Typically developing infants track moving objects with eye and head movements in a smooth and predictive way at 4 mo of age, but this ability is delayed in very preterm infants. We hypothesized that visual tracking ability in very preterm infants predicts later neurodevelopment.
In 67 very preterm infants (gestational age<32 wk), eye and head movements were assessed at 4 mo corrected age while the infant tracked a moving object. Gaze gain, smooth pursuit, head movements, and timing of gaze relative the object were analyzed off line. Results of the five subscales included in the Bayley Scales of Infant Development (BSID-III) at 3 y of age were evaluated in relation to the visual tracking data and to perinatal risk factors.
Significant correlations were obtained between gaze gain and cognition, receptive and expressive language, and fine motor function, respectively, also after controlling for gestational age, severe brain damage, retinopathy of prematurity, and bronchopulmonary dysplasia.
This is the first study demonstrating that the basic ability to visually track a moving object at 4 mo robustly predicts neurodevelopment at 3 y of age in children born very preterm.
Children born very preterm, i.e., with a gestational age < 32 wk, are at increased risk for neurodevelopmental impairments (1,2). In particular, these children show deficits in visuospatial perceptual abilities, which are not explained by their general intelligence level (3,4,5). Cognitive and neurodevelopmental difficulties in very preterm infants can often be predicted already in the neonatal period, e.g., by presence of gray and white matter abnormalities on magnetic resonance imaging at term equivalent age. However, not all infants with brain injury will have a poor outcome, and also infants with no obvious neonatal brain injury may have an adverse neurodevelopment (4,6).
Visual tracking is one of the earliest developing cognitive abilities which are present already soon after birth. Unless the object is large and moving very slowly, newborn infants predominantly use saccades. During the second month after birth, the ability to stabilize gaze on a moving object through smooth pursuit eye movements improves greatly (7) and tracking is achieved by a combination of head and eye movements (7,8). In normally developing infants, horizontal smooth pursuit approaches adult levels around 4 mo of age (8). The contribution of the head increases and at 5 mo infants use the head to follow an object more than adults (7,9). Visual tracking performance has been investigated in a number of clinical conditions in childhood and later, and is associated with cognitive functions as well as with psychiatric disorders (10,11).
In a population-based study of very preterm infants, we used a method of quantitative measurement of eye and head movements in relation to a horizontally oscillating object developed by von Hofsten and Rosander (7,9). The study protocol at 4 mo included evaluation of “smooth pursuit gain”, i.e., the ability to keep the eyes focused on a moving object and to follow it smoothly, and “gaze gain” which refers to the combination of visual tracking through smooth pursuit, head movements, and saccades. To stabilize gaze on the object, eye and head movements need to be coordinated in time and space. In this study, gain is a spatial parameter, which refers to the ratio between gaze, smooth pursuit or head movement amplitudes and the object motion amplitude. Gaze and smooth pursuit should optimally be stabilized on the object which gives a ratio of 1, a ratio less than or larger than 1 indicates that tracking amplitude was smaller (undershooting) or greater than the object amplitude (overshooting) wich are both detrimental to tracking. Thus, “smooth pursuit gain”, “head gain”, and “gaze gain” describes how close smooth pursuit, head or gaze, respectively, anticipated the position of the object. The temporal parameter “timing of gaze” described whether the gaze was lagging or leading the object. To align gaze with the object motion, prediction of the objects direction and velocity is required which also includes prediction of the sinusoidal motion.
We have previously demonstrated that very preterm infants in the present study population had a delayed development of visual tracking at 2 and 4 mo corrected age (12). Several neonatal risk factors correlated with the delayed visual tracking ability, but only presence of periventricular leukomalacia was independently associated with the visual tracking performance (13). In the present study, we hypothesized that visual tracking ability at 4 mo corrected age is an early indicator of neurobehavioral function and correlates with later neurodevelopment, assessed by the Bayley Scales of Infant Development (BSID version III) at 3 y of age.
