• 国家药监局综合司 国家卫生健康委办公厅
  • 国家药监局综合司 国家卫生健康委办公厅

外周血miR-145-5p、miR-223表达与慢性阻塞性肺疾病合并肺结核患者治疗应答及预后的相关性

通讯作者: 陈臻, w15722907113@163.com
DOI:10.12201/bmr.202604.00163
声明:预印本系统所发表的论文仅用于最新科研成果的交流与共享,未经同行评议,因此不建议直接应用于指导临床实践。

Correlation between the Expression of Peripheral Blood miR-145-5p and miR-223 and Treatment Response and Prognosis in Patients with Chronic Obstructive Pulmonary Disease Complicated with Pulmonary Tuberculosis

Corresponding author: Chen Zhen, w15722907113@163.com
  • 摘要:目的? 探讨慢性阻塞性肺疾病(COPD)合并肺结核(PTB)患者外周血微小RNA-145-5p(miR-145-5p)、微小RNA-223(miR-223)表达水平与治疗应答及预后的相关性。方法? 选取2022年3月—2024年3月于该院就诊的COPD合并PTB患者180例作为研究组,另选取同期COPD患者60例、PTB患者60例及健康体检者60例作为对照队列。采用实时荧光定量聚合酶链反应PCR检测所有研究对象基线期外周血miR-145-5p、miR-223表达水平,研究组患者在治疗3个月、6个月动态检测上述指标。比较研究组不同治疗应答及预后结局患者的miR-145-5p、miR-223表达水平,采用受试者工作特征(ROC)曲线分析miR-145-5p、miR-223表达水平对COPD合并PTB患者治疗应答的预测价值,采用多因素Logistic回归分析COPD合并PTB患者预后的影响因素。结果? 研究组基线期外周血 miR-145-5p表达水平显著低于COPD 组、PTB组及健康对照组(P<0.05),miR-223表达水平显著高于上述三组(P<0.05)。治疗6个月后,研究组中治疗有效126例(有效组),治疗无效54例(无效组);有效组治疗后各时间节点miR-145-5p表达水平逐渐升高,miR-223表达水平逐渐降低(P<0.05),无效组上述指标无明显变化(P>0.05)。基线期miR-145-5p联合miR-223预测治疗应答的曲线下面积(AUC)为0.842(95% CI:0.778~0.905),灵敏度88.1%,特异度78.3%,优于单一指标。2年随访期间,研究组复发28例,死亡16例,预后不良组(复发或死亡)基线期miR-145-5p表达更低、miR-223表达更高(P<0.05)。多因素Logistic回归分析显示,基线期miR-145-5p低表达、miR-223高表达、肺结核病灶范围(多肺叶)、IL-6及CRP水平升高是COPD合并PTB患者预后不良的独立危险因素(P<0.05)。结论? COPD合并PTB患者外周血miR-145-5p呈低表达、miR-223呈高表达,二者联合检测可作为评估患者治疗应答及预后的潜在生物标志物,为临床个体化治疗及预后管理提供参考。

    关键词: 慢性阻塞性肺疾病肺结核微小RNA-145-5p微小RNA-223治疗应答预后

     

