Changes in urinary excretion of type-I collagen cross-linked C-telopeptide and N-telopeptide in perimenopausal women

PURPOSE: The overall goal was to develop a simple test of random dot stereoacuity that can be used during the first 24 months of life to measure sensory outcomes following treatment of ophthalmopediatric disorders, both in the context of clinical trials and in the context of clinical management. METHODS: A series of random dot stereoacuity test cards were constructed using vectographic vertical bar stimuli with crossed disparities ranging from 1735 to 45 sec. A two-alternative, forced-choice, preferential-looking test protocol was used to measure stereoacuity in 95 healthy term infants (173 tests) over the 1.5-to-24-month age range. Success rate, validity, and tolerance limits for normal performance as a function of age were evaluated. RESULTS: The success rate was high (158 of 173 tests; 91.3%). The maturation of random dot stereoacuity was similar to that measured in earlier lab-based preferential-looking and visual evoked potential protocols; few infants younger than 2 months of age demonstrated stereopsis although by 12 months, mean stereoacuity was 2.1 log sec (120 sec). A further improvement to 1.7 log sec (56 sec) was seen during months 18 to 24, consistent with data obtained in an earlier operant random dot protocol. Tolerance limits for normal ranged from approximately 1000 sec at 6 months to 100 sec after 12 months. CONCLUSIONS: The infant random dot stereoacuity cards provide a simple, quick, and portable preferential-looking test of random dot stereoacuity for infants that has a high success rate and excellent concordance with stereoacuity outcomes from laboratory-based protocols.     

Predictive eye movements do not discriminate between dyslexic and control children

Pavlidis has suggested that predictive saccadic tracking eye movements distinguish between reading disabled and normal children. We have examined saccadic eye movement tracking in 34 dyslexic and 33 control subjects, between 10 and 12 yr old. The subjects were equivalent in performance IQ (WISC-R), with differences between verbal and performance IQ of less than 30 points. Children with neurological, visual or auditory deficits or histories of emotional problems and hyperactivity were excluded. There were no differences between the groups on the eye movement tracking task when scored objectively by computerized analysis of the eye movement records, or by ranking of the records by an experienced observer. Our results (and those of other recent studies) fail to support Pavlidis' contention that eye movements hold the key to dyslexia.     

Distinguishing schizophrenic patients from healthy controls by quantitative measurement of eye movement parameters

BACKGROUND: Eye tracking dysfunction is a putative trait marker for susceptibility to schizophrenia; however, it cannot be recommended as an additional tool for the diagnosis of schizophrenia, due to low sensitivity and specificity. METHODS: To assess the diagnostic potentials of combinations of eye movement paradigms, four smooth pursuit experiments (1: constant velocity of 15 degrees/sec; 2 and 3: combination with either visual or auditory distractors; 4: constant velocity of 30 degrees/sec) and two saccadic eye movement experiments (1: reflexive saccades; 2: voluntary saccades) were conducted. Fourteen patients with residual schizophrenia and 17 healthy controls were studied. Two sets of discriminant analyses (each with the resubstitution and with the "leaving one out" method) were calculated. RESULTS: In the first set, all 10 characteristic variables were included, whereas for the second set, the three most powerful parameters were selected (two from smooth pursuit tasks and one from a voluntary saccade experiment). This procedure provided the best classification results, regarding concordance between clinical diagnoses and eye movement dysfunction (kappa = .67-.80). CONCLUSIONS: Schizophrenic patients of the residual subtype can be differentiated from healthy individuals with considerable criterion validity on the basis of paradigms from two different ocular motor systems.     

Nucleotide sequences and functional characterization of two tobacco UAG suppressor tRNA(Gln) isoacceptors and their genes

The hypothesis was tested that peak velocity of saccadic eye movements in visual motor tasks varies with variables related to energy regulation. The hypothesis is based on the cognitive-energetical performance model of Sanders. An experimental paradigm was developed in which saccadic peak velocity of task-relevant eye movements is measured while a choice reaction task is carried out. Confounding factors of saccadic amplitude and movement direction were controlled. The task was designed in such a way that in each trial subjects performed a target saccade towards an imperative stimulus and a return saccade after the manual response back to the centre of the screen. For both types of saccades the experimental variables were foreperiod duration (short versus long), knowledge of results (with versus without), postsaccadic demand (low versus high) and time on task (five 30-min intervals). In two experiments, there are main and interaction effects of the task variables on peak saccadic velocity. Return saccades are slower than target saccades, but not in the case of high postsaccadic demand. Knowledge of results increases peak saccadic velocity, but more so for return than for target saccades. Time on task leads to a decrease in peak saccadic velocity, which is much stronger for return than for target saccades; furthermore this effect is more pronounced after short than after long foreperiods. Peak saccadic velocity is changed within seconds. The results support the hypothesis. Peak saccadic velocity of task related eye movements reflects energy regulation during task performance. The paradigm will be developed as a diagnostic tool in workload measurement.     

