# Neuroimaging of acute myocardial injury in stroke: insights into brain lesion locations and network disconnections

**Authors:** Petr Mikulenka, James W. Garrard, Olivia N. Murray, Alistair Perry, George Harston, Michal Mihalovič, Petr Toušek, Tomáš Peisker, Ivana Štětkářová, Davide Carone

PMC · DOI: 10.3389/fneur.2026.1719600 · Frontiers in Neurology · 2026-02-11

## TL;DR

This study finds that acute myocardial injury in stroke patients is linked to specific brain lesion locations and disrupted brain networks, suggesting autonomic dysregulation may play a role.

## Contribution

The study identifies specific brain regions and disconnections associated with acute myocardial injury in stroke patients, offering new insights into the neuroanatomical basis of this condition.

## Key findings

- AMI was associated with lesions in the left insula, basal ganglia, and adjacent white matter.
- AMI was linked to widespread structural disconnection involving central autonomic network regions.
- AMI was more common in older patients, females, and those with higher NIHSS scores.

## Abstract

Acute myocardial injury (AMI) is frequently observed in patients with acute stroke and may be linked to lesion location within the central autonomic network (CAN). However, neuroimaging findings remain inconsistent, and the neuroanatomical basis remains unclear. We investigated associations between lesion location, structural disconnection, and AMI in acute stroke.

In this single-center cohort, patients with ischemic or hemorrhagic stroke were screened for AMI using serial high-sensitivity cardiac troponin I (hs-cTnI) measurements within 48 h of admission. AMI was defined as hs-cTnI levels exceeding the 99th percentile of the reference limit with >20% dynamic change. Stroke lesions were segmented using Brainomix software and overlaid on a diffusion tensor imaging template to generate indirect structural disconnection maps. A voxel-based multivariate method (Sparse Canonical Correlation Analysis) identified associations between AMI and (a) directly damaged areas and (b) disconnected regions.

Among 281 patients (mean age 71.4 ± 12.3 years), 59 (21%) developed AMI. AMI was associated with lesions in the left insula, basal ganglia, and adjacent white matter, as well as with widespread structural disconnection involving CAN regions. It was also significantly associated with older age, female sex, and higher NIHSS scores, but not with atrial fibrillation, diabetes, or hypertension.

In this cohort, AMI affected 21% of stroke patients and was significantly associated with specific lesion locations and widespread structural disconnection, including regions implicated in autonomic regulation, but not with traditional cardiovascular risk factors. These findings support the hypothesis that stroke-induced autonomic dysregulation may contribute to AMI development.

## Linked entities

- **Diseases:** stroke (MONDO:0005098), ischemic stroke (MONDO:1060198), hemorrhagic stroke (MONDO:1060199)

## Full-text entities

- **Genes:** TNNI3 (troponin I3, cardiac type) [NCBI Gene 7137] {aka CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI}
- **Diseases:** inflammation (MESH:D007249), cardiac syndrome X (MESH:D017566), hematoma (MESH:D006406), Hypertension (MESH:D006973), brain lesion (MESH:D001927), brain damage (MESH:D001925), Parkinson's disease (MESH:D010300), acute coronary syndrome (MESH:D054058), ICH (MESH:D002543), TTS (MESH:D054549), Myocardial Infarction (MESH:D009203), diabetes (MESH:D003920), atrial fibrillation (MESH:D001281), ischemic (MESH:D002545), ischemic heart disease (MESH:D017202), ischemic stroke (MESH:D002544), vessel disease (MESH:C536223), hemorrhagic stroke (MESH:D000083302), obstructive sleep apnea (MESH:D020181), arrhythmias (MESH:D001145), lesion (MESH:D009059), infarct (MESH:D007238), hemorrhage (MESH:D006470), tachyarrhythmias (MESH:D013610), AMI (MESH:D056486), myocardial injuries (MESH:D009202), myocarditis (MESH:D009205), Stroke-Heart Syndrome (MESH:D020521), cardiac complications (MESH:D006331), ischemia (MESH:D007511), neurological deficits (MESH:D009461), multiple sclerosis (MESH:D009103), myocardial necrosis (MESH:D009336), pulmonary embolism (MESH:D011655), sepsis (MESH:D018805), contraction band necrosis (MESH:D058745), autonomic (MESH:D001342)
- **Chemicals:** catecholamine (MESH:D002395), cTn (MESH:C403585)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932174/full.md

## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932174/full.md

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Source: https://tomesphere.com/paper/PMC12932174