Search tips
Search criteria 


Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Biol Psychiatry. Author manuscript; available in PMC 2010 June 1.
Published in final edited form as:
PMCID: PMC2879155

Sensorimotor Transformation Deficits for Smooth Pursuit in First-Episode Affective Psychoses and Schizophrenia



Smooth pursuit deficits are an intermediate phenotype for schizophrenia that may result from disturbances in visual motion perception, sensorimotor transformation, predictive mechanisms, or alterations in basic oculomotor control. Which of these components are the primary causes of smooth pursuit impairments and whether they are impaired similarly across psychotic disorders remain to be established.


First-episode psychotic patients with bipolar disorder (n = 34), unipolar depression (n = 24), or schizophrenia (n = 77) and matched healthy participants (n = 130) performed three smooth pursuit tasks designed to evaluate different components of pursuit tracking.


On ramp tasks, maintenance pursuit velocity was reduced in all three patients groups with psychotic bipolar patients exhibiting the most severe impairments. Open loop pursuit velocity was reduced in psychotic bipolar and schizophrenia patients. Motion perception during pursuit initiation, as indicated by the accuracy of saccades to moving targets, was not impaired in any patient group. Analyses in 138 participants followed for 6 weeks, during which patients were treated and psychotic symptom severity decreased, and no significant change in performance in any group was revealed.


Sensorimotor transformation deficits in all patient groups suggest a common alteration in frontostriatal networks that dynamically regulate gain control of pursuit responses using sensory input and feedback about performance. Predictive mechanisms appear to be sufficiently intact to compensate for this deficit across psychotic disorders. The absence of significant changes after acute treatment and symptom reduction suggests that these deficits appear to be stable over time.

Keywords: First-episode psychosis, frontostriatal networks, motion processing, prediction, pursuit eye movements, sensorimotor transformation

Smooth pursuit eye movement deficits are well established in schizophrenia patients and their unaffected relatives and are regarded as intermediate phenotypes for the disorder (14). While some studies suggest that motion perception deficits may contribute to eye-tracking abnormalities (5,6), other data point to deficits in sensorimotor transformation and in extraretinal pursuit generation (79). The present study was designed to evaluate different smooth pursuit components to identify the neural substrates of pursuit impairment and to investigate the specificity of such deficits across affective psychosis and schizophrenia.

Detailed analyses of distinct smooth pursuit components such as visual motion processing, sensorimotor transformation (i.e., the utilization of motion information and feedback about performance accuracy), predictive mechanisms, and basic oculomotor control are required to identify specific alterations within neural systems that can impair eye tracking. Motion perception provides the retinal velocity signal needed to initiate tracking in response to the onset of target motion, especially in the “open loop” period before visual feedback is available about performance accuracy. Pursuit of low predictability target motion relies on ongoing dynamic sensorimotor transformations, while tracking highly predictable oscillating target movement relies more heavily on internally generated predictive models of target motion (10). Core regions of the neural network for smooth pursuit involve extrastriate area V5, which is crucial for motion perception (11), the frontal eye fields (FEF), which play an important role in sensorimotor transformations that control the gain of oculomotor output (12,13), frontostriatal systems that regulate predictive pursuit (14), and cerebellopontine circuitry that controls basic oculomotor function (15). Studies in animal models provide evidence for the distinct roles of these systems in pursuit and paradigms for evaluating their integrity (16). For example, while V5 lesions disrupt motion processing and therefore impair catch-up saccade accuracy (17), FEF lesions impair sensorimotor transformations needed for pursuit maintenance but leave motion perception unimpaired (12,15,18).

In addition to questions about the specific neural system alterations that cause pursuit impairments in schizophrenia, there are also questions about the relative severity of pursuit impairments in other psychotic disorders and whether they are associated with the same specific pursuit abnormalities. Smooth pursuit alterations have been reported in patients with affective psychoses (1924). Studies have reported similar deficits of sensorimotor transformation in mood disorders and schizophrenia (21,23), and there are preliminary data that bipolar patients may be more severely impaired during extraretinal processing for predictive pursuit compared with patients with schizophrenia (25). Limitations of prior studies comparing affective disorders and schizophrenia include small samples, pooling of patients with different affective disorders and those with and without psychotic features, and different medication treatments across affective disorders and schizophrenia that can differentially affect pursuit responses. The present study evaluated first-episode psychotic patients with bipolar disorder, unipolar depression, and schizophrenia, who were antipsychotic-naive or had brief cumulative lifetime exposure to antipsychotics, on a set of pursuit paradigms selected to assess visual motion processing, sensorimotor function, and predictive pursuit mechanisms.

