Details

Autor(en) / Beteiligte

• Rekik, Arwa
• Mrabet, Saloua
• Nasri, Amina
• Abida, Youssef
• Gharbi, Alya
• Gargouri, Amina
• Kacem, Imen
• Gouider, Riadh

Titel

Eye movement study in essential tremor patients and its clinical correlates

Ist Teil von

• Journal of Neural Transmission, 2023-04, Vol.130 (4), p.537-548

Ort / Verlag

Vienna: Springer Vienna

Erscheinungsjahr

2023

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Essential tremor (ET) encompasses a wide spectrum of motor and non-motor features. Eye movement abnormalities were first reported two decades ago as an atypical finding in ET. Today, a growing number of publications about eye movement abnormalities in neurodegenerative diseases have helped understand their pathophysiology and the basis of their phenotypic variability. Thus, addressing such aspect in ET may disentangle, based on the oculomotor network abnormalities, the dysfunctional brain pathways in ET. In this study, we aimed to describe neurophysiological eye movement abnormalities in ET and their clinical correlates in terms of cognition and other associated clinical signs. We conducted a cross-sectional study in a tertiary neurology referral center including consecutive ET patients and cognitively normal healthy controls (HC) matched for age and sex. The study protocol included the assessment of voluntary horizontal saccades, smooth pursuit, anti-saccades and saccadic intrusions. We assessed the associated motor signs, cognitive functions and the presence of rapid eye movement disorder (RBD). Sixty-two ET patients and 66 HC were enrolled in the study. Eye movement examination showed significant abnormalities in comparison with HC (46.7% vs 20%, p  = 0.002). Prolonged saccadic latency (38.7%, p  = 0.033) and altered smooth pursuit (38.7%, p  = 0.033) were the most common abnormalities in ET patients. Anti-saccadic errors (16% vs 0% in HC, p  = 0.034) correlated with the presence of rigidity ( p  = 0.046), bradykinesia ( p  = 0.001), cognitive dysfunction ( p  = 0.006), executive dysfunction ( p  = 0.0002), apraxia ( p  = 0.0001), altered verbal fluency ( p  = 0.013) and altered backward digit span ( p  = 0.045) along with the presence of RBD ( p  = 0.035). Square-wave jerks (11.5% vs 0% in HC, p  = 0.0024) correlated with rest tremor. A distinctive phenotype of ET could emerge out of this study characterized by anti-saccadic errors and a sub-cortical cognitive profile, consecutive to the disruption of the cerebello-thalamo-cortical loop. Patients with anti-saccadic errors could be cognitively vulnerable and in need of a close monitoring of their cognitive efficiency during the disease’s progression. They may as well convert to Parkinson disease if they present with parkinsonism, RBD and square-wave jerks and require, consequently, a close observation of their motor progression.