    Abstract: Objective? To investigate the correlation between the expression levels of peripheral blood microRNA-145-5p (miR-145-5p) and microRNA-223 (miR-223) and treatment response and prognosis in patients with chronic obstructive pulmonary disease (COPD) complicated with pulmonary tuberculosis (PTB).Methods? A total of 180 patients with COPD complicated with PTB treated in this hospital from March 2022 to March 2024 were enrolled as the study group. Meanwhile, 60 COPD patients, 60 PTB patients and 60 healthy subjects during the same period were selected as the control cohort. Quantitative real-time polymerase chain reaction (qRT-PCR) was applied to detect the baseline expression levels of peripheral blood miR-145-5p and miR-223 in all subjects, and the above indicators were dynamically measured in the study group at 3 and 6 months of treatment. The expression levels of miR-145-5p and miR-223 were compared among patients with different treatment responses and prognostic outcomes in the study group. Receiver operating characteristic (ROC) curve was used to analyze the predictive value of miR-145-5p and miR-223 expression levels for treatment response in patients with COPD complicated with PTB. Multivariate Logistic regression analysis was performed to explore the influencing factors for prognosis in these patients.Results? The baseline expression level of peripheral blood miR-145-5p in the study group was significantly lower than that in the COPD group, PTB group and healthy control group (P<0.05), while the expression level of miR-223 was significantly higher than that in the three groups above (P<0.05). After 6 months of treatment, 126 patients in the study group achieved effective treatment (effective group) and 54 had ineffective treatment (ineffective group). In the effective group, the expression level of miR-145-5p gradually increased and that of miR-223 gradually decreased at each time point after treatment (P<0.05), whereas no significant changes were found in the above indicators in the ineffective group (P>0.05). The area under the ROC curve (AUC) of baseline miR-145-5p combined with miR-223 for predicting treatment response was 0.842 (95% CI: 0.778~0.905), with a sensitivity of 88.1% and a specificity of 78.3%, which was superior to single indicator detection. During the 2-year follow-up, 28 patients in the study group experienced recurrence and 16 died. The poor prognosis group (recurrence or death) showed lower baseline miR-145-5p expression and higher miR-223 expression (P<0.05). Multivariate Logistic regression analysis revealed that low baseline expression of miR-145-5p, high baseline expression of miR-223, multi-lobe pulmonary tuberculosis lesion extent, elevated interleukin-6 (IL-6) and C-reactive protein (CRP) levels were independent risk factors for poor prognosis in patients with COPD complicated with PTB (P<0.05).Conclusion? Peripheral blood miR-145-5p is down-regulated and miR-223 is up-regulated in patients with COPD complicated with PTB. Combined detection of the two can serve as potential biomarkers for evaluating treatment response and prognosis of such patients, providing a reference for clinical individualized treatment and prognosis management.

    Key words: chronic obstructive pulmonary disease; pulmonary tuberculosis; microRNA-145-5p; microRNA-223; treatment response; prognosis

    提交时间:2026-04-27

    版权声明:作者本人独立拥有该论文的版权,预印本系统仅拥有论文的永久保存权利。任何人未经允许不得重复使用。
  • 图表

  • 陈翠妍, 梁会营. 基于多模态数据的慢性阻塞性肺疾病筛查集成模型构建. 2026. doi: 10.12201/bmr.202604.00086

    何平, 吴军良, 唐静, 杨静. HBP、IL-6与PCT的检测在慢性阻塞性肺疾病患者中的临床应用价值探讨. 2026. doi: 10.12201/bmr.202604.00134

    王文慧, 李琳浩, 王坤, 李鹏, 徐晓晨, 韩萍. 基于“子盗母气”理论探讨慢阻肺合并营养不良的研究. 2026. doi: 10.12201/bmr.202601.00090

    董丹丹, 马红映. 呼出气冷凝液在慢阻肺中的研究价值与进展. 2025. doi: 10.12201/bmr.202512.00038

    王丽萍, 周杰, 肖玮, 孙增涛. 从“三焦气化-肠道菌群代谢”理解肺肠轴在慢性阻塞性肺疾病的作用机制及治疗策略. 2026. doi: 10.12201/bmr.202601.00005

    祝可欣, 廖思清, 周霞. 慢性肺曲霉病合并咯血的管理. 2025. doi: 10.12201/bmr.202512.00043

    叶贝, 刘顺林. CPNE1、ZWILCH在肺腺癌演进中的表达及与预后的相关性分析. 2024. doi: 10.12201/bmr.202406.00030

    赵静, 黄珺霞, 唐秀花, 王红. HOXA11-AS/miR-149-3p通路在肺鳞状细胞癌中的作用及机制研究. 2022. doi: 10.12201/bmr.202204.00005

    张佳倩, 齐若楠, 马红映, 刘庆兵, 吕丹▲. 纤维蛋白原在慢性阻塞性肺病中的应用价值. 2025. doi: 10.12201/bmr.202511.00035

    陈佳琦, 向红英, 凌迎春. 脑电图定量参数、血清miR-146a-5p对阿尔茨海默病患者认知功能障碍的预测价值分析. 2024. doi: 10.12201/bmr.202412.00027

  • 序号 提交日期 编号 操作
    1 2026-04-10

    10.12201/bmr.202604.00163V1

    下载
  • 公开评论  匿名评论  仅发给作者

引用格式

吴立峥, 王楠, 陈臻. 外周血miR-145-5p、miR-223表达与慢性阻塞性肺疾病合并肺结核患者治疗应答及预后的相关性. 2026. biomedRxiv.202604.00163

访问统计

  • 阅读量:12
  • 下载量: 0
  • 评论数:0

Email This Article

User name:
Email:*请输入正确邮箱
Code:*验证码错误