Methods and Materials


One hundred thirty-five first-episode patients comprising 50 women (38.4%) from inpatient and outpatient services from two sites, the University of Pittsburgh and the University of Illinois at Chicago, met DSM-IV criteria for bipolar I disorder with psychosis (BDP), unipolar depression with psychosis (UDP), or a schizophrenia spectrum disorder (Schiz) (Table 1). The latter group consisted of patients with schizophrenia (n = 69), schizophreniform disorder (n = 4), and schizoaffective disorder, depressed subtype (n = 4). Diagnoses were determined at consensus conferences, which were conducted 4 to 8 weeks after patients had given consent, using all available clinical data, including results from the Structured Clinical Interview for DSM-IV (26). Time since first psychotic symptom did not differ between patient groups [Fgroup(2,120) = 1.02, p =.36] or between sites [Fgroup×site(2,120) = .48, p = .62]. On the Brief Psychiatric Rating Scale (BPRS) (27), psychotic bipolar patients were less symptomatic than other patient groups [F(2,130) = 5.13, p = .007, post hoc: pBDPvsUDP = .01, pBDPvsSchiz < .001] (Table 1). There were no group difference across sites with respect to BPRS scores [Fgroup×site(2,124) = .61, p = .55].

Table 1
Demographic and Clinical Characteristics of Matched Groups of First-Episode Patients with Psychotic Disorders and Healthy Participants

One hundred thirty healthy control participants including 58 women (44.6%) without history of Axis I disorders (Structured Clinical Interview for DSM-IV for Axis I Disorders [SCID-I]) or any known history of psychotic or mood disorder in first-degree relatives were recruited from the surrounding communities via advertisements. There were no group differences across recruitment sites in age [Fgroup×site(3,256) = .34, p = .80] or estimated premorbid IQ [Fgroup×site(3,256) = 1.61, p = .19] ( Table 1).

Inclusion criteria for all participants included: 1) age between 15 and 45 years, 2) no known systemic or neurological disease, 3) no history of head trauma with loss of consciousness > 10 min, and 4) no substance dependence for at least 1 year and no substance abuse for at least 1 month. Only 25 of 135 patients had been treated previously in their lifetime with antipsychotic medication (8 BDP, 6 UDP, 11 Schiz), typically at emergency room visits before entering our clinical service. Accordingly, median cumulative lifetime exposure to antipsychotics in previously treated patients was 1.5 weeks (range up to 6 weeks). Three patients had been treated with mood stabilizers within the prior month (one BDP on valproate for 2 weeks, one UDP on gabapentin for 5 weeks, and one Schiz on valproate for 4 weeks). All preexisting medication was tapered and then discontinued at least 72 hours before testing except for four patients (two BDP, one UDP, one Schiz) who were on antidepressants; the latter are not considered to influence pursuit performance (28). All patients were off benzodiazepines for at least 48 hours before testing. The study was approved by the Institutional Review Boards of the University of Pittsburgh and the University of Illinois at Chicago, and all participants provided written informed consent. Data were collected from 1993 through 2008.

Stimulus Presentation and Eye Movement Measurement

Pursuit tasks were similar at both sites. During testing, participants had a minimum of 20/40 far acuity, with or without correction. Eye movement studies were performed in a darkened black room in which participants were seated with their heads immobilized by a chin rest with forehead and occipital restraints. In Pittsburgh, participants were placed at the center of a circular black arc (1-m radius). The visual stimulus was a red laser spot (3 mm) projected by a mirror and mounted on a rotary stage platform that moved the target across the display arc (New England Affiliated Technologies, Lawrence, Massachusetts). In Chicago, participants sat 1.39 m from the center of a flat screen display (1.82 × 2.44 m) on which a white .5° target was presented on a black background with a cathode-ray tube (CRT) projection system (Christie Digital Marquee 8500, Ultra CRT, Christie Digital Systems, Cypress, California). Participants were instructed via intercom to follow the moving target with their eyes as precisely as possible. Eye movement data were inspected online during testing, and re-alerting instructions were given if participants became inattentive. Eye movement recording was performed using infrared sensors mounted on spectacle frames (Model 210, Applied Science Laboratories, Inc., Bedford, Massachusetts). Fixation targets were presented for 5 sec at 0°, ±3°, 6°, 9°, 12°, and 15° before or after each task to calibrate the eye movement data.

Eye movement data were digitized at 500 Hz and then filtered with a nonlinear transition band between 20 Hz and 65 Hz for eye position and velocity data and 30 Hz and 65 Hz for acceleration data. Data from each trial were visually inspected to eliminate blinks and other artefacts. Saccade onset was defined as the point when eye acceleration exceeded 1000°/sec2 and saccade end points were identified at 25% of peak deceleration. Measurement resolution allowed detection of saccades with amplitudes on the order of .25°. All saccades and a 10-msec interval following the end point of saccades were excluded from data before calculating smooth pursuit gain, which reflects the ratio of eye to target velocity. All eye movement data were scored blind to participant characteristics.

