Abstract:Horizontal vergence eye movements are controlled by two processes, phasic and slow-tonic. Slow-tonic responses are hypothesized to be stimulated by the faster, pulse-step neural output of the phasic system. This suggests that the general behavior of each system should be similar; however, this relationship has yet to be investigated directly. We characterize the relationship between phasic and tonic vergence by quantifying directional asymmetries in the response properties of each mechanism to the same dispari… Show more
“…Vergence stimuli for experiments #2 & 3 were created in a custom-built haploscope, which has been described in detail in our previous work [96]. In this apparatus the participant was seated (head supported and immobilized with a custom chin rest) 12 cm in front of two infrared passing mirrors placed orthogonally to each eyes line of sight.…”
Section: Haploscope Display (Experiments #2 and #3)mentioning
Introduction: The vergence oculomotor system possesses two robust adaptive mechanisms; a fast "dynamic" and a slow "tonic" system that are both vital for single, clear and comfortable binocular vision. The neural substrates underlying these vergence adaptive mechanisms in humans is unclear. Methods: We investigated the role of the posterior cerebellum in convergence adaptation using inhibitory continuous theta-burst repetitive transcranial magnetic stimulation (cTBS) within a double-blind, sham controlled design while eye movements were recorded at 250hz via infrared oculography. Results: In a preliminary experiment we validated our stimulation protocols by reproducing results from previous work on saccadic adaptation during the classic double-step adaptive shortening paradigm. Following this, across a series of three separate experiments we observed a clear dissociation in the effect of cTBS on convergence adaptation. Dynamic adaptation was substantially reduced while tonic adaptation was unaffected. Baseline dynamic fusional vergence response were also unaffected by stimulation. Conclusions: These results indicate a differential role for the posterior cerebellum in the adaptive control of convergence eye movements and provide initial evidence that repetitive transcranial magnetic stimulation is a viable tool to investigate the neurophysiology of vergence control. The results are discussed in the context of the current models of implicit motor adaptation of vergence and their application to clinical populations and technology design in virtual and augmented head mounted display architectures. Significance statement: The cerebellum plays a critical role in the adaptive control of motor systems. Vergence eye movements shift our gaze in depth allowing us to see in 3D and exhibit two distinct adaptive mechanisms that are engaged under a range of conditions including reading, wearing headmounted displays and using a new spectacle prescription. It is unclear what role the cerebellum plays in these adaptive mechanisms. To answer this, we temporarily disrupted the function of the posterior cerebellum using non-invasive brain stimulation and report impairment of only one adaptive mechanism, providing evidence for neural compartmentalization. The results have implications for vergence control models and applications to comfort and experience studies in head-mounted displays and the rehabilitation of clinical populations exhibiting vergence dysfunctions.
“…Vergence stimuli for experiments #2 & 3 were created in a custom-built haploscope, which has been described in detail in our previous work [96]. In this apparatus the participant was seated (head supported and immobilized with a custom chin rest) 12 cm in front of two infrared passing mirrors placed orthogonally to each eyes line of sight.…”
Section: Haploscope Display (Experiments #2 and #3)mentioning
Introduction: The vergence oculomotor system possesses two robust adaptive mechanisms; a fast "dynamic" and a slow "tonic" system that are both vital for single, clear and comfortable binocular vision. The neural substrates underlying these vergence adaptive mechanisms in humans is unclear. Methods: We investigated the role of the posterior cerebellum in convergence adaptation using inhibitory continuous theta-burst repetitive transcranial magnetic stimulation (cTBS) within a double-blind, sham controlled design while eye movements were recorded at 250hz via infrared oculography. Results: In a preliminary experiment we validated our stimulation protocols by reproducing results from previous work on saccadic adaptation during the classic double-step adaptive shortening paradigm. Following this, across a series of three separate experiments we observed a clear dissociation in the effect of cTBS on convergence adaptation. Dynamic adaptation was substantially reduced while tonic adaptation was unaffected. Baseline dynamic fusional vergence response were also unaffected by stimulation. Conclusions: These results indicate a differential role for the posterior cerebellum in the adaptive control of convergence eye movements and provide initial evidence that repetitive transcranial magnetic stimulation is a viable tool to investigate the neurophysiology of vergence control. The results are discussed in the context of the current models of implicit motor adaptation of vergence and their application to clinical populations and technology design in virtual and augmented head mounted display architectures. Significance statement: The cerebellum plays a critical role in the adaptive control of motor systems. Vergence eye movements shift our gaze in depth allowing us to see in 3D and exhibit two distinct adaptive mechanisms that are engaged under a range of conditions including reading, wearing headmounted displays and using a new spectacle prescription. It is unclear what role the cerebellum plays in these adaptive mechanisms. To answer this, we temporarily disrupted the function of the posterior cerebellum using non-invasive brain stimulation and report impairment of only one adaptive mechanism, providing evidence for neural compartmentalization. The results have implications for vergence control models and applications to comfort and experience studies in head-mounted displays and the rehabilitation of clinical populations exhibiting vergence dysfunctions.
