# The Prognostic Value of Left Atrial Size and Strain Assessed by Cardiac Magnetic Resonance in the Coronary Chronic Total Occlusion

**Authors:** Jinfan Tian, Wenxiao Xia, Xueyao Yang, Mingduo Zhang, Huijuan Zuo, Libo Liu, Min Zhang, Yuan Zhou, Ziyu An, Xin Zhao, Lijun Zhang, Yi He, Xiantao Song

PMC · DOI: 10.3390/jcdd13030111 · Journal of Cardiovascular Development and Disease · 2026-02-27

## TL;DR

This study finds that larger left atrial size, measured by MRI, is linked to worse outcomes in patients with a specific heart condition called coronary chronic total occlusion.

## Contribution

The study demonstrates that left atrial maximum volume index is an independent predictor of adverse events in CTO patients with preserved ejection fraction.

## Key findings

- LAVImax was independently associated with MACCE in CTO patients with LVEF ≥ 40%.
- Higher LAVImax quartiles showed significantly increased risk of MACCE compared to the first quartile.
- LA strain parameters did not show a significant association with MACCE after adjustment.

## Abstract

Background: The relationship between left atrial (LA) size, LA strain, and long-term prognosis in patients with coronary chronic total occlusion (CTO) remains unclear. This study aimed to evaluate the association of LA size and LA strain with clinical outcomes in CTO patients using cardiac magnetic resonance (CMR). Methods: This retrospective study included 168 patients with left ventricular ejection fraction (LVEF) ≥ 40%. The primary endpoint was the composite of major adverse cardiovascular and cerebrovascular events (MACCE). Model 1 was established by adjusting for clinically relevant parameters and standard CMR metrics. Models 2–4 were developed using Cox regression based on Model 1, with additional adjustment for each LA strain parameter separately. Results: A total of 168 patients with an LVEF ≥ 40% were analyzed, of whom 39 (23.2%) experienced MACCE during a mean follow-up of 45.9 months (median, 42 months). A preliminary model suggested that LA maximum volume index (LAVImax) was independently associated with MACCE (HR 1.05, 95% CI 1.02–1.08, p = 0.004). Specifically, compared to the first quartile of LAVImax, the second, third, and fourth quartiles were associated with an increased risk of MACCE (Q2: HR 4.50, 95% CI 1.42–14.27, p = 0.011; Q3: HR 4.40, 95% CI 1.29–14.96, p = 0.018; Q4: HR 5.55, 95% CI 1.71–18.06, p = 0.004). In Models 2–4, higher LAVImax remained independently associated with MACCE (all p < 0.05), after adjusting for LA reservoir strain, conduit strain and booster strain, separately. In contrast, none of the LA strain parameters were associated with MACCE. Conclusions: Among CTO patients with LVEF ≥ 40%, LAVImax was independently associated with MACCE.

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** LA (MESH:D059446), MACCE (MESH:D002318), myocardial (MESH:D009202), diabetes (MESH:D003920), Coronary Chronic Total Occlusion (MESH:D054059), injury to (MESH:D014947), ACS (MESH:D054058), stroke (MESH:D020521), infarcted myocardium (MESH:D007238), type 2 diabetes mellitus (MESH:D003924), cardiac death (MESH:D003643), LGE (MESH:C564835), CMR (MESH:D006331), hypertension (MESH:D006973), heart failure (MESH:D006333), LV diastolic dysfunction (MESH:D018487), inflammation (MESH:D007249), three-vessel coronary disease (MESH:D003330), myocardial edema (MESH:D004487), MVD (MESH:C564969), atrial fibrillation (MESH:D001281), hyperlipidemia (MESH:D006949), CTO (MESH:D001157), and cerebrovascular (MESH:D002561), MI (MESH:D009203), Size (MESH:D015875), hypertrophic cardiomyopathy (MESH:D002312), myocardial fibrosis (MESH:D005355), restenosis (MESH:D023903)
- **Chemicals:** gadolinium (MESH:D005682), MRA (MESH:C502936), ACEI (-), aldosterone (MESH:D000450)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13026679/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026679/full.md

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Source: https://tomesphere.com/paper/PMC13026679