Oscillating Task

This task assessed sustained smooth pursuit of predictable oscillating target motion (Figure 1A). The paradigm was similar to an oscillating sinusoidal waveform, except that across the center of the display screen the target moved at a constant speed (29). This was done for three reasons. First, it facilitated measurement of maintenance gain by allowing comparison of average pursuit velocity to a constant stimulus velocity. Second, it provided a more direct comparison with pursuit gain measures on the ramp tasks. Third, it eliminated demands during the constant velocity epochs for ongoing dynamic adjustment of pursuit velocity and acceleration as required when tracking sinusoidal target motion. Oscillating targets moved back and forth across the screen covering ±17° in total. Beyond the positions of ±12°, target speed gradually decelerated to reverse its direction at ±17°, at which point it immediately accelerated again until it reached and maintained a constant speed between ±12°. Blocks of target oscillation with a particular constant target speed (8°, 16°, 24°, or 32°/sec) between ±12° included 13, 15, 23, and 31 side-to-side target movements, respectively. The primary parameter of interest was maintenance gain between ±10° of target sweeps.

Figure 1
Examples of a healthy subject at 8°/sec trials from paradigms used to evaluate smooth pursuit performance: target (dotted), eye position (black, upper trace), and eye velocity data. Saccades and blinks were removed from eye position and velocity ...

Ramp Task

In this task, participants tracked targets that moved at an unpredictable time, direction, and speed from center fixation (Figure 1B). Each trial started with central fixation for 2 sec to 4 sec before targets moved at a constant speed either to the left or the right at one of five target speeds (4°, 8°, 16°, 24°, or 32°/sec). The target was extinguished after reaching ±15° and reappeared at the central fixation position after a 1-sec delay to begin the next trial. Target conditions were presented in a randomized order, with each condition presented four times, resulting in a total of 40 trials (4 repetitions × 5 speeds × 2 directions). In the event that participants reduced pursuit velocity near the end of ramps, such data were removed from analyses before calculating pursuit gain. Parameters of interest were maintenance gain and latency of pursuit initiation (time for pursuit velocity to reach 2°/sec for at least 20 msec if that preceded the first saccade).

Step-Ramp Task

This task was similar to the ramp task except that after initial central fixation for 2 sec to 4 sec, the target stepped 3° to the left or right before continuing in that direction at either 4°, 8°, 16°, or 24°/sec (Figure 1C). This task assesses the use of visual motion information in the “open loop” period before visual feedback about performance influences pursuit responses. It consisted of 32 trials (4 repetitions × 4 speeds × 2 directions) presented in a fixed pseudorandom order. Parameters of primary interest were the position error of the initial catch-up saccade and open loop gain during the first 100 msec of pursuit after the initial catch-up saccade. These parameters together provide data regarding how the oculomotor system uses visual motion information (11). Maintenance gain in the remaining interval of closed loop pursuit beyond the first 100 msec and latency of the initial catch-up saccade were also measured.

Statistical Analysis

Measures of parameters of interest were averaged across identical trials. Since we did not find evidence for an interaction of target direction with group using four-way repeated measures analyses of variance (ANOVAs) (target direction × target speed × site × group), leftward and rightward tracking performance were combined in three-way repeated measures ANOVAs (target speed × site × group). There were no significant interactions of group and site for any parameter of interest, indicating that patient groups performed similarly across sites. The robust effects of target speed on tracking performance are not presented in detail, as target speed effects did not differ across groups (target speed × group) for any parameter of interest. Based on these analyses, measures were averaged across sites and target speeds in figures for presentation of results. For post hoc comparisons to follow up on ANOVA effects, the results of the least significant difference procedure are reported. Spearman’s rank correlations between oculomotor parameters and BPRS ratings, time since first psychotic symptom, and cumulative lifetime exposure to antipsychotic medication did not reveal significant relationships.


Pursuit Maintenance

With the oscillating target task (Figure 2), maintenance gain did not differ between the four groups. In contrast, maintenance gain differed significantly between groups in the step-ramp task: Fgroup(3,251) = 7.52, p < .001, and the ramp task: Fgroup(3,256) = 5.43, p = .001. In the step-ramp task, psychotic bipolar patients had lower maintenance gain than all other participants (post hoc: pBDPvsUDP < .001, pBDPvsSchiz < .001, pBDPvsHealthy < .001), and schizophrenia patients had reduced maintenance gain compared with healthy participants (post hoc: pSchizvsHealthy = .042) (Figure 2). In the ramp task, all patient groups had decreased pursuit gain compared with healthy participants (post hoc: pBDPvsHealthy < .001, pUDPvsHealthy = .016, pSchizvsHealthy = .007), and psychotic bipolar patients had lower maintenance gain than schizophrenia patients (post hoc: pBDPvsSchiz = .002) (Figure 2).

Figure 2
Mean smooth pursuit maintenance gain with oscillating, step-ramp, and ramp tasks measured in first-episode psychosis patients with bipolar disorder (n = 34), unipolar depression (n = 24), schizophrenia (n = 77), and healthy participants (n = 135). Values ...