Patient characteristics ar given in Figure 1 and Table 1. Means and SDs for tracking parameters and BSID III subscale scores are given in Table 2. Figure 2a–d gives examples of visual tracking patterns in two infants.
Gaze gain explained a large part (22–32%) of the variance in the BSID III cognitive, receptive language, expressive language, and fine motor scores (cognition: R2 = 0.315, P < 0.001; receptive language: R2 = 0.224, P = 0.001; expressive language: R2 = 0.285, P < 0.001; fine motor: R2 = 0.218, P = 0.001). An optimal tracking of the object, with the gaze following the complete trajectory of the target without overshoot at the turning points (Figure 3a), was associated with higher scores on all four BSID III subscales.
Smooth pursuit gain was also significantly associated with the cognitive and expressive language subscales, but explained only around 7% of the variance (cognition: R2 = 0.069, P = 0.036; expressive language: R2 = 0.067, P = 0.044). The larger the proportion of the object trajectory that was followed by smooth pursuit eye movements, the higher were the scores in these subscales (Figure 3b). Head gain was significantly associated with the cognitive, expressive language, and fine motor subscales, explaining 7–11% of variance (cognition: R2 = 0.092, P = 0.019; expressive language: R2 = 0.071, P = 0.039; fine motor: R2 = 0.108, P = 0.010). These data indicate that using more head movements for tracking the object at 4 mo was beneficial for later development (Figure 3c).
At 4 mo corrected age, 63 of the 67 very preterm infants lagged the object motion. The timing of gaze in relation to the object was also important for neurodevelopment and explained 13–23% of the variances in the cognitive and language subscales (cognition: R2 = 0.155, P = 0.002; receptive language: R2 = 0.130, P = 0.005; and expressive language: R2 = 0.225, P < 0.001) (Figure 3d).
No tracking parameter was associated with the BSID III gross motor subscale. The frequency of saccades was not related to the BSID III subscales.
Neonatal Risk Factors
Neonatal risk factors associated with the 3-y outcome and determined through univariate linear regressions were gestational age, degree of retinopathy of prematurity, and bronchopulmonary dysplasia, but not presence of severe brain injury (intraventricular hemorrhage 3–4/periventricular leukomalacia) (Table 3).
Gaze Gain and Neonatal Risk Factors
When the neonatal risk factors (gestational age, severe brain damage, retinopathy of prematurity, and bronchopulmonary dysplasia) were entered into a hierarchical regression model together with the visual tracking data, gaze gain explained unique variance not accounted for by the neonatal risk factors (Table 4). The increase in explanatory value by gaze gain (▵R2) was significant. Thus, the effect of gaze gain on neurodevelopmental scores was not the result of clinical risk factors influencing both early visual tracking ability and later development. This was further confirmed as gestational age was entered as sole risk factor in a hierarchical regression model and the increase in explained variance (▵R2) was still significant for all four BSID III subscales (significance levels (P) were found to be between 0.002 and 0.038)
This is the first prospective study evaluating the relationship between early visual tracking and neurodevelopment. Our results demonstrate that integrated neural functional development at 4 mo corrected age, as reflected by visual tracking ability, is significantly related to later neurodevelopment in very preterm infants.
The most important result was that early visual tracking ability predicted cognitive, language, and fine motor development in these children. Gaze gain was the tracking parameter closest associated with the BSID III subscales. Smooth pursuit gain, head gain, and timing of gaze to object motion was related to several BSID subscales. In the regression analysis, gaze gain increased the predictive ability of neonatal risk factors for cognitive, receptive, and expressive language subscale scores, as well as for the fine motor subscale.
Keeping gaze fixed on a target requires sustained attention (11) since both temporal and spatial aspects of tracking have to be precise in order to stabilize the image on the retina (7,14). Visual feedback is too slow to control this system and to generate synchronized behavior and therefore the velocity and direction of the object has to be predicted (9,14,15). In contrast to typically developing infants, who usually demonstrate a lead of gaze relative to the object of 70 to 100 ms (16), a lead was present only in 4 of the 67 very preterm infants. However, the smaller the lag the better the developmental outcome, underlining the importance of adequate timing of gaze to object.
