Ocular Manifestations of Huntington's Disease
- 1 Summary
- 2 Disease Entity
- 3 Clinical Features
- 4 Eye Changes as Biomarkers
- 5 Pathophysiology of HD Manifestations
- 6 Possible Therapy
- 7 References
Huntington’s disease is a genetic disease that usually presents in middle aged patients. It is due to a triplet repeat expansion in the IT15 gene. A genetic test and diagnostic score on the Unified Huntington’s Disease Rating Scale are used to assist in making the diagnosis. Eye symptoms associated with Huntington’s disease include ocular motility problems, like different characteristics of saccades, pursuit and fixation abnormalities, as well as retinal thinning. Eye changes can occur early in Huntington’s, and research is ongoing regarding the utility of eye findings as potential biomarkers. Whilst there is no formal treatment of Huntington’s disease, pridopidine is a drug that has the potential to help with some of the ocular manifestations of the disease.
Huntington’s Disease (HD) is a genetic condition that has autosomal dominant inheritance. The affected gene is IT15and is located at 4p16.3. A (CAG)n expansion in the coding region codes to a polyglutamine repeat and a toxic protein, known as huntingtin. The normal huntingtin protein, which is required for neuronal development, typically has about 35 or fewer triplet repeats, and fully penetrant disease manifests if more than 40 CAGs are present. A range of 36-39 repeats leads to variation in penetrance. Paternal transmission of the mutated gene is also correlated to a higher chance of juvenile-onset Huntington’s Disease.
The prevalence of HD varies across populations ranging from 5.7 per 100,000 in Europe and North America to a lower 0.4 per 100,000 in Asia. The global prevalence is reported to be about 2.1 per 100,000. The disease usually manifests in the fourth or fifth decade of life, but it can it also present in juveniles (<21 years old). Generally, more CAG repeats correlate to earlier onset, yet the exact age of onset is too variable to predict by the triplet expansions alone.
There are two elements to diagnosis of HD. First, a patient should either have a genetic test showing the CAG triplet expansion in the IT15 gene or a family history of the disease. Secondly, “unequivocal signs of HD” outlined in the Unified Huntington’s Disease Rating Scale (UHDRS) should be observed in the patient. Several ocular abnormalities are a part of the UHDRS and include ocular pursuit, saccade initiation, and saccade velocity; these are all tested both horizontally and vertically so that six items on the scale are eye-related. A grade of 0 to 4 is given to each item on the scale - 0 corresponds to the patient not being affected and 4 to being affected most severely. Other modalities testes in the UHDRS include oropharyngeal dysfunction, hand coordination, rigidity, bradykinesia, dystonia, chorea, gait, and balance – the score has 31 items, and a score of up to 124 is possible.
Electro-oculographic recordings of patients with HD show abnormal or inability to perform vertical saccades with lower velocities, amplitudes and longer latencies. These changes are not as distinct in horizontal saccades. A study of 50 patients showed that saccadic abnormalities are common in HD patients, with 62% demonstrating slowed vertical saccades, 56% demonstrating a hypometric and reduced range of vertical saccades, and 89% demonstrating an increased latency. Saccades can be further divided into reflexive (in response to novel stimuli) and voluntary (directly controlled). HD patients often have problems with voluntary saccades - they have difficulty self-directing their eyes upon command. In comparison, patients often have difficulty suppressing reflexive saccades, even when instructed to look away from a novel stimuli place in the visual field, which is thought akin to a ‘visual grasp’ reflex. Patients with an early onset of the disease are characterized by saccadic slowing as the prominent symptom, though initiation (voluntary saccades) may not initially be affected, suggesting multiple contributing factors to saccadic abnormalities. 
Fixation and Pursuit Abnormalities
In HD patients, the balance between reflexive and voluntary saccades is distorted – the inability to appropriately initiate voluntary saccades means that reflexive saccades predominate. This imbalance also manifests in fixation and pursuit abnormalities. Fixation abnormalities refer to patients demonstrating irregular oscillations when focusing on a target. The inability to smoothly pursue a moving target is another symptom, as patients demonstrate both jerky eye movement as a compensatory tactic and similar random oscillations. Fixation and pursuit abnormalities are also common, with a majority of patients presenting with them.
A few recent papers have used optical coherence tomography to measure retinal thickness in HD patients and have obtained varying results. One paper found that even though the average peripapillary retinal nerve fiber layer (RNFL) in patients was similar to that of the control group, the temporal RNFL was significantly thinner in HD patients at 62.3 um vs. the control group at 69.8 um. Though the study could not test for progression, it did note that a longer disease duration showed a significant correlation with thinning. A correlation between a higher UHDRS score and more thinning was noted, but it was not statistically significant. A second study affirmed the presence of temporal RNFL thinning and also suggested that the superior RNFL could be similarly impacted. A third study did not find either temporal or superior RNFL thinning and only observed a significant reduction of macular choroidal thickness. Research into retinal thickness is relatively recent, and more studies are needed for conclusive findings.
Eye Changes as Biomarkers
It is not currently possible to predict the age of onset of HD because of the lack of a marker - the length of CAG repeats does not always correlate to age of onset. A more sensitive test that could objectively trace HD progression would make it easier to understand a therapy’s effectiveness. The following are ocular findings which are being researched as potential biomarkers, although ongoing research is still necessary.
Measuring saccade latency may be a reliable and systematic biomarker for disease progression. A study testing test-retest reliability found that saccade latency had an intraclass correlation coefficient of 0.55-0.87, which corresponds to moderate or high reliability. Another study found that saccade latency could differentiate between patients who manifested HD motor signs and those patients who were premanifest. Moreover, both groups of such patients had a regular 24 ms increase in latency over the 3-year study, suggesting the possibility of saccade latency as a biomarker.
Macular Retinal Thickness
A study that found a decrease in macular retinal thickness also discovered a statistically significant regression equation that correlated average macular retinal thickness with a score on the UHDRS. More research is needed to study both HD’s impact on macular retinal thickness and the sensitivity and specificity of this marker.
Pathophysiology of HD Manifestations
HD can cause region-specific neuronal loss in the brain, especially in the cortex and striatum. Specifically, fewer connections are found between the frontal cortex and caudate nucleus in HD patients, and this pathway corresponds to the one used to initiate voluntary saccades but not reflexive ones. Specific loss of neurons between these brain regions explains saccade initiation, pursuit, and fixation anomalies seen in HD. The parietal lobe can still excite the superior colliculus to initiate voluntary saccades, but the degraded prefrontal-caudate nucleus tract prevents voluntary saccades due to a reduced ability to disinhibit the substantia nigra pars reticulata inhibition of the superior colliculus (see Figure 1).
Though not well studied, one hypothesis suggests that thinning in the temporal thinning may be due to issues in mitochondria trafficking due to it being a similar feature found in mitochondrial disorders.
Pridopidine is a dopaminergic stabilizer that is thought to potentially improve HD symptoms of ocular pursuit, saccade initiation, and velocity at a 90 mg/day dose. A phase 3, randomized, double-blind, placebo-controlled trial found improvement in motor symptoms on the UHDRS, with statistically significant improvements in eye symptoms noted. Further analysis is required into the potential benefits of this medication.
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