Open Loop Pursuit

Open loop gain (Figure 3A) during the first 100 msec of postsaccadic pursuit on the step-ramp task differed significantly between groups [Fgroup(3,248) = 3.16, p = .025], with psychotic bipolar patients (post hoc: pBDPvsHealthy = .008) and schizophrenia patients (post hoc: pSchizvsHealthy = .017) demonstrating lower open loop gain than healthy participants. Spatial error of the initial catch-up saccade on the step-ramp task (Figure 3B) and latency of pursuit initiation on the ramp task did not differ between groups (Figure 3C). The latency of the initial catch-up saccade on the step ramp task differed significantly between groups [Fgroup(3,252) = 3.53, p = .016] with psychotic bipolar patients demonstrating the longest saccade latencies (post hoc: pBDPvsUDP = .001, pBDPvsSchiz = .001, pBDPvsHealthy = .006).

Figure 3
Mean open loop gain on the step-ramp task (A), catch-up saccade accuracy on the step-ramp task (B), and pursuit latency on the ramp task (C) measured in first-episode psychosis patients with bipolar disorder (n = 34), unipolar depression (n = 24), schizophrenia ...

Follow-Up Assessment

A total of 138 participants (18 BDP, 14 UDP, 59 Schiz, and 47 healthy) were available for follow-up testing after 6 weeks of treatment. This subsample did not differ from the full sample in sociodemographic features, baseline clinical ratings, or oculomotor performance. At follow-up, BPRS scores were significantly reduced in all patient groups compared with baseline [Fgroup×time(2,78) = 5.06, p = .009] with improvement in BPRS ratings being significantly greater in patients with psychotic bipolar disorder (−11.4 [SD = 11.7], 23.5% change) and psychotic unipolar depression (−15.0 [SD = 8.6], 30.3% change) than in schizophrenia patients (−6.8 [SD = 9.0], 13.1% change). Most patients (85/91, 93%) were treated with low to moderate doses of antipsychotics including risperidone (n = 69, mean dosage 3.0 mg [SD = 1.9]), olanzapine (n = 6, mean dosage 9.2 mg [SD = 5.8]), haloperidol (n = 4, mean dosage 4.8 mg [SD 2.5]), aripiprazole (n = 3, mean dosage 20 mg [SD 8.7]), quetiapine (n = 2, both on 100 mg), and one patient on perphenazine (4 mg). Furthermore, 18 patients (1 BDP, 9 UPD, 8 Schiz) received antidepressants, and 4 patients (2 BDP, 1 UPD, 1 Schiz) were treated with mood stabilizers at follow-up testing. Exploratory analyses of the pursuit data revealed no patient group differences in change from baseline, i.e., no significant group by time interactions. Tables with means and standard deviations of all parameters for each task from the full baseline sample and the follow-up sample are available in Supplement 1.


This study examined alterations in component aspects of smooth pursuit eye movement responses and their diagnostic specificity in first-episode psychosis patients with either bipolar disorder, unipolar depression, or schizophrenia. By restricting our sample to first-episode patients who were mostly antipsychotic-naive or had been treated previously for only a very short period, we diminished potential confounds that may result from illness chronicity or differential medication treatment across patient groups. Our results demonstrate that the open loop pursuit and pursuit maintenance are impaired in first-episode psychoses and that this is more pronounced in psychotic bipolar disorder than in schizophrenia and psychotic unipolar depression. Motion perception per se as indicated by accuracy of catch-up saccades to moving targets in the step-ramp task was not impaired in any patient group. The lack of abnormality of pursuit responses in the oscillating target task suggests that basic oculomotor systems are intact in these patient groups and that predictive signals are sufficiently intact to compensate for sensorimotor impairments evident in the ramp-tracking tasks. These findings indicate a deficit in frontostriatal networks involved in the dynamic gain control of pursuit responses across psychotic disorders. There were no systematic correlations between oculomotor parameters and psychopathological symptom severity. Follow-up in a subset of participants following acute treatment and clinical stabilization did not reveal any differential recovery from or worsening of deficits across patient groups.