Eye-hand coordination: Oculomotor control in rapid aimed limb movements.

Three experiments are reported in which Ss produced rapid wrist rotations to a target while the position of their eyes was being monitored. In Experiment 1, Ss spontaneously executed a saccadic eye movement to the target around the same time as the wrist began to move. Experiment 2 revealed that wrist-rotation accuracy suffered if Ss were not allowed to move their eyes to the target, even when visual feedback about the moving wrist was unavailable. In Experiment 3, wrist rotations were equally accurate when Ss produced either a saccadic or a smooth-pursuit eye movement to the target. However, differences were observed in the initial-impulse and error-correction phases of the wrist rotations, depending on the type of eye movement involved. The results suggest that aimed limb movements use information from the oculomotor system about both the static position of the eyes and the dynamic characteristics of eye movements. Furthermore, the information that governs the initial impulse is different from that which guides final error corrections. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Detection of cortical activities on eye movement using functional magnetic resonance imaging

Cortical activity during eye movement was examined with functional magnetic resonance imaging. Horizontal saccadic eye movements and smooth pursuit eye movements were elicited in normal subjects. Activity in the frontal eye field was found during both saccadic and smooth pursuit eye movements at the posterior margin of the middle frontal gyrus and in parts of the precentral sulcus and precentral gyrus bordering the middle frontal gyrus (Brodmann's areas 8, 6, and 9). In addition, activity in the parietal eye field was found in the deep, upper margin of the angular gyrus and of the supramarginal gyrus (Brodmann's areas 39 and 40) during saccadic eye movement. Activity of V5 was found at the intersection of the ascending limb of the inferior temporal sulcus and the lateral occipital sulcus during smooth pursuit eye movement. Our results suggest that functional magnetic resonance imaging is useful for detecting cortical activity during eye movement.     

Nitric oxide-mediated renal epithelial cell injury during hypoxia and reoxygenation

If two targets are both on the visual axis of one eye or the other, and binocular fixation is shifted from the farther one to the nearer, the aligned eye consistently makes an initial, seemingly pointless saccade in a temporal direction. The size of those saccades typically differs markedly, depending on whether the targets are aligned with the observer's dominant or non-dominant eye. Pickwell [(1972) Vision Research, 12, 1499-1507] proposed that this binocular asymmetry in oculomotor performance reflects a subject-specific lateral displacement of the egocenter (the "binoculus" of Hering, which has traditionally been assumed to be on the midline). An empirical test of Pickwell's widely endorsed hypothesis has now been conducted and the proposal has been found wanting. In an otherwise darkened room, subjects were required repeatedly to set a small light to a perceived straight-ahead location in the horizontal plane, first for a target at 300 cm distance and then for one at 30 cm. Extrapolation of a line that connects the two averages of those settings to the inter-ocular axis provides an estimate of the subjective egocenter to which visual directions are referred. Contrary to Pickwell's proposal, those locations of the inferred egocenter were usually quite near the midline, and were completely uncorrelated with same-subject data on the extent of saccadic asymmetry at the onset of asymmetrical convergence. The data on perceived straight-ahead underlying this result indicate the availability of extraretinal information about eye orientation that is quite precise at a given moment (median standard deviation of 47 min arc) but conspicuously non-stationary over several-minute intervals (monotonic drifts in sequential settings being very common).     

