实用医学杂志 ›› 2026, Vol. 42 ›› Issue (13): 2388-2395.doi: 10.3969/j.issn.1006-5725.2026.13.015

• 慢性病防治专栏 • 上一篇    

血清OXCT1与XIRP2联合检测对儿童特应性皮炎病情及预后的评估价值

肖君琳1,2,王贵宾3,刘俊峰2,陈逴凡4,莫秀梅2,陈达灿2(),于晓波3   

  1. 1.广州中医药大学第二临床医学院 (广东 广州 510405 )
    2.广州中医药大学第二附属医院(广东省中医院)皮肤科 (广东 广州 510120 )
    3.蛋白质组学国家重点实验室/北京蛋白质组研究中心/国家蛋白质科学中心·北京(凤凰中心)/军事科学院军事医学研究院生命组学研究所 (北京 102206 )
    4.南方医科大学皮肤病医院(广东省皮肤病医院)中西医结合皮肤科 (广东 广州 520091 )
  • 收稿日期:2026-04-09 出版日期:2026-07-10 发布日期:2026-07-14
  • 通讯作者: 陈达灿 E-mail:4910702@163.com
  • 基金资助:
    广东省中医药防治难治性慢病重点实验室项目(2023KT15528);广东省中医院中医药科学技术研究专项项目(YN2022DB02)

Value of combined detection of serum oxct1 and xirp2 with disease severity and prognosis in children with atopic dermatitis

Junlin XIAO1,2,Guibin WANG3,Junfeng LIU2,Chuofan CHEN4,Xiumei MO2,Dachan CHEN2(),Xiaobo YU3   

  1. 1.The Second Clinical Medical College of Guangzhou University of Chinese Medicine,Guangzhou 510405,Guangdong,China
    2.Department of Dermatology the Second Affiliated Hospital of Guangzhou University of Chinese Medicine( Guangdong Provincial Hospital of Traditional Chinese Medicine),Guangzhou 510120,Guangdong,China
    3.State Key Laboratory of Proteomics,Beijing Proteome Research Center,National Center for Protein Sciences,Beijing Institute of Lifeomics,Beijing 102206,Beijing,China
    4.Department of Integrative Chinese and Western Medicine,Dermatology Hospital of Southern Medical University( Guangdong Provincial Dermatology Hospital),Guangzhou 520091,Guangdong,China
  • Received:2026-04-09 Online:2026-07-10 Published:2026-07-14
  • Contact: Dachan CHEN E-mail:4910702@163.com

摘要:

目的 探究血清3-氧酸辅酶A转移酶1(OXCT1)、含Xin肌动蛋白结合重复序列2(XIRP2)与特应性皮炎患儿病情程度、预后的关系。 方法 选取广东省中医院皮肤科门诊治疗的30例中重度特应性皮炎患儿为观察组,根据病情程度分为中度组(n = 15)和重度组(n = 15);根据治疗12周后预后情况分为预后良好组(n = 20)和预后不良组(n = 10)。同时,选取既往无过敏性疾病病史的30例健康儿童为对照组。采用数据非依赖性质谱法测定受试患儿血清蛋白质组水平,得到OXCT1、XIRP2水平;收集特应性皮炎患儿临床资料和IgE、嗜酸性粒细胞水平。对于特应性皮炎患儿预后不良的影响因素,采用logistic回归分析进行识别与验证;针对血清OXCT1、XIRP2对患儿不良预后的预测作用,通过ROC曲线分析予以评价,分析两者单独及联合预测的临床价值。 结果 观察组血清OXCT1水平与对照组相比显著升高、XIRP2水平显著降低(P 0.05);血清OXCT1水平随着特应性皮炎患儿病情的加重而逐渐升高,XIRP2水平随着特应性皮炎患儿病情的加重而逐渐降低(P 0.05);与预后良好组相比,预后不良组临床资料及IgE、嗜酸性粒细胞差异无统计学意义(P 0.05);血清XIRP2为特应性皮炎患儿预后不良的独立危险因素,而血清OXCT1为预后良好的保护因素(P 0.05);血清OXCT1、XIRP2、二者联合预测特应性皮炎患儿发生预后不良的AUC分别为0.940、0.885、0.945,二者联合预测的AUC高于各指标单独预测的AUC。 结论 特应性皮炎患儿血清OXCT1水平明显升高,而XIRP2水平明显降低,二者可能在疾病发生发展及预后转归过程中发挥不同阶段的生物学作用。其中OXCT1为预后良好的保护因素,而XIRP2为预后不良的危险因素,二者联合对特应性皮炎患儿预后具有较好的预测效能。

关键词: 儿童特应性皮炎, 血清3-氧酸辅酶A转移酶1, 含Xin肌动蛋白结合重复序列2

Abstract:

Objective To explore the relationship between serum 3-oxoacid CoA-transferase 1 (OXCT1), Xin actin-binding repeat-containing protein 2 (XIRP2), and the severity and prognosis of atopic dermatitis (AD) in children. Methods Thirty children with moderate-to-severe AD who were treated at the Dermatology Outpatient Department of Guangdong Provincial Hospital of Chinese Medicine were enrolled in the observation group. According to the severity of their conditions, they were divided into a moderate group (n = 15) and a severe group (n = 15). After 12 weeks of treatment, they were further classified into a good prognosis group (n = 20) and a poor prognosis group (n = 10). Meanwhile, 30 healthy children with no previous history of allergic diseases were selected as the control group. Serum proteomic levels were measured by data-independent acquisition mass spectrometry (DIA-MS) to determine the expression levels of OXCT1 and XIRP2. Clinical data, immunoglobulin E (IgE) levels, and eosinophil counts of the AD children were collected. Logistic regression analysis was used to identify the factors influencing the poor prognosis in children with AD. Receiver operating characteristic (ROC) curve analysis was carried out to evaluate the value of serum OXCT1 and XIRP2, either individually or in combination. Results When compared with the control group, the serum OXCT1 level in the observation group showed a significant increase, and the XIRP2 level presented a significant decrease (P 0.05). Serum OXCT1 levels gradually rose as the disease severity worsened, while serum XIRP2 levels gradually declined (P 0.05). In comparison with the good prognosis group, there were no statistically significant differences in clinical data, IgE levels, or eosinophil counts in the poor prognosis groups (P 0.05). Serum XIRP2 was identified as an independent risk factor for poor prognosis in children with AD, whereas serum OXCT1 was identified as an independent protective factor (P 0.05). The area under the ROC curve (AUC) for poor prognosis was 0.940 for OXCT1, 0.885 for XIRP2, and 0.945 for the combination of both markers. The combined prediction AUC remained higher than that of either marker alone. Conclusions Serum OXCT1 levels were significantly elevated, and XIRP2 levels were significantly decreased in children with atopic dermatitis. These two factors may play biological roles at different stages of disease development and prognosis. OXCT1 functions as a protective factor, whereas XIRP2 serves as a risk factor for poor prognosis. The combined assessment of serum OXCT1 and XIRP2 shows good predictive efficacy for the prognosis of children with atopic dermatitis.

Key words: pediatric atopic dermatitis, 3-oxoacid CoA-transferase 1, Xin actin-binding repeat-containing protein 2

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