- Open Access
The diagnostic value of saccades in movement disorder patients: a practical guide and review
© Termsarasab et al. 2015
- Received: 13 May 2015
- Accepted: 1 September 2015
- Published: 15 October 2015
Saccades are rapid eye movements designed to shift the fovea to objects of visual interest. Abnormalities of saccades offer important clues in the diagnosis of a number of movement disorders. In this review, we explore the anatomy of horizontal and vertical saccades, discuss practical aspects of their examination, and review how saccadic abnormalities in hyperkinetic and hypokinetic movement disorders aid in diagnosis, with video demonstration of classic examples. Documentation of the ease of saccade initiation, range of motion and conjugacy of saccades, speed and accuracy of saccades, dynamic saccadic trajectory, and the presence or absence of saccadic intrusions and oscillations are important components of this exam. We also provide a practical algorithm to demonstrate the value of saccades in the differential diagnosis of the movement disorders patient.
- Eye movement
- Ocular motility
- Movement disorders
Saccades are one of the most useful types of eye movements in the evaluation of the movement disorders patient. The presence of characteristic saccadic abnormalities can be enormously helpful in guiding diagnosis in the outpatient clinic. We present a simplified review the anatomy of horizontal and vertical saccades, discuss practical aspects of their examination, and review saccadic abnormalities in hyperkinetic and hypokinetic movement disorders. Further, we provide an algorithm illustrating the value of saccadic abnormalities in the differential diagnosis of the movement disorders patient. The goal is to provide a practical guide to bedside evaluation of saccades in the context of the movement disorders patient. As such, comprehensive coverage of normal and abnormal ocular motor anatomy and physiology are not included and the reader is referred to comprehensive coverage elsewhere [1, 2].
Definition of saccades
There are multiple types of eye movements including smooth pursuit, saccades, vestibular and optokinetic reflexes, and vergence . Saccades refer to fast conjugate eye movements that shift the eyes from one target to another, bringing an object of interest into focus on the fovea  where visual acuity is highest. Saccades are the fastest eye movements (up to about 500 degrees per second) and they are very brief in duration (typically less then 100 msec) . We will review the anatomy, basic clinical features and examination of normal saccades, and then review movement disorders in which saccadic abnormalities aid in diagnosis.
Physiology and anatomy of saccades
Lesions in each controlling component can lead to different pathologies of saccades (Fig. 2). For example, lesions in PPRF (excitatory burst neurons for horizontal saccades) can give rise to decreased propensity to generate strong bursts (or weak action potential bursts), correlating with slow horizontal saccades, as seen in spinocerebellar ataxia type 2 (SCA2) . Lesions of MVN or NPH or their cerebellar feedback circuitry cause problems holding the eyes in lateral gaze after horizontal saccades, giving a clinical picture of gaze-evoked nystagmus [12, 13]. Lesions in RIMLF can lead to vertical supranuclear gaze palsy in PSP  or Niemann-Pick type C (NPC) . Cortical eye field lesions give rise to ocular motor apraxia, such as that seen in Huntington’s disease. Opsoclonus in opsoclonus-myoclonus ataxia syndrome (OMAS) is related to transient impairment in the inhibition through the omnipause neurons in the RIP, though lesions directly in the omnipause neurons cause only saccadic slowing and do not cause opsocolonus . The current mechanisms of such oscillations relate to dysfunction of cerebellar Purkinje cells or to membrane instability and post-saccadic inhibition of burst neurons in the PPRF [17–21].
How to examine saccades
Saccades can be clinically tested in a self-paced or verbally-guided manner. For example, one can examine self-paced saccades by asking the patient to make repeated saccades between two visual targets without verbal commands (such as looking quickly back and forth between two pencils placed to the right and left of central fixation), vs. examining verbally-guided saccades by asking a patient to look at the examiner’s nose and then at a target (such as the examiner’s finger) to the left or right of central fixation only upon verbal command. Further the behavior of purely visually-guided saccades without verbal cue to a target that unexpectedly appears in peripheral visual scene (such as a wiggling finger or a shining light) can be assessed. This reflexive component of saccades can also be assessed by observation of the fast phases of optokinetic nystagmus (OKN).
