Evidence map›Paper›PMID 41917829›Full record

ArticleBMC cardiovascular disorders2026

Development and validation of a nomogram to predict the risk of cardiometabolic multimorbidity in older adults: data from the NHANES database.

Jiao-Yu Cao, Xiao-Juan Zhou, Li-Xiang Zhang

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Article in BMC cardiovascular disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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3 authors.

Jiao-Yu CaoDepartment of Cardiology, Division of Life Science and Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, No.1, Swan Lake Road, Hefei City, Anhui Province, 230001, China.
Xiao-Juan ZhouDepartment of Cardiology, Division of Life Science and Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, No.1, Swan Lake Road, Hefei City, Anhui Province, 230001, China.
Li-Xiang ZhangDepartment of Cardiology, Division of Life Science and Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, No.1, Swan Lake Road, Hefei City, Anhui Province, 230001, China. 15375357537@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo develop and validate a nomogram prediction model for predicting the risk of cardiometabolic multimorbidity(CMM) in older adults, providing a basis for early risk stratification and clinical intervention.

methodsData from seven survey cycles (2005–2018) of the NHANES database were integrated, incorporating 6,338 older adults aged ≥ 65 years who met the inclusion criteria. LASSO regression was employed to screen characteristic variables associated with CMM, followed by multivariate logistic regression analysis to identify independent risk factors and construct the model. The model’s performance was evaluated using the receiver operating characteristic (ROC) curve (AUC) for discrimination, Spiegelhalter’s z-test for calibration, and Decision Curve Analysis (DCA) for clinical utility.

resultsLASSO regression identified 10 characteristic variables, all of which were confirmed as independent predictors via multivariate logistic regression: college education or above (OR = 0.731, 95% CI: 0.611–0.873, P = 0.001), waist circumference (OR = 1.026, 95% CI: 1.021–1.030, P < 0.001), poverty-income ratio > 3 (OR = 0.750, 95% CI: 0.622–0.904, P = 0.003), Patient Health Questionnaire-9 (PHQ-9) score (OR = 1.057, 95% CI: 1.041–1.073, P < 0.001), high-density lipoprotein cholesterol (OR = 0.682, 95% CI: 0.585–0.796, P < 0.001), hemoglobin (OR = 0.884, 95% CI: 0.847–0.922, P < 0.001), red blood cell distribution width (OR = 1.052, 95% CI: 1.005–1.102, P = 0.030), blood urea nitrogen (OR = 1.104, 95% CI: 1.079–1.130, P < 0.001), globulin (OR = 1.026, 95% CI: 1.014–1.038, P < 0.001), and total cholesterol (OR = 0.644, 95% CI: 0.608–0.681, P < 0.001). The AUC of the nomogram was 0.735 (95% CI: 0.723–0.748), and internal 10-fold cross-validation yielded a consistent AUC of 0.736 (95% CI: 0.721–0.748). Spiegelhalter’s z-test (z=-0.399, P = 0.655) indicated good calibration. DCA showed a positive net benefit when the threshold probability for CMM was between 15% and 77%.

conclusionThe nomogram demonstrates satisfactory predictive performance CMM risk in older adults and serves as a valuable quantitative tool for individualized prevention and control.

Indexed as

Cardiovascular DiseasesDecision Support TechniquesNomogramsAgedAged, 80 and overAge FactorsCardiometabolic Risk FactorsDatabases, FactualFemaleHumansMaleMultimorbidityNutrition SurveysPredictive Value of TestsPrognosisReproducibility of ResultsCardiometabolic multimorbidityElderlyNHANESNomogramRisk prediction

Identifiers

PMID41917829
PMCPMC13159309

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.