Development and Validation of a Machine Learning-Based Nomogram for Predicting Severe Pneumocystis jirovecii Pneumonia in Kidney Transplant Recipients

BACKGROUND Pneumocystis jirovecii pneumonia (PJP) is a life-threatening opportunistic infection in kidney transplant recipients (KTRs). Early identification of patients liable to progress to severe disease is critical for improving prognosis. This study aimed to construct and validate a machine learning-based nomogram for predicting the risk of severe PJP in KTRs using routine clinical indicators. MATERIAL AND METHODS A retrospective cohort of 169 KTRs diagnosed with PJP was analyzed. Severe PJP was defined as cases requiring intensive care unit (ICU) admission or death. The cohort was randomized into training (n=120) and testing (n=49) sets. Three machine learning algorithms (Boruta, RFE, and LASSO) were utilized for feature selection. A multivariate logistic regression model was established and visualized as a nomogram. Model performance was evaluated via area under the ROC curve (AUC), calibration plots, and decision curve analysis (DCA). Kaplan-Meier analysis was performed to assess risk stratification. RESULTS Four key predictors were identified: procalcitonin (PCT), (1→3)-ß-D-glucan (G_test), C-reactive protein (CRP), and the time from kidney transplantation to PJP onset (Time KT to PJP). Notably, shorter post-transplant time and elevated biomarkers were associated with greater severity. The nomogram demonstrated robust discrimination with AUCs of 0.935 (training) and 0.886 (testing), alongside excellent calibration. DCA confirmed a significant clinical net benefit. Furthermore, Kaplan-Meier analysis revealed that patients stratified as high-risk by the model had significantly lower survival rates compared to the low-risk group (P<0.0001). CONCLUSIONS We developed a practical nomogram incorporating 4 accessible indicators to accurately predict severe PJP in KTRs. This tool facilitates the early identification of high-risk patients, enabling timely, individualized interventions and the rational allocation of medical resources.

Authors

Institutions

Publication Details

Journal
Annals of Transplantation
Published
2026-02-04
DOI
https://doi.org/10.12659/aot.952235
Primary Topic
Pneumocystis jirovecii pneumonia detection and treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Development and Validation of a Machine Learning-Based Nomogram for Predicting Severe Pneumocystis jirovecii Pneumonia in Kidney Transplant Recipients

Yunchao Wang, Yuchong Zhu, Jie Yang, Lingquan Meng et al.
Annals of Transplantation
Pneumocystis jirovecii pneumonia detection and treatment
article

Development and Validation of a Machine Learning-Based Nomogram for Predicting Severe Pneumocystis jirovecii Pneumonia in Kidney Transplant Recipients

Yunchao Wang, Yuchong Zhu, Jie Yang, Lingquan Meng, Shuo Wang, Xiaohong Cao, Yi-Xiang Wang, Guanbao Tang, Chuanyou Xia
article en

Abstract

BACKGROUND Pneumocystis jirovecii pneumonia (PJP) is a life-threatening opportunistic infection in kidney transplant recipients (KTRs). Early identification of patients liable to progress to severe disease is critical for improving prognosis. This study aimed to construct and validate a machine learning-based nomogram for predicting the risk of severe PJP in KTRs using routine clinical indicators. MATERIAL AND METHODS A retrospective cohort of 169 KTRs diagnosed with PJP was analyzed. Severe PJP was defined as cases requiring intensive care unit (ICU) admission or death. The cohort was randomized into training (n=120) and testing (n=49) sets. Three machine learning algorithms (Boruta, RFE, and LASSO) were utilized for feature selection. A multivariate logistic regression model was established and visualized as a nomogram. Model performance was evaluated via area under the ROC curve (AUC), calibration plots, and decision curve analysis (DCA). Kaplan-Meier analysis was performed to assess risk stratification. RESULTS Four key predictors were identified: procalcitonin (PCT), (1→3)-ß-D-glucan (G_test), C-reactive protein (CRP), and the time from kidney transplantation to PJP onset (Time KT to PJP). Notably, shorter post-transplant time and elevated biomarkers were associated with greater severity. The nomogram demonstrated robust discrimination with AUCs of 0.935 (training) and 0.886 (testing), alongside excellent calibration. DCA confirmed a significant clinical net benefit. Furthermore, Kaplan-Meier analysis revealed that patients stratified as high-risk by the model had significantly lower survival rates compared to the low-risk group (P<0.0001). CONCLUSIONS We developed a practical nomogram incorporating 4 accessible indicators to accurately predict severe PJP in KTRs. This tool facilitates the early identification of high-risk patients, enabling timely, individualized interventions and the rational allocation of medical resources.

Annals of TransplantationVol. 31
Shandong Provincial QianFoShan Hospital (CN), Shandong First Medical University (CN)
Openalex Percentile: Top 66%
Pneumocystis jirovecii pneumonia detection and treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.