Development of a clinical nomogram for predicting sarcopenia in patients with chronic obstructive pulmonary disease based on NHANES data
- PMID: 40809432
- PMCID: PMC12343613
- DOI: 10.3389/fmed.2025.1612403
Development of a clinical nomogram for predicting sarcopenia in patients with chronic obstructive pulmonary disease based on NHANES data
Abstract
Background: The prevalence of sarcopenia in COPD patients is high, and the mutual influence between COPD and sarcopenia creates a vicious cycle. The goal of this research is to create a nomogram model that can forecast when sarcopenia will strike people with COPD.
Methods: 2011 to 2018 data were retrieved from four NHANES database cycles. The 7:3 proportion was applied to split the dataset randomly to separate validation and training datasets. Multivariate logistical regression and LASSO regression were applied to design nomogram design and to select predictors. In addition, multicollinearity existence among final predictor variables remaining in model were tested, among other variables. Calibration curve, decision curve analysis (DCA), and area under receiver operating characteristic curve (AUC) were applied in testing performance in prediction model.
Results: The nomogram was constructed based on four predictive factors: gender, height, BMI, and WWI. The AUC for the training set was 0.94 (95% CI 0.91-0.97), and the AUC for the validation set was 0.91 (95% CI 0.83-0.98), indicating excellent predictive performance. Furthermore, the clinical applicability of the model has been thoroughly validated.
Conclusion: We established a nomogram model to provide an easy and convenient way for early screening of sarcopenia in COPD patients, and to allow for effective guidance to perform early intervention and manage patient prognosis in an optimal way.
Keywords: COPD; NHANES; nomogram; risk factors; sarcopenia.
Copyright © 2025 Fan, Zhao, Luo, Li, Tan and Liu.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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References
-
- GBD 2021 Causes of Death Collaborators. Global burden of 288 causes of death and life expectancy decomposition in 204 countries and territories and 811 subnational locations, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021. Lancet. (2024) 403:2100–32. 10.1016/S0140-6736(24)00367-2 - DOI - PMC - PubMed
LinkOut - more resources
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