ArticleJournal of medical Internet research2026
Machine Learning Analysis of Sex Differences in Cardiovascular-Kidney-Metabolic Risk Factors and Prognosis Among Patients With Moderate-to-Severe Coronary Artery Calcification: Prospective Cohort Study.
Article in Journal of medical Internet research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPatients with coronary artery calcification exhibit notable sex differences in clinical presentation, particularly concerning the role of cardiovascular-kidney-metabolic (CKM) risk factors and their impact on prognoses. However, the precise nature of these sex-specific differences remains incompletely understood.
objectiveThis study aimed to investigate sex disparities in CKM risk factors among patients with moderate-to-severe coronary artery calcification (MSCAC) and elucidate their association with adverse clinical outcomes.
methodsA total of 2418 patients with MSCAC undergoing their first percutaneous coronary intervention were included. Hazard ratios (HRs) were computed to evaluate sex differences in the prognostic significance of various CKM risk factors, including chronic kidney disease (CKD), diabetes mellitus (DM), obesity, hypertension, and hypertriglyceridemia. Four machine learning models-logistic regression, extreme gradient boosting (XGBoost), random forest, and support vector machine-were constructed to predict adverse events. The best-performing model was interpreted using Shapley additive explanations (SHAP) values to identify the relative importance of CKM risk factors and clarify potential sex disparities. Major adverse cardiovascular events (MACEs) were defined as all-cause mortality, nonfatal myocardial infarction, and unplanned repeat revascularization.
resultsAmong the participants, 86.9% (2101/2418) had ≥1 CKM risk factor, while 3.1% (74/2418) had ≥4 risk factors. CKD was independently associated with the occurrence of MACEs in both female patients (HR 2.65, 95% CI 1.50-4.69) and male patients (HR 1.53, 95% CI 1.02-2.60). Notably, the association was stronger in female patients, with a female-to-male multivariate-adjusted HR ratio for CKD of 1.68 (95% CI 1.04-2.97). DM was also associated with MACEs in both sexes, with adjusted HRs of 1.20 (95% CI 1.02-1.92) in female patients and 1.59 (95% CI 1.19-2.12) in male patients. Among the models evaluated, XGBoost demonstrated the highest predictive performance in the test set (area under the curve 0.92; average precision 0.92; F
conclusionsThis study confirmed that CKM risk factors and their influence on prognosis in patients with MSCAC exhibit significant sex differences. The application of machine learning, particularly XGBoost, facilitates a deeper understanding of these disparities and provides a basis for personalized, sex-specific risk assessment and targeted interventions for patients with MSCAC.
Indexed as
Identifiers
What Socratic holds
Registered trials
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 Socratic graph.