# Does a Raised Serum Troponin During a Severe Chronic Obstructive Pulmonary Disease Exacerbation Predict Future Cardiovascular Events?

**Authors:** Nyle Cockell, Nihal Billing, Praanesh Kumareshan, Thapas Nagarajan

PMC · DOI: 10.7759/cureus.79288 · Cureus · 2025-02-19

## TL;DR

High troponin levels during severe COPD flare-ups may predict future heart problems and higher death risk, suggesting the need for early heart monitoring.

## Contribution

This study is the first to investigate the link between admission troponin levels during severe COPD exacerbations and future cardiovascular events.

## Key findings

- Elevated troponin levels were associated with higher cardiovascular event rates at 12 months.
- Patients with high troponin had shorter time to first cardiovascular event.
- Raised troponin was linked to increased 12-month mortality, though not statistically significant.

## Abstract

Background

Cardiovascular (CV) complications are common in chronic obstructive pulmonary disease (COPD), particularly after acute exacerbations (AECOPD). Elevated cardiac biomarkers, such as high-sensitivity troponin I (hsTnI), indicate myocardial injury and commonly rise during AECOPD. While elevated serum troponin during severe AECOPD predicts mortality, the relationship between admission hsTnI levels and future CV event risk has not been investigated.

Aims and objectives

This study evaluated the prognostic value of admission serum troponin during severe AECOPD for future CV events, including new atrial fibrillation (AF), myocardial infarction (MI), or decompensated congestive cardiac failure (CCF) requiring intravenous diuretics.

Methods

This retrospective cohort study analyzed all patients admitted to a single center in 2022 with severe AECOPD and an admission hsTnI measurement. Patients were stratified by hsTnI levels (0-20ng/L and >20ng/L). The primary outcome was CV event incidence at 12 months, with secondary endpoints including event timing, type, and overall mortality.

Results

Patients with elevated hsTnI (n=37) had higher CV event incidence at 12 months compared to those with normal hsTnI (n=44) (24.3% vs 13.6%; OR 2.04, 95% CI 0.65-6.38). The hazard ratio (HR) for events was elevated but not statistically significant (HR 1.992, 95% CI 0.709-5.601, p=0.191). Raised hsTnI was associated with the greatest event risk at one month (OR 3.79 95% CI 0.38-38.1) and remained elevated over 12 months. Time to first event was also shorter in the elevated hsTnI group (3.0 vs 3.7 months, p=0.529).

CCF was the most frequent CV event (77% of all events), followed by MI and AF.​ Elevated hsTnI was associated with 12-month mortality (56.8% vs 36.3%; OR 1.83, 95% CI 0.75-4.48), although the HR did not reach statistical significance (HR 1.767, 95% CI 0.922-3.388, p=0.086).

Discussion

These findings indicate that elevated admission hsTnI during severe AECOPD is associated with increased CV event incidence, earlier time-to-event, and greater mortality over 12 months. Retrospective study design and opportunistic screening limited the ability to infer causality and statistical significance. Selection bias may have influenced the results from the clinical decision-making to measure hsTnI.​ Larger prospective studies with multivariate regression analysis are required to confirm these findings and address confounders.​

Conclusions

Our findings suggest that raised admission troponin levels are associated with CV events following severe AECOPD.  These patients may benefit from early CV risk assessment and preventative strategies.

## Linked entities

- **Diseases:** chronic obstructive pulmonary disease (MONDO:0005002), atrial fibrillation (MONDO:0004981), myocardial infarction (MONDO:0005068)

## Full-text entities

- **Diseases:** CCF (MESH:D006333), myocardial injury (MESH:D009202), MI (MESH:D009203), COPD (MESH:D029424), AF (MESH:D001281), Cardiovascular (CV) complications (MESH:D002318)
- **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/PMC11929144/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC11929144/full.md

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Source: https://tomesphere.com/paper/PMC11929144