留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

血清sCD14、HMGB1水平与口腔正畸患者发生交叉感染的关系研究

方敏 邹英 程春 王卿 米丛波

方敏, 邹英, 程春, 王卿, 米丛波. 血清sCD14、HMGB1水平与口腔正畸患者发生交叉感染的关系研究[J]. 中华全科医学, 2024, 22(11): 1833-1836. doi: 10.16766/j.cnki.issn.1674-4152.003744
引用本文: 方敏, 邹英, 程春, 王卿, 米丛波. 血清sCD14、HMGB1水平与口腔正畸患者发生交叉感染的关系研究[J]. 中华全科医学, 2024, 22(11): 1833-1836. doi: 10.16766/j.cnki.issn.1674-4152.003744
FANG Min, ZOU Ying, CHENG Chun, WANG Qing, MI Congbo. Study of the relationship between serum sCD14, HMGB1 levels and cross-infection in orthodontic patients[J]. Chinese Journal of General Practice, 2024, 22(11): 1833-1836. doi: 10.16766/j.cnki.issn.1674-4152.003744
Citation: FANG Min, ZOU Ying, CHENG Chun, WANG Qing, MI Congbo. Study of the relationship between serum sCD14, HMGB1 levels and cross-infection in orthodontic patients[J]. Chinese Journal of General Practice, 2024, 22(11): 1833-1836. doi: 10.16766/j.cnki.issn.1674-4152.003744

血清sCD14、HMGB1水平与口腔正畸患者发生交叉感染的关系研究

doi: 10.16766/j.cnki.issn.1674-4152.003744
基金项目: 

国家自然科学基金项目 8196030305

详细信息
    通讯作者:

    米丛波,E-mail:615776249@qq.com

  • 中图分类号: R783.5  R446

Study of the relationship between serum sCD14, HMGB1 levels and cross-infection in orthodontic patients

  • 摘要:   目的  探究血清可溶性CD14(sCD14)、高迁移率族蛋白B1(HMGB1)水平与口腔正畸患者发生交叉感染的关系及二者对患者发生交叉感染的预测价值。  方法  以新疆医科大学第一附属医院2018年1月—2022年1月收治的183例口腔正畸患者作为研究对象,其中口腔正畸治疗过程发生交叉感染的患者93例作为感染组,未出现交叉感染的患者90例作为对照组。采用ELISA法检测研究对象血清sCD14、HMGB1水平;多因素logistic回归分析研究口腔正畸患者发生交叉感染的影响因素;ROC曲线分析sCD14、HMGB1与口腔正畸患者发生交叉感染的关系。  结果  与对照组相比,感染组血清sCD14、HMGB1表达水平显著升高(P<0.05);高水平血清sCD14、HMGB1是口腔正畸患者发生交叉感染的独立危险因素;血清sCD14、HMGB1预测口腔正畸患者发生交叉感染的AUC分别为0.769、0.783,两者联合预测口腔正畸患者发生交叉感染的AUC为0.886,均高于sCD14、HMGB1单独检测(P<0.001)。  结论  发生交叉感染的口腔正畸患者血清sCD14、HMGB1水平升高,两者联合检测对口腔正畸患者是否发生交叉感染具有一定的预测价值。

     

  • 图  1  血清sCD14、HMGB1预测口腔正畸患者发生交叉感染的ROC曲线

    Figure  1.  ROC curves of serum sCD14 and HMGB1 for predicting cross-infection in orthodontic patients

    表  1  2组口腔正畸患者基本资料比较

    Table  1.   Comparison of baseline data between two groups of orthodontic patients

    组别 例数 性别[例(%)] 年龄
    (x±s,岁)
    BMI
    (x±s)
    Fascin蛋白
    (x±s,pg/mL)
    IGF
    (x±s,pg/mL)
    男性 女性
    对照组 90 43(47.78) 47(52.22) 21.27±6.83 23.65±5.69 6.22±0.74 0.89±0.21
    感染组 93 48(51.61) 45(48.39) 20.54±6.51 23.71±6.11 4.17±0.57 0.65±0.16
    统计量 0.269a 0.740b 0.069b 21.035b 8.714b
    P 0.604 0.460 0.945 <0.001 <0.001
    注:a为χ2值,bt值。
    下载: 导出CSV

    表  2  2组口腔正畸患者血清sCD14、HMGB1表达水平比较(x±s)