“…50,51 In addition to being slower at baseline than convergence, reflexive divergence responses demonstrated limited recruitment of larger, faster responses after completion of an adaptive lengthening double-step paradigm. 52 This result suggests that a saturation limit in the preprogramed pulse-generating divergence neural mechanism was reached. Beyond this limit, the width of the velocity profile increased in response to the double-step stimuli; however, the overall efficacy of this alterative process was significantly reduced.…”
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confidence: 95%
“…Beyond this limit, the width of the velocity profile increased in response to the double-step stimuli; however, the overall efficacy of this alterative process was significantly reduced. 52 The following study aims to test two separate, but dependent, hypotheses in order to better characterize the oculomotor deficits that underpin the clinical condition of convergence insufficiency. First, individuals with convergence insufficiency will demonstrate a reduced capacity to adaptively lengthen their convergence responses when compared to binocularly normal controls.…”
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confidence: 99%
“…Beyond this limit, the width of the velocity profile increased in response to the double-step stimuli; however, the overall efficacy of this alterative process was significantly reduced. 52 …”
We compared the adaptive capacities of reflexive fusional convergence and divergence in 10 participants with untreated convergence insufficiency (CI) to 10 agematched binocularly normal controls (BNCs) in an effort to elucidate the functional basis of CI. METHODS. Vergence responses were monitored binocularly at 250 Hz using video-based infrared oculography, while single and double-step disparity stimuli were viewed dichoptically. The double-step stimuli were designed to induce an adaptive increase in the convergence or divergence reflexive fusional response dynamics. RESULTS. As expected, convergence responses in the CI population were significantly slower at baseline (BNC 12.0 ± 1.8°/s vs. CI 7.4 ± 2.5°/s; P < 0.001), but divergence response velocities were similar between groups (P = 0.38). Critically, we observed an impaired adaptive change in convergence peak velocities in the CI group when compared to BNCs (-18.2% ± 27.3% vs. 25.4% ± 9.8%; P < 0.001). Adaptive changes in reflexive fusional divergence responses were similar between groups (P > 0.5) and significantly less robust when compared to BNC convergence. CONCLUSIONS. The results support the hypothesis that the adaptive capacities of vergence are related to the strength of the underlying reflexive fusional response. Combined, the evidence suggests that the clinical condition of convergence insufficiency is underpinned by an underdeveloped or perturbated reflexive fusional vergence response mechanism. We relate these observations to different clinical guidelines for the management and treatment of this condition.
“…For example, prior convergence effort diminishes divergence amplitude (Fray 2017), and resting vergence may adapt to the habitual wearing of prismatic spectacles (Sreenivasan and Bobier 2014). Phasic divergence is slower than corresponding phasic convergence (Erkelens and Bobier 2017;Hung et al 1994Hung et al , 1997, although both are proportional to their tonic performance (Erkelens and Bobier 2017). Divergence usually has lower speed and greater latency than convergence (Hung et al 1997;Semmlow and Wetzel 1979), although this asymmetry is reversed in a minority of people (Tyler et al 2012).…”
We employed magnetic resonance imaging (MRI) to quantify human extraocular muscle contractility during centered target fusion, and fusional divergence repeated with each eye viewing monocularly at 20 cm through 8Δ, and at 400 cm through 4Δ base in prism. Contractility, indicated by posterior partial volume (PPV) change, was analyzed in transverse rectus and in medial and lateral superior oblique (SO) muscle compartments, and by cross sectional area change in the inferior oblique (IO). At 20 cm, 3.1±0.5° (SEM) diverging eye abduction in 10 subjects was associated with 4.2±1.5% whole lateral rectus (LR) PPV increase (P<0.05), and 1.7±1.1% overall MR PPV decrease attributable to 3.1±1.8% reduction in the superior compartment (P<0.025), without change in its inferior compartment, or in muscles of the aligned eye. At 400 cm, 2.2±0.5° diverging eye abduction in 9 subjects was associated with 6.1±1.3% whole LR PPV increase (P<10-5) but no change in MR, with compartmentally similar relaxation in the LR and MR of the aligned eye. Unlike convergence, there were no IO or SO contractile changes for divergence to either target, nor any change in rectus pulley positions. Results confirm and extend to proximal divergence the unique role of the superior MR compartment, yet no MR role for far divergence. Co-relaxation of aligned eye LR and MR combined with failure of MR relaxation during divergence is consistent with the limited behavioral range of divergence.
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