Common Sensorimotor Transformation Deficits Across Psychotic Disorders

Our findings document impaired pursuit maintenance in the early course of illness across schizophrenia and psychotic affective disorders on ramp tasks where performance is heavily dependent upon sensorimotor transformation. Open loop pursuit on the step-ramp task was impaired in psychotic bipolar disorder and schizophrenia but not in psychotic unipolar depression. Normal pursuit latencies in all three patient groups make it unlikely that gross attentional impairment caused these pursuit deficits. Also, accuracy of initial catch-up saccade amplitudes in the step-ramp task was not altered in any patient group. Since catch-up saccade accuracy on the step-ramp task requires a precise analysis of target speed to compensate for additional movement that occurs between the time when the saccade is planned and when it is completed, this finding suggests sufficient integrity of visual motion perception to guide eye movements to moving targets (11,21,23,30). While visual motion signals were used effectively to guide catch-up saccades and to drive the onset of pursuit responses, reduced open loop gain in psychotic bipolar and schizophrenia patients provides evidence of a diminished capacity for using this motion information for sensorimotor transformations in the pursuit system. These findings, together with a reduced capacity to use feedback about tracking error to dynamically adjust pursuit responses during the ramp tasks, indicate that alterations in sensorimotor transformation processes represent important causes of pursuit impairments in schizophrenia and psychotic bipolar disorder (9,31).

From a functional neuroanatomy perspective, these findings suggest that motion processing in area V5 is sufficiently intact to guide saccadic responses to moving targets, but the use of this motion information for sensorimotor transformations in the pursuit system is impaired. Functional neuroimaging studies in schizophrenia have not shown a consistent alteration of V5 activation during pursuit (3234), but V5 activity appears to be decoupled from pursuit velocity in schizophrenia patients relative to their association in healthy subjects (35). These observations suggest that a disturbed downstream usage of motion information contributes to pursuit deficits in schizophrenia more than primary alterations in V5 function and motion perception per se. This interpretation is consistent with a model that dysfunctions within frontostriatal networks (8,16), which uses sensory information and extrastriate signals to guide the dynamic regulation of pursuit gain, may represent a final common pathway for alterations in brain function underlying abnormal pursuit eye movements across psychotic disorders.

Imaging studies in schizophrenia support this hypothesis by demonstrating reduced activation during pursuit in a cortical network for sensorimotor transformation that includes the frontal and supplementary eye fields, ventral premotor cortex, basal ganglia, and anterior cingulate (32,34,36). Although not evaluated during smooth pursuit, imaging studies in patients with bipolar disorder using other paradigms have demonstrated abnormalities of frontostriatal networks early in the course of illness (37). Other evidence for shared dysfunction of frontal neural networks across psychotic disorders comes from structural imaging studies showing altered connectivity (38), reduced prefrontal gyrification associated with cognitive impairment (39), and reduced left medial frontal gray matter volume (40) across bipolar disorder and schizophrenia.

Predictive Pursuit

The absence of significantly impaired pursuit of oscillating targets, which relies heavily on internally generated prediction of target motion and rule-based learning, implies that the higher-order cognitive predictive mechanisms for sustained pursuit were sufficiently spared in all patient groups to compensate for sensorimotor transformation impairments seen on the ramp tasks. This intact performance establishes that the basic motor components of oculomotor systems for pursuit are not impaired in these psychotic disorders. Notably, our oscillating task does not require dynamic adjustments of pursuit velocity and acceleration as with sinusoidal tasks or abrupt reversals in target direction as with triangular or trapezoidal waveforms, which have been used to demonstrate pursuit deficits in many previous studies of schizophrenia (3,29,41). Without these task demands, patients were able to precisely match eye velocity to that of the predictable target movement even at high target speeds and perform as well as healthy individuals. Predictive modulation of pursuit could be maintained by sufficiently intact components or compensatory activity in frontostriatal and frontothalamo-cerebellar circuitry that have been shown to modulate prediction, planning, and rule-based learning during pursuit in both healthy individuals and patients with schizophrenia (32,4244).

Diagnostic Specificity

With respect to questions about the relative severity and qualitative differences in pursuit impairments between affective psychoses and schizophrenia, the present findings extend our previous reports by using a wider range of tasks, examination of unipolar and bipolar psychotic patients that has not been done previously, and short-term follow-up after clinical stabilization (21,23). The finding that sensorimotor transformation during pursuit maintenance was most severely impaired in first-episode patients with psychotic bipolar disorder suggests that frontostriatal function is significantly altered in the early course of this illness and may be even more heavily disrupted in this specific way than in schizophrenia. In contrast to other groups, patients with psychotic bipolar disorder needed more time, i.e., had longer latencies, to generate an initial catch-up saccade on the step-ramp task, and yet even with more time for response preparation, they still had the most impaired maintenance gain. The observation of impaired sensorimotor transformation during pursuit in the bipolar patients is consistent with reduced maintenance of manual force steadiness and velocity scaling (45) and persistent neurocognitive deficits early in bipolar disorder (46,47).

Sensorimotor impairments in psychotic bipolar patients may be caused by intrinsic frontostriatal disturbances or the adverse impact of affective (limbic) alterations on these systems (37,40). The latter possibility is consistent with reports from functional magnetic resonance imaging studies using cognitive paradigms in which increased activation of emotional brain areas was associated with reduced prefrontal function in bipolar disorder (48). Our results from follow-up studies of our patients suggest that sensorimotor impairments in the pursuit system persist after clinical stabilization as do neuropsychological deficits (47).