    Table  2.   Comparison of serum sCD14 and HMGB1 expression levels between the two groups of orthodontic patients

    组别 例数 sCD14(ng/mL) HMGB1(pg/mL)
    对照组 90 1.76±0.53 258.05±76.32
    感染组 93 3.02±0.97 421.66±142.51
    t 10.854 9.636
    P <0.001 <0.001
    下载: 导出CSV

    表  3  口腔正畸患者血清sCD14、HMGB1水平与Fascin蛋白、IGF的相关性分析

    Table  3.   Correlation analysis of serum sCD14 and HMGB1 levels with Fascin protein and IGF in orthodontic patients

    项目 sCD14 HMGB1
    r P r P
    Fascin蛋白 -0.454 <0.001 -0.503 0.021
    IGF -0.475 <0.001 -0.492 <0.001
    下载: 导出CSV

    表  4  口腔正畸患者发生交叉感染影响因素的多因素logistic回归分析

    Table  4.   Multivariate logistic regression analysis of factors influencing the occurrence of cross-infection in orthodontic patients

    变量 B SE Waldχ2 P OR 95% CI
    sCD14 0.546 0.218 6.269 0.012 1.726 1.126~2.646
    HMGB1 0.934 0.342 7.460 0.006 2.545 1.302~4.975
    Fascin蛋白 -1.124 0.472 5.670 0.017 0.325 0.129~0.820
    IGF -1.802 0.562 10.279 0.001 0.165 0.055~0.496
    下载: 导出CSV
  • [1] MAZGAEEN L, GURUNG P. Recent advances in lipopolysaccharide recognition systems[J]. Int J Mol Sci, 2020, 21(2): 379-396. doi: 10.3390/ijms21020379
    [2] ADEKOYA M N, ADEYEMI T E, AIKINS E A. COVID-19 risks and extra-protective measures practised among Nigerian orthodontists and orthodontic residents[J]. Niger Postgrad Med J, 2021, 28(2): 88-93. doi: 10.4103/npmj.npmj_576_21
    [3] FU Y J, XU B, HUANG S W, et al. Baicalin prevents LPS-induced activation of TLR4/NF-kB p65 pathway and inflammation in mice via inhibiting the expression of CD14[J]. Acta Pharmacol Sin, 2021, 42(1): 88-96. doi: 10.1038/s41401-020-0411-9
    [4] XUE J M, SUAREZ J S, MINAAI M, et al. HMGB1 as a therapeutic target in disease[J]. J Cell Physiol, 2021, 236(5): 3406-3419. doi: 10.1002/jcp.30125
    [5] WANG S M, ZHANG Y. HMGB1 in inflammation and cancer[J]. J Hematol Oncol, 2020, 24, 13(1): 116-120.
    [6] CAI X F, BISWAS I, PANICKER S R, et al. Activated protein C inhibits lipopolysaccharide-mediated acetylation and secretion of high-mobility group box1 in endothelial cells[J]. J Thromb Haemost, 2019, 17(5): 803-817. doi: 10.1111/jth.14425
    [7] 黄芸, 徐宇红. 口腔正畸中牙槽骨高度的研究进展[J]. 新医学, 2020, 51(12): 907-910.

    HUANG Y, XU Y H. Research progress on alveolar bone height in orthodontics[J]. Journal of New Medicine, 2020, 51(12): 907-910.
    [8] 宋生璋, 程楚昕, 阎转君. 老年口腔正畸感染者病原学分布及相关影响因素分析[J]. 实用老年医学, 2020, 34(3): 266-269.

    SONG S Z, CHENG C X, YAN Z J. Analysis of etiology distribution and related influencing factors in elderly patients with orthodontic infection[J]. Practical Geriatrics, 2020, 34(3): 266-269.
    [9] 张智轶, 安峰, 卢成, 等. 正畸治疗中发生口腔伤口感染的相关危险因素及病原学分析[J]. 中国美容医学, 2021, 30(6): 146-150.