Saccadic gain modification: visual error drives motor adaptation

The brain maintains the accuracy of saccadic eye movements by adjusting saccadic amplitude relative to the target distance (i.e., saccade gain) on the basis of the performance of recent saccades. If an experimenter surreptitiously moves the target backward during each saccade, thereby causing the eyes to land beyond their targets, saccades undergo a gradual gain reduction. The error signal driving this conventional saccadic gain adaptation could be either visual (the postsaccadic distance of the target from the fovea) or motoric (the direction and size of the corrective saccade that brings the eye onto the back-stepped target). Similarly, the adaptation itself might be a motor adjustment (change in the size of saccade for a given perceived target distance) or a visual remapping (change in the perceived target distance). We studied these possibilities in experiments both with rhesus macaques and with humans. To test whether the error signal is motoric, we used a paradigm devised by Heiner Deubel. The Deubel paradigm differed from the conventional adaptation paradigm in that the backward step that occurred during the saccade was brief, and the target then returned to its original displaced location. This ploy replaced most of the usual backward corrective saccades with forward ones. Nevertheless, saccadic gain gradually decreased over hundreds of trials. Therefore, we conclude that the direction of saccadic gain adaptation is not determined by the direction of corrective saccades. To test whether gain adaptation is a manifestation of a static visual remapping, we decreased the gain of 10 degrees horizontal saccades by conventional adaptation and then tested the gain to targets appearing at retinal locations unused during adaptation. To make the target appear in such "virgin territory," we had it jump first vertically and then 10 degrees horizontally; both jumps were completed and the target spot extinguished before saccades were made sequentially to the remembered target locations. Conventional adaptation decreased the gain of the second, horizontal saccade even though the target was in a nonadapted retinal location. In contrast, the horizontal component of oblique saccades made directly to the same virgin location showed much less gain decrease, suggesting that the adaptation is specific to saccade direction rather than to target location. Thus visual remapping cannot account for the entire reduction of saccadic gain. We conclude that saccadic gain adaptation involves an error signal that is primarily visual, not motor, but that the adaptation itself is primarily motor, not visual.     

Peripheral shift reduces visual sensitivity in cat geniculate neurones

The sudden displacement of the retinal image during a saccade raises the visual threshold of human observers to foveal stimuli. The fall in visual sensitivity observed during this phenomenon, known as saccadic suppression, seems to occur very early in the visual processing chain. The lateral geniculate nucleus (LGN) is a likely locus for the multiple retinal and extraretinal interactions occurring during saccadic eye movements, therefore we used the responses of relay cells of adult cats to simulate a psychophysical experiment. We first measured the responses of X and Y relay cells (27 X and 13 Y) to central spots of optimal size and different contrasts. The spots were presented either alone or time locked with the rapid movement of a large, high-contrast peripheral pattern, referred to as shift. We measured the percentage of trials on which the relay cell fired more spikes when the spot (contrast: 0.03-1.0) was present than when it was absent. In experiments with human observers the task was to indicate, by a keypress, which of two otherwise identical temporal intervals contained the spot. The shift reduces the sensitivity (raises the contrast threshold) of neurones in the cat relay cells to brief, stationary targets presented to the receptive-field center. The suppression of visual sensitivity is significantly greater in Y cells than in X cells (average sensitivity ratios 5.6 +/- 5.4 in Y cells, 1.59 +/- 0.9 in X cells: P < 0.001, U test). The shift also reduces the sensitivity of human observers to the same target. This suggests that the LGN is a potential locus for the modulation of visual responses that leads to saccadic suppression.     

Visual search: eye movements and peripheral vision

The visual search task allows investigation of the way in which central processes can influence the programming of saccadic eye movements. In this paper, a simple search task is studied in which a target is presented in a ring-shaped display of eight stimuli. The subject is required to locate the target with a saccadic eye movement. Targets were colored disks and the task was to search for a target of a particular color. Sensory factors (when all nontargets are identical, the target stands out) and central factor (prespecification of the target) both contribute to search efficiency. When the display contains a double target, saccades sometimes land at an intermediate position between the two targets. This shows that the signal delivered by the search procedure is not necessarily highly localized.     

Review of Eye Movements and Vision.

Reviews the book, Eye Movements and Vision by A. L. Yarbus (Lorrin A. Riggs, translation editor; Basil Haigh, translator) (1967). As Riggs says in the introduction to Yarbus's book: The "book is primarily a monograph describing the original researches of the author." The book offers considerably more to the researcher in other areas of vision or visual perception. It discusses major considerations involved in the state of the art of performing eye movement studies. The range of the topics studied is extensive, including work on flicker, color, empty fields, stationary pictures, saccadic movements, nystagmus, visual pursuit of objects, to name a few. The book relates eye movement to a broad spectrum of visual phenomena. There are other plusses on the side of the book--the art work is very good, the translation by Basil Haigh, I found easy to read. In addition, there is a bibliography containing over a hundred and fifty references. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Eye tracking dysfunction in schizophrenia: Characterization of component eye movement abnormalities, diagnostic specificity, and the role of attention.