Saccade initiation: Do the eyes promptly generate saccades after commands? Delayed initiation of saccades, also called prolonged latency, is seen in oculomotor apraxia, and in some neurodegenerative disorders such as Huntington’s disease (HD) . Patients with delayed saccadic initiation often employ head thrusts or eye blinks to generate saccades, and these features may be the sole clinical sign indicating a mild defect in saccadic initiation.
Range of motion and conjugacy of saccades: Do the eyes move to the full gaze extremes up and down and right and left, or is there limitation in the range of motion? Do they move together at the same rate? If there is limited range of motion, the next step is to see if such limitations are present with smooth pursuit and vestibular ocular reflexes (Doll’s eye maneuvers). The hallmark of a supranuclear brainstem saccadic gaze palsy with impaired range of motion, such as that seen with progressive supranuclear palsy (PSP), is a prominent deficit with saccade testing that is improved with smooth pursuit testing and completely overcome with vestibular ocular reflexes.
Speed of saccades: Do the eyes move slowly during the trajectory from the initial position to the target position? A useful clinical pearl is that one should not be able to follow with one’s own eye the full trajectory of a voluntary saccade, due to the very fast speed of normal saccades. It is important to examine vertical and horizontal saccades independently, as different disorders selectively affect horizontal vs. vertical saccades. Assessment of diagonal saccades (from up and right to down and left, for example) may also be helpful.
Accuracy of saccades: Do the eyes move accurately to the new target? Are saccades hypermetric or hypometric? Is there correction of the saccade to target, and is this correction accurate?
Saccadic intrusions or oscillations: These saccades occur when patients are fixating in the eye primary position, or they may be superimposed during smooth pursuit. Examples include square wave jerks, macrosaccadic oscillations and ocular flutter/opsoclonus. When square wave jerks occur nearly continuously, they are called square wave oscillations. The main distinguishing features between these movements are their size, whether they move away from and back to midline or oscillate about the midline, their trajectory, and whether or not there is an intersaccadic interval between movements. Square wave jerks consist of a small saccade away from and back to midline with an intersaccadic interval between movements. Macrosaccadic oscillations consist of back-to-back saccades with an intersaccadic interval between movements that oscillate in a crescendo-decrescendo pattern about the midline. Ocular flutter consists of back-to-back saccades without an intersaccadic interval that oscillate about the midline in the horizontal direction only. Opsoclonus is similar to ocular flutter but occurs in all planes (horizontal, vertical, and torsional). Further, one must ask if there are saccadic intrusions during fixation in primary position. Saccadic intrusions are abnormalities of ocular fixation, spontaneous unwanted saccades on regular fixation of a target. A clinical pearl to heighten sensitivity of detection of saccadic intrusions is to have the patient look in lateral extreme gaze and then back to center, as saccadic intrusions are often provoked by gaze shifts. Finally, it should be noted if saccadic intrusions are present during smooth pursuit.
Saccades in movement disorders
Hypokinetic movement disorders
Saccades have an important diagnostic role in differentiating parkinsonian disorders (Video segment 1). Their most obvious utility is in PSP, where vertical supranuclear gaze palsy (VSGP) including slowing of vertical saccades is a crucial diagnostic feature. Multiple system atrophy (MSA) also has saccadic abnormalities as described below, whereas saccades are relatively normal in Parkinson’s disease (PD).
Parkinson’s disease (PD). Hypometric vertical and/or horizontal saccades can sometimes be seen, especially on self-paced saccades [23–25], but these may need special eye movement recording techniques to detect. Clinically (with gross observation at the bedside), saccadic abnormalities are subtle except in severe cases.
Multiple system atrophy (MSA). Patients with MSA, especially of the cerebellar type (or MSA-C, olivopontocerebellar atrophy), can have square wave jerks  and saccadic dysmetria. Saccadic hypometria [24, 26] and hypermetric saccades (reflecting fastigial nucleus involvement) may also be seen. Saccadic breakdown of smooth pursuit is also common with cerebellar involvement , though a very non-specific finding. Although the scope of this article focuses on saccades and does not encompass a comprehensive review of nystagmus and abnormalities of other types of eye movements, it is important to note the presence or absence of gaze-evoked or downbeat nystagmus (DBN), which may only be seen when the patient is placed in a supine position (eg. positioning DBN), in a patient with parkinsonism. If present, these would suggest cerebellar involvement and, thus, might be the main clue to a diagnosis of MSA.
