Development and validation of a clinical prediction model for overactive bladder in type 2 diabetes: a pathophysiology-informed approach

Overactive bladder (OAB) is a highly prevalent and burdensome complication of type 2 diabetes mellitus (T2DM), with a pathophysiology distinct from idiopathic OAB. Current management relies on symptom-based diagnosis, lacking tools for proactive risk stratification that reflect its multifactorial origins in neuropathy, microvascular injury, and inflammation. In this retrospective cohort study, we developed and temporally validated a clinical prediction model using data from 1531 patients with T2DM. The model was derived via multivariable logistic regression with backward selection in a development cohort (n = 810, Jan 2018-Dec 2021) and tested in an independent validation cohort (n = 721, Jan 2022-Feb 2025). OAB was defined by the Overactive Bladder Symptom Score (OABSS). Model performance was assessed by discrimination (AUC), calibration, and decision curve analysis (DCA). SHapley Additive exPlanations (SHAP) analysis elucidated variable contributions. Seven readily available clinical parameters were retained in the final model: diabetic peripheral neuropathy (DPN), HbA1c, urinary albumin-to-creatinine ratio (UACR) category, neutrophil-to-lymphocyte ratio (NLR), age, the Triglyceride-Glucose (TyG) Index, and post-void residual volume (PVR). The model demonstrated excellent discrimination (AUC 0.880 [0.844–0.917] in development; 0.858 [0.814–0.902] in validation) and was well-calibrated. Decision curve analysis confirmed clinical utility across a wide risk threshold range. SHAP analysis identified DPN as the strongest predictor, validating the model’s alignment with the underlying pathophysiological hierarchy. We developed and validated a practical, pathophysiology-informed prediction model that accurately stratifies the risk of OAB in patients with T2DM. This tool integrates key domains of diabetic complications into a single assessment, enabling a shift towards proactive, personalized risk communication and targeted surveillance for high-risk individuals.

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Journal
European journal of medical research
Published
2026-03-23
DOI
https://doi.org/10.1186/s40001-026-04289-w
Primary Topic
Urinary Bladder and Prostate Research
Type
article
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article

Development and validation of a clinical prediction model for overactive bladder in type 2 diabetes: a pathophysiology-informed approach

Meiyuan Lv, Zhihua Zhang, Dongfeng Yi, Liangbing Liu et al.
European journal of medical research
Urinary Bladder and Prostate Research
article

Development and validation of a clinical prediction model for overactive bladder in type 2 diabetes: a pathophysiology-informed approach

Meiyuan Lv, Zhihua Zhang, Dongfeng Yi, Liangbing Liu, Guangxu Fu
article en

Abstract

Overactive bladder (OAB) is a highly prevalent and burdensome complication of type 2 diabetes mellitus (T2DM), with a pathophysiology distinct from idiopathic OAB. Current management relies on symptom-based diagnosis, lacking tools for proactive risk stratification that reflect its multifactorial origins in neuropathy, microvascular injury, and inflammation. In this retrospective cohort study, we developed and temporally validated a clinical prediction model using data from 1531 patients with T2DM. The model was derived via multivariable logistic regression with backward selection in a development cohort (n = 810, Jan 2018-Dec 2021) and tested in an independent validation cohort (n = 721, Jan 2022-Feb 2025). OAB was defined by the Overactive Bladder Symptom Score (OABSS). Model performance was assessed by discrimination (AUC), calibration, and decision curve analysis (DCA). SHapley Additive exPlanations (SHAP) analysis elucidated variable contributions. Seven readily available clinical parameters were retained in the final model: diabetic peripheral neuropathy (DPN), HbA1c, urinary albumin-to-creatinine ratio (UACR) category, neutrophil-to-lymphocyte ratio (NLR), age, the Triglyceride-Glucose (TyG) Index, and post-void residual volume (PVR). The model demonstrated excellent discrimination (AUC 0.880 [0.844–0.917] in development; 0.858 [0.814–0.902] in validation) and was well-calibrated. Decision curve analysis confirmed clinical utility across a wide risk threshold range. SHAP analysis identified DPN as the strongest predictor, validating the model’s alignment with the underlying pathophysiological hierarchy. We developed and validated a practical, pathophysiology-informed prediction model that accurately stratifies the risk of OAB in patients with T2DM. This tool integrates key domains of diabetic complications into a single assessment, enabling a shift towards proactive, personalized risk communication and targeted surveillance for high-risk individuals.

European journal of medical research
The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture (CN)
Peace, Justice and strong institutions
Openalex Percentile: Top 12%
Urinary Bladder and Prostate Research
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