Abstract

BackgroundOculomotor dysfunction is one of the most replicated findings in schizophrenia. However the association between saccadic abnormalities and particular clinical syndromes remains unclear. The assessment of saccadic movements in schizophrenia patients as well as in clinical high-risk state for psychosis individuals (CHR) as a part of schizophrenia continuum may be useful in validation of saccadic movements as a possible biomarker.MethodsThe study included 156 patients who met the ICD-10 criteria for schizophrenia: 42 individuals at clinical high-risk-state for psychosis and 61 healthy controls. The schizophrenia patients had three subgroups based on the sum of the global SAPS and SANS scores: (1) patients with predominantly negative symptoms (NS, n = 62); (2) patients with predominantly positive symptoms (PS, n = 54) (3) patients with predominantly disorganization symptoms (DS, n = 40). CHR subjects were characterized by the presence of one of the groups of criteria: (1) Ultra High Risk criteria, (2) Basic Symptoms criteria or (3) negative symptoms and formal thought disorders. Horizontal eye movements were recorded by using videonystagmograph. We measured peak velocity, latency and accuracy in prosaccade, antisaccade and predictive saccade tasks as well as error rates in the antisaccade task.ResultsSchizophrenia patients performed worse than controls in predictive, reflexive and antisaccade tasks. Oculomotor parameters of NS were different from the other groups of patients. Latencies of predictive and reflexive saccades were significantly longer than in controls only in the NS group. The accuracy of predictive saccades was also different from controls only in the NS schizophrenia group. More prominent loss of accuracy of reflexive saccades was found in the DS group and it significantly differed from the one in other groups. Participants from DS group made more errors in antisaccade task compared to NS and PS groups. CHR subjects performed worse than controls as measured by the accuracy of reflexive saccades and antisaccades.ConclusionsThe study confirms the existence of different relations between the symptom dimensions of schizophrenia and saccades tasks performances. Saccadic abnormalities were revealed in the clinical (schizophrenia) and pre-clinical (clinical high risk) populations that provide further evidence for assessing saccadic abnormalities as a possible neurobiological marker for schizophrenia.

Highlights

  • Oculomotor dysfunction is one of the most replicated findings in schizophrenia

  • Comparison of schizophrenia patients and controls revealed no difference in velocity of reflexive (451.85, SD = 39.35 in control, 454.84, SD = 40.28 in SCH; p > 0.05) and predictive saccades

  • Latencies of predictive saccades were longer in schizophrenia patients compared to controls (250.83, SD = 32.32 in control, 273.24, SD = 64.93 in SCH; p < 0.05) as well as latencies of reflexive saccades (242.53, SD = 23.99 in control, 265.56, SD = 65.68 in SCH; p < 0.01)

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Summary

Introduction

Oculomotor dysfunction is one of the most replicated findings in schizophrenia. The association between saccadic abnormalities and particular clinical syndromes remains unclear. Schizophrenia is а severe mental disorder which usually begins in adolescence and often has a chronic deteriorating course. Diagnosis of schizophrenia is based on the detection of clinical symptoms and depends on the clinician’s interpretation of patients’ subjective experience [2]. Researchers are trying to find more objective tests (biomarkers) to detect schizophrenia, to make a prognosis, to predict response to treatment. Some potential biomarkers for schizophrenia have been proposed, such as markers associated with inflammation, immune processes and with metabolic disorders or neuroendocrine/neurotrophin/ neurotransmitter alterations [5,6,7], as well as abnormalities in neural activity [5, 8]

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