To characterize oculomotor components and diagnostic specificity of eye tracking abnormalities in schizophrenia, we examined a large consecutively admitted series of psychotic patients and matched controls. The most common abnormality in schizophrenic patients was low gain (slow) pursuit eye movements (47% of cases). Pursuit and saccadic eye movement abnormalities were no more severe in schizophrenic Ss than in those with affective psychoses, except that high rates of catch-up saccades were unique to schizophrenic Ss (17% of cases). These findings indicate that impaired pursuit eye movements are a major cause of eye tracking impairments in schizophrenia, that tracking dysfunctions commonly occur in affective psychoses, and that markedly high rates of catch-up saccades during eye tracking may be specific to schizophrenia. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

An enquiry into the relationship between activation and performance using saccadic eye movement parameters

Saccadic eye movement was measured in three studies in a tracking task in which increasing stimulus jumping frequency indicates increasing difficulty. In the first study, after taking a benzodiazepine 16 subjects showed decreased saccadic velocity (activation indicator), but their reaction times and anticipatory behaviour (performance indicators) did not parallel this decline, although the saccadic amplitudes did. In the second deactivation study 23 subjects worked on somewhat boring oculomotor tasks for 2 h and showed the same decrease in saccadic velocity but showed almost no performance decline. In the third study a large sample of 254 subjects performed the same short tracking task, which offered the detailed analysis of the correspondence of the saccadic activation indicator to saccadic performance indicators. Almost all correlations were zero correlations. Thus, while performance seems to be practically independent of changing activation, the latter is dependent upon performance from one moment to the next. Stable differences were found between anticipatory and reactive saccades, which indicate an immediate change of saccadic velocity when the response mode changes. Therefore a reformulation of the relationship between performance and activation is proposed. Performance is stabilized by 'concentration' in a two-stage regulation process, i.e., it resists changing activation (for example through fatigue). In the second stage, the 'effort loop', additional brainstem activation is demanded when concentration alone fails to reach the goals that were set by the subject for his performance.     

Evidence for a global scanpath strategy in viewing abstract compared with realistic images

Scanpaths, the repetitive sequences of saccadic eye movements, occurred when subjects viewed slide projections of both realistic and abstract art. Variance analysis demonstrated that global/local eye movement indices were lower for local scanning by professional art viewers who relied on more global viewing, particularly in abstract images. Non-professional, unsophisticated subjects carried their local scanpath patterns from realistic images on to abstract images. The blink rate of professional subjects viewing abstract images was also significantly lower, indicating increased visual effort. Non-professional viewers showed no difference in blink rates.     

Gain adaptation of eye and head movement components of simian gaze shifts

Gain adaptation of eye and head movement components of simian gaze shifts. J. Neurophysiol. 78: 2817-2821, 1997. To investigate the site of gaze adaptation in primates, we reduced the gain of large head-restrained gaze shifts made to 50 degrees target steps by jumping the target 40% backwards during a targeting saccade and then tested gain transfer to the eye- and head-movement components of head-unrestrained gaze shifts. After several hundred backstep trials, saccadic gain decreased by at least 10% in 8 of 13 experiments, which were then selected for further study. The minimum saccadic gain decrease in these eight experiments was 12.8% (mean = 18.4%). Head-unrestrained gaze shifts to ordinary 50 degrees target steps experienced a gain reduction of at least 9.3% (mean = 14.9%), a mean gain transfer of 81%. Both the eye and head components of the gaze shift also decreased. However, average head movement gain decreased much more (22.1%) than eye movement gain (9.2%). Also, peak head velocity generally decreased significantly (20%), but peak eye velocity either increased or remained constant (average increase of 5.6%). However, the adapted peak eye and head velocities were appropriate for the adapted, smaller gaze amplitudes. Similar dissociations in eye and head metrics occurred when head-unrestrained gaze shifts were adapted directly (n = 2). These results indicated that head-restrained saccadic gain adaptation did not produce adaptation of eye movement alone. Nor did it produce a proportional gain change in both eye and head movement. Rather, normal eye and head amplitude and velocity relations for a given gaze amplitude were preserved. Such a result could be explained most easily if head-restrained adaptation were realized before the eye and head commands had been individualized. Therefore, gaze adaptation is most likely to occur upstream of the creation of separate eye and head movement commands.     

