Fu Xuemin, Wu Luling, Xun Jingna, Pütz Benno, Zheng Zhihang, Li Yanpeng, Shen Yinzhong, Lu Hongzhou, Chen Jun, Müller-Myhsok Bertram
Statistical Genetics, Max Planck Institute of Psychiatry, Munich, Germany.
Department of Infectious Diseases and Immunology, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Front Cell Infect Microbiol. 2025 May 2;15:1542707. doi: 10.3389/fcimb.2025.1542707. eCollection 2025.
HIV-associated cryptococcosis is marked by unpredictable disease trajectories and persistently high mortality rates worldwide. Although improved risk stratification and tailored clinical management are urgently needed to enhance patient survival, such strategies remain limited.
We analyzed clinical and immunological data from 98 HIV-related cryptococcosis cases, employing machine learning techniques to model disease severity and predict survival outcomes. Our approach included unsupervised clustering, elastic net regularized Cox regression, and random survival forests. Model performance was rigorously assessed using the C-index, Brier score, Calibration and time-dependent AUC, with validation executed through a comprehensive, multi-replicated nested cross-validation framework.
Through cytokine profiling, we identified an immune phenotype characterized by excessive inflammatory response (EXC), associated with greater disease severity, more frequent neurological symptoms, and poorer survival outcomes compared to the other two immune phenotypes, highlighting its potential significance in risk stratification. To further support clinical decision-making, we developed an elastic net regularized Cox regression model, achieving superior predictive accuracy with a mean C-index of 0.78 for 36-month outcomes and a mean Brier score of 0.13, outperforming both random survival forest and traditional Cox models. Time-dependent AUC analysis validated the model's robustness, with AUC values of 0.84 at 12 months and 0.79 at 36 months, indicating its reliability and potential clinical utility.
This study presents comprehensive and multidimensional approaches to overcome the challenges commonly encountered in real-world clinical settings. By applying cytokine-based clustering, we illustrate the potential for more nuanced severity stratification, offering a fresh perspective on disease progression. In parallel, our penalized survival model provides a step forward in personalized risk assessment, supporting informed clinical decisions and customized patient management. These findings suggest promising directions for individualized healthcare solutions, leveraging machine learning to enhance survival predictions in HIV-related cryptococcosis.
与HIV相关的隐球菌病具有不可预测的疾病发展轨迹,且在全球范围内死亡率持续居高不下。尽管迫切需要改善风险分层并进行针对性的临床管理以提高患者生存率,但此类策略仍然有限。
我们分析了98例与HIV相关的隐球菌病病例的临床和免疫学数据,采用机器学习技术对疾病严重程度进行建模并预测生存结果。我们的方法包括无监督聚类、弹性网络正则化Cox回归和随机生存森林。使用C指数、Brier评分、校准和时间依赖性AUC对模型性能进行了严格评估,并通过全面、多重复的嵌套交叉验证框架进行验证。
通过细胞因子谱分析,我们确定了一种以过度炎症反应(EXC)为特征的免疫表型,与其他两种免疫表型相比,该表型与更高的疾病严重程度、更频繁的神经症状和更差的生存结果相关,凸显了其在风险分层中的潜在重要性。为进一步支持临床决策,我们开发了一种弹性网络正则化Cox回归模型,对于36个月的结果,平均C指数为0.78,平均Brier评分为0.13,预测准确性更高,优于随机生存森林模型和传统Cox模型。时间依赖性AUC分析验证了该模型的稳健性,12个月时AUC值为0.84,36个月时为0.79,表明其可靠性和潜在的临床实用性。
本研究提出了全面且多维度的方法来克服现实临床环境中常见的挑战。通过基于细胞因子的聚类,我们展示了进行更细致的严重程度分层的潜力,为疾病进展提供全新视角。同时,我们的惩罚生存模型在个性化风险评估方面向前迈进了一步,支持明智的临床决策和个性化的患者管理。这些发现为个性化医疗解决方案指明了有前景的方向,利用机器学习提高与HIV相关的隐球菌病的生存预测。