ArticleFrontiers in cardiovascular medicine2026
Identification of key metabolic indicators associated with the comorbidity of ischemic stroke and diabetes mellitus using an optimal interpretable clinlabomics model.
Article in Frontiers in cardiovascular medicine, 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
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: To identify candidate metabolic biomarkers and establish a Clinlabomics model for early precise screening of ischemic stroke (IS) with diabetes mellitus (DM) comorbidity population. Methods: A total of 2,587 IS patients were retrospectively enrolled and classified into IS-DM comorbidity and IS-only groups. A total of 16 metabolic indicators were collected, and candidate indicators were identified using univariate and multivariate logistic regression along with restricted cubic spline (RCS) analysis. The dataset was randomly split into training and test sets at a 7:3 ratio, and an additional 406 patients constituted a temporal validation set. Clinlabomics models were constructed using 11 machine learning (ML) algorithms. Model performance was evaluated using F1-score, accuracy (ACC) and area under the curve (AUC) to select the optimal algorithm, and SHapley Additive exPlanations (SHAP) analysis was performed to quantify feature contributions. Results: Multivariate logistic regression showed that 12 metabolic indicators were closely associated with IS-DM comorbidity. Notably, the triglyceride glucose (TyG) index (OR = 4.76, 95% CI: 4.01-5.64, Conclusions: This study successfully identified 9 candidate metabolic indicators of IS-DM comorbidity. The Clinlabomics model established by rpart algorithm presents excellent performance in identifying the IS-DM population.
Indexed as
Identifiers
What OpenQuestion 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 OpenQuestion graph.