Swallowing and choking difficulties as potential markers of FXTAS progression in FMR1 premutation carriers
Fragile X-associated tremor/ataxia syndrome (FXTAS) affects motor and coordination pathways and is linked to swallowing and choking difficulties, which can lead to aspiration pneumonia, a leading cause of death in late-stage FXTAS. Despite their severity, these issues are under-investigated. This study examined their association with FXTAS stages and potential as markers of disease progression in FMR1 premutation (PM) carriers. A secondary analysis of Genotype-Phenotype cohort data (2017-2025, MIND Institute, UC Davis) examined swallowing/choking problems, FXTAS stage, neuroimaging, and psychological distress (Symptom Checklist-90-Revised; SCL-90-R). Associations between independent and dependent variables were tested using Generalized Estimating Equation (GEE) regression due to their correlated data. The study included 169 PM carriers (mean age 65 ± 10.9 years; 54% male), with approximately 35% reporting swallowing/choking difficulties. After adjusting for age and sex, individuals in the severe stage of FXTAS (stage 4-5) had a significantly higher risk of swallowing/choking problems compared to those without FXTAS (adjusted odds ratio [aOR] = 4.17; 95%CI = 1.28-13.58). PM carriers with swallowing/choking problems showed a significantly increased association with magnetic resonance imaging (MRI) findings of moderate to severe abnormalities in several brain regions, including cerebral atrophy (aOR = 2.69, p = 0.027), cerebellar atrophy (aOR = 3.34, p = 0.013), cerebellar white matter hyperintensity (aOR = 3.33, p = 0.012), and pons white matter hyperintensity (aOR = 3.93, p = 0.035). Swallowing/choking problems are common in FXTAS, particularly in later stages, and may represent an important clinical marker of disease progression. These patients should be referred to speech-language pathologists for evaluation and treatment. Such interventions could reduce morbidity-mortality associated with these problems.
Authors
- Flora Tassone (ORCID: https://orcid.org/0000-0002-6388-9180)
- Andrea L.C. Schneider (ORCID: https://orcid.org/0000-0003-0026-5052)
- Nell Maltman (ORCID: https://orcid.org/0000-0001-7874-9925)
- Narueporn Likhitweerawong (ORCID: https://orcid.org/0000-0002-1175-0021)
- Federica Alice Maria Montanaro (ORCID: https://orcid.org/0000-0001-7293-2315)
- Jessica Klusek (ORCID: https://orcid.org/0000-0002-2818-0344)
- Ellery Santos (ORCID: https://orcid.org/0000-0001-6301-7262)
- Udayakumar Narasimhan (ORCID: https://orcid.org/0000-0003-2402-7390)
- Waralee Dejputtawat
- Junyi Wang (ORCID: https://orcid.org/0000-0003-0464-4543)
- Randi J. Hagerman
Institutions
- University of Arizona (US)
- University of South Carolina (US)
- Child Development Center (QA)
- Nakornping Hospital (TH)
- University of California Davis Medical Center (US)
- UC Davis Health (US)
- Department of Health Services (US)
- Chiang Mai University (TH)
- University of Bari Aldo Moro (IT)
- University of California, Davis (US)
Publication Details
- Journal
- Scientific Reports
- Published
- 2025-11-26
- DOI
- https://doi.org/10.1038/s41598-025-25959-5
- Primary Topic
- Genetics and Neurodevelopmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Intellectual and Developmental Disabilities Research Center