Evidence mapPaperPMID 41555416Full record

ArticleEuropean journal of medical research2026

Unveiling the relationship between stress-hyperglycemia ratio and cardiometabolic multimorbidity risk using interpretable machine learning.

Shouxin Wei, Sijia Yu, Chuan Qian, Yunsheng Lan, Huang Xufeng

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Article in European journal of medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Shouxin Wei *Department of Gastrointestinal Surgery, Suining Central Hospital, Suining, China. weishouxin@sns120.cn.
Sijia Yu *Department of General Practice, Suining Central Hospital, Suining, China.
Chuan Qian *Department of Gastrointestinal Surgery, Suining Central Hospital, Suining, China.
Yunsheng LanDepartment of Gastrointestinal Surgery, Suining Central Hospital, Suining, China.
Huang XufengDepartment of Data Visualization, Faculty of Informatics, University of Debrecen, Debrecen, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiometabolic multimorbidity (CMM) is the simultaneous manifestation of multiple cardiovascular and metabolic diseases, and it has arisen as a substantial worldwide healthcare issue. The stress-hyperglycemia ratio (SHR) represents a novel biomarker that is strongly associated with the prognosis of various diseases; however, its role in CMM remains insufficiently understood. This research aims to examine the association between SHR and CMM risk and assess its clinical utility in risk assessment.

methodsThis cross-sectional study utilized data from the National Health and Nutrition Examination Survey (NHANES), with a total of 12,279 participants meeting the inclusion criteria. A weighted logistic regression model was used to examine the correlation between SHR and CMM. Furthermore, machine learning (ML) techniques were applied to develop a CMM prediction model, and the validity of the findings was confirmed by several sensitivity analysis, including external validation using the China Health and Retirement Longitudinal Survey (CHARLS). In addition, mediation analysis was performed to investigate the potential mediating roles of body mass index (BMI) and waist circumference (WC).

resultsA substantial positive relationship was identified between SHR and CMM risk. For 1-unit rise in SHR, the risk of CMM rose by 21.131 (OR = 22.131 [10.688, 45.823]). Smooth curve fitting analysis indicated a U-shaped correlation between SHR and CMM risk. When SHR is below 0.841, CMM risk decreases as SHR increases (OR = 0.001 [0.000, 0.004]); however, when SHR exceeds 0.841, CMM risk increases sharply as SHR rises (OR = 116.890 [70.086, 194.951]). The findings of the mediation study demonstrated that BMI and WC moderated the association between SHR and CMM risk. Furthermore, the gradient boosting machine (GBM) model demonstrated robust predictive performance with an Area Under the Curve (AUC) of 0.880 (95% CI 0.866-0.894), while shapley additive explanations identified age, SHR, and WC as the top three predictors with the most significant impact on the model outcomes. Sensitivity analyses consistently validated the findings, with the external validation in the CHARLS cohort confirming a significant positive association (OR = 1.389, [1.026, 1.880].

conclusionsThis study identified a U-shaped non-linear relationship between SHR and CMM risk, underscoring the potential clinical value of SHR in the early diagnosis and risk assessment of CMM. The predictive model developed using machine learning methods can significantly aid clinicians in conducting personalized risk assessments for CMM.

Indexed as

Cardiometabolic multimorbidityCHARLSMachine learning modelsNHANESStress–hyperglycemia ratio

Identifiers

PMID41555416
PMCPMC12895724

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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 Socratic graph.