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Tolerability of SGLT2 inhibitors in patients with Fabry disease: An observational study
Isabel Mattig1,2,3,4, Berit Zirkelbach1,2, Carina Bonnekoh2
1Deutsches Herzzentrum der Charité, Department of Cardiology, Angiology and Intensive Care Medicine, Charitéplatz 1, 10117, Berlin, Germany.
Insights
Sodium glucose cotransporter 2 (SGLT2) inhibitors show an acceptable safety profile for managing heart failure (HF) in Fabry disease (FD) patients. Further research is needed to confirm their clinical benefits in this specific population.
Area of Science:
- Cardiology
- Nephrology
- Genetics
Background:
- Fabry disease (FD) commonly involves cardiac complications, including heart failure (HF).
- Current HF management in FD follows general guideline recommendations.
- The role of specific HF medications, like sodium glucose cotransporter 2 (SGLT2) inhibitors, in FD requires further investigation.
Purpose of the Study:
- To investigate the use and safety of HF medications, particularly SGLT2 inhibitors, in patients with Fabry disease.
- To analyze the impact of SGLT2 inhibitors on cardiac and renal biomarkers and echocardiographic parameters in FD patients.
Main Methods:
- Retrospective analysis of 99 FD patients' HF medication, laboratory, and echocardiographic data.
- Assessment of SGLT2 inhibitor use, side effects, and outcomes at baseline and follow-up.
- Propensity score matching was employed to compare patient groups.
Main Results:
- SGLT2 inhibitors were used in 20% of the analyzed FD cohort.
- 15 FD patients on SGLT2 inhibitors demonstrated stable cardiac and renal biomarkers over a median follow-up of 663 days.
- Echocardiographic parameters showed mixed trends; left ventricular ejection fraction slightly decreased in the SGLT2 inhibitor group but significantly reduced in the non-SGLT2 inhibitor group.
Conclusions:
- SGLT2 inhibitors appear to have an acceptable safety profile in this exploratory cohort of Fabry disease patients with heart failure.
- No clear clinical benefit of SGLT2 inhibitors could be concluded due to study limitations.
- Further prospective studies are warranted to elucidate the efficacy and long-term outcomes of SGLT2 inhibitors in FD management.
Abstract:
Cardiac involvement of Fabry disease (FD) includes heart failure (HF) treated according to general guideline recommendations. The retrospective study investigates HF medication in FD focusing on sodium glucose cotransporter 2 (SGLT2) inhibitors. HF medication, laboratory and echocardiographic measurements as well as side effects of SGLT2 inhibitors were analyzed at baseline and the last available follow-up. The analysis included 99 FD patients treated with angiotensin converting enzyme (ACE) inhibitors or angiotensin II type 1 receptor blocker (ARB) (50%), beta-blocker (31%), SGLT2 inhibitors (20%), diuretics (12%), angiotensin receptor-neprilysin inhibitors (ARNI) (2%), and mineralocorticoid receptor antagonists (MRA) (1%). After 663 (457-725) days, 15 FD patients treated with SGLT2 inhibitors showed stable cardiac and renal biomarkers. Echocardiographic parameters did not reveal a consistent pattern: Left ventricular ejection fraction (LVEF) showed a slight decrease in the SGLT2 inhibitor group and a significant reduction in patients without SGLT2 inhibitors. Left atrial volume index (LAVI) and tricuspid annular plane systolic excursion (TAPSE) showed an upward trend in the SGLT2 inhibitor group, whereas LAVI declined and TAPSE remained unchanged in patients without SGLT2 inhibitors. After propensity score matching, there were no inter- or intragroup differences. The most common side effects comprised polyuria, hypovolemia, and vertigo. Overall, these exploratory findings suggest an acceptable safety profile of SGLT2 inhibitors in this FD cohort, without allowing clear conclusions regarding clinical benefit.
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