# Takotsubo cardiomyopathy in myasthenia gravis: a systematic review of case reports with subtype-based analysis

**Authors:** Hideya Itagaki, Takuro Hagino, Tomoyuki Endo

PMC · DOI: 10.1186/s12245-026-01145-w · 2026-02-12

## TL;DR

This paper reviews cases of Takotsubo cardiomyopathy in myasthenia gravis patients, highlighting its severity and clinical features.

## Contribution

The study provides a systematic review and subtype-based analysis of a rare condition in MG patients.

## Key findings

- Apical TTC was the most common subtype, occurring in 71.8% of cases.
- Myasthenic crisis was the most frequent TTC trigger, reported in 37.5% of cases.
- High mortality (17.5%) and ICU admission rates (97.4%) were observed in these patients.

## Abstract

Takotsubo cardiomyopathy (TTC) is a stress-induced cardiac disorder characterized by transient left ventricular dysfunction. Myasthenia gravis (MG), an autoimmune neuromuscular disease, can precipitate TTC during exacerbations such as myasthenic crises. However, the clinical features and outcomes of TTC associated with MG remain unclear.

We conducted a systematic review by the PRISMA guidelines. A comprehensive search of PubMed, Web of Science, and Google Scholar was performed up to May 31, 2025, using terms related to TTC and MG. Case reports and series were included if they described patients with confirmed diagnoses of both MG and TTC, with MG exacerbation occurring at the time of TTC onset. Data were extracted and compared between apical and non-apical TTC subtypes. Statistical analyses included the Mann-Whitney U test and chi-squared or Fisher’s exact test, as appropriate.

A total of 38 articles comprising 40 cases were included. The median age was 69 years; 67.5% of the participants were female. Apical TTC was the most common subtype (71.8%). Myasthenic crisis was the most frequent TTC trigger (37.5%), while chest pain was reported in only 17.5% of cases. Mechanical ventilation and ICU admission were required in 95% and 97.4% of cases, respectively. Overall mortality was 17.5%. No significant differences were found between TTC subtypes; apical cases showed numerically higher troponin levels, which should be interpreted cautiously.

TTC associated with MG exacerbation is a rare but serious condition with high rates of respiratory failure, ICU admission, and mortality. Emergency and critical care physicians should suspect TTC in MG patients presenting with hemodynamic instability or ECG abnormalities, even in the absence of chest pain.

The online version contains supplementary material available at 10.1186/s12245-026-01145-w.

## Linked entities

- **Diseases:** Takotsubo cardiomyopathy (MONDO:0019018), myasthenia gravis (MONDO:0009688)

## Full-text entities

- **Diseases:** MG (MESH:D009157), TTC (MESH:D054549), autoimmune neuromuscular disease (MESH:D009468), respiratory failure (MESH:D012131), left ventricular dysfunction (MESH:D018487), chest pain (MESH:D002637), myasthenic crises (MESH:D013224), cardiac disorder (MESH:D006331), Myasthenic crisis (MESH:D020294)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12998353/full.md

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Source: https://tomesphere.com/paper/PMC12998353