Stereoscopic depth perception in the owl

It is unclear whether the neural algorithm that underlies stereoscopic vision in birds incorporates both low level (camouflage breaking) and high level (depth ordering) comparisons of information available to each of the eyes. Both visual functions were successfully tested by examining transitive inference performance in two barn owls trained to discriminate static Julesz random dot stereograms, thus demonstrating a capacity to detect relative depth using fine retinal disparity as the sole cue for discrimination. Our behavioral tests provide strong evidence that the barn owl possesses global stereopsis comparable to that found in the macaque monkey--the owl's best stereoacuity was 2 min of arc.     

Anticipatory saccades during smooth pursuit eye movements and familial transmission of schizophrenia

BACKGROUND: Smooth pursuit eye movement (SPEM) abnormalities are a putative marker of genetic risk for schizophrenia. Accurate SPEM performance requires the subject to activate neural systems responsible for smooth pursuit tracking, while simultaneously suppressing activity of neurons responsible for saccadic movements that would move the eye ahead of the target. This study examined whether specific aspects of SPEM dysfunction cosegregate with genetic risk in parents of schizophrenic probands. METHODS: Eighteen probands and their parents had SPEM recorded. Parents with an ancestral history of schizophrenia were hypothesized to be more likely than their spouses without such a history to carry a genetic risk for schizophrenia. RESULTS: Ten families had a single parent with a positive ancestral history for schizophrenia. The frequency of anticipatory saccades, which were mostly small, and the fraction of total eye movement that they represented were the only measures that differentiated the more likely genetic carrier parents in these families from their spouses and age-matched normals. CONCLUSIONS: Failure to suppress saccadic anticipation of target motion during smooth pursuit appears an aspect of SPEM dysfunction related to presumed genetic risk for schizophrenia.     

Attending to Eye Movements and Retinal Eccentricity: Evidence for the Activity Distribution Model of Attention Reconsidered.

When testing between spotlight and activity distribution models of visual attention, D. LaBerge, R. L. Carlson, J. K. Williams, and B. G. Bunney (1997) used an experimental paradigm in which targets are embedded in 3 brief displays. This paradigm, however, may be confounded by retinal eccentricity effects and saccadic eye movements. When the retinal eccentricities of the targets are equated and eye position is monitored, the pattern of results reported by LaBerge et al., which supported the activity distribution model, is not found. This result underscores the importance of considering targets' eccentricity and people's inclination to make saccadic eye movements in certain types of visual cognition tasks. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Guidance of eye movements during conjunctive visual search: The distractor-ratio effect.

The distractor-ratio effect refers to the finding that search performance in a conjunctive visual search task depends on the relative frequency of two types or subsets of distractors when the total number of items in a display is fixed. Previously, Shen, Reingold, and Pomplun (2000) examined participants' patterns of eye movements in a distractor-ratio paradigm and demonstrated that on any given trial saccadic endpoints were biased towards the smaller subset of distractors and participants flexibly switched between different subsets across trials. The current study explored the boundary conditions of this tendency to flexibly search through a smaller subset of distractors by examining the influence of several manipulations known to modulate search efficiency, including stimulus discriminability (Experiment 1), within-dimension versus cross-dimension conjunction search and distractor heterogeneity (Experiment 2). The results indicated that the flexibility of visual guidance and saccadic bias exemplified by the distractor-ratio effect is a robust phenomenon that mediates search efficiency by adapting to changes in the relative informativeness of stimulus dimensions and features. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Structure, promoter analysis and chromosomal assignment of the human APEX gene

Measures of functional vision are needed to assess elderly low vision patients, their success in using devices, and their ability to manage outside the treatment setting. A new test devised to measure functional ability through the performance of everyday tasks was administered to 94 patients who had acuities of 20/100 or worse in their better eye. Consisting of three versions and four subtests: spot reading, short-term text reading, identifying paper currency and clock reading, the test used standardized items and was timed. In a multiple regression model predicting test performance higher scores were associated with better near acuity (P = .002), higher education (P = .022) and higher levels of self-reported visual skills (P = .072). These predictors plus distance acuity, age and sex only accounted for 35 percent of the variance in test scores. Repeated administration of the test to a different group of 21 patients showed the test to be reliable (intraclass correlation = .85, P < .01) and to have no practice or version effects or differences between raters. This new test may be useful for natural history studies and clinical trials involving low vision patients but further evaluation of its sensitivity to change over time is required.