Progressive supranuclear palsy (PSP) and its mimics
Square wave jerks are common in PSP and are often prominent , accompanying the VSGP that defines the illness. In PSP, vertical gaze is typically more affected than horizontal gaze, as the primary pathology is in the midbrain affecting the vertical gaze center or RIMLF. Downgaze may be affected prior to upgaze, but not always. At onset patients may have only slow vertical saccades without limitation of vertical gaze , one of the earliest sign of VSGP in PSP. Some patients manifest only progressive vertical gaze slowing and never progress to a limitation of the vertical range of motion in the course of their disease . Careful examination of saccadic velocity is needed to make this diagnosis with confidence [28, 29]. During vertical saccades, especially upgaze, the eyes may follow a curved rather than a linear trajectory, giving the feature of so-called “round-the-house” saccades [24, 30]. This is not specific to PSP, but in fact can be seen in any condition that leads to slowing of vertical saccades relative to horizontal saccades. OKNs are reduced or absent in PSP, vertical more than horizontal . The eyes may appear to follow the OKN stripes, and a common scenario is for only the slow phases of OKN to be generated without any accompanying reflexive saccadic fast phases.
While a VSGP is required for the diagnosis of PSP, a growing list of disorders also include this feature, such as corticobasal degeneration (CBD) or corticobasal syndrome (CBS) [32, 33], frontotemporal dementia , Creutzfeldt-Jakob disease [35–39], Kufor-Rakeb syndrome (PARK9 due to ATP13A2 mutations) [40, 41], Perry syndrome due to DCTN1 mutations , Niemann-Pick type C , Whipple’s disease , and Gaucher’s disease type 3 (horizontal saccades can also be affected, or even more severe) , among others. In Whipple’s disease, in addition to VSGP, patients can have oculomasticatory myorhythmia [45, 46] and pendular convergent-divergent nystagmus .
Corticobasal degeneration (CBD)
Patients with pathologically confirmed CBD or CBS can have VSGP as mentioned above, although a more typical saccadic abnormality is oculomotor apraxia.
Hyperkinetic movement disorders
Opsoclonus-myoclonus ataxia syndrome (OMAS). Patients with OMAS usually present with vertigo, oscillopsia or ataxia with or without myoclonus . Opsoclonus is a diagnostic feature of this entity (Video segment 2), and can be seen even when eyelids are closed . Opsoclonus is a type of saccadic intrusion/oscillation with spontaneous back-to-back saccades in all trajectories (horizontal, vertical, torsional) without an intersaccadic interval. Both eyes are conjugate during the saccadic intrusions. Ocular flutter refers to a similar movement occurring only in the horizontal trajectory, but there is no functional or clinical difference between opsoclonus and flutter. Opsoclonus and ocular flutter may be post-infectious [49–51] (usually treated with immunomodulating agents such as intravenous steroids, immunoglobulin or Rituximab [52–54]), paraneoplastic [55–58], or due to brainstem encephalitis. In children, an underlying neuroblastoma must be excluded [57, 59, 60].
Oculopalatal Myoclonus (OPM). Oculomotor abnormalities in oculopalatal myoclonus are not saccadic (Video segment 2), but the entity merits mention because of its clinical similarity. As in OMAS, eye movement abnormalities in OPM may be more prominent when eyelids are closed. Pendular nystagmus, often with a predominant vertical trajectory occurring at the same frequency as palatal myoclonus (2–3 Hz), is characteristic [61–65].