In contrast to psychotic bipolar disorder and schizophrenia, we found sensorimotor transformation in psychotic unipolar depression to be impaired only during pursuit maintenance on the ramp task. This finding is in line with findings that frontostriatal networks may be affected differently and perhaps less severely in psychotic unipolar depression compared with psychotic bipolar disorder and schizophrenia (21,49).

Future Perspectives

The present findings point to several promising directions of research. First, the study highlights the presence of sensorimotor deficits across psychotic disorders that require further investigation to determine their pathophysiology and potential familiality. Second, the findings point to alterations in frontostriatal systems that support visual sensorimotor transformations across psychotic disorders, suggesting that disturbances in this circuitry, whether via similar or different etiologic mechanisms, may be a common final pathway related to pursuit impairments associated with psychotic disorders (50). Functional neuroimaging studies using smooth pursuit paradigms may better define the underlying alterations in neural systems that lead to shared sensorimotor deficits across psychotic disorders. Third, the especially robust alterations of pursuit in psychotic bipolar patients require further investigation and replication. While our follow-up data suggest persistent deficits, longer-term follow-up is needed to establish if this is a stable trait or changes differentially relative to other psychotic disorders over the course of illness. Last, the observation that patients in all groups could perform our oscillating target task without impairment may be heuristically important, and future studies may follow up on this observation to identify the specific neurophysiological impairments in the pursuit system that impair pursuit on other tasks in patients with psychotic disorders while leaving pursuit performance on this task unaffected.

Supplementary Material

Supplementary Data


This study was supported by National Institutes of Health (NIH) Grants MH62134, MH45156, and MH01433 and the NIH/National Center for Research Resources (NCRR)/General Clinical Research Centers Grant M01 RR00056; by Janssen Grant RIS-INT-35; and by a Feodor Lynen Fellowship provided by the Alexander von Humboldt Foundation (RL). The contents of this work are solely the responsibility of the authors and do not necessarily represent the official views of NIH.

We thank Gretchen Haas, Ph.D., Cameron Carter, M.D., and Debra Montrose, Ph.D. and the clinical core staff of the Center for the Neuroscience of Mental Disorders in Pittsburgh (director: David Lewis, M.D.) and Cherise Rosen Ph.D., Robert Marvin, M.D., Ovideo DeLeon, M.D., and Peter Weiden, M.D., in Chicago for their assistance in diagnostic and psychopathological assessments.


Dr. Sweeney is a consultant to Pfizer. Drs. Lencer, Reilly, Sprenger, and Keshavan and Ms. Harris report no biomedical financial interests or potential conflicts of interest.

Supplementary material cited in this article is available online.


