IMT)将患者分为粥样硬化组(IMT≥1.5 mm,n=56)和非粥样硬化组(IMT<1.5 mm,n=112),比较两组患者临床资料及血清IL-17、LL-37的差异,采用Pearson检验分析血清IL-17、LL-37与IMT的相关性,采用logistic回归分析颈动脉粥样硬化的影响因素,采用ROC曲线分析血清指标对颈动脉粥样硬化的诊断价值。结果 粥样硬化组的银屑病皮损面积和严重程度指数及血清低密度脂蛋白胆固醇(low-density lipoprotein cholesterol,LDLC)、C反应蛋白、尿酸、IL-17、LL-37水平高于非粥样硬化组(P<0.05);血清IL-17、LL-37与颈动脉IMT呈显著正相关关系(P<0.05);IL-17升高(OR=1.255)、LL-37升高(OR=1.014)、LDLC升高(OR=13.278)是颈动脉粥样硬化的危险因素(P<0.05);IL-17、LL-37、LDLC诊断颈动脉粥样硬化的曲线下面积分别为0.861、0.848、0.702;IL-17、LL-37诊断颈动脉粥样硬化的曲线下面积高于LDLC(P<0.05),IL-17与LL-37曲线下面积比较的差异无统计学意义(P>0.05)。结论 中重度斑块型银屑病患者血清IL-17、LL-37升高与颈动脉粥样硬化相关,IL-17、LL-37作为颈动脉粥样硬化诊断标志物的诊断效能优于LDLC。

关键词: 中重度斑块型银屑病, 颈动脉粥样硬化, 血清白介素-17, 抗菌肽LL-37, 危险因素

Abstract: Objective To investigate the relationship between serum interleukin-17 (IL-17), cathelicidin antimicrobial peptide LL-37 levels and carotid atherosclerosis in patients with moderate-to-severe plaque psoriasis. Methods A total of 168 patients with moderate-to-severe plaque psoriasis admitted between June 2023 and December 2024 were selected and serum IL-17 and LL-37 levels were measured.According to cartid intima-media thickness(IMT), patients were divided into atherosclerosis group (IMT ≥1.5 mm, n=56) and non-atherosclerosis group (IMT <1.5 mm, n=112). Clinical data and serum IL-17 and LL-37 levels were compared between the two groups. We used Pearson correlation analysis to evaluate the association between serum IL-17, LL-37 levels and IMT. Additionally, logistic regression analysis was applied to determine the factors affecting carotid atherosclerosis. Additionally, receiver operating characteristic (ROC) curve analysis was conducted to evaluate the diagnostic efficacy of serum biomarkers for carotid atherosclerosis. Results The Psoriasis Area and Severity Index score and levels of low-density lipoprotein cholesterol (LDLC), C-reactive protein, uric acid, IL-17 and LL-37 in serum of the atherosclerosis group were higher than those of the non-atherosclerosis group (P<0.05). Serum IL-17 and LL-37 showed significant positive correlations with carotid IMT (P<0.05). Elevated IL-17 (OR=1.255), elevated LL-37 (OR=1.014), and elevated LDLC (OR=13.278) were risk factors for carotid atherosclerosis (P<0.05). The areas under the curve (AUC) of IL-17, LL-37, LDLC for diagnosing carotid atherosclerosis were 0.861, 0.848, 0.702, respectively. The AUCs for IL-17 and LL-37 in diagnosing carotid atherosclerosis were higher than those for LDLC (P<0.05), and there was no statistically significant difference in the AUCs between IL-17 and LL-37 (P>0.05). Conclusion Elevated serum IL-17 and LL-37 levels are associated with carotid atherosclerosis in patients with moderate-to-severe plaque psoriasis. The diagnostic efficacy of IL-17 and LL-37 as diagnostic markers for carotid atherosclerosis is superior to that of LDLC.

Key words: moderate-to-severe plaque psoriasis, carotid atherosclerosis, serum interleukin-17, LL-37, risk factors

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