Huntington’s disease (HD). Oculomotor findings are an important early diagnostic clue in HD patients. The main abnormality is impairment of saccade initiation [22, 66, 67], with or without slowing of saccadic velocity (Video segment 2). Slowed saccadic initiation refers to a delay when a patient is asked to perform saccadic eye movements: the latency from the command to initiation of saccades is long, and vertical saccades are generally more affected than horizontal . Importantly, HD patients also have impairment in anti-saccade tasks: when the examiner confronts the patient, showing a finger on either the left or right side and asks the patient to look at the side contralateral to the appearance of the examiner’s fingers, HD patients make more errors than controls [22, 68–70]. This finding is not, however, pathognomonic for HD and has been seen in many other disorders, including PSP and Dementia with Lewy Bodies.
Neuroacanthocytosis. There is no comprehensive description of eye movement abnormalities in neuroacanthocytosis in the literature. Anecdotally, patients can have eye movement abnormalities similar to HD, but saccades tend to be relatively preserved compared to the degree of motor and neuropsychiatric impairment (as opposed to HD where eye movement abnormalities are a cardinal early sign) (Video segment 2). One study showed square-wave jerks, and hypometric horizontal and vertical saccades, as well as limited vertical gaze on eye movement recordings .
Spinocerebellar ataxia (SCA). Saccades are very important diagnostic clues in some types of SCA (Video segment 3). Slowing of saccades, especially on horizontal gaze, is a hallmark clinical feature of spinocerebellar ataxia type 2 (SCA2), first described by Wadia and Swami , though slow saccades have also been described in other types, such as SCA1 and SCA7. In our experience, this feature may guide clinicians to pursue initial targeted investigation for the SCA2 gene, instead of ordering the entire ataxia panel. In SCA3, there may be abnormalities of vestibular eye movements, and supranuclear ophthalmoplegia . In SCA6 (typically a pure cerebellar syndrome) and other pure cerebellar SCAs, there may be downbeat and/or gaze-evoked and rebound nystagmus . In SCA8, there are hypermetric saccades . It is worth noting that the horizontal slow saccades of SCA2 and the vestibular deficits of SCA3 are the most suggestive ocular findings of a specific genetic defect. The other SCAs manifest ‘cerebellar eye movements’ including saccadic dysmetria, cerebellar nystagmus, and impaired smooth pursuit in various patterns with substantial overlap in phenotypes. In addition to saccades, examination of optic fundi is also helpful. For example, pigmentary maculopathy is seen in SCA7 [75–78]. Frequent macrosaccadic oscillations are seen in spinocerebellar ataxia with saccadic intrusions (SCASI) [79, 80].
Recessive cerebellar ataxia
Saccades may be very useful diagnostically in recessive forms of cerebellar ataxia (Video segment 3). In Friedreich’s ataxia, prominent fixation instability may take the form of macrosaccadic oscillations or nearly continuous square wave jerks , while interestingly cerebellar atrophy is not seen until the very late stages of the illness . Oculomotor apraxia, an impairment of higher cortical control of eye movements with delayed initiation of saccades and other voluntary eye movements such as smooth pursuit, typically affects horizontal more than vertical gaze. Patients may employ head thrusts or eye blinks to generate saccades, but they are able to generate saccades if given enough time. Oculomotor apraxia can be seen in ataxia with oculomotor apraxia types 1 and 2 (AOA1 and AOA2) and ataxia-telangiectasia (AT) [83–87]. In AT, hypometric saccades, alternating skew deviation, gaze-evoked nystagmus, downbeat nystagmus, upbeat nystagmus, periodic alternating nystagmus, and square wave jerks can be seen [88–90]. In AT and AOA1, after rotating a patient in a chair, there is prolonged post-rotational nystagmus with fast phase (beating) to the direction of vestibulo-ocular reflex (VOR) slow phase . Other clinical and laboratory features are helpful to further distinguish these conditions including careful examination of conjunctiva, palate, pinna or skin in other regions to look for oculocutaneous telangiectasia (seen in AT), elevated alpha-fetoprotein (elevated in AT and AOA2), hypoalbuminemia and hypercholesterolemia (in AOA1 and AOA2).
Algorithmic approach to movement disorders by utilizing saccades
Saccades are a very useful part of the clinical examination in movement disorder patients. Clinicians should be familiar with the appropriate examination of saccades and interpretation of findings of abnormal saccades.
Written informed consent was obtained from the patients for publication of all video segments. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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