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中国艾滋病合并肺结核患者抗结核治疗不良结局预测列线图

A nomogram for predicting unfavorable outcomes of antituberculosis treatment among individuals with AIDS combined with pulmonary tuberculosis in China.

作者信息

Han Xiaoxu, Sun Jin, Gao Yuan, Yan Hongxia, He Xiangchuan, Ma Yuanyuan, Xu Peng, Ding Ning, Zhang Xin, Ren Meixin, Jiang Taiyi, Zhang Tong, Su Bin

机构信息

Beijing Key Laboratory for HIV/AIDS Research, Clinical and Research Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Sino-French Joint Laboratory for HIV/AIDS Research, Sino-French Joint Laboratory for Research on Humoral Immune Response to HIV Infection, Beijing Youan Hospital, Capital Medical University, Beijing, China.

出版信息

Front Immunol. 2025 May 29;16:1594107. doi: 10.3389/fimmu.2025.1594107. eCollection 2025.

DOI:10.3389/fimmu.2025.1594107
PMID:40510348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12158956/
Abstract

BACKGROUND

Acquired Immune Deficiency Syndrome (AIDS) combined with tuberculosis (TB) is one of the key factors affecting global TB control, and timely and effective treatment is essential to improve the prognosis in this population. However, data from the WHO have shown that patients with AIDS combined with TB have a lower anti-TB treatment success rate than HIV-negative individuals do, which may lead to an increased incidence of treatment relapse and drug resistance. Therefore, exploring the risk factors affecting the outcome of anti-TB treatment in patients with AIDS combined with TB and developing relevant predictive models will help clinicians rapidly identify patients at greater risk of treatment failure, which is highly valuable for clinical management.

METHODS

We conducted a retrospective cohort study including inpatients with AIDS combined with pulmonary tuberculosis (PTB) who were treated at Beijing Youan Hospital between January 2020 and January 2024. The baseline data and laboratory test data of all enrolled patients were collected from the electronic medical records system. We randomly divided the participants into a training set and a validation set at a ratio of 2:1 and established a LASSO Cox model on the basis of the training set to identify risk factors affecting the outcome of anti-TB treatment. The selected prognostic factors were then used to construct the final Cox model, which was visualized using a nomogram. The receiver operating characteristic (ROC) curves, concordance index (C-index), and calibration curves of the training set and validation set were used to evaluate the discrimination ability and consistency of the model, respectively. Decision curve analysis (DCA) was used to assess the clinical applicability of the prognostic models. Patients were subsequently risk stratified according to the optimal cutoff value selected by X-tile software for better clinical decision-making by clinicians.

RESULTS

A total of 203 inpatients with AIDS combined with PTB were enrolled in this study, including 141 (69.5%) with treatment success and 62 (30.5%) with unfavorable outcome. The results of the LASSO Cox regression model revealed that the CRP/albumin ratio (CAR), extrapulmonary disseminated tuberculosis, other pulmonary infectious diseases, and pulmonary cavitation were independent risk factors for unfavorable outcomes in patients with AIDS combined with PTB, whereas the CD4 T-cell counts was a protective factor affecting patient outcomes. The five variables in the final Cox regression model were further used to establish a predictive nomogram. The AUC (0.760 for the training set and 0.811 for the validation set) and C-index (0.765 for the training set and 0.768 for the validation set) showed that the model we constructed had good discrimination ability. The calibration curves indicated high consistency between the predictions and the actual observations in both the training set and the validation set. DCA for the training set and validation set revealed that the nomogram had clinical applicability. Patients were risk-stratified according to the total nomogram score, and the patients were divided into three groups: low risk (total points <358), medium risk (358 ≤ total points <373), and high risk (total points ≥373). Clinicians should focus on patients whose total score is more than 358 points.

CONCLUSION

We identified prognostic factors for unfavorable anti-TB treatment outcomes and constructed a predictive nomogram to assess the risk of treatment failure in patients with AIDS combined with PTB. Our model performed satisfactorily and can be used for the clinical screening and management of high-risk patients.

摘要

背景

获得性免疫缺陷综合征(AIDS)合并结核病(TB)是影响全球结核病控制的关键因素之一,及时有效的治疗对于改善该人群的预后至关重要。然而,世界卫生组织的数据显示,AIDS合并TB患者的抗结核治疗成功率低于HIV阴性个体,这可能导致治疗复发和耐药发生率增加。因此,探索影响AIDS合并TB患者抗结核治疗结局的危险因素并建立相关预测模型,将有助于临床医生快速识别治疗失败风险较高的患者,这对临床管理具有重要价值。

方法

我们进行了一项回顾性队列研究,纳入2020年1月至2024年1月在北京佑安医院接受治疗的AIDS合并肺结核(PTB)住院患者。所有纳入患者的基线数据和实验室检查数据均从电子病历系统中收集。我们将参与者按2:1的比例随机分为训练集和验证集,并在训练集的基础上建立LASSO Cox模型,以识别影响抗结核治疗结局的危险因素。然后,将选定的预后因素用于构建最终的Cox模型,并使用列线图进行可视化。训练集和验证集的受试者工作特征(ROC)曲线、一致性指数(C指数)和校准曲线分别用于评估模型的区分能力和一致性。决策曲线分析(DCA)用于评估预后模型的临床适用性。随后,根据X-tile软件选择的最佳截断值对患者进行风险分层,以便临床医生做出更好的临床决策。

结果

本研究共纳入203例AIDS合并PTB住院患者,其中141例(69.5%)治疗成功,62例(30.5%)治疗结局不佳。LASSO Cox回归模型结果显示,C反应蛋白/白蛋白比值(CAR)、肺外播散性结核、其他肺部感染性疾病和肺空洞是AIDS合并PTB患者治疗结局不佳的独立危险因素,而CD4 T细胞计数是影响患者结局的保护因素。最终Cox回归模型中的五个变量进一步用于建立预测列线图。AUC(训练集为0.760,验证集为0.811)和C指数(训练集为0.765,验证集为0.768)表明,我们构建的模型具有良好的区分能力。校准曲线表明,训练集和验证集的预测结果与实际观察结果高度一致。训练集和验证集的DCA显示,列线图具有临床适用性。根据列线图总分对患者进行风险分层,患者分为三组:低风险(总分<358)、中风险(358≤总分<373)和高风险(总分≥373)。临床医生应关注总分超过358分的患者。

结论

我们确定了抗结核治疗结局不佳的预后因素,并构建了预测列线图以评估AIDS合并PTB患者的治疗失败风险。我们的模型表现令人满意,可用于高危患者的临床筛查和管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/428cea1a917c/fimmu-16-1594107-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/b6b51727e112/fimmu-16-1594107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/ab20efcd2466/fimmu-16-1594107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/72218745e998/fimmu-16-1594107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/0204f41f90a8/fimmu-16-1594107-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/250506d01cd4/fimmu-16-1594107-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/428cea1a917c/fimmu-16-1594107-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/b6b51727e112/fimmu-16-1594107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/ab20efcd2466/fimmu-16-1594107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/72218745e998/fimmu-16-1594107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/0204f41f90a8/fimmu-16-1594107-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/250506d01cd4/fimmu-16-1594107-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7249/12158956/428cea1a917c/fimmu-16-1594107-g006.jpg

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