Successful tracking depends on the ability to coordinate saccades, smooth pursuit, and head movements into precise gaze gain and timing. Smooth visual tracking relies on smooth pursuit as well as on head movements (17). If smooth pursuit is poorly developed, head movements can compensate for this at moderate target velocities. It is therefore important not to restrain the movements of the head in the assessment, as this might compromise the gaze tracking.
Visual identification of objects and actions is important for the capability to communicate around them, and thus development of language accompanies that of visual processing (18). Our results are in line with those of Ellis et al. (19) who found that the ability to anticipate a visual sequence at 6 mo predicted receptive and expressive vocabulary at 2 y.
Fine motor function is dependent on eye-hand coordination, which matures early in life; at 4 mo, the child reaches successfully for both moving and stationary objects (20). When reaching, the child prepares to grasp the object by predictive timing of opening and closing of the hand (21). These adjustments are visually guided and it was therefore expected that early visual skills should be closely related to fine motor abilities.
The gross motor subscale showed no significant relationship with early visual tracking ability. The visual mechanisms required for gross motor development may differ from those underlying cognitive and language functions. Another possibility is that the BSID III gross motor subscale relies less on visual tracking abilities since no moving objects are included among the tasks at this age level. In the Swedish EXPRESS study, a national population-based study of infants born before 27 gestational weeks, the gross motor subscale identified fewer children with disability at 2.5 y corrected age (prevalence 7%) than the other BSID III subscales (prevalence 11–15%) (22). It was also the only subscale in the present study that was not associated with clinical risk factors.
Visual attention and ability to follow moving targets, as assessed early in life through direct observation, has previously been shown to be associated with 12-mo outcome in preterm infants (23). In addition, cortical visual function measured with visual event-related potentials responses to visual fixational shifts at 3–7 mo corrected age predicted results on the Griffiths scale at 2 y of age (3). Fixational shifts were delayed in very preterm infants without diagnosed brain damage and the authors suggested that evaluation of visual functioning might be a sensitive indicator of later subtle neurodevelopmental problems. Recently, neonatal visual fixation was demonstrated to predict visuomotor performance at 2 y, and visual reasoning at 5 y of age (24).
Visual tracking ability relies on the function of the dorsal neural pathway, where information about spatial relationships, motion perception and control of motor actions are integrated with attention, motives, and comprehension (3,25). At 4 mo of age, cortical processing of motion is still dominated by the direct pathway from retina to pulvinar and middle temporal area. For smooth pursuit, it is assumed that the frontal eye field is critical, as well as cerebellar areas via pontine nuclei. Subcortical nuclei (superior colliculus and substatia nigra) are also crucial for eye movements (18,26). Lesions in these subcortical areas and basal ganglia give severe effects on eye movements (27). In addition, the prefrontal cortex is involved in predictive aspects of tracking (8). Retinopathy of prematurity and diffuse or localized white matter injury are prevalent in very preterm infants, and these conditions may affect the dorsal pathway and the maturation of both the pulvinar to middle temporal visual area and the primary visual pathways (26,27,28). It was shown in very preterm infants that reduced occipital cortical volumes at term equivalent age were associated with poor visual motion perception at 2 y of age (29). Abnormal visual tracking ability is present in many behavioral and psychiatric disorders, such as autism, attention deficit hyperactivity disorder, developmental coordination disorders, and dyslexia (3,4,10,26,30), which also constitute a risk for children born very preterm. Visual tracking assessments and longitudinal follow-up studies may contribute to an increased understanding of the relation between neurodevelopmental profiles, and behavioral and psychiatric disorders in these children.
In the present study, only four infants were diagnosed with severe brain injury, and probably due to this low number, there were no significant associations between neonatal brain injury, visual tracking parameters, and 3-y outcome. A limitation was that no cerebral magnetic resonance images were performed in the neonatal period, and consequently mild to moderate white matter injury may not have been detected. However, cranial ultrasound examinations were performed by experienced pediatric radiologists at 35–36 gestational weeks and near term these examinations should be able to identify major white matter injury associated with adverse outcome (31,32).
