- McLennan, Yingratana A;
- Mosconi, Matthew W;
- McKenzie, Forrest J;
- Famula, Jessica;
- Krawchuk, Bennet;
- Kim, Kyoungmi;
- Clark, Courtney J;
- Hessl, David;
- Rivera, Susan M;
- Simon, Tony J;
- Tassone, Flora;
- Hagerman, Randi J
Background
Quantitative measurement of eye movements can reveal subtle progression in neurodegenerative diseases.Objective
To determine if quantitative measurements of eye movements may reveal subtle progression of fragile X-associated tremor and ataxia (FXTAS).Methods
Prosaccade (PS) and antisaccade (AS) behavior was analyzed in 25 controls, 57 non-FXTAS carriers, and 46 carriers with FXTAS.Results
Symptomatic individuals with FXTAS had longer AS latencies, increased rates of AS errors, and increased AS dysmetria relative to non-FXTAS carriers and controls. These deficits, along with PS latency and velocity, were greater in advanced FXTAS stages.Conclusion
AS deficits differentiated FXTAS from non-FXTAS premutation carriers implicating top-down control and frontostriatal deterioration. However, the absence of group differences between non-FXTAS carriers and controls in AS and PS markers suggests saccade performance may not be a sensitive enough measure for detecting conversion to FXTAS, but instead more helpful as translational biomarkers of FXTAS progression.