# The Prognostic Ability of ECG Findings in Predicting Cardiovascular Events: A Five‐Year Nested Case—Cohort Study in an Iranian Population (Shiraz Heart Study)

**Authors:** Seyed Alireza Mirhosseini, Pouria Azami, Raziye Saeedizade, Mehrab Sayadi, Mahya Beykihosseinabadi, Mohammad Keshavarz, Masood Dindari Parizi, Mahsa Borjzadehgashtaseb, Mohammadjavad Nobakhti, Armin Attar, MohammadJavad Zibaeenezhad

PMC · DOI: 10.1002/hsr2.71830 · Health Science Reports · 2026-02-28

## TL;DR

This study shows that specific ECG findings can predict cardiovascular events in an Iranian population over five years, improving risk assessment beyond traditional methods.

## Contribution

The study identifies ST-segment coving and PR interval as novel independent ECG predictors of cardiovascular events in a Middle Eastern cohort.

## Key findings

- ST-segment coving and shorter PR interval were independent predictors of cardiovascular events in multivariable models.
- The 22-variable model and LASSO model both showed excellent discrimination with AUCs above 0.96.
- ECG markers added prognostic value beyond traditional ASCVD risk scores.

## Abstract

Electrocardiographic (ECG) markers may provide incremental prognostic value for cardiovascular disease (CVD) events beyond traditional ASCVD risk scores. This study aimed to evaluate the association between baseline ECG parameters and the incidence of cardiovascular events over 5 years in a nested case‐control cohort.

We analyzed 442 participants from the Shiraz Heart Study, including 221 individuals who experienced CVD events and 221 ASCVD risk‐matched event‐free controls. Detailed ECG parameters and clinical variables were evaluated. Multivariable logistic regression, including a prespecified 22‐variable model and LASSO penalized regression, was used to identify independent ECG predictors. Model performance was assessed using bootstrap‐corrected area under the curve (AUC).

In multivariable analyses, ST‐segment coving (OR 7.57, 95% CI 2.09–27.4, p = 0.002) and shorter PR interval (OR 0.98 per ms decrease, 95% CI 0.95–1.00, p = 0.036) remained independent predictors of incident CVD events in the prespecified 22‐variable model, which was constructed based on clinical relevance and supported by univariable analyses. This model demonstrated excellent discrimination (bootstrap‐corrected AUC 0.97, 95% CI 0.96–0.98). In the parsimonious four‐variable LASSO model, ST‐segment coving (OR 4.31, 95% CI 1.38–13.0) and PR interval (OR 0.977, 95% CI 0.961–0.992) remained independent predictors, and model performance remained robust (bootstrap‐corrected AUC 0.96, 95% CI 0.94–0.98). Other ECG features, including prolonged QTc, abnormal R‐wave progression, left ventricular hypertrophy, and T‐wave inversions, were significant in univariable analyses but did not remain independent predictors in multivariable models.

Baseline ECG parameters provide independent prognostic information for cardiovascular events beyond traditional ASCVD risk factors. These findings highlight the potential of ECG markers to enhance risk stratification, although external validation in larger and diverse populations is warranted before clinical implementation.

## Linked entities

- **Diseases:** cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Diseases:** wave abnormalities (MESH:C535500), COPD (MESH:D029424), corrected QT interval (OMIM:610141), SHS (MESH:D006331), thyrotoxicosis (MESH:C566386), stroke (MESH:D020521), sinus tachycardia (MESH:D013616), ST (MESH:D000072657), arrhythmias (MESH:D001145), heart failure (MESH:D006333), -Ganong-Levine (MESH:D008151), ischemia (MESH:D007511), premature atrial contraction (MESH:D018880), QT prolongation (MESH:D008133), arrhythmic (OMIM:212500), death (MESH:D003643), left ventricular hypertrophy (MESH:D017379), hypertension (MESH:D006973), ASCVD (MESH:D050197), chronic liver disease (MESH:D008107), Wolff-Parkinson-White (MESH:D014927), repolarization abnormalities (MESH:D000014), RAD (MESH:C535729), AV block (MESH:D054537), DM (MESH:D009223), chronic kidney disease (MESH:D051436), CVD (MESH:D002318), MI (MESH:D009203), cancer (MESH:D009369), diabetes (MESH:D003920), bundle branch blocks (MESH:D002037), atrial fibrillation (MESH:D001281), ischemic (MESH:D002545)
- **Chemicals:** cholesterol (MESH:D002784), alcohol (MESH:D000438), TG (MESH:D013866), HDL-C (-), triglycerides (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12949821/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949821/full.md

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Source: https://tomesphere.com/paper/PMC12949821