The present data demonstrates that visual tracking ability at 4 mo corrected age, and especially gaze gain, is an independent predictor of later neurodevelopment in very preterm infants, explaining around 30% of cognitive function and expressive language function at 3 y of age. Gestational age was found to be an important and independent risk factor where low gestational age predicts low performance on BSID. Cognitive testing at school age could confirm the sustainability of the tracking results over time. Further studies are required to investigate whether measures of tracking ability should be included in the clinical routine for a better assessment of early neurological functioning. A visual tracking recording is clinically feasible, since it is quick to perform and not distressing for the infant and could be readily interpreted by a trained nurse or physician.
The LOngitudinal VISual follow-up of visuomotor development (LOVIS) study population included all very preterm infants in the County of Uppsala born at Uppsala University Hospital between January 2004 and December 2007 (12). A total of 145 very preterm infants were eligible for the study; Figure 1 describes the steps for inclusion of the 67 infants who had visual tracking assessments at 4 mo corrected age and later follow up with the BSID III. The gestational age ranged from 22 + 2 to 31 + 6 wk and birth weight from 520 to 2,030 g. Cranial ultrasound was performed at least twice in the neonatal period, at 2–7 d and at 35–36 gestational weeks, and all infants were regularly screened for retinopathy of prematurity. Bronchopulmonary dysplasia was defined as need for additional oxygen at 36 gestational weeks. Clinical routines have been described previously (13). The final study group did not differ from the initial LOVIS cohort neither in perinatal characteristics nor in the BSID III scores. The study was approved by the Regional Ethics committee at Uppsala University (Ups 03-665). Parental consent was collected for the clinical examinations and for the visual tracking assessments.
Visual Tracking Assessments
The child was placed securely in a baby seat inside a white cylinder (1 m diameter and 1 m high), and thereby shielded from distractors. A happy face (7 cm diameter) with a camera at its nose moved horizontally according to a sinusoidal pattern at 0.25 Hz along a track on the inside of the cylinder surface (Figure 4). The camera made it possible to observe the child via a monitor, in order to ensure wellbeing and attention to the task. Two amplitudes of object motion were used, 12.5° and 25° of visual angle, and each trial lasted 35 s.
Horizontal eye movements were recorded through electro-oculography (DatAid, Umeå, Sweden) (see refs. (7,9) for detailed description). Miniature skin electrodes (Beckman, Grass technologies, West Warwick, RI) were placed at the outer canthi and the ground at the ear lobe or the forehead. A preamplifier was placed on the head of the infant, to minimize drift and noise. The electro-oculography was calibrated for each infant and the precision of eye position measurement was 0.4°.
Infants could move their heads rather freely during the trials. The movements of the head and the object were measured by an optoelectronic camera system (Qualysis Proreflex, Gothenburg, Sweden) utilizing infrared light and small (diameter 5 mm) passive reflective markers. Measurement frequency was set to 240 Hz in synchrony with the electro-oculography. All infants tracked the object. In the rare case that an infant temporarily lost attention this section of tracking was not included in the analysis.
Neurodevelopmental follow up with the BSID III, performed at 29–41 (median 32) months’ corrected age, was part of the standard clinical routine. The BSID III assesses the child’s abilities within five subscales (mean = 100, SD = 15): cognition, receptive language, expressive language, fine motor, and gross motor functions. The cognitive subscale includes tasks such as shape perception, complexity of play behavior, simple visual logic, and comparisons. The receptive language subscale is based on identifying objects and actions in pictures, while the expressive language subscale is obtained through observation, naming of, and conversations around pictures. In the fine motor tasks, the child is asked to stack and string blocks and to handle a pencil and scissors. Stability, coordination, and balance are targeted in the gross motor tasks.