1. Thaker GK. Neurophysiological endophenotypes across bipolar and schizophrenia psychosis. Schizophr Bull. 2008;34:760–773. [PMC free article] [PubMed]
2. Calkins ME, Iacono WG, Ones DS. Eye movement dysfunction in first-degree relatives of patients with schizophrenia: A meta-analytic evaluation of candidate endophenotypes. Brain Cogn. 2008;68:436–461. [PubMed]
3. O’Driscoll GA, Callahan BL. Smooth pursuit in schizophrenia: A meta-analytic review of research since 1993. Brain Cogn. 2008;68:359–370. [PubMed]
4. Levy DL, Holzman PS, Matthysse S, Mendell NR. Eye tracking dysfunction and schizophrenia: A critical perspective. Schizophr Bull. 1993;19:461–536. [PubMed]
5. Chen Y, Levy DL, Nakayama K, Matthysse S, Palafox G, Holzman PS. Dependence of impaired eye tracking on deficient velocity discrimination in schizophrenia. Arch Gen Psychiatry. 1999;56:155–161. [PubMed]
6. Clementz BA, McDowell JE, Dobkins KR. Compromised speed discrimination among schizophrenia patients when viewing smooth pursuit targets. Schizophr Res. 2007;95:61–64. [PMC free article] [PubMed]
7. Hong LE, Turano KA, O’Neill H, Hao L, Wonodi I, McMahon RP, et al. Refining the predictive pursuit endophenotype in schizophrenia. Biol Psychiatry. 2008;63:458–464. [PMC free article] [PubMed]
8. Sweeney JA, Luna B, Srinivasagam NM, Keshavan MS, Schooler NR, Haas GL, et al. Eye tracking abnormalities in schizophrenia: Evidence for dysfunction in the frontal eye fields. Biol Psychiatry. 1998;44:698–708. [PubMed]
9. Hong LE, Turano KA, O’Neill HB, Hao L, Wonodi I, McMahon RP, et al. Is motion perception deficit in schizophrenia a consequence of eye-tracking abnormality? Biol Psychiatry. 2008;65:1079–1085. [PMC free article] [PubMed]
10. Burke MR, Barnes GR. Brain and behavior: A task-dependent eye movement study. Cereb Cortex. 2008;18:126–135. [PubMed]
11. Newsome WT, Wurtz RH, Komatsu H. Relation of cortical areas MT and MST to pursuit eye movements. II. Differentiation of retinal from extraretinal inputs. J Neurophysiol. 1988;60:604–620. [PubMed]
12. MacAvoy MG, Gottlieb JP, Bruce CJ. Smooth-pursuit eye movement representation in the primate frontal eye field. Cereb Cortex. 1991;1:95–102. [PubMed]
13. Rosano C, Krisky CM, Welling JS, Eddy WF, Luna B, Thulborn KR, et al. Pursuit and saccadic eye movement subregions in human frontal eye field: A high-resolution fMRI investigation. Cereb Cortex. 2002;12:107–115. [PubMed]
14. Sweeney JA, Luna B, Keedy SK, McDowell JE, Clementz BA. fMRI studies of eye movement control: Investigating the interaction of cognitive and sensorimotor brain systems. Neuroimage. 2007;36(suppl 2):T54–T60. [PMC free article] [PubMed]
15. Lencer R, Trillenberg P. Neurophysiology and neuroanatomy of smooth pursuit in humans. Brain Cogn. 2008;68:219–228. [PubMed]
16. MacAvoy MG, Bruce CJ. Comparison of the smooth eye tracking disorder of schizophrenics with that of nonhuman primates with specific brain lesions. Int J Neurosci. 1995;80:117–151. [PubMed]
17. Newsome WT, Wurtz RH, Dursteler MR, Mikami A. Deficits in visual motion processing following ibotenic acid lesions of the middle temporal visual area of the macaque monkey. J Neurosci. 1985;5:825–840. [PubMed]
18. Heide W, Kurzidim K, Kompf D. Deficits of smooth pursuit eye movements after frontal and parietal lesions. Brain. 1996;119:1951–1969. [PubMed]
19. Abel LA, Friedman L, Jesberger J, Malki A, Meltzer HY. Quantitative assessment of smooth pursuit gain and catch-up saccades in schizophrenia and affective disorders. Biol Psychiatry. 1991;29:1063–1072. [PubMed]
20. Blackwood DH, Sharp CW, Walker MT, Doody GA, Glabus MF, Muir WJ. Implications of comorbidity for genetic studies of bipolar disorder: P300 and eye tracking as biological markers for illness. Br J Psychiatry Suppl. 1996 Jun;:85–92. [PubMed]
21. Lencer R, Trillenberg P, Trillenberg-Krecker K, Junghanns K, Kordon A, Broocks A, et al. Smooth pursuit deficits in schizophrenia, affective disorder and obsessive-compulsive disorder. Psychol Med. 2004;34:451–460. [PubMed]
22. Flechtner KM, Steinacher B, Sauer R, Mackert A. Smooth pursuit eye movements in schizophrenia and affective disorder. Psychol Med. 1997;27:1411–1419. [PubMed]
23. Sweeney JA, Luna B, Haas GL, Keshavan MS, Mann JJ, Thase ME. Pursuit tracking impairments in schizophrenia and mood disorders: Step-ramp studies with unmedicated patients. Biol Psychiatry. 1999;46:671–680. [PubMed]
24. Kathmann N, Hochrein A, Uwer R, Bondy B. Deficits in gain of smooth pursuit eye movements in schizophrenia and affective disorder patients and their unaffected relatives. Am J Psychiatry. 2003;160:696–702. [PubMed]
25. Moates AF, Ivleva E, Cole D, Gonzales R, Cullum M, Hong LE, et al. The relationship between oculomotor measures of predictive pursuit and neurophysiological measures of working memory in patients with schizophrenia and bipolar disorder. Schizophr Bull. 2009;35:63.
26. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 4. Washington, DC: American Psychiatric Publishing; 1994.
27. Rhoades HM, Overall JE. The semistructured BPRS interview and rating guide. Psychopharmacol Bull. 1988;24:101–104. [PubMed]
28. Reilly JL, Lencer R, Bishop JR, Keedy S, Sweeney JA. Pharmacological treatment effects on eye movement control. Brain Cogn. 2008;68:415–435. [PMC free article] [PubMed]
29. Lencer R, Sprenger A, Harris MSH, Reilly JL, Keshavan MS, Sweeney JA. Effects of second-generation antipsychotic medication on smooth pursuit performance in antipsychotic-naive schizophrenia. Arch Gen Psychiatry. 2008;65:1146–1154. [PMC free article] [PubMed]
30. Clementz BA. Saccades to moving targets in schizophrenia: Evidence for normal posterior cortex functioning. Psychophysiology. 1996;33:650–654. [PubMed]
31. Chen Y, Levy DL, Sheremata S, Holzman PS. Bipolar and schizophrenic patients differ in patterns of visual motion discrimination. Schizophr Res. 2006;88:208–216. [PMC free article] [PubMed]
32. Nagel M, Sprenger A, Nitschke M, Zapf S, Heide W, Binkofski F, et al. Different extraretinal neuronal mechanisms of smooth pursuit eye movements in schizophrenia: An fMRI study. Neuroimage. 2007;34:300–309. [PubMed]
33. Tregellas JR, Tanabe JL, Martin LF, Freedman R. fMRI of response to nicotine during a smooth pursuit eye movement task in schizophrenia. Am J Psychiatry. 2005;162:391–393. [PubMed]
34. Hong LE, Tagamets M, Avila M, Wonodi I, Holcomb H, Thaker GK. Specific motion processing pathway deficit during eye tracking in schizophrenia: A performance-matched functional magnetic resonance imaging study. Biol Psychiatry. 2005;57:726–732. [PubMed]
35. Lencer R, Nagel M, Sprenger A, Heide W, Binkofski F. Reduced neuronal activity in the V5 complex underlies smooth-pursuit deficit in schizophrenia: Evidence from an fMRI study. Neuroimage. 2005;24:1256–1259. [PubMed]
36. Keedy SK, Ebens CL, Keshavan MS, Sweeney JA. Functional magnetic resonance imaging studies of eye movements in first episode schizophrenia: Smooth pursuit, visually guided saccades and the oculomotor delayed response task. Psychiatry Res. 2006;146:199–211. [PubMed]
37. Strakowski SM, Delbello MP, Adler CM. The functional neuroanatomy of bipolar disorder: A review of neuroimaging findings. Mol Psychiatry. 2005;10:105–116. [PubMed]
38. Sussmann JE, Lymer GK, McKirdy J, Moorhead TW, Maniega SM, Job D, et al. White matter abnormalities in bipolar disorder and schizophrenia detected using diffusion tensor magnetic resonance imaging. Bipolar Disord. 2009;11:11–18. [PubMed]
39. McIntosh AM, Moorhead TW, McKirdy J, Hall J, Sussmann JE, Stanfield AC, et al. Prefrontal gyral folding and its cognitive correlates in bipolar disorder and schizophrenia. Acta Psychiatr Scand. 2009;119:192–198. [PubMed]
40. Janssen J, Reig S, Parellada M, Moreno D, Graell M, Fraguas D, et al. Regional gray matter volume deficits in adolescents with first-episode psychosis. J Am Acad Child Adolesc Psychiatry. 2008;47:1311–1320. [PubMed]
41. Thaker GK, Ross DE, Buchanan RW, Adami HM, Medoff DR. Smooth pursuit eye movements to extra-retinal motion signals: Deficits in patients with schizophrenia. Psychiatry Res. 1999;88:209–219. [PubMed]
42. Middleton FA, Strick PL. Basal ganglia and cerebellar loops: Motor and cognitive circuits. Brain Res Brain Res Rev. 2000;31:236–250. [PubMed]
43. Burke MR, Barnes GR. Sequence learning in two-dimensional smooth pursuit eye movements in humans. J Vis. 2007;7:1–12. [PubMed]
44. Schmid A, Rees G, Frith C, Barnes G. An fMRI study of anticipation and learning of smooth pursuit eye movements in humans. Neuroreport. 2001;12:1409–1414. [PubMed]
45. Lohr JB, Caligiuri MP. Abnormalities in motor physiology in bipolar disorder. J Neuropsychiatry Clin Neurosci. 2006;18:342–349. [PubMed]
46. Pavuluri MN, West A, Hill SK, Jindal K, Sweeney JA. Neurocognitive function in pediatric bipolar disorder: 3-year follow-up shows cognitive development lagging behind healthy youths. J Am Acad Child Adolesc Psychiatry. 2009;48:299–307. [PMC free article] [PubMed]
47. Hill SK, Reilly JL, Harris MS, Rosen C, Marvin RW, Deleon O, et al. A comparison of neuropsychological dysfunction in first-episode psychosis patients with unipolar depression, bipolar disorder, and schizophrenia. Schizophr Res. 2009;113:167–175. [PMC free article] [PubMed]
48. McIntosh AM, Whalley HC, McKirdy J, Hall J, Sussmann JE, Shankar P, et al. Prefrontal function and activation in bipolar disorder and schizophrenia. Am J Psychiatry. 2008;165:378–384. [PubMed]
49. Strakowski SM, Adler CM, DelBello MP. Volumetric MRI studies of mood disorders: Do they distinguish unipolar and bipolar disorder? Bipolar Disord. 2002;4:80–88. [PubMed]
50. Blackwood DH, Pickard BJ, Thomson PA, Evans KL, Porteous DJ, Muir WJ. Are some genetic risk factors common to schizophrenia, bipolar disorder and depression? Evidence from DISC1, GRIK4 and NRG1. Neurotox Res. 2007;11:73–83. [PubMed]