    ZHANG Z Y, AN F, LU C, et al. Related risk Factors and Etiology Analysis of Oral Wound Infection During Orthodontics[J]. Chinese Journal of Aesthetic Medicine, 2021, 30(6): 146-150.
    [10] CHENG H C, YEN Y C, MING-FANG YEN A, et al. Factors affecting infection control measures performed by dental workers[J]. J Dent Sci, 2023, 18(2): 722-729. doi: 10.1016/j.jds.2022.11.023
    [11] SHI S, ZHENG H C, ZHANG Z G. Roles of Fascin mRNA expression in colorectal cancer: meta-analysis and bioinformatics analysis[J]. Mol Clin Oncol, 2020, 13(2): 119-128. doi: 10.3892/mco.2020.2069
    [12] 朱利娟, 张立娜. 青少年口腔正畸中微型种植体支抗的应用效果及对骨桥蛋白Fascin蛋白水平的影响[J]. 中国药物与临床, 2021, 21(7): 1120-1122.

    ZHU L J, ZHANG L N. Effectiveness of the application of miniature implant supports in adolescent orthodontics and the effect on the level of Fascin protein, a bone bridging protein[J]. Chinese Remedies & Clinics, 2021, 21(7): 1120-1122.
    [13] KOFFI K A, DOUBLIER S, RICORT J M, et al. The role of GH/IGF axis in dento-alveolar complex from development to aging and therapeutics: a narrative review[J]. Cells, 2021, 10(5): 1181. DOI: 10.3390/cells10051181.
    [14] ALMALKI A, THOMAS J T, ALOTAIBI S, et al. Association between chronological age and IGF-1, IGFBP-3, and CTX levels in saliva of children through younger adult population with varying periodontal status[J]. Children (Basel), 2022, 9(9): 1301-1312.
    [15] MALDEGHEM I V, NUSMAN C M, VISSER D H. Soluble CD14 subtype (sCD14-ST) as biomarker in neonatal early-onset sepsis and late-onset sepsis: a systematic review and meta-analysis[J]. BMC Immunol, 2019, 20(1): 17. DOI: 10.1186/s12865-019-0298-8.
    [16] GÓMEZ-RIAL J, CURRÁS-TUALA M J, RIVERO-CALLE I, et al. Increased serum levels of sCD14 and sCD163 indicate a preponderant role for monocytes in COVID-19 immunopathology[J]. Front Immunol, 2020, 11(1): 560381. DOI: 10.3389/fimmu.2020.560381.
    [17] YANG K, PAN Y, YAN B, et al. Serum sCD14 as a biomarker for significant liver inflammation in chronic hepatitis B patients with normal or mildly elevated ALT[J]. Clin Lab, 2021, 67(10). DOI: 10.7754/Clin.Lab.2021.210130.
    [18] WATANABE M, TOYOMURA T, WAKE H, et al. Cationic ribosomal proteins can inhibit pro-inflammatory action stimulated by LPS+HMGB1 and are hindered by advanced glycation end products[J]. Biotechnol Appl Biochem, 2024, 71(2): 264-271. doi: 10.1002/bab.2538
    [19] FENG Y P, HU S Y, LIU L, et al. HMGB1 contributes to osteoarthritis of temporomandibular joint by inducing synovial angiogenesis[J]. J Oral Rehabil, 2021, 48(5): 551-559. doi: 10.1111/joor.13129
    [20] ZHANG T, WU K Y, MA N, et al. The C5a/C5aR2 axis promotes renal inflammation and tissue damage[J]. JCI Insight, 2020, 5(7): e134081. DOI: 10.1172/jci.insight.134081.
    [21] LAI W X, LI X Y, KONG Q, et al. Extracellular HMGB1 interacts with RAGE and promotes chemoresistance in acute leukemia cells[J]. Cancer Cell Int, 2021, 21(1): 700-720. doi: 10.1186/s12935-021-02387-9
    [22] 胡慧婷, 袁静芝, 史清海, 等. 血清sCD14, HMGB1联合检测在肺部感染疾病中的临床诊断价值[J]. 国际检验医学杂志, 2020, 41(3): 270-273.

    HU H T, YUAN J Z, SHI Q H, et al. Clinical diagnostic value of combined detection of serum sCD14 and HMGB1 in pulmonary infection[J]. International Journal of Laboratory Medicine, 2020, 41(3): 270-273.
  • 加载中
图(1) / 表(4)
计量
  • 文章访问数:  22
  • HTML全文浏览量:  10
  • PDF下载量:  1
  • 被引次数: 0
出版历程
  • 收稿日期:  2024-04-11
  • 网络出版日期:  2024-12-31

目录

    /

    返回文章
    返回