All children were tested by a licensed psychologist, who was blind to the results of the early visual tracking performance but could not, due to the clinical circumstances, be blind to gestational age.
Ophthalmologic and orthoptic assessment was performed at 30 mo corrected age (33). In the present study, 64 of the 67 children were examined at 2.5 y, two at 6.5 y, and one at 1 y corrected age. Four children had strabismus and eight had major refractive errors in at least one eye (defined as myopia of < −3 diopters hypermetropia > +3 diopters, astigmatismus ≥ 2 diopters, and/or anisometropia ≥ 2 diopters). Four of the latter children were wearing glasses at the examination. No child was visually impaired, i.e., blind or only able to fixate a torch when tested binocularly, regardless of degree of retinopathy of prematurity.
Data from electro-oculography and Qualysis were synchronized to obtain data of head and eye movements in relation to the moving object. The analysis was performed by FYSTAT designed for time series (DatAid, Umeå, Sweden) or Matlab (Mathworks, Natick, MA). Gaze gain, smooth pursuit gain, head gain, and timing of gaze, were calculated from the average of the high and low amplitude trials (7,9). Before the calculation of smooth pursuit, the saccades exceeding 40°/s were eliminated from the eye movement data (7).
Gaze gain and head gain were defined as their spatial position relative to that of the object. The smooth pursuit gain was defined as its spatial position to head slip, i.e., the difference between head and object positions or the proportion of the target trajectory that needs to be covered by the eye to obtain perfect gain.
Timing (phase) was calculated by cross correlations, where the time difference between gaze and object motion was estimated (Figure 2). Finally, the number of large saccades (>100°/s) were counted from the eye velocity file.
Statistical analysis was carried out with IBM SPSS Statistics, version 20.0. Armonk, NY, and graphs were created in GNU Octave 3.8.1. (Open source).
Similar to findings in the EXPRESS study (22), the BSID III language and motor subscales in this study differed in mean and SDs as compared to BSID III reference data (Table 1). Therefore, we used the results of each subscale in the analysis instead of language and motor indexes.
Associations between tracking parameters and BSID III results were analyzed through hierarchical regression models and effect size (R2) and significance levels (P values, two-tailed) were noted. Quadratic regression models were used for evaluating relationships between gaze gain and the BSID III subscales since both too low and too high gaze gain values means suboptimal tracking. All remaining parameters were analyzed with linear regression.
To test if adding gaze gain to a model of neonatal risk factors increased the capacity to predict neurodevelopmental outcome, a linear hierarchical regression analysis was conducted. To adjust for the nonlinear relationship between gaze gain and the BSID III sub scores, the gaze variable was squared. Gaze gain was then entered both as squared and nonsquared in step two of the hierarchical regression model. Following common praxis to include 1/10 as many covariates as subjects, this meant that four neonatal risk factors could be entered into the first step of the hierarchical regression model. These risk factors were selected among factors of known relevance for neurodevelopment (34). Several of the neonatal risk factors were highly correlated with each other and collinearity diagnosis showed that birth weight and gestational age were too strongly interdependent to be entered into the same regression analysis. The degree of prematurity (gestational age) was selected as being more relevant for the study, along with bronchopulmonary dysplasia, retinopathy of prematurity, and severe brain injury (presence of intraventricular hemorrhage 3–4 and/or periventricular leukomalacia).
Statement of Financial Support
Financial support was obtained from the Linnéa and Josef Carlsson Foundation, Helsingborg, Sweden, the Jerring Foundation, Stockholm, Sweden, the Gillbergska Foundation, Uppsala, Sweden, and Uppsala University Funds, Uppsala, Sweden.
None of the authors have any conflict of interest or any financial ties to products in this study.
We thank all children and parents who participated in the study; twenty-one children also participated in the EXPRESS study. We acknowledge the work by the following: Jonina Hreinsdottir, Lisa Strömbeck-Sandlund, Cecilia Ewald, Uwe Ewald, Bo Strömberg, Olga Kuchokova, and Ingela Helling.
About this article
Italian Journal of Pediatrics (2017)