# Risk factors, stroke rates and aspirin prescribing trends in the Canadian Fabry disease initiative cohort

**Authors:** Emilie T. Théberge, Caroline Selvage, Anita Thomas, Kaye M. LeMoine, Rebecca Robichaud, Lily Zhou, Darwin F. Yeung, Michael L. West, Sandra Sirrs, Anna Lehman

PMC · DOI: 10.1186/s13023-025-04098-0 · Orphanet Journal of Rare Diseases · 2025-11-07

## TL;DR

This study examines stroke rates and aspirin use in a Canadian cohort of Fabry disease patients, finding higher stroke rates in males and those with severe genetic variants, and a decline in aspirin prescriptions after 2018.

## Contribution

The study provides new insights into stroke risk and aspirin use in Fabry disease patients, highlighting sex and genetic variant differences.

## Key findings

- Stroke/TIA rates were significantly higher in male patients compared to females.
- Patients with severe GLA variants had higher stroke/TIA rates than those with attenuated variants.
- Fewer patients were prescribed aspirin for primary prevention after 2018.

## Abstract

Fabry disease (FD) is an X-linked disorder caused by deleterious variants in GLA. Cardiovascular disease (CVD) causes premature mortality in FD. Hope for aspirin (acetylsalicylic acid, ASA) to reduce CVD risks in FD as primary prevention may have been tempered by the 2018 ARRIVE, ASCEND, and ASPREE clinical trials. It is unclear how new ASA guidance applies to FD patients, who have a high rate of young-onset, small vessel stroke compared with the general population.

Longitudinal data spanning 2007–2023 from patients in the Canadian Fabry Disease Initiative (CFDI) were analyzed retrospectively. Incident stroke and transient ischemic attack (TIA), other CVD events, FD-specific risk factors, and ASA/antiplatelet (“ASA/AP”) prescription before and after 2018 were compared between groups who never had an event (“primary prevention group”) to those who had incident stroke/TIA during the study. Stroke/TIA rates were compared within CFDI by sex and GLA variant severity, and in the CFDI compared to Canadian statistics by sex. Ten-year atherosclerotic CVD (ASCVD) risk was calculated using the 2013 ACC/AHA risk calculator. ASA/AP prescription rate was compared before and after 2018.

Out of 641 patients, 57 had an incident stroke/TIA during the study, and 193 with complete data remained in the primary prevention group. Stroke/TIA rates were significantly higher among male patients (0.026 events per patient-year) than females (0.0098 events per patient-year), and higher among patients with severe GLA variants (males: 0.031 events per patient-year, females: 0.0096 events per patient-year) compared to those with attenuated variants (males: 0.011 events per patient-year, females: 0.0088 events per patient-year). No patients under 60 years at their incident stroke/TIA had high (≥ 10%) calculated 10-year ASCVD risk. Fewer patients were prescribed ASA/AP for primary prevention after 2018.

There was a high incidence of stroke/TIA in the younger CFDI cohort compared to the general Canadian population, despite low levels of traditional vascular risk factors as represented in 10-year estimated ASCVD risk. Primary prevention use of ASA has declined.

The online version contains supplementary material available at 10.1186/s13023-025-04098-0.

## Linked entities

- **Genes:** GLA (galactosidase alpha) [NCBI Gene 2717]
- **Chemicals:** acetylsalicylic acid (PubChem CID 2244), aspirin (PubChem CID 2244)
- **Diseases:** Fabry disease (MONDO:0010526), cardiovascular disease (MONDO:0004995), stroke (MONDO:0005098), transient ischemic attack (MONDO:0005264), atherosclerotic cardiovascular disease (MONDO:1060134)

## Full-text entities

- **Genes:** GLA (galactosidase alpha) [NCBI Gene 2717] {aka GALA}
- **Diseases:** ASCVD (MESH:D050197), FD (MESH:D000795), X-linked disorder (MESH:D040181), CVD (MESH:D002318), vessel stroke (MESH:C536223), Stroke (MESH:D020521), TIA (MESH:D002546)
- **Chemicals:** ASA (MESH:D001241), AP (MESH:D000667)
- **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/PMC12595872/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12595872/full.md

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Source: https://tomesphere.com/paper/PMC12595872